Presence of Listeria monocytogenes in Ready-to-Eat Artisanal Chilean Foods

Ready-to-eat (RTE) artisanal foods are very popular, but they can be contaminated by Listeria monocytogenes. The aim was to determine the presence of L. monocytogenes in artisanal RTE foods and evaluate its food safety risk. We analyzed 400 RTE artisanal food samples requiring minimal (fresh products manufactured by a primary producer) or moderate processing (culinary products for sale from the home, restaurants such as small cafés, or on the street). Listeria monocytogenes was isolated according to the ISO 11290-1:2017 standard, detected with VIDAS equipment, and identified by real-time polymerase chain reaction (PCR). A small subset (n = 8) of the strains were further characterized for evaluation. The antibiotic resistance profile was determined by the CLSI methodology, and the virulence genes hlyA, prfA, and inlA were detected by PCR. Genotyping was performed by pulsed-field gel electrophoresis (PFGE). Listeria monocytogenes was detected in 7.5% of RTE artisanal foods. On the basis of food type, positivity in minimally processed artisanal foods was 11.6%, significantly different from moderately processed foods with 6.2% positivity (p > 0.05). All the L. monocytogenes strains (n = 8) amplified the three virulence genes, while six strains exhibited premature stop codons (PMSC) in the inlA gene; two strains were resistant to ampicillin and one strain was resistant to sulfamethoxazole-trimethoprim. Seven strains were 1/2a serotype and one was a 4b strain. The sampled RTE artisanal foods did not meet the microbiological criteria for L. monocytogenes according to the Chilean Food Sanitary Regulations. The presence of virulence factors and antibiotic-resistant strains make the consumption of RTE artisanal foods a risk for the hypersensitive population that consumes them.


Introduction
Foodborne diseases are a major public health problem worldwide. The y have an impact on consumer health and the economies of importing countries [1]. The incidence of foodborne diseases has been increasing because of factors such as changes in industrial production, food globalization, new economic treaties, and more recently, the need to consume fresher, healthier, and ready-to-eat

Sampling
A total of 400 samples of artisanal foods (with minimal and moderate processing) were analyzed because they were considered to be at risk by the health authority. Minimally processed foods are home-produced and moderately processed foods originate in family-owned shops with good manufacturing practices (GMP). Samples included cheeses (n = 90), cooked meats (artisanal ham, pâté, sausages, blood sausages) (n = 235), pre-processed fruit and vegetables (chopped fruit, fruit salads with strawberries, melon, and peaches, and leafy vegetable salads) (n = 35), meals and mixed dishes with raw and/or cooked ingredients (n = 40) sampled as part of the Emerging Pathogens Program of the Chilean Health Authority.

Isolation and Enumeration of Listeria monocytogenes
Isolation was performed according to the ISO 11290-1:2017 method with two-stage enrichment. First, 25 g of each food sample was inoculated in 225 mL half Fraser broth (Basingstoke, Oxoid, UK) for initial selective enrichment and homogenized in a stomacher (Seward 400, Radnor, PA, USA). Incubation followed at 30 ± 1 • C for 25 ± 1 h and 0.1 mL of the broth culture was inoculated in 10 mL of full-strength Fraser broth for the second enrichment, which was cultured at 37 • C for 24 ± 2 h. A loopful (1 mL) of each of the half-and full-strength Fraser broths were plated on the chromogenic Listeria agar Ottaviani and Agosti (ALOA agar) (Merck, Darmstadt, Germany). The plates were incubated at 37 • C for 24 to 48 h. Five typical colonies from each ALOA agar were restreaked on tryptic soy agar supplemented with 0.6% yeast extract (TSA-YE) (Sigma, Darmstadt, Germany) as a nonselective medium and incubated at 37 • C for 24 to 48 h. The colonies from TSA-YE were verified by Gram staining, catalase reactions, oxidase tests, carbohydrate utilization, CAMP tests, and motility at 20 to 25 • C. Listeria monocytogenes was enumerated in the samples according to the methodology described in the ISO 11,290-2:2017 Microbiology of the food chain standard-Horizontal method for the detection and enumeration of L. monocytogenes and Listeria spp.-Part 2: Enumeration method [17,18].

Detection of Listeria monocytogenes
After the incubation period, described in the previous point, an immunoenzymatic assay was performed with the VIDAS L. monocytogenes equipment (Vitek Immunodiagnostic Assay System, bioMerieux Vitek Inc., Hazelwood, MO, USA) according to the manufacturer's instructions. Measurement and interpretation were automatically performed by the equipment, reporting the detection as positive or negative according to the validated AOAC (Official Method of Analysis N • 2004.2) protocol for food matrices.

Phenotypic Identification of Listeria monocytogenes
Phenotypic identifcation was performed using the API Listeria gallery (bioMérieux, Marcy-l'Étoile, France) according to the manufacturer's instructions. It was incubabed at 35 ± 1 • C for 24 h. The resulting numerical profile was evaluated with the APIWEB program provided by the manufacturer. Listeria monocytogenes ATCC 35152 was used as a control.

Molecular Identification of Listeria monocytogenes
The genomic DNA of the suspected strains was extracted and purified with an UltraClean Microbial DNA Isolation Kit (Mo Bio Laboratories, Qiagen, Carlsbad, CA, USA). Strains were confirmed as L. monocytogenes by hlyA gene amplification [19] with the Stratagene Mx3000P real-time PCR System equipment (Agilent Technologies, Santa Clara, CA, USA) using the commercial Brilliant II SYBR Green QRT-PCR Master Mix [20] (Agilent Technologies, Santa Clara, CA, USA). Amplified products were sent for sequencing to Macrogen, Korea. The y were then analyzed with the Gentle software and assembled with PRABI-Doua (France). The free BLASTn (NCBI) database was used to identify the strains.

Antibiotic Resistance Profile
The disc diffusion method was applied based on the recommendations by the Clinical and Laboratory Standards Institute [21]. The commercial antibiotic discs consisted of 10 µg ampicillin, 10 µg penicillin, 25 µg sulfamethoxazole-trimethoprim, 15 µg erythromycin, 30 µg vancomycin, and 30 µg chloramphenicol. The strain resistance/susceptibility profiles were characterized by measuring the inhibition zone and interpreting inhibition diameters according to the manufacturer's instructions and using S. pneumoniae ATCC 49619 as a reference microorganism of the CLSI guideline. In addition, Escherichia coli ATCC 25922 and L. monocytogenes ATCC 7644 were used as controls.

Detection of Virulence Genes
The method described by Aznar and Alarcón [22] was used to amplify conserved regions of three characteristic virulence genes, that is, listeriolysin O (hlyA), positive regulatory factor A (prfA), and internalin A (inlA) ( Table 1). The genomic DNA of the suspected strains was extracted and purified with the UltraClean Microbial DNA Isolation Kit (Mo Bio Laboratories, Qiagen, Carlsbad, CA, USA) and mixed with GoTaq Green Master Mix (Promega, Madison, WI, USA) in a thermocycler (Fermelo Biotec, People's Republic of China). The amplified products of each gene were sent for sequencing to Macrogen, Korea. The y were then analyzed with the Gentle software and assembled with PRABI-Doua (France). The L. monocytogenes strain ATCC 19115 was used as the positive control, while the L. innocua ATCC 33090 strain was used as the negative control. The amplified products were sent for sequencing to Macrogen, Korea. Sequences were assembled with the Gentle software and aligned with ClustaW. The consensus sequences were compared with the BLAST database available at https://BLAST.ncbi.nlm.nih.gov/BLAST.cgi.

Serotype and Sequence Type (ST) of Listeria monocytogenes
The L. monocytogenes strains were sequenced at the Institute of Medical Microbiology and Hygiene AGES-Austrian Agency for Health and Food Safety, Austria. This information allowed us to determine the serotypes by the extraction of specific sequence targets of the genome [26] using the L. monocytogenes 5-plex PCR Serogroup task templates of the SeqSphere+ v. 7.2.0 (2020-7) software with fragments from five DNA regions (lmo118, lmo0737, ORF2110, ORF2829, and prs as an internal amplification control) according to the description by Doumith et al. [27] and Lee et al. [28].
The STs were determined from whole-genome sequencing (WGS) with Task templates for available MLST schemes from the SeqSphere+ v. 7.2.0 (2020-7) software; the ST was determined in the isolates with fragments from the seven housekeeping genes abcZ, bglA, cat, dapE, dat, Idh, and ihkA [29,30] and with the profiles of the Institut Pasteur MLST Listeria database (http://bigsdb.pasteur.fr/Listeria/Listeria.html).

Pulsed-Field Gel Electrophoresis (PFGE)
Pulsed-field gel electrophoresis (PFGE) was carried out following the Centers for Disease Control and Prevention (CDC) standardized PulseNet protocol for L. monocytogenes (www.cdc.gov/pulsenet) [31] with AscI and ApaI as the restriction endonuclease. The PFGE patterns were analyzed with the Gel ComparII Software (Bionumerics 2011 Applied Maths NV), which uses the standard strain Salmonella enterica serovar Braenderup H9812 loaded in three lanes in each gel to normalize the images. The strain ATCC 19115 was used as the L. monocytogenes control. Matching and the dendrogram from the unweighted pair-group method with arithmetic mean (UPGMA) analysis of the PFGE patterns was performed by the Dice coefficient with a 1.5% tolerance window.

Estimation of Listeria monocytogenes Concentration at the End of Product Shelf Life
The approach described by Aguirre et al. [32] was used to determine the biological variability of micropopulations and the distribution of L. monocytogenes at the end of the shelf life of most of the contaminated food group. Kinetic data were fitted to various distributions with the @Risk 4.5 software for Excel (Palisade Corporation, Newfield, NY, USA). The goodness of fit was compared by three different methods: X2, Anderson Darling, and Kolmogorov-Smirnov.
The best-fitted distributions, based on the mentioned criteria, were introduced into an exponential model with lag to describe the growth of individually treated and untreated cells using Monte Carlo simulations as described by Koutsoumanis and Lianou [33] expressed as where N t is the total number of cells at time t, N o is the intial number of cells in the population at t = 0, N g (Binomial N o , Pg), and Pg is the mean probability of growth [34].

Bioinformatics and Statistical Analyses
Sequencing products were analyzed with the Gentle software and aligned with ClustaW. A phylogenic tree was constructed by the maximum likelihood method with the MEGA7 software. Central tendency measurements were used for statistical description and the Mann-Whitney test was used for comparison with the STATA 15.0 software with a significance level of α = 0.05.

Detection and Quantification of Listeria monocytogenes
Of the 400 analyzed samples, 30 (7.5%) were positive for L. monocytogenes by the VIDAS system. The highest positivity was 17.5% (7/40) for prepared meals and dishes, followed by 8.6% (3/35) for pre-processed fruit and vegetables, 8.5% (20/235) for cooked meats, and 0% (0/90) for cheese and fresh cheese. on the basis of food type, the highest proportion was 11.6% for artisanal foods with minimal processing, which was significantly higher than 6.2% for moderately processed foods (p > 0.05) ( Table 2). As for pathogen quantification, minimally processed RTE artisanal foods such as cooked meats and pre-processed fruit had the highest counts with 5.7 × 10 2 and 2.2 × 10 3 CFU/g, respectively. Meanwhile, prepared meals and dishes with moderate processing had the lowest counts with 1.6 × 10 2 CFU/g ( Table 3). In addition, 8.5% of the samples exceeded these limits (100 CFU/g) at the beginning of their shelf life.
Due to economic limitations, only eight strains were selected, four minimally processed (1116, 1259, 1310, and 1383) and four moderately processed isolates (1202, 1263, 1264, and 1310). An in-depth study of phenotypic and genotypic characterization was conducted with these isolates.

Phenotypic Identification with API Listeria
The eight selected strains were identified as L. monocytogenes. Seven strains had the same API Listeria numerical profile, number 6510, and only one strain (1383) had a different number, that is, 6410. This occurred because strain 1383 was unable to acidify D-arabitol (DARL).

Molecular Identification
All the strains were identified as L. monocytogenes when the hly gene was amplified. This was also confirmed with BLASTn, which identified L. monocytogenes at a 99% and 100% identification level ( Figure 1).

Antibiotic Resistance Profile
Of the eight analyzed strains, three were susceptible to all the tested antibiotics (1202, 1259, and 1263), three strains had intermediate susceptibility to ampicillin (1116, 1310, and 1540), one strain was resistant to ampicillin (1383), and one strain was resistant to ampicillin and sulfamethoxazole-trimethoprim (1264).

Virulence Factors
All the L. monocytogenes strains were positive to the three evaluated virulence genes (hlyA, prfA, and inlA). As for sequencing the inlA gene, six of the eight L. monocytogenes strains exhibited mutations resulting in premature stop codons (PMSC) associated with changes in amino acids. Strain 1259 exhibited a type 6 mutation (Table 3); four new mutations were detected in strains 1116, 1263, 1264, 1310, and 1383, which could not be identified because they are not described or published in the current literature ( Figure 2).

Pulsed-Field Gel Electrophoresis (PFGE)
Culture purity was initially corroborated by Gram stain and the macroscopic characteristics of the colonies. Two colonies were selected for characterization by PFGE, designated as "a" and "b", from the samples in which different colonies were detected (D-1263, G-1383, K-1202, L-1310). The PFGE was used to characterize 13 bacterial isolates. In the association dendogram created on the basis of the similarity of DICE between isolates and the UPGMA association method, eight groups of pulse types had similarities greater than 90% and four included more than two bacterial isolates. From the last four groups, two only consisted of isolates from the same sample (L 1310a and L 1310b; K 1202a and K 1202b), one shared strains between samples (G 1383b and H 1540), and one shared isolates from the same and another sample (D 1263a, D 1263b, and E 1264). In addition, strain 1383, which exhibited different morphological colonies as to size and color, had two different pulsetypes. The other three strains in which two colonies were selected for analysis had identical pulsetypes (Figure 3).

Discussion
The importance of wholesome and RTE food for a healthier population has been demonstrated in recent decades [36]. The se artisanally processed RTE foods are increasingly popular because of social and environmental interests; however, there is no clear definition or specific regulations associated with them since this type of food is linked to individual producers or very low scale production resulting in dissimilar quality and safety standards [37]. The growing need to consume healthier foods has also produced certain health risks associated with their contamination by different pathogenic microorganisms such as L. monocytogenes, which is particularly relevant.
The 7.5% positivity encountered in our study concurs with other studies that have analyzed similar foods with raw or cooked ingredients, pre-processed fruit and vegetables, and minimal or moderate processing ( Table 2). In Morocco, Amajoud et al. [38] found L. monocytogenes prevalence of 16.6% in salad dressings and 2.7% in beef. Another study of raw materials used in salads and prepared dishes conducted in Iran reported a prevalence of 14% in cucumber, 12% in dressings, 10% in lettuce, and 6% in meat products [39]. Segura and Chávez [40] indicated 8% of RTE fruit salad samples were contaminated with L. monocytogenes in Peru. In Turkey, the prevalence of L. monocytogenes in RTE vegetables varied between 5% and 15% [41]; this is similar to positivity encountered in Malaysia where 15% contamination was also revealed in this type of food [42]. Studies conducted in the United States demonstrated that L. monocytogenes contamination in RTE fruit salad varied between 0.5% and 2.4% [43]. Meanwhile, another study in Spain showed that the presence of L. monocytogenes was only 0.7% in minimally processed RTE fruit salad [44]. The se prevalence values of L. monocytogenes in RTE foods are very similar to those found in our study, except for the United States; our values fluctuated between 17.5% for prepared meals and dishes and 8.5% for pre-processed fruit and vegetables. In addition, these positivity values of L. monocytogenes are consistent with the type of manufacturing process for the minimally or moderately processed RTE foods. The presence of L. monoctogenes is directly associated with or without the implementation of adequate manufacturing and hygiene practices used by the producers of RTE foods in the different countries where such foods are produced.
Several authors postulate that a high inoculum is required to become ill from L. monocytogenes. However, it has been found that counts greater than 100 CFU of viable cells in the case of high-risk groups, or 10 000 CFU in the case of the healthy population with a strong immune system, would be sufficient to cause the disease [45,46]. Under this premise, if foods are able to bear the growth of L. monocytogenes, the possibility of reaching a disease-causing dose is greater. Another empirically-based epidemiological risk model using eight RTE products resulted in infective doses between 10 2 and 10 6 CFU/g. Another model using data on the incidence of listeriosis and prevalence of this pathogen in smoked fish obtained a minimal dose that caused listeriosis with 10 4 CFU/g [47]. In our study, we used the Monte Carlo simulation to estimate that 39% (95% CI) of the evaluated RTE foods would exceed the limit of 100 CFU/g allowed in Chile for products that promote the development of L. monocytogenes [11] at the end of their shelf life (Figure 4). In addition, these high counts can increase the risk of disease associated with L. monocytogenes, which is a concern if we consider that counts in the initial food evaluation already showed that 8.5% of samples exceeded these limits (100 CFU/g) at the beginning of their shelf life. This shows the need for greater control because there are cases of the disease each year in the province where this study was carried out, and there were two fatal cases in 2019 [48]. A key aspect to consider is that strict safety protocols, such as the HACCP system or GMP, are not applied in the manufacturing process of these types of artisanal RTE foods, which has a direct impact on their final safety [49]. Our results show that the highest counts were in the group of minimally processed RTE cooked meats, and the lowest count was in this same food group with moderate processing, which corroborates our hypothesis of the need to implement a safety system to guarantee safe food for the population.
Another significant aspect evaluated in our study was the antibiotic resistance profile. The importance of this test is related to the treatment of listeriosis, which still uses antibiotics [50]. In general, most of the Listeria spp. isolated from food and clinical samples and environments are sensitive to antibiotic therapy, which is usually used against Gram-positive bacteria, including tetracyclines, ampicillin, penicillin G, imipenem, amoxicillin, sulfonamides, aminoglycosides, macrolides, chloramphenicol, and glycopeptides [51]. It should be noted that bacteria are very versatile in adapting and generating resistance to antibiotics [52]. The results of our study revealed susceptibility to the tested antibiotics, and two strains (1264 and 1383a) were resistant to ampicillin and sulfamethoxazole-trimethoprim (STX). Strains 1116, 1310, and 1540 showed intermediate resistance to ampicillin, which is a concern because previous studies in Chile have indicated that L. monocytogenes is susceptible to ampicillin [53]. This is particularly relevant because ampicillin, amoxicillin, and gentamicin are still used to treat listeriosis [54]. Only strain 1264 was resistant to the antibiotic sulfamethoxazole-trimethoprim in the present study (Table 3). However, antibiotic resistance among bacteria transmitted by food, including L. monocytogenes, has evolved in recent decades. Yucel et al. [55] reported 66% resistance to ampicillin and STX in strains of L. monocytogenes isolated from raw and cooked meats. Conter et al. [56] found resistance to ampicillin in two strains of L. monocytogenes isolated from RTE salmon. Jamali et al. [57] observed that the resistance among L. monocytogenes strains from fish products was 20.9% to 27.9% resistant to tetracycline and ampicillin, respectively. Kuan et al. [58] tested the antibiotic resistance of 58 L. monocytogenes strains from vegetable farms and retail markets in Malaysia and found 5.2% resistance to STX. Arslan and Baytur [59] detected 6.1% resistance to ampicillin and 12.1% to STX in L. monocytogenes strains isolated from retail meat This resistance is pertinent because the STX antibiotic is usually used to treat listeriosis in persons who are allergic to penicillin [60]. In addition, the emerging resistance to penicillin of strains from clinical samples poses another major public health problem because penicillin is the gold standard to treat human listeriosis [61]. The refore, encountering ampicillin and sulfamethoxazole-trimethoprim resistant strains and intermediate resistance to ampicillin in our study should alert authorities and food producers to the potential danger associated with the consumption of these artisanal RTE products.
Some studies have observed that between 8% and 21% of natural L. monocytogenes isolates, both food and environmental, are either attenuated in their virulence or are totally avirulent [62]. In our study, the eight analyzed L. monocytogenes strains were positive to the three virulence genes used. This finding is especially relevant for the prognosis and future severity of the disease in individuals who consume contaminated RTE foods and develop the disease from this pathogen, as occurs in this part of Chile. The hlyA gene is a virulence factor that encodes for listeriolysin O, a pore-forming cytolysin, which allows entry into host cells [63]; this toxin can be easily detected with blood agar in hemolysis tests [64]. The virulence factor hlyA is only present in virulent species of Listeria spp. [65], which is frequently used to evaluate the presence of virulence factors in L. monocytogenes strains isolated from RTE foods [66]. Virulence factors are regulated by other genes, which are also virulence factors. Thus, the PrfA protein is an absolutely indispensable virulence factor for the expression of virulence in pathogenic species of L. monocytogenes, which also depends on environmental conditions such as high temperature (37 • C) and stress conditions [67]. The presence of the hlyA and prfA genes in all the L. monocytogenes strains evaluated in our study constitutes an additional risk for people who frequently consume this type of food. The inlA gene, also used in the present study, is another relevant virulence factor for the entry of the bacterium into the organism and which participates in the adhesion process between the bacterial wall and intestinal cells of the individual [68]. The two main invasion proteins of L. monocytogenes are InlA and InlB. The y are members of a protein superfamily called internalins (Inl), and 41 genes that encode for proteins of this type have been detected in the L. monocytogenes genome [69]. A relevant aspect associated with the inlA gene is the presence of PMSC. The PMSC have been associated with impaired virulence, which affects their ability to invade human cells. In addition, mounting evidence suggests that all the inlA gene PMSC mutations are more frequent in L. monocytogenes strains isolated from food than in clinical strains [70]. In our study, only six of the eight evaluated strains exhibited PMSC. We also identified that the inlA gene in strain 1259 is a mutation known as type 6 ( Table 3). We detected four mutations that could not be identified because they are not described or published in the current literature, which is why we believe they are new mutations ( Figure 2). Likewise, a very interesting finding was the presence of mutations in strain 1383 serotype 4b. The PMSC have only appeared in the inlA gene in serotype 4b in publications since 2019. Zamani et al. [71] found a strain of L. monocytogenes serotype 4b with PMSC. This strain had PMSC in nucleotide 1380, truncated inlA gene, and replacement mutation G → A; it is categorized as PMSC number 8. Upham et al. [72] genomically analyzed clinical and food strains and detected that the prevalence of the inlA gene PMSC mutations in genomes of food strains was significantly higher (p < 0.0001) than in clinical strains. However, a three-codon deletion in the inlA gene associated with a highly invasive phenotype was more prevalent in genomes from clinical strains, mainly from serotype 4b, than from food strains (p < 0.001). The se aspects encountered in the literature are consistent with our reported findings and further in-depth study is required.
Serotype identification is important because not all L. monocytogenes serotypes are pathogens. The re are currently 13 serotypes of which 4b, 1/2a, and 1/2b are the most frequently associated with the development of listeriosis in more than 98% of human cases [73]; however, other authors include serotype 1/2c [74]. According to our comparative analysis, the strains found in our study belong to serotypes 1/2a and 4b. Toledo et al. [75] analyzed 38 clinical and non-clinical isolates in Chile and found that 65% of the clinical isolates belonged to the serogroup IVb (which includes serotype 4b), while serogroups IIa and IIb represented 17% and 13% of the isolates, respectively. Among the isolates of the non-clinical samples, serogroup IVb was also the most common (33%). Ulloa et al. [76] and Paduro et al. [77] analyzed strains of L. monocytogenes isolated in clinical cases and foods and reported that the most common serotype was 4b followed by 1/2a. In South America, Braga et al. [78] found that serotypes 1/2b and 4b were the most prevalent, 45.8% and 41.7%, respectively, in RTE foods in Uruguay. Meanwhile, in Colombia, serotype 4b occurred in more than 50% of the RTE food isolates, followed by 10.8% for 1/2c and 9.5% for 1/2a [79]. In Brazil, various authors have encountered a high prevalence of serotype 4b in RTE foods, while serotypes 1/2a and 1/2c were found in unprocessed and processed RTE foods [80][81][82].
In the present study, ST 8 and ST 388 were identified by MLST; these STs have been found in L. monocytogenes isolated from RTE foods such as salmon and poultry products, cooked meats, and vegetables, which are raw materials widely used in sandwiches, salads, and prepared foods sampled in our study [83][84][85]. The use of MLST in L. monocytogenes is still limited in South America; Chile and Brazil have reported the use of this molecular typing technique on this pathogen. Chile reported the presence of ST 8 in a clinical case isolate and another in RTE foods in 2018. Ulloa et al. [76] encountered ST 8 in clinical cases and foods and ST 388 was first mentioned in a clinical case. In Brazil, Oxaran et al. [86] reported ST 8 for the first time in cheese commercialized in the country. Camargo et al. [87] detected ST 8 in raw Brazilian beef; when compared with 270 existing ST profiles in South America, they determined that ST 8 had only been reported in Chile and Brazil, and ST 388 was not found in any other country. Several authors state that L. monocytogenes ST 8 is one of the most persistent STs in RTE food processing plants. This persistence promotes the risk of recontamination by L. monocytogenes in food; future studies are therefore required concerning the factors that confer this persistence in L. monocytogenes strains so as to develop preventive control measures [88].
Two groups of L. monocytogenes were observed when revising the phylogenetic tree of the hlyA gene of the strains under study and adding for comparison two hlyA genes of L. monocytogenes clinical strains. The group of strains 1116, 1202, 1259, 1264, 1310, and 1540 are genetically related, whereas strains 1263 and 1383 are less related to the former group and between strains (66%) when compared with L. monocytogenes strains (Figure 1). This genotypic difference could not be corroborated by PFGE because they were different pulsetypes. The PFGE was the gold standard of molecular typing, however, WGS is now considered as the standard. However, PFGE is still used in research because the comparison of the restriction patterns provides information on the relationship between the different isolates. In our study, we observed two unrelated clusters (45.1%) with eight well-related pulsetype subgroups (>90%). As previously mentioned, isolates 1202, 1263, 1310, and 1383 were evaluated in duplicate (referred to as "a" and "b") because there were small macroscopic morphological differences between them. This variability can be due specifically to the isolation method and subsequent recovery that was used; however, the duplicate strain sent for WGS did not show a mixture of strains according to the initial information provided by the institution that sequenced the genome of our L. monocytogenes strains. The refore, strains 1202, 1263, and 1310 exhibited an identical pulsetype (Figure 3). The remaining strain (1383) originating in cooked meats exhibited two unrelated pulsetypes. The pulsetype of strain 1383a was more related to the pulsetype of strain 1310 from pre-processed fruit, while the pulsetype of strain 1383b was related to the pulsetype of strain 1540, both from cooked meats. Another study conducted in Chile analyzed 94 pulsetypes of L. monocytogenes and we detected a great electrophoretic similarity when we compared the ST 8 and ST 388 strains from that study [76] with our strains 1263 and 1383, that is, the same STs and serotypes. This scenario suggests the persistence of L. monocytogenes over time, as described by other authors such as Kudsen et al. [88]. Likewise, WGS technologies emerge as the best typing tool for L. monocytogenes isolates in epidemiological research. Sequencing the whole bacterial genome provides an unparalleled depth of information to compare between species and subspecies and generate information on aspects such as virulence factors, sequence types, and antimicrobial resistance genes. This type of sequencing is far more comprehensive than the insight provided by PFGE [89].
The limitation of this study is related to the use of only eight strains of L. monocytogenes due to economic reasons. This situation restricts our knowledge of the phenotypic and genotypic characteristics of L. monocytogenes in the foods under study, which are associated with disease and mortality in Chile. However, these eight strains were randomly selected and represented eight independent samples found positive for L. monocytogenes from producers who manufacture different artisanal RTE foods. Although it is not possible to extrapolate this information to the positives of the analyzed samples, it provides us with a focused approach to reality regarding the source, quantification, virulence, and antibiotic resistance profile of the L. monocytogenes strains; this information is not available for this type of food. It is relevant that this research was authorized by the health authority. The refore, the results in terms of the prevalence of L. monocytogenes in the food groups will improve targeted sampling of at-risk foods that promote the growth of this pathogen, as classified by the Chilean Sanitary Food Regulations.

Conclusions
The sampled foods did not comply with the microbiological criteria according to the Chilean Food Sanitary Regulations for Listeria monocytogenes. Higher than permissible counts, presence of virulence factors, serotypes associated with cases, and antibiotic-resistant strains mean that consuming moderately and minimally processed ready-to-eat foods is a tangible risk of disease for the particularly hypersensitive population that consumes them. In addition, more active food control and surveillance must be established by the health authorities. Education programs on preventive measures are needed for population groups at higher risk of listeriosis.