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Review

Microbial Interactions within the Cheese Ecosystem and Their Application to Improve Quality and Safety

by
Baltasar Mayo
*,
Javier Rodríguez
,
Lucía Vázquez
and
Ana Belén Flórez
Departamento de Microbiología y Bioquímica, Instituto de Productos Lácteos de Asturias (IPLA), Consejo Superior de Investigaciones Científicas (CSIC), Paseo Río Linares s/n, 33300 Villaviciosa, Spain
*
Author to whom correspondence should be addressed.
Foods 2021, 10(3), 602; https://doi.org/10.3390/foods10030602
Submission received: 25 February 2021 / Accepted: 9 March 2021 / Published: 12 March 2021
(This article belongs to the Special Issue Recent Advances and Trends in the Dairy Field)
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Abstract

:
The cheese microbiota comprises a consortium of prokaryotic, eukaryotic and viral populations, among which lactic acid bacteria (LAB) are majority components with a prominent role during manufacturing and ripening. The assortment, numbers and proportions of LAB and other microbial biotypes making up the microbiota of cheese are affected by a range of biotic and abiotic factors. Cooperative and competitive interactions between distinct members of the microbiota may occur, with rheological, organoleptic and safety implications for ripened cheese. However, the mechanistic details of these interactions, and their functional consequences, are largely unknown. Acquiring such knowledge is important if we are to predict when fermentations will be successful and understand the causes of technological failures. The experimental use of “synthetic” microbial communities might help throw light on the dynamics of different cheese microbiota components and the interplay between them. Although synthetic communities cannot reproduce entirely the natural microbial diversity in cheese, they could help reveal basic principles governing the interactions between microbial types and perhaps allow multi-species microbial communities to be developed as functional starters. By occupying the whole ecosystem taxonomically and functionally, microbiota-based cultures might be expected to be more resilient and efficient than conventional starters in the development of unique sensorial properties.

1. General Introduction

Cheese is a fermented milk product that dates back to Neolithic times. Traditionally, cheese was a milk-derived food that served as a means of preserving milk and its remarkable nutritive properties. Currently, the Codex Alimentarius defines cheese as “a ripened or unripened, soft, semi-hard, hard, or extra-hard, dehydrated milk-derived product in which the whey protein/casein ratio does not exceed that of milk” [1]. Thus, cheese is the generic name for a group of milk-derived food products that come in a great variety of forms, sizes, textures, aromas, and tastes. The use of milk from distinct species (cows, sheep, goats, yaks, buffalos, moose, llamas) or their mixtures and the different technological operations employed in coagulation (e.g., acidification or the addition of animal rennet- or microbial- and plant-derived coagulants), the cutting of the coagulum (from rice grain to walnut size), whey drainage, washing, heating (from 30 °C to 55 °C), pressing, salting (between 1% and 5% NaCl), ripening, dehydration, immersion (in oil, wine or brine), wrapping (with ash or flour, etc.), and the addition of spices (pepper, cumin, clover, rosemary, aromatic herbs, garlic, etc.) or colorants (chlorophylls, paprika, annatto) make cheese one of the most diverse of all foodstuffs [2,3] (Figure 1).
The sensorial properties of cheese depend on the milk type used, the feed given to the providing animal, the manufacturing practices involved, the ripening environment, the duration of ripening, and the type, numbers and activity of the microorganisms in the forming product [4,5]. Microorganisms are responsible for the fermentation of milk and for the many biochemical reactions occurring during manufacturing and ripening, which give rise to the distinctive cheese-associated textures and flavors.
In the wake of the booming amount of microbial data obtained through state-of-the-art molecular methods, this review presents updated knowledge on the composition of the cheese microbiota and summarizes the microbial interactions taking place in the cheese ecosystems. The review shows a strong focus on the biotic and abiotic factors driving the development and succession of the microbial populations and points out the potential use of this knowledge to improve the sensorial properties and safety concerns of cheese.

2. Cheese Starters and Adjunct Cultures

Milk can be coagulated by heating, by the formation or addition of acid, by the use of a natural coagulant (such as rennet), or a combination of these treatments (Figure 1). Spontaneous acidification is caused by the growth of lactic acid bacteria (LAB), a diverse bacterial group the members of which generate lactic acid as the main end-product of lactose fermentation. The typical LAB are arranged into the genera Lactococcus, Lactobacillus, Leuconostoc, and Pediococcus [6,7]. Via the action of complex anabolic and catabolic systems, the growth of LAB modifies the constituents of the milk (carbohydrates, proteins and lipids) [8]. These modifications do not involve nutritional or sensorial losses; rather, they increase the bioavailability and diversity of nutrients and improve the quality and complexity of flavor profiles [9]. LAB naturally present in milk or on manufacturing tools and in the environment [10,11,12,13,14,15,16] are still relied upon in many traditional fermentations [17,18,19,20,21,22,23,24,25,26,27,28]. However, improvement in milk hygiene (mainly by refrigeration and pasteurization practices) and the need for standardization have promoted the generalized use of starters [11,13], i.e., selected strains of different LAB species deliberately added to the milk to control the fermentation and standardize the quality of the fermented product (Table 1). Not surprisingly, in the search for improved starters, most microbial studies of cheese have focused on the isolation and characterization of new LAB strains of species such as Streptococcus (S.) thermophilus, Lactococcus (Lc.) lactis, Lactobacillus (Lb.) sp., and Leuconostoc (Leuc.) sp. [24,29,30,31,32,33,34,35,36,37,38]. In the industry, however, the term “starter” refers to all microorganisms added to the milk with a technological purpose, e.g., for improving the appearance, texture, and/or flavor of the final product, and thus also covers LAB species not involved in acidification, the so-called non-starter LAB (NSLAB) [39,40]. In certain cheeses, it also covers bacteria of the genera Propionibacterium (Emmental, Gruyère), Brevibacterium, and Corynebacterium (smear-ripened cheeses), molds and yeasts such as Penicillium (P.) roqueforti (blue-veined varieties), P. camemberti (white moldy varieties), Geotrichum (G.) candidum, Debaryomyces (D.) hansenii (moldy and smear-ripened cheeses), and others [39,40]. These secondary types of microorganisms are usually referred to as adjunct and/or ripening cultures (Table 1).

3. Cheese Microbiology

The microbial composition of cheese and the microbial succession of the microorganisms in the cheese matrix have traditionally been assessed by culturing methods [25,26,41,42,43,44,45,46,47,48,49]. These rely on the isolation and cultivation of microorganisms before their identification and typing. However, culturing has repeatedly been shown unreliable for the exhaustive microbial characterization of many food ecosystems [50,51,52]. For example, the selective isolation of certain microbial taxa may require unknown growth factors and/or growth conditions that are not reproduced in the laboratory media [53]. Besides, cheese can have a low pH, a reduced aw, and is commonly kept under harsh storage conditions (e.g., at low temperatures or in strong brine), all of which might leave certain microbes in a physiologically viable but non-cultivable state [54]. Further, microbes present in low numbers can be outcompeted in culture by numerically abundant species, impeding the effective detection of the former [45,55,56,57]. The culture techniques can therefore underestimate the microbial diversity present and sometimes even fail to detect some majority microbial groups.
Helping to overcome the problems of culturing, numerous culture-independent, molecular methods based on the amplification of nucleic acids by polymerase chain reaction (PCR) have been developed, such as denaturing gradient gel electrophoresis (DGGE) [23,57,58,59,60,61], temporal temperature gradient electrophoresis (TTGE) [45,62], real-time quantitative PCR (qPCR) [63,64], single strand conformation polymorphism (SSCP) [65,66], the construction and analysis of gene libraries [46,66], and others [67]. The basis, similarities, differences and main outputs of such techniques, all of which have been extensively used to investigate the microbiology of cheese and dairy systems, are schematically depicted in Figure 2. As an example of the value of using such molecular techniques, Leuc. lactis and Mycoplasma agalactiae, constituting subdominant populations in two farmhouse goats’ milk cheeses and detected by PCR-TTGE, could never be recovered from cultures [45]. Similarly, although many Arthrobacter and Brevibacterium species were detected by PCR-DGGE in the smear-ripened Limburger cheese, only strains of Arthrobacter (Arthr.) arilaitensis and Brevibacterium (Brev.) aurantiacum have been retrieved by culturing [42]. Further, during the microbial typing of natural whey cultures for water-buffalo Mozzarella cheese production, Lb. fermentum, a majority population as judging by PCR-DGGE, was not recovered in culture [58]. Nonetheless, different LAB species have been found dominant in most cheeses both by culturing and molecular techniques, but only the latter were able to associate cheese ecosystems with occasional subdominant populations and minority microorganisms such as Agrococcus and Leucobacter [56], Massilia sp. [57], and Bifidobacterium sp. [68].
More recently, the advent of high throughput sequencing (HTS) of DNA has promoted the emergence of new, culture-independent technologies [69,70,71,72,73]. For metagenomics purposes, HTS can be used in two distinct ways: gene-specific sequencing (targeted sequencing) and the sequencing of all the microbial nucleic acids present (shotgun sequencing) (Figure 2). Compared to earlier molecular methods, HTS techniques analyze a vastly greater number of nucleic acid molecules, allowing for a much more comprehensive description of a cheese’s microbial constituents. After a pioneering use of pyrosequencing [68,74,75,76,77], Ilumina [73,78] and PacBio [79,80] technologies are currently the gold standard HTS techniques. Surprisingly, HTS has uncovered an unprecedented microbial diversity in cheeses. For example, 132 genera of the Bacteria and Archaea domains have been identified on the surface of a Swiss smear-ripened cheese [81]. Also, 238 species belonging to 14 phyla and 140 genera were recently identified in a Kazakh cheese [80], and up to 574 operational taxonomic units (OTUs) have been reported in traditional Mexican Cotija cheese [82].
LAB reads usually account for > 90% of the sequences (Lactobacillus, Leuconostoc, Weissella, Enterococcus, and Lactococcus) detected within the inner part of the cheese, but only less than 30% of reads from certain surfaces [83]. The HTS-based discovery of sequences belonging to microbes previously undetected in the dairy environment [84,85] may allow for the isolation and characterization of new biotypes by conventional [86] and novel cultivation techniques (“culturomics”) [53,87]. Further, the integration of data from culturing and culture-independent techniques (including genomics, metagenomics, metatranscriptomics, and metabolomics) is expected to provide insights into the cause–effect relationships between microbes and the metabolites that shape the sensorial descriptors of cheese, such as organic acids, fatty acids, amino acids, volatile compounds, etc. [88,89]. Certainly, while the inventory and succession of bacteria, yeasts, and molds in some cheeses are known, the functional features of the different populations are yet to be understood. By and large, most studies have been descriptive, and relatively little is known about the mechanisms that govern the architecture and dynamics of microbial populations or the molecular interactions between their members. Indeed, the activity in the cheese matrix of some uncultured/uncharacterized microbes may have a huge impact on the overall quality and safety of some cheeses [90,91]. However, understanding the technological importance and biological significance of such phenotypic microbial diversity and the genetic redundancy in cheese remains a challenge.

4. The Cheese Microbiota

Whether fermented in a natural manner, or with the aid of starter and/or adjunct cultures, most cheeses contain a complex mixture of microbial populations—including technologically-relevant, spoilage, opportunistic and pathogenic organisms—that develops and changes throughout manufacturing and ripening [11,92,93]. All these microbes constitute the microbiota of the cheeses (Table 2). Both intrinsic (substrates, vitamins, cofactors, the presence of inhibitory/activator compounds, pH, redox potential) and extrinsic factors (oxygen availability, temperature, salt, relative humidity) drive the numbers and spatial and temporal distribution of the members of the microbiota [89,94]. The populations of the microbiota are composed of prokaryotic Archaea and Bacteria, eukaryotic yeasts and fungi [74,81,82,95,96], and viruses (mainly bacteriophages) [97,98,99]. The microbiota of cheese can be as simple as that of yogurt and other kinds of fermented milks, with perhaps just one or a very small number of LAB species present, such as in Petit-Suisse (S. thermophilus and Lb. delbrueckii subsp. bulgaricus) [100] and Quark (Lc. lactis subsp. lactis and Lc. lactis subsp. cremoris) [101]. More often, however, the cheese microbiota is composed of a consortium of diverse microorganisms and varies widely from one variety to another, although the dominant microbial types for each cheese type (soft, hard, natural rind, smear-ripened, blue-veined, etc.) are usually similar [42,102,103,104]. The microbiota becomes particularly complex in blue-veined and smear-ripened varieties (Table 2). As in other ecosystems, the diversity of the microbiota in cheese is governed by classical ecological processes, such as dispersion, diversification, environmental selection, and ecological drift (Figure 3). Microbial diversity and numbers are also influenced by the environmental interaction of biotic (natural fermentation, use or not of starters, presence of contaminating microbes and microbial metabolites) and abiotic factors (technological processes and environmental conditions), which modulate the implantation, development and, more importantly, the activity of the different microbes (Figure 3). Together, these variables determine the growth and function of the microorganisms and, therefore, some of the key biochemical changes they drive during ripening that lead to the unique appearance, texture, aroma and taste properties of each cheese variety, as well as their safety quality [4,8,105].
Cheese bacteria belong mainly to the phyla Firmicutes (LAB, enterococci, staphylococci), Actinobacteria (corynebacteria, propionibacteria, bifidobacteria), and Proteobacteria (enterobacteria) [55,56,83,104,107]. The archaeal taxa include members of Thermocladium, Sulfurisphaera, Methanohalobium, and others; these are minority populations (< 0.5% relative abundance) and have only ever been detected by molecular methods [57,81,82]. Among the eukaryotes, the dominant yeasts belong to the genera Geotrichum, Debaryomyces, Kluyveromyces, Candida, and Yarrowia, and the filamentous fungi are molds such as P. camemberti, P. roqueforti and other Penicillium species, which are abundant in mold-ripened cheese varieties [12,47,106,112,113]. Other filamentous fungi such as Fusarium domesticum, Scopulariopsis (Sc.) flava and Sc. casei are also found in low numbers on the surface of most cheeses [12,14,96]. Except for P. roqueforti, all these other mold species are only known from cheese, suggesting they are adapted (“domesticated”) to this particular habitat. In particular, P. camemberti derives from the wild ancestor Penicillium commune in a quick adaptation process that involves reduced reproductive output, reduced mycotoxin production, reduced pigmentation and, significantly, a change in the volatile compound profile from earthy to cheesy [114]. The genetic basis of this rapid “evolution” has proven to be through gene regulation instead of genome changes [114]. Lc. lactis subpopulations of the lactis and cremoris subspecies in dairy environments are also thought to be adapted through domestication processes [115,116]. These, and the domesticated strains of other LAB species found only in milk and dairy products, seem to have emerged recently due to the selective pressure imposed by the dairy technologies [117].
Though highly variable between varieties, the concentration of bacteria in ripened cheese may exceed 109 colony forming units (cfu)/g [5,25,108,118], while those of yeasts and filamentous fungi range widely between 102 and 107 cfu/g [5,28,96,106,113,119]. Depending on the microbial taxon, maximum numbers are reached by the end of the fermentation (e.g., Lc. lactis), between day 7 to 17 (e.g., Lactobacillus spp.) after one to two months of ripening (e.g., filamentous fungi). Once the highest level is reached, numbers are declining slightly but consistently afterward. Variations in the composition and/or dynamics of the microbial communities making up the typical microbiota of a given cheese can lead to serious technological and sensorial defects [84,85,120,121,122] and even pose food safety risks [123,124].

5. Microbial Interactions in Cheese

In nature, microorganisms live in complex communities, in which different direct and indirect, cooperative and competitive microbial interactions can occur (Figure 3). Microbial interactions are mediated through a variety of molecular and physiological mechanisms, of which trophic interactions (cross-feeding) and the exchange of metabolites are the most typical. Trophic food chains enable multiple groups of organisms to survive on limited resources, increasing community diversity [125,126]. Conversely, some microbes can be inhibited or killed by metabolic substances or antimicrobial compounds produced by other components of the microbiota [127,128,129]. In general, the interactions between the different microorganisms impact the final composition and diversity of the cheese microbiota, but particularly its functionality [130,131]. In the context of milk fermentation, direct interactions refer to parasitism and apply mostly to phage-bacteria predation [132]. Under the changing environmental conditions throughout manufacture and ripening, bacteriophages are considered key players in the dynamics of the cheese microbial communities [133]. Phage predation ensures bacterial diversity by suppressing abundant strains (by the “kill the winner” theory), stabilizing the overall functionality of the host community [134]. Phages may have a tremendous effect on the fermentation, in which LAB populations need to attain high cell numbers in a very short time [132]. A fermentation failure leads usually to a subsequent improper ripening process downgrading the sensory properties of the final product. Regardless of this importance, due to the inanimate living nature of the phages, the direct bacteriophage–bacteria interactions are outside the scope of this review. Many different types of indirect interactions between the other microbial types exist [135,136], although, as in other ecosystems, the four main types in cheese involve competition, amensalism, commensalism, and mutualism [137,138,139,140].

5.1. Competition

In competition, two or more microorganisms compete for nutrient and energy resources in a manner that negatively affects both. The success of LAB in milk is due to their efficient use of the nutrients found in this medium, which include lactose (a rare sugar outside milk, the utilization of which requires specific transport and degradation machinery [141]), and the ability to degrade milk proteins (caseins) and efficiently take up the released amino acids and peptides [140]. Other organisms are limited by the inability of using lactose and/or the small amounts of freely available nitrogenous substrates [142,143]. Iron and zinc are also thought to be limiting micronutrients in dairy products [84]. Some microorganisms, such as Arthrobacter, Corynebacterium, yeasts, etc., produce siderophores to help take up these essential trace elements, while siderophore-deficient bacteria such as Brevibacterium and Microbacterium, etc., have molecular systems that help them to “steal” siderophores from their producers [84,144]. Understanding these interactions is essential, for instance, to selecting starter species and strains (or mixtures of strains) with efficient metal acquisition systems [145,146], which will allow them to strive for growth in dairy systems.

5.2. Amensalism

Amensalism involves interactions in which one type of microorganism negatively affects another without being affected itself. This type of relationship is commonly seen in dairy fermentations, where strains of many LAB species produce organic acids (lactic and acetic acids) that are effective inhibitors of susceptible microorganisms [128,129]. In addition to reducing the pH when released into the surrounding medium, they also have a direct inhibitory effect resulting from their undissociated forms by diffusing through the cell membranes and releasing H+ ions that acidify the cell cytoplasm [147]. Some other LAB antimicrobials, such as bacteriocins, H2O2, and fatty acids, are also thought to inhibit the growth of some organisms [148]. Bacteriocin-producing strains typically synthesize dedicated systems that protect them from these products’ harmful effects. In practice, bacteriocin-producing strains are used as “protective cultures” [149] to inhibit the development of pathogens and spoilage microorganisms in cheese. Indeed, they have been tested as inhibitors of Listeria (L.) monocytogenes [150,151,152,153,154,155,156], Staph. aureus [157,158], Salmonella sp. [159], Clostridium sp. [160,161,162], and other undesirable microbes [163]. Despite their technological use, bacteriocins may have physiological functions beyond their inhibitory activity [164,165]. Some authors [166] have suggested that subinhibitory levels may play subtle roles in guiding the succession of microbes in food fermentations.
Occasionally, the antimicrobial activity is associated with a microbial consortium rather than any single strain. For example, strong antilisterial activity exerted by some undefined consortia from the rind of smear-ripened cheeses has been repeatedly reported [167,168,169,170,171]. Via addition and erosion experiments (i.e., adding or removing one strain at a time from a mixture), attempts have been made to establish the “minimum community” showing an inhibitory property [169]. Interestingly, some minimal communities have been shown to exert greater antilisterial activity than the initial complex smear. After partial purification, an antimicrobial produced by one such minimum community proved to be a small, extremely thermo- and protease-stable molecule [168].
Certain LAB also have antifungal activity [147]. The nature and quantity of antifungal compounds produced are species- and strain-dependent. Organic acids (phenyllactic, hydroxyphenyllactic), fatty acids (decanoic, coriolic), cyclopeptides, hydrogen peroxide, and diacetyl have all been found to inhibit certain fungi [128]. The production of antifungal compounds, however, is not limited to bacteria. As such, the yeast Williopsis saturnus (with the killer phenotype) has been reported to inhibit the galactose-fermenting spoilage yeasts Saccharomyces (Sc.) cerevisiae and Kluyveromyces (K.) marxianus [172]. Negative yeast–yeast interactions unrelated to antimicrobials, but rather of a metabolic nature, have also been reported. In co-cultures of D. hansenii and Yarrowia (Y.) lipolytica, the latter yeast causes a shift from respiratory to fermentative metabolism in the former [173].

5.3. Commensalism

Commensalism occurs when a microorganism in a mixture is favored by the interactions that occur in that mixture, while other organisms experience neither negative nor positive effects. It has long been recognized that the proteolytic activity of proteinase-positive LAB cultures enables non-proteolytic species and strains to grow in milk [174,175]. The same interaction has also been reported between the LAB components of the traditional Dutch starter culture known as Ur [133]. In this starter, culturing and typing techniques have identified eight genetic lineages as the microbial components, including five strains of Lc. lactis subsp. cremoris, two of Lc. lactis subsp. lactis biovar diacetylactis, and one of Leuc. mesenteroides. Genome analysis and in silico reconstruction of metabolic maps of the different species and strains of the consortium suggested that γ-aminobutyric acid (GABA) excreted by Lc. lactis as part of its acid stress response might serve as a substrate for succinate formation by Leuc. mesenteroides. In contrast, this species did not appear to contribute to the growth of Lc. lactis strains [133]. Likewise, in Swiss-type cheeses, propionic acid bacteria (PAB) utilize the lactate produced by LAB, generating the typical “eyes” of these cheeses [2,4], without any apparent benefit for the latter population. The presence of lactate alone, however, cannot explain all the beneficial effects of LAB on PAB. The growth of the latter bacteria might also be enhanced by amino acids and peptides released by the LAB proteolytic system [176]. Similarly, the stimulation of LAB growth by yeasts without apparent profit of the eukaryotic microorganisms has also been reported [177,178,179]. In French Cantalet cheese, the use of yeasts as adjunct cultures has been found to promote the survival of Lc. lactis cells during ripening, and to enhance the formation of the cheese’s aroma [180]. This relationship might not be strictly commensal, however, since the yeasts might also benefit from LAB growth by using the glucose and/or galactose sugars released by some LAB species [177].
The regulation of color development in cheese rinds of a Muenster-type cheese by Brevibacterium (Brev.) linens via the activity of accompanying yeast species may, however, be understood as an outcome of true commensalism [181].

5.4. Mutualism

Mutualism is the relationship in which all the microorganisms involved benefit from their interactions. The most typical mutualistic interplay between LAB bacteria in dairy products is the so-called “protocooperation” that takes place in yogurt between S. thermophilus and Lb. delbrueckii subsp. bulgaricus [140,166]. This relies on casein proteolysis by Lb. delbrueckii subsp. bulgaricus via its surface caseinolytic proteinase PrtB, whose activity supplies amino acids to S. thermophilus. This latter bacterium, in turn, provides formic acid and carbon dioxide to the former organism [182]. Recently, it has been shown that urease activity in S. thermophilus is also essential in this cooperation [183]. Urease deficiency causes a shortage of ammonium and CO2, compounds that affect the growth of S. thermophilus and Lb. delbrueckii subsp. bulgaricus, respectively. Additional interactions between the two microbes might include the supply of purine precursors (xanthine, uracil) by Lb. delbrueckii subsp. bulgaricus to S. thermophilus, and a reduction in the formation of reactive oxygen species (ROS) by S. thermophilus in response to H2O2 production by Lb. delbrueckii subsp. bulgaricus via the Fenton reaction [166]. Cooperation between other LAB species, such as that seen between Lc. lactis and Lb. casei in the proteolysis of milk proteins during cheese ripening, has also been reported [184].
Cooperative cross-feeding between LAB and yeast species isolated from cheese has been abundantly described [185,186]. Yeasts can provide LAB with essential vitamins [180] or with carbon (2-oxoglutarate) and nitrogen (amino acids) sources, while LAB can provide lactic acid to non-lactose fermenting yeasts as a preferred energy substrate [187,188]. A better understanding of the metabolic activities of yeasts and LAB species and their possible interactions in cheese rind has recently been gained by combining the results of metagenomic, metatranscriptomic, and metabolomic analyses [189]. In the rind of a cheese model involving a synthetic microbiota composed of Lc. lactis, Brev. aurantiacum, Glutamicibacter (G.) arilaitensis (formerly Arthr. arilaitensis), Corynebacterium casei, Hafnia (H.) alvei and Staph. equorum, plus the yeasts D. hansenii, G. candidum and K. lactis, several mutualistic interactions were observed [188]. Lc. lactis and the yeast K. lactis, the most active species on day one, enabled the rapid fermentation of lactose, and the lactate produced was rapidly consumed by the yeast species D. hansenii and G. candidum. The ensuing deacidification of the matrix by the yeasts allowed the ensuing development of all five acid-sensitive bacteria [189].
The biotic interactions between D. hansenii and strains of the acid-sensitive species Brev. aurantiacum and H. alvei have also been recently assessed in a mini-cheese model [190]. Transcriptomic profiling of the cheeses produced with different combinations of these three species revealed potential mechanisms of interaction involving iron acquisition, proteolysis, lipolysis, sulfur metabolism, and D-galactonate catabolism. Confirming the previous results by Dugat-Bony et al. [189], the growth of D. hansenii increased the pH, allowing for the development of Brev. aurantiacum and H. alvei [190]. Further, strong mutualistic interactions between the two bacteria were also observed. Brev. aurantiacum benefited from the production of siderophores by H. alvei, while H. alvei growth was stimulated by sulfur amino acids and other energy compounds released from casein and triglycerides via the proteases and lipases secreted by Brev. aurantiacum [190]. Some of these interactions are of industrial interest since proteolysis increases the pool of methionine, the substrate for the formation of volatile sulfur compounds by H. alvei, which increase cheese flavor.
None of the above microbial interactions rules out others occurring [135,136]. Indeed, many and complex interactions between and within the different components of the cheese microbiota surely take place at the same time throughout manufacturing and ripening. For example, commensalistic and amensalistic interactions have been observed during the investigation of the interactions between the cheese microbes Lc. lactis, Y. lipolytica, and Staph. xylosus [191]. The numbers of Y. lipolytica were dramatically reduced by the presence of Staph. xylosus, whereas, although some changes in gene expression were observed, the growth of the lactic acid bacterium was not affected by the presence of either Staph. xylosus or Y. lipolytica [191]. Similarly, LAB and adventitious non-starter organisms may compete for citrate in cheese, while cooperation in terms of proteolysis and lipolysis may occur; all these interactions can lead to increased flavor formation [192,193,194]. Growth-detrimental interactions between S. thermophilus and Lb. delbrueckii subsp. bulgaricus in yogurt have also been reported. Strains of either species can produce bacteriocins that inhibit those of their partner [195,196].

6. Dynamics of Microbial Communities in Cheese

Microbial interactions determine the development, dynamics and activity of the microbial communities that compose the cheese microbiota, which may also influence cheese quality and safety [63,192,197,198]. Microbial communities often express emergent properties that cannot be predicted based on their individual members [199]. The robustness of microbiota may also be promoted by the taxonomic, genetic and functional redundancy seen in complex microbial communities [200]. To understand the causes and consequences of the microbial interactions affecting community dynamics and functionality, strategies are required that will help identify the patterns of microorganisms that determine the processes shaping the outcomes of the microbial interactions. These strategies must also assist in unraveling the molecular mechanisms underlying the interactions [201]. In this regard, the assistance of a vast array of state-of-the-art “omic” techniques is crucial [61,202]. For example, metagenomic surveys of the microbiota of cheeses [17,74,80,82,83,95,103,107,117,118,203,204,205] can help uncover patterns of community composition, while transcriptomic profiling [173,184,189,190,191,198,206] can be used to study microorganisms in a pairwise fashion and thus dissect interaction mechanisms. Besides, metabolomic techniques [115,116,207] can be used to identify the actual chemical mediators of these interactions [85,166,189,190,208,209]. The knowledge gathered through all these techniques may provide tools for managing and manipulating the microbiota and, consequently, can contribute to cheese quality and safety [210].
It has been consistently noted that the dominant microbial populations in different cheese varieties remain the same irrespective of whether the cheese is made from raw or pasteurized milk [42,102,103,211]. This suggests that cheese-specific environmental factors allow the consistent assembly of certain microbes in each particular cheese type [201,212]. Recently, the rind microbiota of a large set of cheeses with natural, smear, and bloomy rinds, although varied and complex, has been reported to be composed of easily tractable microbial communities [205]. Intensive sampling of cheeses from Europe and the USA made at different times of year has shown the assemblage of rind microbial communities to be very consistent. More importantly, in a simple in vitro system (10% cheese curd agar), Wolfe et al. [205] demonstrated that the different patterns of community composition and succession in cheese rinds can be easily reconstructed from a small pool of the commonest abundant taxa (seven bacteria and four fungal species) simply by changing the inoculum size and the rind washing and drying processes followed. Moisture was found to be the best predictor of the cheese rind community’s composition. In bloomy rinds, the numbers of Galactomyces and four genera of highly abundant Proteobacteria species were found to positively correlate with the moisture level [205], while molds, Actinobacteria, and Staphylococcus species, which are all abundant in dry, natural rinds, were negatively associated with this parameter. The same research group also showed that motile bacteria from rind microbial communities (Serratia, Halomonas, Vibrio, Psychrobacter, and others) use the humidity associated with the physical networks created by the co-occurring filamentous fungi for dispersal [208]. The latter study highlights how fungal-mediated bacterial dispersal can promote the growth of motile organisms over that of non-motile community members. In addition to shaping the composition of the cheese rind microbiota, this interaction could have quality and safety implications, depending on whether motile microbes are of technological relevance (H. alvei, Psychrobacter sp., etc.) or are pathogens (L. monocytogenes) [208].
By analyzing the spread of three closely related Staphylococcus species in cheese rind biofilms, it has been shown that biotic interactions can drive the patterns of microbial species distribution [209]. Surprisingly, based on growth and competition assays in the laboratory, Staph. equorum (the most abundant Staphylococcus in cheese) proved to be a slower colonizer and weaker competitor than Staph. xylosus and Staph. saprophyticus [208]. However, Staph. equorum was shown to be promoted by fungi, particularly by those of the genus Scopulariopsis [209]. Comparative genomic and transcriptomic experiments indicated that the potential mechanism underlying this bacterium–fungus interaction was based on iron utilization. Filamentous fungi release siderophores into the cheese matrix, and the bacterium responds by overexpressing siderophore-binding proteins [209]. This reaction provides Staph. equorum with an exclusive and inexpensive iron source.
Nine synthetic microbial communities consisting of different strains of three bacterial species (Staph. equorum, Brev. aurantiacum, and Brachybacterium alimentarium) have been reported to show different responses to abiotic (high salt) and biotic (the presence of the fungus Penicillium) disturbances [213]. Some combinations of strains showed no response, while others showed a substantial shift in community composition. These differing responses were shown to correlate with differences in pigment production (light yellow to orange) and with the volatile organic compounds emitted from the rinds (nutty to sulfury) [213]. This suggests that taxonomic profiling alone may not predict well the assembly, dynamics, and functions of cheese microbiomes. However, the results stress the importance of the microbial interactions in the flavor formation in the cheese rind. Chemicals triggering the assemblage of a community do not necessarily need to be physically close to the microbial responder. Indeed, volatile compounds produced by fungi have recently been found to stimulate the growth of Vibrio casei [214]. The latter study showed how volatile compounds may affect the development of a microbial community in cheese and demonstrated the feasibility of using airborne chemicals to control the composition (and thus activity) of the cheese microbiota.
Together, the above studies highlight how easily tractable microbial communities within the cheese microbiota can link the results of in vitro experiments with in situ observations [215]. Such associations might help determine the ecological processes contributing to species distribution and the abundance of microorganisms in cheese. A difficulty in inferring hypotheses regarding the relationships of ecological processes and microbial communities and in testing them experimentally is the inability to mirror accurately under laboratory settings the natural conditions encountered during cheese manufacturing and ripening [84,189,190,208,210]. However, understanding the mechanisms behind these interactions, and the environmental conditions that induce them, is a prerequisite for engineering communities for applied purposes [197,216]. The knowledge obtained in this regard might serve to support cheesemakers’ empirical observations, such as that the use of fresh milk with low levels of psychrotrophs prevents the development of the spoilage fungus Mucor during ripening [217], and that lowering the humidity of the curd favors the growth of G. candidum while inhibiting that of Mucor [218]. An advantage might also be taken of biotic interactions between the typical members of the cheese microbiota to inhibit the dynamics of cheese-borne pathogens such as L. monocytogenes and enteropathogenic Escherichia coli [219].

7. Microbiota-Based Starters

Despite the enormous advances made in resolving microbial safety hazards and spoilage issues, the dairy industry still faces important technological challenges beyond the phage infection, such as the need for improved science-based strategies to control cheese defects including the formation of splits associated with secondary fermentation [10,121,220], the appearance of calcium lactate crystals [122], and discolorations [84,120,221]. Reducing the presence of pathogens in raw milk-made cheeses [123,221], controlling spore-formers in cheeses made from pasteurized milk [11,13,138], and reducing the production and accumulation of biogenic amines in cheese [124] also need to be pursued. However, as has been repeatedly reported [207,222,223], the outcomes produced by the raw milk microbiota in cheeses during ripening cannot be reproduced by simply adding starter and ripening cultures. One solution for developing multipurpose functional starters would be to identify, isolate and characterize competitive microorganisms within dominant and key functional populations (the so-called “core microbiota”) in each cheese type, and return them in a synthetic mixture for cheese manufacture and ripening [215,224].
Multi-species synthetic microbial communities are widely used in several biotechnological processes, as these may have properties that a single species or microbial strain alone could never show [225]. The main aim of a multi-species community culture is to occupy the ecosystem from a taxonomic viewpoint, but especially from a functional perspective [88,226]. This idea has proven successful in the inhibition of pathogens in plant roots, where, as shown above for the antilisterial activity of some cheese rind smears, the inhibition induced is deemed to be a property that emerges at the microbial community level [227]. The use of multispecies communities also shows promise for the treatment of intestinal disorders associated with microbial dysbiosis [228]; synthetic communities might soon be able to replace the unappealing treatments of fecal transplantation. To these ends, metagenomic data of the concerned ecosystem of interest can be examined by software tools [229] and in-network analyses [230,231] to search the samples for interactions between taxonomic units and biological samples. The relative abundance of biotypes, occurrence and exclusion patterns could also be scrutinized via correlation with the presence and concentration of key taste and aroma compounds [88,118]. Such analyses can help identify the core microbiota and key environmental factors that influence microbial colonization, development and activity. Using this strategy, Wang et al. [88] identified five genera as the core microbiota—Lactobacillus, Saccharomyces, Pichia, Geotrichum, and Candida—involved in the fermentation of a sorghum-derived liquor. Four yeast species (Pichia kudriavzevii, G. candidum, Candida vini, and Sc. cerevisiae) and one bacterium (Lb. acetotolerans) were then employed as representatives of each genus in experimental liquor manufacture. After fermentation, the synthetic mix was shown to have a flavor dynamics similar to that produced under standard conditions [88].
Synthetic microbial communities from cheese rinds containing various types of bacteria and fungi have already been used as smearing starters for the manufacture of smear-ripened cheeses [12,42,56,206]. Traditional smearing, in fact, involves an “old to young smearing” procedure, in which smears from mature cheeses dispersed in water or a saline solution are used to inoculate—as an undefined rind starter—the surface of young cheeses [39]. Some synthetic smear starters have been conceived [232] and typically contain three to six strains of deacidifying fungal species (usually D. hansenii and G. candidum) and acid-susceptible bacteria (G. arilaitensis, Brev. aurantiacum, Brev. linens, and/or C. casei). Occasionally, Gram-negative bacteria such as H. alvei, Proteus vulgaris or Psychrobacter celer can also be included, aiming at enhancing the production of volatile sulfur compounds [233,234]. At present, the design of such cultures is mostly empirical, and neither the biotic interactions between the different taxa involved nor the effects of abiotic factors are currently taken into account, which very commonly results in a colonization failure [145,235,236]. Scientifically sound, microbiota-based, multi-species starters composed of LAB and non-LAB species, and, if required, of eukaryotic organisms, would provide enzymatic activities that LAB alone do not possess, thus contributing to expanding the textural and flavor patterns of the cheeses produced with them. These starters might more easily resist the phage attack and reduce colonization by adventitious spoilage and pathogenic organisms.

8. Conclusions and Prospects

Abundant knowledge on the composition, diversity, and structure of the microbial communities in cheese has been accrued over recent decades via the use of HTS techniques. The diversity and number of species present within the microbial communities of different cheese varieties create the potential for a multitude of inter- and intra-species interactions, most of which, however, are currently unknown. Indeed, the interactions that have already been studied are limited to a few community members and a small number of exchanged metabolites. Even less is known about the molecular bases facilitating and regulating these exchanges. Neither do we have much knowledge regarding the conditions that allow the cheese microbiota to form and develop under the influence of biotic and abiotic factors, nor of how any of this translates into the improvement of cheese manufacture and ripening. As a consequence, successful cheese fermentations cannot be predicted, and technological failures of microbial origin are commonly inexplicable. In this regard, establishing chemical and/or microbial biomarkers to trace the milk fermentation would certainly be a valuable tool, which might contribute to enhancing cheese quality.
To get the most out of the omics revolution in cheesemaking, computational pipelines have to be developed to infer putative mechanisms of interaction between the many microbial populations. Constructing and using simple microbial communities in model systems might help unravel how microorganisms from complex consortia interact in their communities, and what influence they imprint on the sensorial properties of cheese. Confirmation is also required that the processes and mechanisms identified in model systems also work at the natural ecosystem scale, that is, at the cheese level. To that end, model communities should mimic natural populations as closely as possible; this will help throw light on the mechanisms involved in microbial colonization, functioning, and endurance of the different biotypes. Understanding microbial interactions of the biotypes with biotic and abiotic factors in cheese could help design strain mixtures as improved starter cultures. Knowledge of how microbes assemble into communities and the practical implications of these in cheesemaking could ultimately be used to improve the overall cheese quality and safety.

Author Contributions

B.M., J.R., L.V. and A.B.F. reviewed the literature and drafted parts of the manuscript. B.M. set parts together, homogenized the style, and produced the final draft. B.M., J.R., L.V. and A.B.F. reviewed and amended the draft to attain the final version. All authors have read and agreed to the published version of the manuscript.

Funding

Research on the microbiology of traditional dairy products in the authors’ laboratory is currently supported by projects from the Spanish Ministry of Science and Innovation (PID2019-110549RB-I00/AEI/10.13039/501100011033) and Asturias Principality (IDI/2018/000114). A Ph.D. grant of the Severo Ochoa Program from Asturias Principality was awarded to J.R. (BP19-098).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

References

  1. Codex Standard 283-1978. Codex General Standard for Cheese; Adopted in 1973; Revision 1999; Amendments 2006; Codex Alimentarius Commission: Rome, Italy, 2013. [Google Scholar]
  2. Fox, P.F.; Guinee, T.P.; Cogan, T.M.; McSweeney, P.L.H. Principal families of cheese. In Fundamentals of Cheese Science; Fox, P.F., Guinee, T.P., Cogan, T.M., McSweeney, P.L.H., Eds.; Springer: Boston, MA, USA, 2017; pp. 27–69. [Google Scholar]
  3. Kosikowski, F.V.; Mistry, V.V. Cheese and Fermented Milk Foods, 3rd ed.; Kosikowski, F.V., Ed.; LLC: Westport, CT, USA, 1997. [Google Scholar]
  4. Fox, P.F.; Guinee, T.P.; Cogan, T.M.; McSweeney, P.L.H. Microbiology of cheese ripening. In Fundamentals of Cheese Science; Fox, P.F., Guinee, T.P., Cogan, T.M., McSweeney, P.L.H., Eds.; Springer: Boston, MA, USA, 2017; pp. 333–390. [Google Scholar]
  5. Montel, M.C.; Buchin, S.; Mallet, A.; Delbes-Paus, C.; Vuitton, D.A.; Desmasures, N.; Berthier, F. Traditional cheeses: Rich and diverse microbiota with associated benefits. Int. J. Food Microbiol. 2014, 177, 136–154. [Google Scholar] [CrossRef]
  6. Bintis, T. Lactic acid bacteria as starter cultures: An update in their metabolism and genetics. AIMS Microbiol. 2018, 4, 665–684. [Google Scholar] [CrossRef]
  7. Carr, F.J.; Chill, D.; Maida, N. The lactic acid bacteria: A literature survey. Crit. Rev. Microbiol. 2002, 28, 281–370. [Google Scholar] [CrossRef] [PubMed]
  8. Smit, G.; Smit, B.A.; Engels, W.J. Flavour formation by lactic acid bacteria and biochemical flavour profiling of cheese products. FEMS Microbiol. Rev. 2005, 29, 591–610. [Google Scholar] [CrossRef] [PubMed]
  9. Fardet, A.; Dupont, D.; Rioux, L.E.; Turgeon, S.L. Influence of food structure on dairy protein, lipid and calcium bioavailability: A narrative review of evidence. Crit. Rev. Food Sci. Nutr. 2019, 59, 1987–2010. [Google Scholar] [CrossRef] [PubMed]
  10. Metzger, S.A.; Hernandez, L.L.; Suen, G.; Ruegg, P.L. Understanding the milk microbiota. Vet. Clin. North Am. Food Anim. Pract. 2018, 34, 427–438. [Google Scholar] [CrossRef]
  11. Boor, K.J.; Wiedmann, M.; Murphy, S.; Alcaine, S. A 100-Year Review: Microbiology and safety of milk handling. J. Dairy Sci. 2017, 100, 9933–9951. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Irlinger, F.; Layec, S.; Hélinck, S.; Dugat-Bony, E. Cheese rind microbial communities: Diversity, composition and origin. FEMS Microbiol. Lett. 2015, 362, 1–11. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  13. Quigley, L.; O’Sullivan, O.; Stanton, C.; Beresford, T.P.; Ross, R.P.; Fitzgerald, G.F.; Cotter, P.D. The complex microbiota of raw milk. FEMS Microbiol. Rev. 2013, 37, 664–698. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  14. Lavoie, K.; Touchette, M.; St-Gelais, D.; Labrie, S. Characterization of the fungal microflora in raw milk and specialty cheeses of the province of Quebec. Dairy Sci. Technol. 2012, 92, 455–468. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  15. Mounier, J.; Goerges, S.; Gelsomino, R.; Vancanneyt, M.; Vandemeulebroecke, K.; Hoste, B.; Brennan, N.M.; Scherer, S.; Swings, J.; Fitzgerald, G.F.; et al. Sources of the adventitious microflora of a smear-ripened cheese. J. Appl. Microbiol. 2006, 101, 668–681. [Google Scholar] [CrossRef] [PubMed]
  16. Desmasures, N.; Bazin, F.; Guéguen, M. Microbiological composition of raw milk from selected farms in the Camembert region of Normandy. J. Appl. Microbiol. 1997, 83, 53–58. [Google Scholar] [CrossRef] [PubMed]
  17. Aldrete-Tapia, A.; Escobar-Ramírez, C.M.; Tamplin, M.L.; Hernández-Iturriaga, M. Characterization of bacterial communities in Mexican artisanal raw milk "Bola de Ocosingo" cheese by high-throughput sequencing. Front. Microbiol. 2018, 9, 2598. [Google Scholar] [CrossRef] [PubMed]
  18. Frétin, M.; Martin, B.; Rifa, E.; Isabelle, V.M.; Pomiès, D.; Ferlay, A.; Montel, M.C.; Delbès, C. Bacterial community assembly from cow teat skin to ripened cheeses is influenced by grazing systems. Sci. Rep. 2018, 8, 200. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  19. Haastrup, M.K.; Johansen, P.; Malskær, A.H.; Castro-Mejía, J.L.; Kot, W.; Krych, L.; Arneborg, N.; Jespersen, L. Cheese brines from Danish dairies reveal a complex microbiota comprising several halotolerant bacteria and yeasts. Int. J. Food Microbiol. 2018, 285, 173–187. [Google Scholar] [CrossRef] [PubMed]
  20. Lucchini, R.; Cardazzo, B.; Carraro, L.; Negrinotti, M.; Balzan, S.; Novelli, E.; Fasolato, L.; Fasoli, F.; Farina, G. Contribution of natural milk culture to microbiota, safety and hygiene of raw milk cheese produced in alpine malga. Ital. J. Food Saf. 2018, 7, 6967. [Google Scholar] [CrossRef] [PubMed]
  21. Quijada, N.M.; Mann, E.; Wagner, M.; Rodríguez-Lázaro, D.; Hernández, M.; Schmitz-Esser, S. Autochthonous facility-specific microbiota dominates washed-rind Austrian hard cheese surfaces and its production environment. Int. J. Food Microbiol. 2018, 267, 54–61. [Google Scholar] [CrossRef] [Green Version]
  22. Santarelli, M.; Bottari, B.; Lazzi, C.; Neviani, E.; Gatti, M. Survey on the community and dynamics of lactic acid bacteria in Grana Padano cheese. Syst. Appl. Microbiol. 2013, 36, 593–600. [Google Scholar] [CrossRef]
  23. Edalatian, M.R.; Habibi, M.B.; Mortazavi, S.A.; Alegría, A.; Nassiri, M.R.; Bassam, M.R.; Mayo, B. Microbial diversity of the traditional Iranian cheeses Lighvan and Koozeh, as revealed by polyphasic culturing and culture-independent approaches. Dairy Sci. Technol. 2012, 92, 75–90. [Google Scholar] [CrossRef] [Green Version]
  24. Feutry, F.; Oneca, M.; Berthier, F.; Torre, P. Biodiversity and growth dynamics of lactic acid bacteria in artisanal PDO Ossau-Iraty cheeses made from raw ewe’s milk with different starters. Food Microbiol. 2012, 29, 33–42. [Google Scholar] [CrossRef]
  25. Alegría, A.; Álvarez-Martín, P.; Sacristán, N.; Fernández, E.; Delgado, S.; Mayo, B. Diversity and evolution of majority microbial populations during manufacturing and ripening of Casín, a Spanish traditional, starter-free cheese made of raw cow’s milk. Int. J. Food Microbiol. 2009, 136, 44–51. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Callon, C.; Berdagué, J.L.; Dufour, E.; Montel, M.C. The effect of raw milk microbial flora on the sensory characteristics of Salers-type cheeses. J. Dairy Sci. 2005, 88, 3840–3850. [Google Scholar] [CrossRef] [Green Version]
  27. Morales, P.; Fernández-García, E.; Gaya, P.; Núñez, M. Formation of volatile compounds by wild Lactococcus lactis strains isolated from raw ewes’ milk cheese. Int. Dairy J. 2003, 13, 201–209. [Google Scholar] [CrossRef]
  28. Baruzzi, F.; Matarante, A.; Morea, M.; Cocconcelli, P.S. Microbial community dynamics during the Scamorza Altamurana cheese natural fermentation. J. Dairy Sci. 2002, 85, 1390–1397. [Google Scholar] [CrossRef]
  29. Moser, A.; Schafroth, K.; Meile, L.; Egger, L.; Badertscher, R.; Irmler, S. Population dynamics of Lactobacillus helveticus in Swiss Gruyère-type cheese manufactured with natural whey cultures. Front. Microbiol. 2018, 9, 637. [Google Scholar] [CrossRef]
  30. Castro, R.D.; Oliveira, L.G.; Sant’Anna, F.M.; Luiz, L.M.P.; Sandes, S.H.C.; Silva, C.I.F.; Silva, A.M.; Nunes, A.C.; Penna, C.F.A.M.; Souza, M.R. Lactic acid microbiota identification in water, raw milk, endogenous starter culture, and fresh Minas artisanal cheese from the Campo das Vertentes region of Brazil during the dry and rainy seasons. J. Dairy Sci. 2016, 99, 6086–6096. [Google Scholar] [CrossRef]
  31. Solieri, L.; Bianchi, A.; Giudici, P. Inventory of non-starter lactic acid bacteria from ripened Parmigiano Reggiano cheese as assessed by a culture dependent multiphasic approach. Syst. Appl. Microbiol. 2012, 35, 270–277. [Google Scholar] [CrossRef]
  32. Nieto-Arribas, P.; Seseña, S.; Poveda, J.M.; Palop, L.; Cabezas, L. Genotypic and technological characterization of Leuconostoc isolates to be used as adjunct starters in Manchego cheese manufacture. Food Microbiol. 2010, 27, 85–93. [Google Scholar] [CrossRef] [PubMed]
  33. van Hoorde, K.; van Leuven, I.; Dirinck, P.; Heyndrickx, M.; Coudijzer, K.; Vandamme, P.; Huys, G. Selection, application and monitoring of Lactobacillus paracasei strains as adjunct cultures in the production of Gouda-type cheeses. Int. J. Food Microbiol. 2010, 144, 226–235. [Google Scholar] [CrossRef] [PubMed]
  34. Henri-Dubernet, S.; Desmasures, N.; Guéguen, M. Diversity and dynamics of lactobacilli populations during ripening of RDO Camembert cheese. Can. J. Microbiol. 2008, 54, 218–228. [Google Scholar] [CrossRef]
  35. Sánchez, I.; Seseña, S.; Poveda, J.M.; Cabezas, L.; Palop, L. Genetic diversity, dynamics, and activity of Lactobacillus community involved in traditional processing of artisanal Manchego cheese. Int. J. Food Microbiol. 2006, 107, 265–273. [Google Scholar] [CrossRef]
  36. Dasen, A.; Berthier, F.; Grappin, R.; Williams, A.G.; Banks, J. Genotypic and phenotypic characterization of the dynamics of the lactic acid bacterial population of adjunct-containing Cheddar cheese manufactured from raw and microfiltered pasteurised milk. J. Appl. Microbiol. 2003, 94, 595–607. [Google Scholar] [CrossRef] [PubMed]
  37. Corroler, D.; Mangin, I.; Desmasures, N.; Gueguen, M. An ecological study of lactococci isolated from raw milk in the camembert cheese registered designation of origin area. Appl. Environ. Microbiol. 1998, 64, 4729–4735. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  38. Desmasures, N.; Mangin, I.; Corroler, D.; Guéguen, M. Characterization of lactococci isolated from milk produced in the Camembert region of Normandy. J. Appl. Microbiol. 1998, 85, 999–1005. [Google Scholar] [CrossRef] [PubMed]
  39. Fox, P.F.; Guinee, T.P.; Cogan, T.M.; McSweeney, P.L.H. Starter cultures. In Fundamentals of Cheese Science; Fox, P.F., Guinee, T.P., Cogan, T.M., McSweeney, P.L.H., Eds.; Springer: Boston, MA, USA, 2017; pp. 121–183. [Google Scholar]
  40. Parente, E.; Cogan, T.M. Starter cultures: General aspects. In Cheese: Chemistry, Physics and Microbiology, 3rd ed.; Fox, P.O., Ed.; Elsevier: Oxford, UK, 2004; pp. 123–147. [Google Scholar]
  41. Giello, M.; La Storia, A.; Masucci, F.; Di Francia, A.; Ercolini, D.; Villani, F. Dynamics of bacterial communities during manufacture and ripening of traditional Caciocavallo of Castelfranco cheese in relation to cows’ feeding. Food Microbiol. 2017, 63, 170–177. [Google Scholar] [CrossRef]
  42. Cogan, T.M.; Goerges, S.; Gelsomino, R.; Larpin, S.; Hohenegger, M.; Bora, N.; Jamet, E.; Rea, M.C.; Mounier, J.; Vancanneyt, M.; et al. Biodiversity of the surface microbial consortia from Limburger, Reblochon, Livarot, Tilsit, and Gubbeen cheeses. Microbiol. Spectr. 2014, 2, 219–256. [Google Scholar] [CrossRef] [Green Version]
  43. Mounier, J.; Monnet, C.; Jacques, N.; Antoinette, A.; Irlinger, F. Assessment of the microbial diversity at the surface of Livarot cheese using culture-dependent and independent approaches. Int. J. Food Microbiol. 2009, 133, 31–37. [Google Scholar] [CrossRef] [Green Version]
  44. Dolci, P.; Alessandria, V.; Rantsiou, K.; Rolle, L.; Zeppa, G.; Cocolin, L. Microbial dynamics of Castelmagno PDO, a traditional Italian cheese, with a focus on lactic acid bacteria ecology. Int. J. Food Microbiol. 2008, 122, 302–311. [Google Scholar] [CrossRef]
  45. Martín-Platero, A.M.; Valdivia, E.; Maqueda, M.; Martín-Sánchez, I.; Martínez-Bueno, M. Polyphasic approach to bacterial dynamics during the ripening of Spanish farmhouse cheese, using culture-dependent and -independent methods. Appl. Environ. Microbiol. 2008, 74, 5662–5673. [Google Scholar] [CrossRef] [Green Version]
  46. Delbès, C.; Ali-Mandjee, L.; Montel, M.C. Monitoring bacterial communities in raw milk and cheese by culture-dependent and -independent 16S rRNA gene-based analyses. Appl. Environ. Microbiol. 2007, 73, 1882–1891. [Google Scholar] [CrossRef] [Green Version]
  47. Rea, M.C.; Görges, S.; Gelsomino, R.; Brennan, N.M.; Mounier, J.; Vancanneyt, M.; Scherer, S.; Swings, J.; Cogan, T.M. Stability of the biodiversity of the surface consortia of Gubbeen, a red-smear cheese. J. Dairy Sci. 2007, 90, 2200–2210. [Google Scholar] [CrossRef] [PubMed]
  48. Brennan, N.M.; Ward, A.C.; Beresford, T.P.; Fox, P.F.; Goodfellow, M.; Cogan, T.M. Biodiversity of the bacterial flora on the surface of a smear cheese. Appl. Environ. Microbiol. 2002, 68, 820–830. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  49. Callon, C.; Millet, L.; Montel, M.C. Diversity of lactic acid bacteria isolated from AOC Salers cheese. J. Dairy Res. 2004, 71, 231–244. [Google Scholar] [CrossRef] [PubMed]
  50. Ercolini, D. High-throughput sequencing and metagenomics: Moving forward in the culture-independent analysis of food microbial ecology. Appl. Environ. Microbiol. 2013, 79, 3148–3155. [Google Scholar] [CrossRef] [Green Version]
  51. Quigley, L.; O’Sullivan, O.; Beresford, T.P.; Ross, R.P.; Fitzgerald, G.F.; Cotter, P.D. Molecular approaches to analysing the microbial composition of raw milk and raw milk cheese. Int. J. Food Microbiol. 2011, 150, 81–94. [Google Scholar] [CrossRef]
  52. Jany, J.L.; Barbier, G. Culture-independent methods for identifying microbial communities in cheese. Food Microbiol. 2008, 25, 839–848. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  53. Overmann, J.; Abt, B.; Sikorski, J. Present and future of culturing bacteria. Ann. Rev. Microbiol. 2017, 71, 711–730. [Google Scholar] [CrossRef] [PubMed]
  54. Kumar, S.S.; Ghosh, A.R. Assessment of bacterial viability: A comprehensive review on recent advances and challenges. Microbiology 2019, 165, 593–610. [Google Scholar] [CrossRef]
  55. Yunita, D.; Dodd, C.E.R. Microbial community dynamics of a blue-veined raw milk cheese from the United Kingdom. J. Dairy Sci. 2018, 101, 4923–4935. [Google Scholar] [CrossRef] [PubMed]
  56. Larpin-Laborde, S.; Imran, M.; Bonaïti, C.; Bora, N.; Gelsomino, R.; Goerges, S.; Irlinger, F.; Goodfellow, M.; Ward, A.C.; Vancanneyt, M.; et al. Surface microbial consortia from Livarot, a French smear-ripened cheese. Can. J. Microbiol. 2011, 57, 651–660. [Google Scholar] [CrossRef]
  57. Feligini, M.; Panelli, S.; Buffoni, J.N.; Bonacina, C.; Andrighetto, C.; Lombardi, A. Identification of microbiota present on the surface of Taleggio cheese using PCR-DGGE and RAPD-PCR. J. Food Sci. 2012, 77, M609–M615. [Google Scholar] [CrossRef]
  58. Ercolini, D.; Moschetti, G.; Blaiotta, G.; Coppola, S. The potential of a polyphasic PCR-DGGE approach in evaluating microbial diversity of natural whey cultures for water-buffalo Mozzarella cheese production: Bias of culture-dependent and culture-independent analyzes. Syst. Appl. Microbiol. 2001, 24, 610–617. [Google Scholar] [CrossRef] [PubMed]
  59. Dolci, P.; Zenato, S.; Pramotton, R.; Barmaz, A.; Alessandria, V.; Rantsiou, K.; Cocolin, L. Cheese surface microbiota complexity: RT-PCR-DGGE, a tool for a detailed picture? Int. J. Food Microbiol. 2013, 162, 8–12. [Google Scholar] [CrossRef] [PubMed]
  60. Flórez, A.B.; Mayo, B. Microbial diversity and succession during the manufacture and ripening of traditional, Spanish, blue-veined Cabrales cheese, as determined by PCR-DGGE. Int. J. Food Microbiol. 2006, 110, 165–171. [Google Scholar] [CrossRef] [PubMed]
  61. Randazzo, C.L.; Torriani, S.; Akkermans, A.D.; de Vos, W.M.; Vaughan, E.E. Diversity, dynamics, and activity of bacterial communities during production of an artisanal Sicilian cheese as evaluated by 16S rRNA analysis. Appl. Environ. Microbiol. 2002, 68, 1882–1892. [Google Scholar] [CrossRef] [Green Version]
  62. Roth, E.; Miescher Schwenninger, S.; Hasler, M.; Eugster-Meier, E.; Lacroix, C. Population dynamics of two antilisterial cheese surface consortia revealed by temporal temperature gradient gel electrophoresis. BMC Microbiol. 2010, 10, 74. [Google Scholar] [CrossRef] [Green Version]
  63. Bertani, G.; Levante, A.; Lazzi, C.; Bottari, B.; Gatti, M.; Neviani, E. Dynamics of a natural bacterial community under technological and environmental pressures: The case of natural whey starter for Parmigiano Reggiano cheese. Food Res. Int. 2020, 129, 108860. [Google Scholar] [CrossRef]
  64. Agrimonti, C.; Bottari, B.; Sardaro, M.L.S.; Marmiroli, N. Application of real-time PCR (qPCR) for characterization of microbial populations and type of milk in dairy food products. Crit. Rev. Food Sci. Nutr. 2019, 59, 423–442. [Google Scholar] [CrossRef] [PubMed]
  65. Hermet, A.; Mounier, J.; Keravec, M.; Vasseur, V.; Barbier, G.; Jany, J.L. Application of capillary electrophoresis single-stranded conformation polymorphism (CE-SSCP) analysis for identification of fungal communities in cheese. Food Microbiol. 2014, 41, 82–90. [Google Scholar] [CrossRef]
  66. Duthoit, F.; Godon, J.J.; Montel, M.C. Bacterial community dynamics during production of registered designation of origin Salers cheese as evaluated by 16S rRNA gene single-strand conformation polymorphism analysis. Appl. Environ. Microbiol. 2003, 69, 3840–3848. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  67. Sánchez, J.I.; Rossetti, L.; Martínez, B.; Rodríguez, A.; Giraffa, G. Application of reverse transcriptase PCR-based T-RFLP to perform semi-quantitative analysis of metabolically active bacteria in dairy fermentations. J. Microbiol. Methods 2006, 65, 268–277. [Google Scholar] [CrossRef] [PubMed]
  68. Alegría, A.; Szczesny, P.; Mayo, B.; Bardowski, J.; Kowalczyk, M. Biodiversity in Oscypek, a traditional Polish cheese, determined by culture-dependent and -independent approaches. Appl. Environ. Microbiol. 2012, 78, 1890–1898. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  69. Afshari, R.; Pillidge, C.J.; Dias, D.A.; Osborn, A.M.; Gill, H. Cheesomics: The future pathway to understanding cheese flavour and quality. Crit. Rev. Food Sci. Nutr. 2020, 60, 33–47. [Google Scholar] [CrossRef] [PubMed]
  70. Cao, Y.; Fanning, S.; Proos, S.; Jordan, K.; Srikumar, S. A review on the applications of Next Generation Sequencing technologies as applied to food-related microbiome studies. Front. Microbiol. 2017, 8, 1829. [Google Scholar] [CrossRef] [PubMed]
  71. Kergourlay, G.; Taminiau, B.; Daube, G.; Champomier Vergès, M.C. Metagenomic insights into the dynamics of microbial communities in food. Int. J. Food Microbiol. 2015, 213, 31–39. [Google Scholar] [CrossRef] [PubMed]
  72. Mayo, B.; Rachid, C.T.C.C.; Alegría, A.; Leite, A.M.O.; Peixoto, R.S.; Delgado, S. Impact of next generation sequencing techniques in Food Microbiology. Curr. Genom. 2014, 15, 293–309. [Google Scholar] [CrossRef] [Green Version]
  73. Bokulich, N.A.; Mills, D.A. Next-generation approaches to the microbial ecology of food fermentations. BMB Rep. 2012, 45, 377–389. [Google Scholar] [CrossRef] [Green Version]
  74. Ercolini, D.; De Filippis, F.; La Storia, A.; Iacono, M. “Remake” by high-throughput sequencing of the microbiota involved in the production of water buffalo Mozzarella cheese. Appl. Environ. Microbiol. 2012, 78, 8142–8145. [Google Scholar] [CrossRef] [Green Version]
  75. Lusk, T.S.; Ottensen, A.R.; White, J.R.; Allard, M.W.; Brown, E.W.; Kase, J.E. Characterization of microflora in Latin-style cheeses by next-generation sequencing technology. BCM Microbiol. 2012, 12, 254. [Google Scholar] [CrossRef] [Green Version]
  76. Quigley, L.; O’Sullivan, O.; Beresford, T.P.; Ross, R.P.; Fitzgerald, G.F.; Cotter, P.D. High-throughput sequencing for detection of subpopulations of bacteria not previously associated with artisanal cheeses. Appl. Environ. Microbiol. 2012, 78, 5717–5723. [Google Scholar] [CrossRef] [Green Version]
  77. Masoud, W.; Takamiya, M.; Vogensen, F.K.; Lillevang, S.; Al-Soud, W.A.; Sørensen, S.J.; Jakobsen, M. Characterization of bacterial populations in Danish raw milk cheeses made with different starter cultures by denaturing gradient gel electrophoresis and pyrosequencing. Int. Dairy J. 2010, 21, 142–148. [Google Scholar] [CrossRef]
  78. Yeluri Jonnala, B.R.; McSweeney, P.L.H.; Sheehan, J.J.; Cotter, P.D. Sequencing of the cheese microbiome and its relevance to industry. Front. Microbiol. 2018, 9, 1020. [Google Scholar] [CrossRef] [Green Version]
  79. Jin, H.; Mo, L.; Pan, L.; Hou, Q.; Li, C.; Darima, I.; Yu, J. Using PacBio sequencing to investigate the bacterial microbiota of traditional Buryatian cottage cheese and comparison with Italian and Kazakhstan artisanal cheeses. J. Dairy Sci. 2018, 101, 6885–6896. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  80. Li, J.; Zheng, Y.; Xu, H.; Xi, X.; Hou, Q.; Feng, S.; Wuri, L.; Bian, Y.; Yu, Z.; Kwok, L.Y.; et al. Bacterial microbiota of Kazakhstan cheese revealed by single molecule real time (SMRT) sequencing and its comparison with Belgian, Kalmykian and Italian artisanal cheeses. BMC Microbiol. 2017, 17, 13. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  81. Ritschard, J.S.; Amato, L.; Kumar, Y.; Müller, B.; Meile, L.; Schuppler, M. The role of the surface smear microbiome in the development of defective smear on surface-ripened red-smear cheese. AIMS Microbiol. 2018, 4, 622–641. [Google Scholar] [CrossRef]
  82. Escobar-Zepeda, A.; Sanchez-Flores, A.; Quirasco Baruch, M. Metagenomic analysis of a Mexican ripened cheese reveals a unique complex microbiota. Food Microbiol. 2016, 57, 116–127. [Google Scholar] [CrossRef] [PubMed]
  83. Ceugniez, A.; Taminiau, B.; Coucheney, F.; Jacques, P.; Delcenserie, V.; Daube, G.; Drider, D. Use of a metagenetic approach to monitor the bacterial microbiota of “Tomme d’Orchies” cheese during the ripening process. Int. J. Food Microbiol. 2017, 247, 65–69. [Google Scholar] [CrossRef] [PubMed]
  84. Cleary, J.L.; Kolachina, S.; Wolfe, B.E.; Sanchez, L.M. Coproporphyrin III produced by the bacterium Glutamicibacter arilaitensis binds zinc and is upregulated by fungi in cheese rinds. mSystems 2018, 3, e00036-18. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  85. Kamelamela, N.; Zalesne, M.; Morimoto, J.; Robbat, A.; Wolfe, B.E. Indigo- and indirubin-producing strains of Proteus and Psychrobacter are associated with purple rind defect in a surface-ripened cheese. Food Microbiol. 2018, 76, 543–552. [Google Scholar] [CrossRef] [PubMed]
  86. Delgado, D.; Rachid, C.T.C.C.; Fernández, E.; Rychlik, T.; Alegría, A.; Peixoto, R.S.; Mayo, B. Diversity of thermophilic bacteria in raw, pasteurized and selectively-cultured milk, as assessed by culturing, PCR-DGGE and pyrosequencing. Food Microbiol. 2013, 36, 103–111. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  87. Ito, T.; Skizuka, T.; Kishi, N.; Yamahita, A.; Kuroda, M. Conventional culture methods with commercially available media unveil the presence of novel culturable bacteria. Gut Microbes 2018, 10, 77–91. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  88. Wang, S.; Wu, Q.; Nie, Y.; Wu, J.; Xu, Y. Construction of a synthetic microbiota for reproducible flavor compound metabolism in Chinese light-aroma-type liquor produced by solid-state fermentation. Appl. Environ. Microbiol. 2019, 85, e03090-18. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  89. De Pasquale, I.; Di Cagno, R.; Buchin, S.; De Angelis, M.; Gobbetti, M. Spatial distribution of the metabolically active microbiota within Italian PDO ewes’ milk cheeses. PLoS ONE 2016, 11, e0153213. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  90. Almeida, M.; Hébert, A.; Abraham, A.L.; Rasmussen, S.; Monnet, C.; Pons, N.; Delbès, C.; Loux, V.; Batto, J.M.; Leonard, P.; et al. Construction of a dairy microbial genome catalog opens new perspectives for the metagenomic analysis of dairy fermented products. BMC Genom. 2014, 15, 1101. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  91. Bonaïti, C.; Irlinger, F.; Spinnler, H.E.; Engel, E. An iterative sensory procedure to select odor-active associations in complex consortia of microorganisms: Application to the construction of a cheese model. J. Dairy Sci. 2005, 88, 1671–1684. [Google Scholar] [CrossRef]
  92. Mayo, B.; Ammor, M.S.; Delgado, S.; Alegría, A. Fermented milk products. In Fermented Food and Beverages of the World; Tmang, J.P., Kilasapathy, K., Eds.; Taylor & Francis: Abingdon, UK, 2010; pp. 263–288. [Google Scholar]
  93. Wouters, J.T.M.; Ayad, E.H.E.; Hugenholtz, J.; Smit, G. Microbes from raw milk for fermented dairy products. Int. Dairy J. 2002, 12, 91–109. [Google Scholar] [CrossRef]
  94. Sheedan, A.; O’Cuinn, G.; Fitzgerald, R.J.; Wilkinson, M.G. Distribution of microbial flora, intracellular enzymes and compositional indices throughout a 12 kg Cheedar cheese block during ripening. Int. Dairy J. 2009, 19, 321–329. [Google Scholar]
  95. Alessandria, V.; Ferrocino, I.; De Filippis, F.; Fontana, M.; Rantsiou, K.; Ercolini, D.; Cocolin, L. Microbiota of an Italian Grana-like cheese during manufacture and ripening, unraveled by 16S rRNA-based approaches. Appl. Environ. Microbiol. 2016, 82, 3988–3995. [Google Scholar] [CrossRef] [Green Version]
  96. Ropars, J.; Cruaud, C.; Lacoste, S.; Dupont, J. A taxonomic and ecological overview of cheese fungi. Int. J. Food Microbiol. 2012, 155, 199–210. [Google Scholar] [CrossRef]
  97. Oliveira, J.; Mahony, J.; Hanemaaijer, L.; Kouwen, T.R.H.M.; van Sinderen, D. Biodiversity of bacteriophages infecting Lactococcus lactis starter cultures. J. Dairy Sci. 2018, 101, 96–105. [Google Scholar] [CrossRef] [PubMed]
  98. Alexeeva, S.; Guerra-Martínez, J.A.; Spus, M.; Smid, E.J. Spontaneously induced prophages are abundant in a naturally evolved bacterial starter culture and deliver competitive advantage to the host. BMC Microbiol. 2018, 18, 120. [Google Scholar] [CrossRef]
  99. Mahony, J.; Moscarelli, A.; Kelleher, P.; Lugli, G.A.; Ventura, M.; Settanni, L.; van Sinderen, D. Phage biodiversity in artisanal cheese wheys reflects the complexity of the fermentation process. Viruses 2017, 9, 45. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  100. Cardarelli, H.R.; Saad, S.M.; Gibson, G.R.; Vulevic, J. Functional petit-suisse cheese: Measure of the prebiotic effect. Anaerobe 2007, 13, 200–207. [Google Scholar] [CrossRef] [PubMed]
  101. Ferreiro, T.; Martínez, S.; Gayoso, L.; Rodríguez-Otero, J.L. 2016. Evolution of phospholipid contents during the production of quark cheese from buttermilk. J. Dairy Sci. 2016, 99, 4154–4159. [Google Scholar] [CrossRef] [PubMed]
  102. Lee, J.; Seo, Y.; Ha, J.; Kim, S.; Choi, Y.; Oh, H.; Lee, Y.; Kim, Y.; Kang, J.; Park, E.; et al. Influence of milk microbiota on Listeria monocytogenes survival during cheese ripening. Food Sci. Nutr. 2020, 8, 5071–5076. [Google Scholar] [CrossRef] [PubMed]
  103. Delcenserie, V.; Taminiau, B.; Delhalle, L.; Nezer, C.; Doyen, P.; Crevecoeur, S.; Roussey, D.; Korsak, N.; Daube, G. Microbiota characterization of a Belgian protected designation of origin cheese, Herve cheese, using metagenomic analysis. J. Dairy Sci. 2014, 97, 6046–6056. [Google Scholar] [CrossRef] [Green Version]
  104. Fuka, M.M.; Wallisch, S.; Engel, M.; Welzl, G.; Havranek, J.; Schloter, M. Dynamics of bacterial communities during the ripening process of different Croatian cheese types derived from raw ewe’s milk cheeses. PLoS ONE 2013, 8, e80734. [Google Scholar] [CrossRef] [Green Version]
  105. Fox, P.F.; Guinee, T.P.; Cogan, T.M.; McSweeney, P.L.H. Biochemistry of cheese ripening. In Fundamentals of Cheese Science; Fox, P.F., Guinee, T.P., Cogan, T.M., McSweeney, P.L.H., Eds.; Springer: Boston, MA, USA, 2017; pp. 391–442. [Google Scholar]
  106. Laurencík, M.; Sulo, P.; Sláviková, E.; Piecková, E.; Seman, M.; Ebringer, L. The diversity of eukaryotic microbiota in the traditional Slovak sheep cheese-bryndza. Int. J. Food Microbiol. 2008, 127, 176–179. [Google Scholar] [CrossRef]
  107. Flórez, A.B.; Álvarez-Martín, P.; López-Díaz, T.M.; Mayo, B. Microbiological characterisation of the traditional Spanish blue-veined Cabrales cheese: Identification of dominant lactic acid bacteria. Eur. Food Res. Technol. 2006, 223, 503–508. [Google Scholar] [CrossRef]
  108. Pangallo, D.; Saková, N.; Koreňová, J.; Puškárová, A.; Kraková, L.; Valík, L.; Kuchta, T. Microbial diversity and dynamics during the production of May bryndza cheese. Int. J. Food Microbiol. 2014, 170, 38–43. [Google Scholar] [CrossRef]
  109. De Pasquale, I.; Calasso, M.; Mancini, L.; Ercolini, D.; La Storia, A.; De Angelis, M.; Di Cagno, R.; Gobbetti, M. Causal relationship between microbial ecology dynamics and proteolysis during manufacture and ripening of protected designation of origin (PDO) cheese Canestrato Pugliese. Appl. Environ. Microbiol. 2014, 80, 4085–4094. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  110. Afshari, R.; Pillidge, C.J.; Read, E.; Rochfort, S.; Dias, D.A.; Osborn, A.M.; Gill, H. New insights into cheddar cheese microbiota-metabolome relationships revealed by integrative analysis of multi-omics data. Sci. Rep. 2020, 10, 3164. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  111. Salazar, J.K.; Carstens, C.K.; Ramachandran, P.; Shazer, A.G.; Narula, S.S.; Reed, E.; Ottesen, A.; Schill, K.M. Metagenomics of pasteurized and unpasteurized Gouda cheese using targeted 16S rDNA sequencing. BMC Microbiol. 2018, 18, 189. [Google Scholar] [CrossRef] [PubMed]
  112. Ceugniez, A.; Taminiau, B.; Coucheney, F.; Jacques, P.; Delcenserie, V.; Daube, G.; Drider, D. Fungal diversity of “Tomme d’Orchies” cheese during the ripening process as revealed by a metagenomic study. Int. J. Food Microbiol. 2017, 258, 89–93. [Google Scholar] [CrossRef] [Green Version]
  113. Ceugniez, A.; Drider, D.; Jacques, P.; Coucheney, F. Yeast diversity in a traditional French cheese “Tomme d’orchies” reveals infrequent and frequent species with associated benefits. Food Microbiol. 2015, 52, 177–184. [Google Scholar] [CrossRef]
  114. Bodinaku, I.; Shaffer, J.; Connors, A.B.; Steenwyk, J.L.; Biango-Daniels, M.N.; Kastman, E.K.; Rokas, A.; Robbat, A.; Wolfe, B.E. Rapid phenotypic and metabolomic domestication of wild Penicillium molds on cheese. mBio 2019, 10, e02445-19. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  115. Laroute, V.; Tormo, H.; Couderc, C.; Mercier-Bonin, M.; Le Bourgeois, P.; Cocaign-Bousquet, M.; Daveran-Mingot, M.L. From genome to phenotype: An integrative approach to evaluate the biodiversity of Lactococcus lactis. Microorganisms 2017, 5, 27. [Google Scholar] [CrossRef] [PubMed]
  116. Cavanagh, D.; Fitzgerald, G.F.; McAuliffe, O. From field to fermentation: The origins of Lactococcus lactis and its domestication to the dairy environment. Food Microbiol. 2015, 47, 45–61. [Google Scholar] [CrossRef] [PubMed]
  117. Douglas, G.L.; Klaenhammer, T.R. Genomic evolution of domesticated microorganisms. Annu. Rev. Food Sci. Technol. 2010, 1, 397–414. [Google Scholar] [CrossRef] [PubMed]
  118. Zheng, X.; Liu, F.; Shi, X.; Wang, B.; Li, K.; Li, B.; Zhuge, B. Dynamic correlations between microbiota succession and flavor development involved in the ripening of Kazak artisanal cheese. Food Res. Int. 2018, 105, 733–742. [Google Scholar] [CrossRef]
  119. Flórez, A.B.; Álvarez-Martín, P.; López-Díaz, T.M.; Mayo, B. Morphotypic and molecular identification of filamentous fungi from Spanish blue-veined Cabrales cheese and technological characterisation of Penicillium roqueforti and Geotrichum candidum strains. Int. Dairy J. 2007, 17, 350–357. [Google Scholar] [CrossRef]
  120. Guzzon, R.; Carafa, I.; Tuohy, K.; Cervantes, G.; Vernetti, L.; Barmaz, A.; Larcher, R.; Franciosi, E. Exploring the microbiota of the red-brown defect in smear-ripened cheese by 454-pyrosequencing and its prevention using different cleaning systems. Food Microbiol. 2017, 62, 160–168. [Google Scholar] [CrossRef] [PubMed]
  121. Bassi, D.; Puglisi, E.; Cocconcelli, P.S. Understanding the bacterial communities of hard cheese with blowing defect. Food Microbiol. 2015, 52, 106–118. [Google Scholar] [CrossRef] [PubMed]
  122. Agarwal, S.; Sharma, K.; Swanson, B.G.; Yüksel, G.U.; Clark, S. Nonstarter lactic acid bacteria biofilms and calcium lactate crystals in Cheddar cheese. J. Dairy Sci. 2006, 89, 1452–1466. [Google Scholar] [CrossRef]
  123. Rosengren, A.; Fabricius, A.; Guss, B.; Sylvén, S.; Lindqvist, R. Occurrence of foodborne pathogens and characterization of Staphylococcus aureus in cheese produced on farm-dairies. Int. J. Food Microbiol. 2010, 144, 263–269. [Google Scholar] [CrossRef] [PubMed]
  124. Linares, D.M.; Del Río, B.; Ladero, V.; Martínez, N.; Fernández, M.; Martín, M.C.; Alvarez, M.A. Factors influencing biogenic amines accumulation in dairy products. Front. Microbiol. 2012, 3, 180. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  125. Thommes, M.; Wang, T.; Zhao, Q.; Paschalidis, I.C.; Segrè, D. Designing metabolic division of labor in microbial communities. mSystems 2019, 4, e00263-18. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  126. Embree, M.; Liu, J.K.; Al-Bassam, M.M.; Zengler, K. Networks of energetic and metabolic interactions define dynamics in microbial communities. Proc. Natl. Acad. Sci. USA 2015, 112, 15450–15455. [Google Scholar] [CrossRef] [Green Version]
  127. O’Connor, P.M.; Kuniyoshi, T.M.; Oliveira, R.P.; Hill, C.; Ross, R.P.; Cotter, P.D. Antimicrobials for food and feed; a bacteriocin perspective. Curr. Opin. Biotechnol. 2020, 61, 160–167. [Google Scholar] [CrossRef] [PubMed]
  128. Leyva Salas, M.; Mounier, J.; Maillard, M.B.; Valence, F.; Coton, E.; Thierry, A. Identification and quantification of natural compounds produced by antifungal bioprotective cultures in dairy products. Food Chem. 2019, 301, 125260. [Google Scholar] [CrossRef] [PubMed]
  129. Silva, C.C.G.; Silva, S.P.M.; Ribeiro, S.C. Application of bacteriocins and protective cultures in dairy food preservation. Front. Microbiol. 2018, 9, 594. [Google Scholar] [CrossRef] [PubMed]
  130. Baran, R.; Brodie, E.L.; Mayberry-Lewis, J.; Hummel, E.; Da Rocha, U.N.; Chakraborty, R.; Bowen, B.P.; Karaoz, U.; Cadillo-Quiroz, H.; Garcia-Pichel, F. Exometabolite niche partitioning among sympatric soil bacteria. Nat. Commun. 2015, 6, 8289. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  131. Koropatkin, N.M.; Cameron, E.A.; Martens, E.C. How glycan metabolism shapes the human gut microbiota. Nat. Rev. Microbiol. 2012, 10, 323–335. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  132. Mahony, J.; McDonnell, B.; Casey, E.; van Sinderen, D. Phage-host interactions of cheese-making lactic acid bacteria. Annu. Rev. Food Sci. Technol. 2016, 7, 267–285. [Google Scholar] [CrossRef]
  133. Erkus, O.; de Jager, V.C.L.; Spus, M.; van Alen-Boerritger, I.J.; van Rijswijck, I.M.H.; Hazelwood, L.; Janssen, P.W.M.; van Hijum, S.A.F.T.; Kleerebezem, M.; Smid, E.J. Multifactorial diversity sustains microbial community stability. ISME J. 2013, 7, 2126–2136. [Google Scholar] [CrossRef] [PubMed]
  134. Rodríguez-Valera, F.; Martín-Cuadrado, A.B.; Rodríguez-Brito, B.; Pasic, L.; Thingstad, T.F.; Rohwer, F.; Mira, A. Explaining microbial population genomics through phage predation. Nat. Rev. Microbiol. 2009, 7, 828–836. [Google Scholar] [CrossRef] [PubMed]
  135. Braga, R.M.; Dourado, M.N.; Araújo, W.L. Microbial interactions: Ecology in a molecular perspective. Braz. J. Microbiol. 2016, 47, 86–98. [Google Scholar] [CrossRef] [Green Version]
  136. Pacheco, A.R.; Segrè, D. A multidimensional perspective on microbial interactions. FEMS Microbiol. Lett. 2019, 366, fnz125. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  137. Smid, E.J.; Lacroix, C. Microbe-microbe interactions in mixed culture food fermentations. Curr. Opin. Biotechnol. 2013, 24, 148–154. [Google Scholar] [CrossRef] [PubMed]
  138. Irlinger, F.; Mounier, J. Microbial interactions in cheese: Implications for cheese quality and safety. Curr. Opin. Biotechnol. 2009, 20, 142–148. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  139. Mounier, J.; Monnet, C.; Vallaeys, T.; Arditi, R.; Sarthou, A.S.; Hélias, A.; Irlinger, F. Microbial interactions within a cheese microbial community. Appl. Environ. Microbiol. 2008, 74, 172–181. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  140. Sieuwerts, S.; de Bok, F.A.; Hugenholtz, J.; van Hylckama Vlieg, J.E. Unraveling microbial interactions in food fermentations: From classical to genomics approaches. Appl. Environ. Microbiol. 2008, 74, 4997–5007. [Google Scholar] [CrossRef] [Green Version]
  141. Iskandar, C.F.; Cailliez-Grimal, C.; Borges, F.; Revol-Junelles, A.M. Review of lactose and galactose metabolism in Lactic Acid Bacteria dedicated to expert genomic annotation. Trends Food Sci. Technol. 2019, 88, 121–132. [Google Scholar] [CrossRef]
  142. Upadhyay, V.K.; McSweeney, P.L.H.; Magboul, A.A.A.; Fox, P.F. Proteolysis in cheese during ripening. In Cheese Chemistry, Physics and Microbiology; Fox, P.F., McSweeney, P.L.H., Cogan, T.M., Guinee, T.P., Eds.; Elsevier Academic Press: London, UK, 2004; Volume 1, pp. 391–434. [Google Scholar]
  143. Liu, M.; Bayjanov, J.R.; Renckens, B.; Nauta, A.; Siezen, R.J. The proteolytic system of lactic acid bacteria revisited: A genomic comparison. BMC Genom. 2010, 11, 36. [Google Scholar] [CrossRef] [Green Version]
  144. Noordman, W.H.; Reissbrodt, R.; Bongers, R.S.; Rademaker, J.L.W.; Bockelmann, W.; Smit, G. Growth stimulation of Brevibacterium sp. by siderophores. J. Appl. Microbiol. 2006, 101, 637–646. [Google Scholar] [CrossRef]
  145. Özcan, E.; Seven, M.; Şirin, B.; Çakır, T.; Nikerel, E.; Teusink, B.; Toksoy Öner, E. Dynamic co-culture metabolic models reveal the fermentation dynamics, metabolic capacities and interplays of cheese starter cultures. Biotechnol. Bioeng. 2020, 1–15. [Google Scholar] [CrossRef]
  146. Monnet, C.; Back, A.; Irlinger, F. Growth of aerobic ripening bacteria at the cheese surface is limited by the availability of iron. Appl. Environ. Microbiol. 2012, 78, 3185–3192. [Google Scholar] [CrossRef] [Green Version]
  147. Schnürer, J.; Magnusson, J. Antifungal lactic acid bacteria as biopreservatives. Trends Food Sci. Technol. 2005, 16, 70–78. [Google Scholar] [CrossRef]
  148. Arqués, J.L.; Rodríguez, E.; Langa, S.; Landete, J.M.; Medina, M. Antimicrobial activity of lactic acid bacteria in dairy products and gut: Effect on pathogens. Biomed. Res. Int. 2015, 2015, 584183. [Google Scholar] [CrossRef] [PubMed]
  149. Garnier, L.; Mounier, J.; Lê, S.; Pawtowski, A.; Pinon, N.; Camier, B.; Chatel, M.; Garric, G.; Thierry, A.; Coton, E.; et al. Development of antifungal ingredients for dairy products: From in vitro screening to pilot scale application. Food Microbiol. 2019, 81, 97–107. [Google Scholar] [CrossRef] [PubMed]
  150. Martinez, R.C.; Staliano, C.D.; Vieira, A.D.; Villarreal, M.L.; Todorov, S.D.; Saad, S.M.; Franco, B.D. Bacteriocin production and inhibition of Listeria monocytogenes by Lactobacillus sakei subsp. sakei 2a in a potentially synbiotic cheese spread. Food Microbiol. 2015, 48, 143–152. [Google Scholar] [CrossRef]
  151. Imran, M.; Bré, J.M.; Vernoux, J.P.; Desmasures, N. Reduced growth of Listeria monocytogenes is not associated with individual microbial strains. Food Microbiol. 2013, 33, 30–39. [Google Scholar] [CrossRef]
  152. Loessner, M.; Guenther, S.; Steffan, S.; Scherer, S. A pediocin-producing Lactobacillus plantarum strain inhibits Listeria monocytogenes in a multispecies cheese surface microbial ripening consortium. Appl. Environ. Microbiol. 2003, 69, 1854–1857. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  153. McAuliffe, O.; Hill, C.; Ross, R.P. Inhibition of Listeria monocytogenes in cottage cheese manufactured with a lacticin 3147-producing starter culture. J. Appl. Microbiol. 1999, 86, 251–256. [Google Scholar] [CrossRef]
  154. Ennahar, S.; Assobhel, O.; Hasselmann, C. Inhibition of Listeria monocytogenes in a smear-surface soft cheese by Lactobacillus plantarum WHE 92, a pediocin AcH producer. J. Food Prot. 1998, 61, 186–191. [Google Scholar] [CrossRef] [PubMed]
  155. Núñez, M.; Rodríguez, J.L.; García, E.; Gaya, P.; Medina, M. Inhibition of Listeria monocytogenes by enterocin 4 during the manufacture and ripening of Manchego cheese. J. Appl. Microbiol. 1997, 83, 671–677. [Google Scholar] [CrossRef] [PubMed]
  156. Wan, J.; Harmark, K.; Davidson, B.E.; Hillier, A.J.; Gordon, J.B.; Wilcock, A.; Hickey, M.W.; Coventry, M.J. Inhibition of Listeria monocytogenes by piscicolin 126 in milk and Camembert cheese manufactured with a thermophilic starter. J. Appl. Microbiol. 1997, 82, 273–280. [Google Scholar] [CrossRef] [PubMed]
  157. Delbès-Paus, C.; Dorchies, G.; Chaabna, Z.; Callon, C.; Montel, M.C. Contribution of hydrogen peroxide to the inhibition of Staphylococcus aureus by Lactococcus garvieae in interaction with raw milk microbial community. Food Microbiol. 2010, 27, 924–932. [Google Scholar] [CrossRef] [PubMed]
  158. Rilla, N.; Martínez, B.; Rodríguez, A. Inhibition of a methicillin-resistant Staphylococcus aureus strain in Afuega’l Pitu cheese by the nisin Z-producing strain Lactococcus lactis subsp. lactis IPLA 729. J. Food Prot. 2004, 67, 928–933. [Google Scholar] [CrossRef] [PubMed]
  159. Ferrari Ida, S.; de Souza, J.V.; Ramos, C.L.; da Costa, M.M.; Schwan, R.F.; Dias, F.S. Selection of autochthonous lactic acid bacteria from goat dairies and their addition to evaluate the inhibition of Salmonella typhi in artisanal cheese. Food Microbiol. 2016, 60, 29–38. [Google Scholar] [CrossRef] [PubMed]
  160. Garde, S.; Ávila, M.; Arias, R.; Gaya, P.; Núñez, M. Outgrowth inhibition of Clostridium beijerinckii spores by a bacteriocin-producing lactic culture in ovine milk cheese. Int. J. Food Microbiol. 2011, 150, 59–65. [Google Scholar] [CrossRef] [PubMed]
  161. Mathot, A.G.; Beliard, E.; Thuault, D. Streptococcus thermophilus 580 produces a bacteriocin potentially suitable for inhibition of Clostridium tyrobutyricum in hard cheese. J. Dairy Sci. 2003, 86, 3068–3074. [Google Scholar] [CrossRef]
  162. Rilla, N.; Martínez, B.; Delgado, T.; Rodríguez, A. Inhibition of Clostridium tyrobutyricum in Vidiago cheese by Lactococcus lactis ssp. lactis IPLA 729, a nisin Z producer. Int. J. Food Microbiol. 2003, 85, 23–33. [Google Scholar] [CrossRef]
  163. Bassi, D.; Gazzola, S.; Sattin, E.; Dal Bello, F.; Simionati, B.; Cocconcelli, P.S. Lactic acid bacteria adjunct cultures exert a mitigation effect against spoilage microbiota in fresh cheese. Microorganisms 2020, 8, 1199. [Google Scholar] [CrossRef]
  164. Murado, M.A.; Vazquez, J.A. Biphasic toxicodynamic features of some antimicrobial agents on microbial growth: A dynamic mathematical model and its implications on hormesis. BMC Microbiol. 2010, 10, 220. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  165. Davies, J. Are antibiotics naturally antibiotics? J. Ind. Microbiol. Biotechnol. 2006, 33, 496–499. [Google Scholar] [CrossRef] [PubMed]
  166. Herve-Jimenez, L.; Guillouard, I.; Guedon, E.; Boudebbouze, S.; Hols, P.; Monnet, V.; Maguin, E.; Rul, F. Postgenomic analysis of Streptococcus thermophilus cocultivated in milk with Lactobacillus delbrueckii subsp. bulgaricus: Involvement of nitrogen, purine, and iron metabolism. Appl. Environ. Microbiol. 2009, 75, 2062–2073. [Google Scholar] [CrossRef] [Green Version]
  167. Callon, C.; Saubusse, M.; Didienne, R.; Buchin, S.; Montel, M.C. Simplification of a complex microbial antilisterial consortium to evaluate the contribution of its flora in uncooked pressed cheese. Int. J. Food Microbiol. 2011, 145, 379–389. [Google Scholar] [CrossRef] [Green Version]
  168. Bleicher, A.; Stark, T.; Hofmann, T.; Bogovic Matijasić, B.; Rogelj, I.; Scherer, S.; Neuhaus, K. Potent antilisterial cell-free supernatants produced by complex red-smear cheese microbial consortia. J. Dairy Sci. 2010, 93, 4497–4505. [Google Scholar] [CrossRef] [PubMed]
  169. Imran, M.; Desmasures, N.; Vernoux, J.P. From undefined red smear cheese consortia to minimal model communities both exhibiting similar anti-listerial activity on a cheese-like matrix. Food Microbiol. 2010, 27, 1095–1103. [Google Scholar] [CrossRef] [PubMed]
  170. Monnet, C.; Bleicher, A.; Neuhaus, K.; Sarthou, A.S.; Leclercq-Perlat, M.N.; Irlinger, F. Assessment of the anti-listerial activity of microfloras from the surface of smear-ripened cheeses. Food Microbiol. 2010, 27, 302–310. [Google Scholar] [CrossRef] [PubMed]
  171. Maoz, A.; Mayr, R.; Scherer, S. Temporal stability and biodiversity of two complex antilisterial cheese-ripening microbial consortia. Appl. Environ. Microbiol. 2003, 69, 4012–4018. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  172. Liu, S.Q.; Tsao, M. Inhibition of spoilage yeasts in cheese by killer yeast Williopsis saturnus var. saturnus. Int. J. Food Microbiol. 2009, 131, 280–282. [Google Scholar] [CrossRef] [PubMed]
  173. Malek, R.; Bonnarme, P.; Irlinger, F.; Frey-Klett, P.; Onésime, D.; Aubert, J.; Loux, V.; Beckerich, J.M. Transcriptomic response of Debaryomyces hansenii during mixed culture in a liquid model cheese medium with Yarrowia lipolytica. Int. J. Food Microbiol. 2018, 264, 53–62. [Google Scholar] [CrossRef] [PubMed]
  174. Senaka Ranadheera, C.; Evans, C.A.; Adams, M.C.; Baines. S.K. Probiotic viability and physico-chemical and sensory properties of plain and stirred fruit yogurts made from goat’s milk. Food Chem. 2012, 135, 1411–1418. [Google Scholar] [CrossRef] [PubMed]
  175. Juillard, V.; Richard, J. Indirect interaction in milk between proteolytic and isogenic nonproteolytic strains of Lactococcus lactis. II. Effect of pre-culturing by a proteolytic strain. Lait 1991, 71, 55–64. [Google Scholar] [CrossRef] [Green Version]
  176. Baer, A.; Ryba, I. Influence of casein proteolysis by starter bacteria, rennet and plasmin on the growth of propionibacteria in Swiss-type cheese. Lait 1995, 75, 391–400. [Google Scholar] [CrossRef] [Green Version]
  177. Sudun, W.; Arakawa, K.; Miyamoto, M.; Miyamoto, T. Interaction between lactic acid bacteria and yeasts in airag, an alcoholic fermented milk. Anim. Sci. J. 2013, 84, 66–74. [Google Scholar] [CrossRef]
  178. Álvarez-Martín, P.; Flórez, A.B.; Hernández-Barranco, A.; Mayo, B. Interaction between dairy yeasts and lactic acid bacteria strains during milk fermentation. Food Control 2008, 1, 62–70. [Google Scholar] [CrossRef]
  179. Ruiz-Barba, J.L.; Jiménez-Díaz, R. Availability of essential B-group vitamins to Lactobacillus plantarum in green olive fermentation brines. Appl. Environ. Microbiol. 1995, 61, 1294–1297. [Google Scholar] [CrossRef] [Green Version]
  180. De Freitas, I.; Pinon, N.; Maubois, J.L.; Lortal, S.; Thierry, A. The addition of a cocktail of yeasts species to Cantalet cheese changes bacterial survival and enhances aroma compound formation. Int. J. Food Microbiol. 2009, 129, 37–42. [Google Scholar] [CrossRef]
  181. Leclercq-Perlat, M.N.; Corrieu, G.; Spinnler, H.E. The color of Brevibacterium linens depends on the yeast used for cheese deacidification. J. Dairy Sci. 2004, 87, 1536–1544. [Google Scholar] [CrossRef]
  182. Sieuwerts, S.; Molenaar, D.; van Hijum, S.A.F.T.; Beerthuyzen, M.; Stevens, M.J.A.; Janssen, P.W.M.; Ingham, C.J.; de Bok, F.A.M.; de Vos, W.M.; van Hylckama Vlieg, J.E.T. Mixed-culture transcriptome analysis reveals the molecular basis of mixed-culture growth in Streptococcus thermophilus and Lactobacillus bulgaricus. Appl. Environ. Microbiol. 2010, 76, 7775–7784. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  183. Yamauchi, R.; Maguin, E.; Horiuchi, H.; Hosokawa, M.; Sasaki, Y. The critical role of urease in yogurt fermentation with various combinations of Streptococcus thermophilus and Lactobacillus delbrueckii ssp. bulgaricus. J. Dairy Sci. 2019, 102, 1033–1043. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  184. Desfossés-Foucault, E.; LaPointe, G.; Roy, D. Transcription profiling of interactions between Lactococcus lactis subsp. cremoris SK11 and Lactobacillus paracasei ATCC 334 during Cheddar cheese simulation. Int. J. Food Microbiol. 2014, 178, 76–86. [Google Scholar] [CrossRef]
  185. Viljoen, B.C. The interaction between yeasts and bacteria in dairy environments. Int. J. Food Microbiol. 2001, 69, 37–44. [Google Scholar] [CrossRef]
  186. van den Tempel, T.; Nielsen, M.S. Effects of atmospheric conditions, NaCl and pH on growth and interactions between moulds and yeasts related to blue cheese production. Int. J. Food Microbiol. 2000, 57, 193–199. [Google Scholar] [CrossRef]
  187. Ponomarova, O.; Gabrielli, N.; Sévin, D.C.; Mülleder, M.; Zirngibl, K.; Bulyha, K.; Andrejev, S.; Kafkia, E.; Typas, A.; Sauer, U.; et al. Yeast creates a niche for symbiotic lactic acid bacteria through nitrogen overflow. Cell Syst. 2017, 5, 345–357. [Google Scholar] [CrossRef] [Green Version]
  188. Castellote, J.; Fraud, S.; Irlinger, F.; Swennen, D.; Fer, F.; Bonnarme, P.; Monnet, C. Investigation of Geotrichum candidum gene expression during the ripening of Reblochon-type cheese by reverse transcription-quantitative PCR. Int. J. Food Microbiol. 2015, 194, 54–61. [Google Scholar] [CrossRef]
  189. Dugat-Bony, E.; Straub, C.; Teissandier, A.; Onésime, D.; Loux, V.; Monnet, C.; Irlinger, F.; Landaud, S.; Leclercq-Perlat, M.N.; Bento, P.; et al. Overview of a surface-ripened cheese community functioning by meta-omics analyses. PLoS ONE 2015, 10, e0124360. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  190. Pham, N.P.; Landaud, S.; Lieben, P.; Bonnarme, P.; Monnet, C. Transcription profiling reveals cooperative metabolic interactions in a microbial cheese-ripening community composed of Debaryomyces hansenii, Brevibacterium aurantiacum, and Hafnia alvei. Front. Microbiol. 2019, 10, 1901. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  191. Mansour, S.; Bailly, J.; Landaud, S.; Monnet, C.; Sarthou, A.S.; Cocaign-Bousquet, M.; Leroy, S.; Irlinger, F.; Bonnarme, P. Investigation of associations of Yarrowia lipolytica, Staphylococcus xylosus, and Lactococcus lactis in culture as a first step in microbial interaction analysis. Appl. Environ. Microbiol. 2009, 75, 6422–6430. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  192. Blaya, J.; Barzideh, Z.; LaPointe, G. Symposium review: Interaction of starter cultures and nonstarter lactic acid bacteria in the cheese environment. J. Dairy Sci. 2018, 101, 3611–3629. [Google Scholar] [CrossRef]
  193. De Pasquale, I.; Di Cagno, R.; Buchin, S.; De Angelis, M.; Gobbetti, M. Microbial ecology dynamics reveal a succession in the core microbiota involved in the ripening of pasta filata Caciocavallo Pugliese cheese. Appl. Environ. Microbiol. 2014, 80, 6243–6255. [Google Scholar] [CrossRef] [Green Version]
  194. Settanni, L.; Moschetti, G. Non-starter lactic acid bacteria used to improve cheese quality and provide health benefits. Food Microbiol. 2010, 27, 691–697. [Google Scholar] [CrossRef] [PubMed]
  195. Rossi, F.; Marzotto, M.; Cremonese, S.; Rizzotti, L.; Torriani, S. Diversity of Streptococcus thermophilus in bacteriocin production; inhibitory spectrum and occurrence of thermophilin genes. Food Microbiol. 2013, 35, 27–33. [Google Scholar] [CrossRef]
  196. Simova, E.D.; Beshkova, D.M.; Angelov, M.P.; Dimitrov, Z.P. Bacteriocin production by strain Lactobacillus delbrueckii ssp. bulgaricus BB18 during continuous prefermentation of yogurt starter culture and subsequent batch coagulation of milk. J. Ind. Microbiol. Biotechnol. 2008, 35, 559–567. [Google Scholar] [CrossRef] [PubMed]
  197. Medlock, G.L.; Carey, M.A.; McDuffie, D.G.; Mundy, M.B.; Giallourou, N.; Swann, J.R.; Kolling, G.L.; Papin, J.A. Inferring metabolic mechanisms of interaction within a defined gut microbiota. Cell Syst. 2018, 7, 245–257. [Google Scholar] [CrossRef] [Green Version]
  198. De Filippis, F.; Genovese, A.; Ferranti, P.; Gilbert, J.A.; Ercolini, D. Metatranscriptomics reveals temperature-driven functional changes in microbiome impacting cheese maturation rate. Sci. Rep. 2016, 6, 21871. [Google Scholar] [CrossRef] [Green Version]
  199. Fischer, C.N.; Trautman, E.P.; Crawford, J.M.; Stabb, E.V.; Handelsman, J.; Broderick, N.A. Metabolite exchange between microbiome members produces compounds that influence Drosophila behabiour. eLife 2017, 6, e18855. [Google Scholar] [CrossRef]
  200. Acinas, S.G.; Klepac-Ceraj, V.; Hunt, D.E.; Pharino, C.; Ceraj, I.; Distel, D.L.; Polz, M.F. Fine-scale phylogenetic architecture of a complex bacterial community. Nature 2004, 430, 551–554. [Google Scholar] [CrossRef] [PubMed]
  201. Cosetta, C.M.; Wolfe, B.E. Causes and consequences of biotic interactions within microbiomes. Curr. Opin. Microbiol. 2019, 50, 35–41. [Google Scholar] [CrossRef]
  202. O’Donnell, S.T.; Ross, R.P.; Stanton, C. The progress of multi-omics technologies: Determining function in lactic acid bacteria using a systems level approach. Front. Microbiol. 2020, 10, 3084. [Google Scholar] [CrossRef]
  203. Castellanos-Rozo, J.; Pérez Pulido, R.; Grande, M.J.; Lucas, R.; Gálvez, A. Analysis of the bacterial diversity of Paipa cheese (a traditional raw cow’s milk cheese from Colombia) by high-throughput sequencing. Microorganisms 2020, 8, 218. [Google Scholar] [CrossRef] [Green Version]
  204. Gonçalves, M.T.P.; Benito, M.J.; Córdoba, M.G.; Egas, C.; Merchán, A.V.; Galván, A.I.; Ruiz-Moyano, S. Bacterial communities in Serpa cheese by culture dependent techniques, 16S rRNA gene sequencing and high-throughput sequencing analysis. J. Food Sci. 2018, 83, 1333–1341. [Google Scholar] [CrossRef] [PubMed]
  205. Wolfe, B.E.; Button, J.E.; Santarelli, M.; Dutton, R.J. Cheese rind communities provide tractable systems for in situ and in vitro studies of microbial diversity. Cell 2014, 158, 422–433. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  206. Monnet, C.; Dugat-Bony, E.; Swennen, D.; Beckerich, J.M.; Irlinger, F.; Fraud, S.; Bonnarme, P. Investigation of the activity of the microorganisms in a Reblochon-style cheese by metatranscriptomic analysis. Front. Microbiol. 2016, 7, 536. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  207. Valente, N.I.P.; Rudnitskaya, A.; Oliveira, J.A.B.P.; Gaspar, E.M.M.; Gomes, M.T.S.R. Cheeses made from raw and pasteurized cow’s milk analysed by an electronic nose and an electronic tongue. Sensors 2018, 18, 2415. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  208. Zhang, Y.; Kastman, E.K.; Guasto, J.S.; Wolfe, B.E. Fungal networks shape dynamics of bacterial dispersal and community assembly in cheese rind microbiomes. Nat. Commun. 2018, 9, 336. [Google Scholar] [CrossRef] [Green Version]
  209. Kastman, E.K.; Kamelamela, N.; Norville, J.W.; Cosetta, C.M.; Dutton, R.J.; Wolfe, B.E. Biotic interactions shape the ecological distributions of Staphylococcus species. mBio 2016, 7, e01157-16. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  210. Wolfe, B.E. Using cultivated microbial communities to dissect microbiome assembly: Challenges, limitations, and the path ahead. mSystems 2018, 3, e00161-17. [Google Scholar] [CrossRef] [Green Version]
  211. Park, W.; Yoo, J.; Oh, S.; Ham, J.S.; Jeong, S.G.; Kim, Y. Microbiological characteristics of Gouda cheese manufactured with pasteurized and raw milk during ripening using Next Generation Sequencing. Food Sci. Anim. Resour. 2019, 39, 585–600. [Google Scholar] [CrossRef]
  212. Wolfe, B.E.; Dutton, R.J. Towards an ecosystem approach to cheese microbiology. Microbiol. Spectr. 2013, 1, CM0012-2012. [Google Scholar] [CrossRef] [Green Version]
  213. Niccum, B.A.; Kastman, E.K.; Kfoury, N.; Robbat, A., Jr.; Wolfe, B.E. Strain-level diversity impacts cheese rind microbiome assembly and function. mSystems 2020, 5, e00149-20. [Google Scholar] [CrossRef]
  214. Cosetta, C.M.; Kfoury, N.; Robbat, A.; Wolfe, B.E. Fungal volatiles mediate cheese rind microbiome assembly. Environ. Microbiol. 2020, 22, 4745–4760. [Google Scholar] [CrossRef] [PubMed]
  215. Cosetta, C.M.; Wolfe, B.E. Deconstructing and reconstructing cheese rind microbiomes for experiments in Microbial Ecology and Evolution. Curr. Protoc. Microbiol. 2020, 56, e95. [Google Scholar] [CrossRef]
  216. Tveit, A.T.; Urich, T.; Frenzel, P.; Svenning, M.M. Metabolic and trophic interactions modulate methane production by Arctic peat microbiota in response to warming. Proc. Natl. Acad. Sci. USA 2015, 112, E2507–E2516. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  217. Tormo, J.; Barral, J. Accidents de Fromagerie. 2004. Available online: http://www.accident-fromagerie.fr/spip.php (accessed on 20 November 2020).
  218. Le Bars-Bailly, S.; Bailly, J.D.; Brugere, H. Mold-realted failings in cheesemaking. Rev. Med. Vet. 1999, 150, 413–430. [Google Scholar]
  219. Salazar, J.K.; Gonsalves, L.J.; Natarajan, V.; Shazer, A.; Reineke, K.; Mhetras, T.; Sule, C.; Carstens, C.K.; Schill, K.M.; Tortorello, M.L. Population dynamics of Listeria monocytogenes, Escherichia coli O157:H7, and native microflora during manufacture and aging of Gouda cheese made with unpasteurized milk. J. Food Prot. 2020, 21, 266–276. [Google Scholar] [CrossRef]
  220. Daly, D.F.M.; McSweeney, P.L.H.; Sheehan, J.J. Split defect and secondary fermentation in Swiss-type cheeses—A review. Dairy Sci. Technol. 2010, 90, 3–26. [Google Scholar] [CrossRef]
  221. Sattin, E.; Andreani, N.A.; Carraro, L.; Fasolato, L.; Balzan, S.; Novelli, E.; Squartini, A.; Telatin, A.; Simionati, B.; Cardazzo, B. Microbial dynamics during shelf-life of industrial Ricotta cheese and identification of a Bacillus strain as a cause of a pink discolouration. Food Microbiol. 2016, 57, 8–15. [Google Scholar] [CrossRef] [PubMed]
  222. McAuliffe, O.; Kilcawley, K.; Stefanovic, E. Symposium review: Genomic investigations of flavor formation by dairy microbiota. J. Dairy Sci. 2019, 102, 909–922. [Google Scholar] [CrossRef] [Green Version]
  223. Alonso, R.; Picón, A.; Gaya, P.; Núñez, M. Proteolysis, lipolysis, volatile compounds and sensory characteristics of Hispanico cheeses made using frozen curd from raw and pasteurized ewe milk. J. Dairy Res. 2013, 80, 51–57. [Google Scholar] [CrossRef] [PubMed]
  224. Topisirovic, L.; Kojic, M.; Fira, D.; Golic, N.; Strahinic, I.; Lozo, J. Potential of lactic acid bacteria isolated from specific natural niches in food production and preservation. Int. J. Food Microbiol. 2006, 112, 230–235. [Google Scholar] [CrossRef]
  225. Minty, J.J.; Singer, M.E.; Scholz, S.A.; Bae, C.H.; Ahn, J.H.; Foster, C.E.; Liao, J.C.; Lin, X.N. Design and characterization of synthetic fungal-bacterial consortia for direct production of isobutanol from cellulosic biomass. Proc. Natl. Acad. Sci. USA 2013, 110, 14592–14597. [Google Scholar] [CrossRef] [Green Version]
  226. Ben-Harb, S.; Saint-Eve, A.; Panouillé, M.; Souchon, I.; Bonnarme, P.; Dugat-Bony, E.; Irlinger, F. Design of microbial consortia for the fermentation of pea-protein-enriched emulsions. Int. J. Food Microbiol. 2019, 293, 124–136. [Google Scholar] [CrossRef]
  227. Hu, J.; Wei, Z.; Friman, V.P.; Gu, S.H.; Wang, X.F.; Eisenhauer, N.; Yang, T.J.; Ma, J.; Shen, Q.R.; Xu, Y.C.; et al. Probiotic diversity enhances rhizosphere microbiome function and plant disease suppression. mBio 2016, 7pii, e01790-16. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  228. Vázquez-Castellanos, J.F.; Biclot, A.; Vrancken, G.; Huys, G.R.; Raes, J. Design of synthetic microbial consortia for gut microbiota modulation. Curr. Opin. Pharmacol. 2019, 49, 52–59. [Google Scholar] [CrossRef] [PubMed]
  229. Carriço, J.A.; Rossi, M.; Moran-Gilad, J.; van Domselaar, G.; Ramirez, M. A primer on microbial bioinformatics for nonbioinformaticians. Clin. Microbiol. Infect. 2018, 24, 342–349. [Google Scholar] [CrossRef] [Green Version]
  230. Mataragas, M.; Alessandria, V.; Ferrocino, I.; Rantsiou, K.; Cocolin, L. A bioinformatics pipeline integrating predictive metagenomics profiling for the analysis of 16S rDNA/rRNA sequencing data originated from foods. Food Microbiol. 2018, 76, 279–286. [Google Scholar] [CrossRef] [PubMed]
  231. Parente, E.; Cocolin, L.; De Filippis, F.; Zotta, T.; Ferrocino, I.; O’Sullivan, O.; Neviani, E.; De Angelis, M.; Cotter, P.D.; Ercolini, D. FoodMicrobionet: A database for the visualisation and exploration of food bacterial communities based on network analysis. Int. J. Food Microbiol. 2016, 219, 28–37. [Google Scholar] [CrossRef] [PubMed]
  232. Bockelmann, W. Secondary cheese starter cultures. In Technology of Cheesemaking; Law, B.A., Tamime, A.Y., Eds.; Wiley-Blackwell: Oxford, UK, 2010; pp. 193–230. [Google Scholar] [CrossRef]
  233. Irlinger, F.; Yung, S.A.; Sarthou, A.S.; Delbès-Paus, C.; Montel, M.C.; Coton, E.; Coton, M.; Helinck, S. Ecological and aromatic impact of two Gram-negative bacteria (Psychrobacter celer and Hafnia alvei) inoculated as part of the whole microbial community of an experimental smear soft cheese. Int. J. Food Microbiol. 2012, 153, 332–338. [Google Scholar] [CrossRef] [PubMed]
  234. Deetae, P.; Mounier, J.; Bonnarme, P.; Spinnler, H.E.; Irlinger, F.; Helinck, S. Effects of Proteus vulgaris growth on the establishment of a cheese microbial community and on the production of volatile aroma compounds in a model cheese. J. Appl. Microbiol. 2009, 107, 1404–1413. [Google Scholar] [CrossRef] [PubMed]
  235. Goerges, S.; Mounier, J.; Rea, M.C.; Gelsomino, R.; Heise, V.; Beduhn, R.; Cogan, T.M.; Vancanneyt, M.; Scherer, S. Commercial ripening starter microorganisms inoculated into cheese milk do not successfully establish themselves in the resident microbial ripening consortia of a South German red smear cheese. Appl. Environ. Microbiol. 2008, 74, 2210–2217. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  236. Feurer, C.; Vallaeys, T.; Corrieu, G.; Irlinger, F. Does smearing inoculum reflect the bacterial composition of the smear at the end of the ripening of a French soft, red-smear cheese? J. Dairy Sci. 2004, 87, 3189–3197. [Google Scholar] [CrossRef]
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Figure 1. Schematic diagram of the cheese manufacturing processes and types of the resulting cheese varieties.
Figure 1. Schematic diagram of the cheese manufacturing processes and types of the resulting cheese varieties.
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Figure 2. Flow chart of different microbial culture-independent molecular methods, including the main steps and final outputs, applied in cheese microbiology.
Figure 2. Flow chart of different microbial culture-independent molecular methods, including the main steps and final outputs, applied in cheese microbiology.
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Figure 3. A succession of the microbial communities of the microbiota at the cheese surface, and ecological processes and environmental biotic and abiotic factors (including technological procedures) that influence microbial colonization, development and activity.
Figure 3. A succession of the microbial communities of the microbiota at the cheese surface, and ecological processes and environmental biotic and abiotic factors (including technological procedures) that influence microbial colonization, development and activity.
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Table
Table 1. Current common species used as “starters” in industrial dairy fermentations.
Table 1. Current common species used as “starters” in industrial dairy fermentations.
Microbial Group/SpeciesCheeseType of StarterMain Role/s
Lactic acid bacteria
Lc. lactis subsp. lactis
Lc. lactis subsp. cremoris		Most cheesesPrimaryAcidification, flavor development
S. thermophilus
Lb. delbrueckii subsp. lactis		Italian and Swiss typesPrimaryAcidification, flavor development
Leuc. mesenteroides subsp. cremoris
Leuc. lactis		Soft and semi-hardSecondary/adjunctFlavor development, CO2 production
Lb. helveticusSemi-hard, hardSecondary/adjunctFlavor development, health benefits
Lb. casei/Lb. paracaseiArtisanalSecondary/adjunctFlavor development
Lb. plantarumArtisanalSecondary/adjunctFlavor development
Propionibacteria
Propionibacterium freudenreichiiSwiss-typeSecondary/ripeningHole formation, flavor development
Other bacteria
Brevibacterium linensSmear-ripenedSecondary/ripeningColor, flavor development
Corynebacterium caseiSmear-ripenedSecondary/ripeningFlavor development
Fungi
P. camembertiWhite moldySecondary/ripeningAspect, texture, and flavor development
P. roquefortiBlue-veinedSecondary/ripening
G. candidumSmear-ripenedSecondary/ripening
Compiled and modified from Fox et al. [39] and Parente and Cogan [40].
Table
Table 2. Non-exhaustive compilation of microbial studies of traditional cheeses, technologies applied, and dominant populations identified or detected.
Table 2. Non-exhaustive compilation of microbial studies of traditional cheeses, technologies applied, and dominant populations identified or detected.
Cheese/Type, Country (Milk Type)TechniqueMicrobial TargetNo. of SpecimensMain Families/Genera/Species (Relative Abundance); Sampling PointReference
Culturing
Bryndza/soft Feta-type, Slovakia (Sheep)CulturingFungi5 speciesGeotrichum candidum > Kluyveromyces marxianus > Pichia fermentans > Candida inconspicua > Trichosporon cutaneumLaurencík et al. [106]
Cabrales/blue-veined, Spain (Cow, sheep, and goat)CulturingLAB15 speciesLc. lactis subsp. lactis > Lb. plantarum > Leuc. mesenteroides > Leuc. citreum > Enterococcus > Lb. paracaseiFlórez et al. [107]
Gubbeen/smear-ripened, Ireland (Cow)CulturingCorynebacteria39 speciesCorynebacterium casei (50.2%) > Corynebacterium mooreparkense (26%) > Microbacterium gubbeenense (12.8%); cheese rindBrennan et al. [48]
May bryndza/soft, Slovakia (Sheep)CulturingBacteria
Fungi		5 species
17 species		Lc. lactis subsp. cremoris > Lc. lactis subsp. lactis > Mannheimia glucosida
G. candidum > Penicillium > Beauveria brongniartii > Alternaria alternata		Pangallo et al. [108]
Rinds of 33 cheeses/smear-ripened, various countries (Cow, sheep, or goat)Culturing, sequencingMicrobes104 bacterial genera, 39 fungal generaStaphylococcus (78%) > Brevibacterium (75%) > Corynebacterium (75%) > Arthrobacter (66%) > Lactococcus (50%) > Enterococcus (41%) > Brachybacterium (38%) > Microbacterium (38%) > Psychrobacter (33%) > Halomonas (31%) > Lactobacillus (25%) > Streptococcus (22%) > Marinilactibacillus (22%) > Pseudoalteromonas (22%) > Agrococcus (19%) > Micrococcus (19%) > Vibrio (19%) > Vagococcus (16%) > Facklamia (16%)
Debaryomyces (86%) > Yarrowia (57%) > Candida (54%) > Geotrichum (49%) > Kluyveromyces (32%) > Pichia (22%) > Penicillium (19%) > Scopulariopsis (8%) > Fusarium (8%)		Irlinger et al. [12]
Scamorza Altamurana/pasta filata, Italy (Cow)CulturingLAB10 speciesLb. delbrueckii > Streptococcus macedonicus > S. thermophilus > Enterococcus durans > Lb. fermentum > Lb. paracaseiBaruzzi et al. [28]
Culturing and molecular methods
Casín/kneaded, Spain (Cow)Culturing
DGGE		Bacteria14 speciesLc. lactis subsp. lactis > Lactococcus garvieae > Staphylococcus saprophyticus > Klebsiella > Lb. plantarumAlegría et al. [25]
Bacteria (V1-V2 16S rDNA)14 OTUsLc. lactis, Streptococcus parauberis, S. thermophilus, Lc. garvieae, Lb. plantarum, Enterobacter, Corynebacterium variabile, Lb. paracasei, Macrococcus caseolyticus
Castelmagno/semi-hard, Italy (Cow)Culturing
PCR-DGGE		LAB
Bacteria (V1 16S rDNA)		11 species
7 OTUs		Lc. lactis subsp. lactis > Lb. plantarum > Lc. paracasei >Enterococcus faecium >E. durans
Lb. plantarum, Lb. kefiranofaciens, Lactobacillus, Lc. lactis, Streptococcus agalactiae, M. caseolyticus		Dolci et al. [44]
Cueva de la Magahá/hard, Spain (Goat)Culturing
PCR-TTGE		Bacteria
Bacteria (V3 16S rDNA)		10 species
8 species		Lb. paracasei > Lb. plantarum > Lb. brevis > Lactobacillus > Enterococcus
Lb. plantarum, Lb. brevis, Lc. Lactis, S. thermophilus, Staphylococcus equorum, Lb. curvatus, Lb. paracasei		Martín-Platero et al. [45]
Grana Padano/hard, Italy (Cow)LH-PCRLAB6 speciesLb. rhamnosus > Lb. paracasei > Lb. delbrueckii > Pediococcus acidilacticiSantarelli et al. [22]
Livarot/smear-ripened, France (Cow)Culturing
Cloning		Bacteria/yeasts
Bacteria (V4 16S rDNA)		8 bacteria, 5 yeasts species
8 species		M. gubbeenense > Leucobacter komagatae > Halomonas; cheese rind
Candida catenulata > Candida intermedia > G. candidum > Geotrichum > Yarrowia lipolytica; cheese rindHalomonas > L. komagatae > M. gubbeenense; cheese rind		Mounier et al. [43]
Nottinghamshire/blue-veined, UK (Cow)Culturing
PCR-DGGE		Bacteria
Bacteria (V3, V4-V5, V6-V8 16S rDNA)		12 species
11 OTUs		Lc. lactis subsp. lactis > E. faecalis > Kokuria > Lactobacillus
Lc. lactis, Lb. plantarum, Staph. equorum		Yunita and Dodd [55]
Ragusano/pasta filata, Italy (Cow)PCR-DGGEBacteria (V6-V8, V1-V3 16S rDNA or rRNA)12 speciesS. thermophilus, Lb. fermentum, Lb. delbrueckii, Lc. lactis, Leuc. mesenteroides, Lb. casei, Enterococcus hirae > E. faecalisRandazzo et al. [61]
Salers/semi-hard, France (Cow)PCR-SSCPBacteria (V2 16S rDNA)9 OTUsE. faecium, Leuconostoc, Enterobacteriaceae, Bacillus thuringiensis, S. thermophilus, Leuc. pseudomesenteroides, Lb. pentosus, Corynebacterium variabilis, Brachybacterium nesterenkoviiDuthoit et al. [66]
Saint Nectaire/smear-ripened, France (Cow)Culturing
SSCP-PCR		Bacteria
Bacteria		21 species
12 OTUs		Lc. lactis > Staphylococcus fleurettii > E. faecalis > S. thermophilus > Marinilactibacillus psychrotolerans > Chryseobacterium > Klebsiella
Lc. lactis, S. thermophilus, Clostridium confusum, Nocardioides dubius, Arthrobacter psychrolactophilus, Enterobacter agglomerans		Delbès et al. [46]
Molecular methods/high throughput sequencing
Artisan cheeses/various, Ireland (Cow, goat, or sheep)PyrosequencingBacteria (V4 16S rDNA)5 phyla
21 genera		Lactococcus (50–90%) > Lactobacillus > Leuconostoc > Pseudomonas > Psychrobacter > Staphylococcus > Arthrobacter > Faecalibacterium; common to 62 cheesesQuigley et al. [76]
Buryatian/soft, Kazakhstan (Cow)PacBio sequencingMicrobes7 phyla, 82 genera, 145 speciesLactococcus (51.46%) > Streptococcus (17.81%) > Pseudomonas (5.48%) > Acetobacter (4.83%) > Klebsiella (3.36%) > Lactobacillus (2.36%) > Acinetobacter (1.84%) > Raoultella (1.63%)Jin et al. [79]
Canestrato Pugliese/hard, Italy (Sheep)PyrosequencingBacteria (V1-V3 16S rDNA)28 generaLactococcus (87.2%) > Lactobacillus (4.8%; mainly Lb. plantarum and Lb. sakei) > Leuconostoc (3.9%)De Pasquale et al. [109]
Cheddar/semi-hard, UK (Cow)Illumina sequencingBacteria (V4 16S rDNA)159 OTUsStreptococcus > Lactococcus > Lactobacillus > Staphylococcus (70%); interiorAfshari et al. [110]
Gouda-like cheese/semi-hard, USA (Cow)Illumina sequencingBacteria (V4 16S rDNA)36 generaBacillaceae > Lactococcus > Lactobacillus > Streptococcus > StaphylococcusSalazar et al. [111]
Cotija/hard, Mexico (Cow)Illumina sequencingMicrobes31 phyla, 574 generaLb. plantarum > Leuc. mesenteroides > Weissella paramesenteroides (>80%)
Aerococcus > Enterococcus > Lactococcus > Staphylococcus (<10%)		Escobar-Zepeda et al. [82]
Grana/hard, Italy (Cow)RT-PCR-DGGE
Pyrosequencing		Bacteria (V1 16S rDNA)
Bacteria (V1-V3 16S rDNA)		16 OTUs
25 genera		Lb. helveticus, Lb. delbrueckii, S. thermophilus, Lb. acidophilus, Lb. rhamnosus, Acetobacter baumanii, Propionibacterium
Lb. helveticus > Propionibacterium > Lb. delbrueckiii > Lb. casei > Lb. rhamnosus > S. thermophilus > Staphylococcus > Lb. brevis		Alessandria et al. [95]
Artisanal cheeses/soft, Kazakhstan (Cow)PacBio sequencingMicrobes14 phyla, 140 genera, 238 speciesLc. lactis (28.93%) > Lb. helveticus (26.43%) > S. thermophilus (12.18%) > Lb. delbrueckii (12.15%)Li et al. [80]
Ocosingo/semi-hard, Mexico (Cow)PyrosequencingBacteria (V1 16S rDNA)162 OTUsS. thermophilus > Lc. lactis > Lb. helveticus > Lb. delbrueckii > Lb. plantarum (70%); interiorAldrete-Tapia et al. [17]
Tomme d’Orchies/semi-hard, France (Cow)Illumina sequencingBacteria (V1-V3 16S rDNA)10 species core, 21 species surfaceLactococcuss > Streptococcus (66%); interior
Lactobacillus > Lactococcus > Corynebacterium > Micrococcales > Psychrobacter (80%); surface		Ceugniez et al. [83]
Tomme d’Orchies/semi-hard, France (Cow)Illumina sequencingFungi 5.8S-ITS230 OTUsY. lipolytica > G. candidum/Galactomyces geotrichum (99%); interior
Y. lipolytica > G. candidum/Galactomyces geotrichum (98%); surface		Ceugniez et al. [112]
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Mayo, B.; Rodríguez, J.; Vázquez, L.; Flórez, A.B. Microbial Interactions within the Cheese Ecosystem and Their Application to Improve Quality and Safety. Foods 2021, 10, 602. https://doi.org/10.3390/foods10030602

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Mayo B, Rodríguez J, Vázquez L, Flórez AB. Microbial Interactions within the Cheese Ecosystem and Their Application to Improve Quality and Safety. Foods. 2021; 10(3):602. https://doi.org/10.3390/foods10030602

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Mayo, Baltasar, Javier Rodríguez, Lucía Vázquez, and Ana Belén Flórez. 2021. "Microbial Interactions within the Cheese Ecosystem and Their Application to Improve Quality and Safety" Foods 10, no. 3: 602. https://doi.org/10.3390/foods10030602

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