Phenotypic and Genotypic Virulence Characterisation of Staphylococcus pettenkoferi Strains Isolated from Human Bloodstream and Diabetic Foot Infections
by
, , , , , , and
Chloé Magnan
1,
Nour Ahmad-Mansour
2,
Cassandra Pouget
1,
Madjid Morsli
1,
Sylvaine Huc-Brandt
2,
Alix Pantel
1,
Catherine Dunyach-Remy
1,
Albert Sotto
3,
Virginie Molle
2 and
Jean-Philippe Lavigne
1,* 1
Bacterial Virulence and Chronic Infections, INSERM U1047, Department of Microbiology and Hospital Hygiene, University of Montpellier, CHU Nîmes, CEDEX 09, 30029 Nîmes, France
2
Laboratory of Pathogen Host Interactions, University of Montpellier, CNRS, UMR 5235, 34095 Montpellier, France
3
Bacterial Virulence and Chronic Infections, INSERM U1047, Department of Infectious Diseases, University of Montpellier, CHU Nîmes, CEDEX 09, 30029 Nîmes, France
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2022, 23(24), 15476; https://doi.org/10.3390/ijms232415476
Submission received: 25 October 2022
/
Revised: 30 November 2022
/
Accepted: 2 December 2022
/
Published: 7 December 2022
(This article belongs to the Special Issue Current and New Knowledge of Biofilm Formation by Staphylococci)
Abstract
:Staphylococcus pettenkoferi is a recently described coagulase-negative Staphylococcus identified in human diseases, especially in infections of foot ulcers in patients living with diabetes mellitus. To date, its pathogenicity remains underexplored. In this study, whole-genome analysis was performed on a collection of 29 S. pettenkoferi clinical strains isolated from bloodstream and diabetic foot infections with regard to their phylogenetic relationships and comprehensive analysis of their resistome and virulome. Their virulence was explored by their ability to form biofilm, their growth kinetics and in an in vivo zebrafish embryo infection model. Our results identified two distinct clades (I and II) and two subclades (I-a and I-b) with notable genomic differences. All strains had a slow bacterial growth. Three profiles of biofilm formation were noted, with 89.7% of isolates able to produce biofilm and harbouring a high content of biofilm-encoding genes. Two virulence profiles were also observed in the zebrafish model irrespective of the strains’ origin or biofilm profile. Therefore, this study brings new insights in S. pettenkoferi pathogenicity.
1. Introduction
Diabetes mellitus is considered as a global epidemic with almost 550 million adults affected worldwide, a number predicted to rise to 640 million by 2030 [1]. Diabetic foot ulcers (DFU) represent a significant complication of diabetes mellitus, affecting 34% of patients during their lifetime [2]. Initially superficial, these chronic wounds are responsible for frequent infections (more than 50% of cases) [3] spreading to soft tissues and bone structures in 44 to 68% of cases [2]. Bone infection leads to diabetic foot osteomyelitis (DFOM), a real public health problem responsible for one amputation every 20 s worldwide [4]. DFOM and amputations participate in reducing the life quality of patients, increasing the morbidity and mortality, and represent a costly issue for health care systems [2,4,5,6].
The majority of these chronic wounds are polymicrobial [7]. Culturomic and metagenomic approaches revealed that DFU and DFOM ecology is established by a predominance of Firmicutes and particularly Staphylococus aureus and coagulase-negative Staphylococcus (CoNS) [7,8,9]. While S. aureus is clearly implicated in the unfavourable course of these wounds [10], the role of CoNS in infected DFUs remains poorly understood, even though their pathogenicity has been reported [11,12,13,14]. Twelve of the fifty CoNS species, including Staphylococcus lugdunensis, Staphylococcus saprophyticus, Staphylococcus schleiferi and Staphylococcus epidermidis, have been identified as true pathogens and are at the origin of endogenous or nosocomial infections involving bacteremia, pneumonia, urinary tract infection, wound infection and osteomyelitis. These bacteria, constituting the cutaneous commensal microbiota, are considered as opportunists and present different virulence potentials. It is therefore essential to investigate their role in bacterial pathogenicity.
First described in 2002 [15], Staphylococcus pettenkoferi is a CoNS increasingly described in human pathology, especially in bloodstream infection [16,17,18,19,20,21,22,23,24] and osteomyelitis [13]. This skin commensal and opportunistic bacterium mainly infects immunocompromised patients or patients with comorbidities such as diabetes mellitus [24,25]. Thus, S. pettenkoferi is notably a frequent bacterium isolated from DFOM, suggesting that it could also be involved in the pathophysiology of these infections [26]. Recently, our team described the virulence of one clinical strain isolated from this condition and, notably, its ability to proliferate in phagocytes and to persist inside macrophages and its virulence was confirmed in the zebrafish model of infection [27].
In this study, we performed a genomic comparison and established the biofilm, resistance and virulence potential of a collection of clinical S. pettenkoferi strains isolated from both bloodstream and infected DFUs.
2. Results
2.1. Genetic Diversity of Clinical S. pettenkoferi Strains
We analysed a collection of 29 S. pettenkoferi strains isolated from infected DFUs or DFOM (n = 22) and blood cultures (n = 7) between July 2018 and June 2022 at Nîmes University Hospital (France). S. pettenkoferi genome sequences of these clinical strains, the reference strain CIP 107711 and five available S. pettenkoferi draft genomes, including the genome reference FDAARGOS_288 (CP022096), were used for genome-based phylogenetic comparison (Figure 1). Whole-genome sequencing (WGS) bioinformatic data are summarised in Table S1.
Two main clades were determined. Clade I contained two subclades. Six strains from both origins (SP165, NSP008P, NSP009P, NSP019P, NSP003H and NSP005H) clustered together with CIP 107711, 1286_SHAE and 1H7 in subclade I-a. Subclade I-b included the genome reference FDAARGOS_288 and 589_SHAE draft genome and was composed of 15 other clinical strains isolated from DFUs (NSP004P, NSP007P, NSP010P, NSP011P, NSP012P, NSP013P, NSP015P, NSP016P, NSP017P, NSP018P, NSP021P, NSP022P, NSP023P, NSP024P and NSP026P) and four bloodstream isolates (NSP001H, NSP002H, NSP004H and NSP007H). Clade II included the four other clinical strains (NSP008H, NSP003P, NSP020P and NSP025P). Inter-clade diversity was <5% sequence divergence from each other. In contrast, intra-clade diversity was <3%, <2% and <1% for I-a, I-b and II, respectively.
2.2. Resistome of S. pettenkoferi Strains
The main characteristics and resistance profiles of the 29 S. pettenkoferi clinical isolates are listed in Table 1.
Thirteen resistance-associated genes were reported after genomic analysis of the 29 S. pettenkoferi genomes (Table S2). Resistome comparisons between strains isolated from infected DFUs and blood cultures are summarised in Table 2.
No difference was noted between the resistome content and the results of susceptibility testing. Moreover, this resistome content was not significantly different between strains isolated from blood culture and infected DFUs. Eleven clinical isolates (41.4%) were resistant to penicillin G (with the presence of the blaZ gene) and only one strain (SP165) carried the mecA gene and was methicillin-resistant. All isolates were susceptible to gentamicin. The only resistance to aminosides was the presence of the ant(9)-Ia gene, encoding an aminoglycoside nucleotidyltransferase, and presenting in three strains isolated from infected DFUs. The SP165 strain was resistant to rifampicin with a mutation in the rpoB gene (p.H481N). NSP009P was resistant to tetracyclin, with the tet(K) gene detected in its genome. The ermA gene, conferring resistance to erythromycin and clindamycin, was only detected in 10.3% (n = 3) of the strains, while the vgaA gene, conferring resistance to streptogramin A and related antibiotics, was identified in 20.7% (n = 6) of the strains. Concerning resistance to quinolones, 20.7% (n = 6) of the genomes harboured a mutation in gyrA (corresponding to p.S84L in gyrase A protein) and 76.7% (n = 23) in the glrA (corresponding to p.S80Y in topoisomerase IV subunit A protein) gene. Strains isolated from infected DFUs more frequently possessed a grlB mutation (corresponding to pE422D in topoisomerase IV subunit B protein) than strains isolated from blood cultures (59% vs. 14.3%, respectively). The fusB gene was detected in 26.7% (n = 8) of the genomes. Among the 14 strains resistant to fosfomycin, 10 harboured the fosB gene, which was found in 37.9% (n = 11) of the studied genomes. Five isolates (17.2%) were multidrug resistant (i.e., resistant to ≥3 antimicrobial groups) (SP165, NSP009P, NSP004P, NSP012P and NSP001H).
2.3. Biofilm Capacity of S. pettenkoferi Strains
2.3.1. Ability to Form Early Biofilm
The ability of 29 S. pettenkoferi clinical strains to form biofilms was analysed by the Biofilm Ring Test® (Biofilm Control, Saint-Beauzire, France) and compared against the CIP 107711 reference strain. Biofilm formation index values (BFI) evaluating S. pettenkoferi adhesion ability were distributed in three distinct groups: BFI values = 0 at 4 h of incubation for Group 1; BFI values < 5 at 5 h of incubation for Group 2; and BFI values ≥ 5 at 5 h of incubation for Group 3 (Figure 2). Interestingly, the majority of S. pettenkoferi strains (n = 17, 58.6%) were able to produce an early biofilm after 4 h of incubation in BHI and were thus classed to Group 1. Group 2 contained nine (31.0%) strains isolated from infected DFU which required a longer incubation time to reach BFI values near 2 at 5 h (a value considered as fixed biofilm in this assay). Finally, three (10.3%) strains constituting Group 3 presented low adherence and potential of biofilm formation. The reference strain CIP 107711 represented our negative for biofilm production with BFI values around 20 during the whole experiment. The three groups showed significant differences in the change in BFI values over time (Mann-Whitney test; p < 0.001). Interestingly, all strains isolated from blood cultures belonged to Group 1, with strong production of early biofilm.
2.3.2. Biofilm-Related Genes within S. pettenkoferi Genomes
Biofilm was further studied by determining the biofilm-encoding genes in all 29 S. pettenkoferi genomes. The coding sequences (CDS) annotated were assigned functions based on Best DIAMOND Hit using the UniProt Reference Clusters (UniRef50) database. The prevalence of these biofilm-associated genes in the 29 studied S. pettenkoferi genomes according to the biofilm production of the strains and their origin (blood cultures or DFUs) are presented in Table 3.
All strains harboured the atlE gene, encoding for autolysin E, a major contributor to primary attachment to abiotic surfaces; the BUY34_0850 gene encoding for phenol soluble modulin beta protein (known for its major role in biofilm detachment); the splF and htrA genes encoding for serine proteases involved in biofilm structuration; and the clpP gene encoding for ClpP protease, implicated in S. epidermidis biofilm development. The poly-N-acetylglucosamine (PNAG) production is dependent on the presence of the intracellular adhesion (ica) operon for which the icaA, icaB and icaC genes were identified in all strains, while icaD and icaR were absent. We also noted a high presence of the most important biofilm regulators genes (agrA and agrC, being part of the Agr quorum sensing system; the rsbUVW-sigB operon; mgrA; sarA; luxS; lytSR; alrRS; cidA; and lgrA).
Interestingly, no significant differences were observed between the presence of biofilm-encoding genes and the profile of the biofilm producers, nor between the origin of the strains (DFU and blood culture) and the clades. Finally, a previous study on S. saprophyticus strain MS1146 described the presence of the uafB gene, encoding for an adhesin involved in biofilm, on the pSSAP1 plasmid [28] (Table S3). Notably, this plasmid and the uafB gene were present in strains belonging to the two biofilm-producing groups (9/17, 52.9% in Group 1 and 4/9, 44.4% in Group 2) but absent in bacteria belonging to the Group 3.
2.4. Fitness of S. pettenkoferi Strains
Based on our biofilm results, we selected three strains isolated from infected DFUs representing the three groups identified by the BRT® experiments: NSP003P (clade II, biofilm Group 1, NSP009P (clade I-a, biofilm Group 2) and NSP0023P (clade I-b, biofilm Group 3), as well as one strain isolated from blood cultures, NSP004H (clade I-b, biofilm Group 1). S. aureus reference strain Newman [29] was used as control. Growth profiles of these strains were monitored for over 24 h (Figure 3).
The growth of S. aureus Newman was significantly faster than the S. pettenkoferi strains as illustrated by the maximum absorbances measures in the stationary phase (Ym) (Ym, S. aureus Newman = 1.644, Ym, NSP003P = 1.234, Ym NSP009P = 1.062, Ym NSP023P = 1.086 and Ym, NSP004H = 0.953 respectively, disjoint interval confidence; Table S4). The comparison between each S. pettenkoferi strain showed that NSP0023P presented a significantly higher Ym whereas NSH004H had the lowest. No significant differences between strains were observed for the lag times (K) and inflexion points (1/K) excepted for NSP023P and S. aureus Newman (K NSP023P = 0.246 and K S. aureus Newman = 0.194; 1/K NSP023P = 4.066 and 1/K S. aureus Newman = 5.147, disjoint interval confidence).
Moreover, a significant difference in slopes was observed between all the S. pettenkoferi strains compared to S. aureus Newman (Wilcoxon test; p = 0.009), confirming that bacterial growth was slower for S. pettenkoferi strains. Different growth rates were also observed between NSP004H and NSP003P with a significant slope observed for NSP004H, indicative of a lower growth rate (Dunn test; p = 0.03).
2.5. Virulence Study of S. pettenkoferi Strains Using a Zebrafish Embryos Model
In vivo virulence of the four selected S. pettenkoferi strains (NSP003P, NSP009P, NSP023P and NSP004H) with different biofilm productions and origins was tested using the bath infection model of wounded zebrafish embryos, as previously described for S. pettenkoferi [27]. The viability of zebrafish embryos was monitored for 48 h and we observed that mortalities in injured larvae infected with S. pettenkoferi began at 18 hpi for all strains (Figure 4). Strains showed different virulence profiles: deaths increased up to 95% by 24 hpi for the NSP009P strain, while embryos infected by NSP003P, NSP0023P and NSP004H showed a mortality of around 50% at 36 h (Log-rank Mantel–Cox statistical test, p < 0.001). S. pettenkoferi NSP009P was two times more virulent than the other three strains with less than 5% embryo survival at 24 hpi. Interestingly, NSP009P displayed the same virulence profile as for the S. pettenkoferi SP165 isolate previously described [27].
2.6. Genomic Analysis of Putative Virulence Factors of the S. pettenkoferi Strains
Due to the evidence that the S. pettenkoferi strains are virulent and presented two profiles, we investigated their virulome content. A total of 44 putative homologues were identified by genomics analyses (Table 4). Most detected genes were related to immune system evasion and invasiveness (e.g., capA, eno, katA, tuf, esXA and five genes encoding for the T7SSb apparatus), whereas most of the toxins-encoding genes were absent (e.g., hly, hlb, hlg, sea, sel, seg, tst-1, etA, etB, etD and lukDE).
However, three CDSs annotated as haemolysin H1U, delta haemolysin and haemolysin III were identified in 15 (51.7%), 23 (79.3%) and 29 (100%) of all the genomes, respectively. Haemolysin H1U homologue was present in almost all bloodstream isolates (n = 6/7) and was only present in biofilm-producing strains.
Additional predicted virulence factors identified in all genomes were associated with lipoprotein maturation (lspA and lgt), proteases (clp proteases), iron scavenging (isdF) and nuclease activity (nucH). Moreover, two-component systems (TCS) involved in virulence regulation (saeSR and vraSR) were identified. Conserved virulence factor B and C were present in all genomes, and two isolates (NSP008P and NSP0023P) harboured, in addition, the virE gene.
Overall, no significant differences were observed in the virulome content, in the biofilm profiles, or related to the origin of the studied strains. Moreover, regarding the NSP009P strain, which presented a highly virulent profile in the zebrafish model, we could not identify any difference in its virulome content in comparison to the less virulent NSP004H, NSP003P and NSP023P strains. Interestingly, using an alignment of the NSP004H, NSP003P, NSP023P and SP165 genomes against the NSP009P genome, we could characterize conserved genomic regions between the two more virulent strains (SP165 and NSP009P) and the others (Figure 5). Seven regions were identified that will require further investigations to identify putative virulence trends that could explain their different virulence profiles. Genomic diversity was investigated by pangenome and SNP analysis (Figures S1 and S2). These analyses confirmed the genomic diversity of the five studied S. pettenkoferi isolates (Figure S1). The two most virulent strains (NSP009P and SP165) were clustered together (Figure S2). A similar clustering was also observed with the two less virulent strains NSP004H and NSP023P. Comparison between phenotype (biofilm and zebrafish) and genotype results targeting genes encoding biofilm (Table S5) and virulence factors (Table S6) did not identify any specific virulence traits in the two most virulent strains These strains shared conserved coding regions which will require further investigation (Figure S2).
3. Discussion
Chronic non-healing wounds are a major complication of diabetes mellitus, associated with severe outcomes such as high morbidity and health care costs [4,30]. Polymicrobial colonisation, biofilm formation, and collaboration between pathogenic and colonising bacteria are hypothesised to impair healing of DFUs, thus contributing to severe complications such as osteomyelitis and amputation [2,3].
The microbial community present on foot ulcers in patients living with diabetes is highly complex and diverse, with CoNS frequently isolated from DFOM specimens [8,9]. Whereas CoNS have long been considered as colonising bacteria belonging to cutaneous commensal microbiota, some species such as S. lugdunensis have been identified as true pathogens [14]. However, the role of each CoNS species in infected DFUs remains unclear to date [14,31]. Among them, S. pettenkoferi was reported to cause severe infections [13,16,17,18,19,20,21,22,23,24], predominantly in immunocompromised patients. Recently, we determined the pathogenicity of one S. pettenkoferi clinical isolate from DFOM, and demonstrated its in vivo virulence associated with a large production of biofilm [27]. Here, we confirm that S. pettenkoferi is a pathogen by studying a collection of 29 S. pettenkoferi clinical isolates from blood cultures and infected DFU.
Biofilm formation is an important pathophysiological hallmark in DFU, involving most of the bacteria present in chronic wounds, and inducing prolonged inflammation and chronicity of the lesions, as well as the development of antibiotic resistance resulting in difficulties treating these wounds [32]. It has been established that CoNS participate in biofilm formation that could contribute to the chronicity of DFU. However, biofilm-related studies tend to only focus on S. epidermidis, as this species is the most frequently isolated [33]. Few studies have evaluated the biofilm formation of S. pettenkoferi and, surprisingly, the previous investigations on clinical, animal or environmental isolates reported no production of biofilm [34,35]. We corroborated that the reference strain CIP 107711 was unable to form biofilm as previously published [35]. However, our results showed that clinical S. pettenkoferi strains were able to form biofilm, as previously published for one isolate, SP165 [27]. We could classify the strains in three different groups with distinct biofilm behaviours: a large majority of strains (n = 17 and the SP165 isolate) corresponding to fast and high producers, a second group of strains (n = 9) with an intermediate profile, and three strains with a low potential for biofilm formation. This classification confirmed that most clinical S. pettenkoferi strains (n = 26, 89.7%) were able to form biofilm. Notably, all strains isolated from blood cultures belonged to the faster biofilm producers group, which is consistent with previous studies showing that 52–100% of CoNS species isolated from bloodstream formed a biofilm [36,37,38].
To corroborate our results, S. pettenkoferi genome analysis identified genes known to participate in biofilm formation. All S. pettenkoferi genomes harboured the atlE gene encoding for the homologous autolytic enzyme AtlE, described in S. epidermidis [39]. This protein is a major contributor to primary attachment to abiotic surfaces and a critical enzyme required for the release of eDNA, a component of the staphylococcal in vitro biofilm matrix [40]. Moreover, the NSP012P and NSP023P strains possessed the gene encoding for the Bap homologue protein (Bhp), described in S. epidermidis [41]. In S. aureus, this protein has been identified as the main determinant for successful surface adherence, as well as intercellular accumulation during biofilm development [42,43]. In addition, the PNAG, a polysaccharide synthesized by products of the icaADBC locus, is a well-known mechanism of intercellular adhesion in staphylococcal biofilms. Some genes of this locus (the icaA, icaB and icaC homologue genes) were identified in all studied strains, although the icaD and icaR genes were absent. Interestingly, a similar analysis was reported by Dutta et al. (2018) in S. pettenkoferi isolated from a cat peritonitis case [34]. The icaADBC locus organisation may differ between staphylococci, as S. lugdunensis also does not contain the icaR gene [44]. Moreover, the ica operon expression can be activated by sarA and partially by the sigmaB and srrAB two-component systems [45], and such homologues of major staphylococcal biofilm-regulator-encoding genes were detected in the S. pettenkoferi genomes. This included positive regulators such as sigmaB (sigB), expressed from and regulated by the rsbUVW-sigB operon also present in S. pettenkoferi genomes; sarA, critical for biofilm formation mainly through repression of proteases; and mgrA and luxS, two negative regulators. However, the major regulatory system of staphylococcal biofilm formation is the accessory gene regulator (Agr), known to regulate the production of proteases and phenol-soluble modulins (PSMs), main contributors to biofilm maturation and disassembly in S. aureus and S. epidermidis [46,47]. Phenol-soluble modulin beta (PSMβ) protein and ClpP protease homologues were also annotated in all S. pettenkoferi genomes. PSMβ is a key effector in biofilm structuring and dispersion, both in vitro and in vivo [48]. A role in biofilm development has also been identified for the S. epidermidis protease ClpP and its expression is regulated by the agr system [49]. Finally, the pSSAP1 plasmid described in the S. saprophyticus strain MS1146 and containing the adhesin-encoding gene uafB was also detected in all the strains. The UafB adhesin is known to contribute to cell surface hydrophobicity and to mediate adhesion to fibronectin and fibrinogen [28]. Therefore, this adhesin could play a role in biofilm formation in S. pettenkoferi strains, as it is present in 50% of the biofilm producers’ genomes and absent in the non-producer group.
In accordance with Ahmad-Mansour et al. [27], we confirmed that S. pettenkoferi strains showed relatively slow growth compared to S. aureus. One hypothesis predicts a positive association between the evolution of host immunity and pathogen virulence involving an increase in replication rates in response to host resistance [50]. Remarkably, a specific set of putative virulence factors (e.g., capA, katA and nucH) involved in immune evasion were identified in all S. pettenkoferi strains. These immune evasion determinants and the slow growth replication of S. pettenkoferi may be involved in its persistence during host infection.
Our study confirmed that S. pettenkoferi is a virulent pathogen in the zebrafish model of infection, which represents an important animal model to study host–pathogen interactions in vivo [51]. Zebrafish embryos possess a fully functional innate immune system and have been used for their ability to closely mimic human diseases [52]. Bacterial infections in zebrafish embryos are most frequently performed by microinjection. As S. pettenkoferi was isolated from chronic wounds, we used an adapted model where a bath infection model was chosen with larvae fin excision to mimic “sterile” wounding damage and inflammation [53]. Immersion following the larvae injury model was recently validated to study S. pettenkoferi virulence [27]. The studied strains with different origins and biofilm production ability showed virulence in this model. However, two clear virulence profiles were observed with one strain (NSP009P) being highly virulent, as previously published for the SP165 isolate [27], while the other three studied strains displayed a less virulent profile. However, no difference was observed in virulome content nor in biofilm behaviour. In addition, our genome phylogenetic analysis obtained by WGS data confirmed the presence of distinct clusters and subclusters, each comprising closely related S. pettenkoferi isolates from the two different clinical origins. A previous phylogenetic study between 25 S. pettenkoferi strains showed that clinical isolates were closely related to environmental isolates, irrespective of their geographic origin [35]. Interestingly, despite the single geographical origin of the strains analysed in this study, a similar repartition between their strains and our strains was observed except for clade II, absent in this previous study. This clade corresponds to a new group of S. pettenkoferi, genetically distant from the other strains, and will require phylogenetic investigations on a larger scale. More importantly, no links could be highlighted between biofilm production groups nor with strain origin and cluster membership. However, the two highly virulent strains SP165 and NSP009P are closely related in the same clade, I-a, with seven conserved regions, though more investigation is needed to determine if these regions could correspond to pathogenicity islands.
4. Materials and Methods
4.1. Bacterial Strains
All S. pettenkoferi strains belonged to the collection of the Department of Microbiology at Nîmes University Hospital (France). Twenty-two S. pettenkoferi strains were isolated from infected DFUs or DFOM and seven from blood cultures between July 2018 and June 2022. Bacterial identification was obtained by mass spectrometry (Vitek-MS®, Biomérieux, Marcy-l’Étoile, France). Antimicrobial susceptibility testing was performed by the disc diffusion test according to the European Committee for Antimicrobial Susceptibility Testing (EUCAST) recommendations [54]. Vancomycin, teicoplanin and daptomycin MICs were determined using broth microdilution procedures (UMIC) (Bruker, Champs-sur-Marne, France). The S. pettenkoferi reference strain CIP 107711 (Culture Collection University of Gothenburg, Department of Clinical Bacteriology, University of Gothenburg, Sweden) was used as control in biofilm assays. The S. aureus reference strain Newman [29] was used as control in growth curves tests.
4.2. Whole-Genome Sequencing and Bioinformatics Analysis
S. pettenkoferi strains were cultivated aerobically at 37 °C for 48 h on Columbia sheep blood agar plates (5%) (Biomérieux). Following the manufacturer’s instructions, genomic DNA was extracted using the DNeasy UltraClean Microbial Kit (Qiagen, Aarhus, Denmark). Whole-genome sequencing (WGS) was carried out using Illumina MiSeq sequencing equipment (Illumina, San Diego, CA, USA) using paired-end (PE) read libraries (PE250) made with an Illumina DNA Library Prep Kit (Illumina) according to the manufacturer’s instructions. To examine data quality, raw readings were processed using FastQC (v.0.11.9). Sequencing reads were quality-trimmed and assembled de novo using CLC Genomics Workbench 22.0.2 (Qiagen) with default parameters to include only contigs > 1000 nt. Each S. pettenkoferi contig sequence was then annotated with Find Prokaryotic Genes, Annotate CDS with Best DIAMOND Hit and Annotate CDS with Pfam Domains functions within the Functional Analysis tool of the Microbial Genomics Module on the CLC Genomics Workbench with settings as previously described [55]. Virulence and biofilm genes were identified from each annotated S. pettenkoferi genome. ResFinder (2022-06-22), PointFinder for S. aureus (2019-08), CARD and the NCBI Bacterial Antimicrobial Resistance Reference Gene (2021-08) databases were also used to identify antimicrobial resistance genes [56,57,58]. Sequences obtained were aligned by using the multisequence alignment tool in CLC Genomics Workbench 22.0 with default parameters. Phylogenetic relationships were inferred from this alignment using a distance matrix generated under the assumptions of the Jukes and Cantor model [59]. The phylogenetic tree was constructed by using the neighbour-joining method implemented in the software [60]. WGS was subjected to other investigations, such as circular genome representation using the Proksee programme with CGView.js as its genome drawing engine [61]. Whole-genome bioinformatic data are summarised in Table S1. All the identified genomics sequences have been deposited on the GenBank website accession bioproject: PRJNA870410.
4.3. Kinetics of Early Biofilm Formation
To evaluate the capacity of S. pettenkoferi to form biofilm, we used the Biofilm Ring Test® technique (Biofilm Control, Saint-Beauzire, France) following the manufacturer’s recommendations [62]. This assay is based on the measurement of the mobility of superparamagnetic microbeads embedded in biofilms subjected to a magnetic field. Standardised bacterial cultures were deposited on 96-well microtiter plates (Falcon 96 Flat Bottom Transparent, Coming, USA) containing magnetic beads (TON004). The plates were incubated without shaking at 37 °C. After incubation, 100 µL of liquid contrast (LIC001) solution was added on the top of each well, and plates were inserted for 1 min onto a magnetic block and then into a reader (an Epson Scanner modified for microplate reading). Images of each well were acquired at 3 h, 4 h and 5 h. Data were analysed using the BFC Elements 3.0 software (Biofilm Control), giving a result in the form of a Biofilm Formation Index (BFI). Each experiment was performed in triplicate. A negative control was systematically included in each experiment corresponding to Brain Heart Infusion (BHI) medium and beads without bacterial suspension. BFI values were calculated for each well, ranging from 0 (total bead immobilisation, i.e., strongly adherent cells/strong biofilm formation) to 20 (no bead aggregation, i.e., non-adherent cells/no biofilm formation in the experiment conditions). A high BFI value (>7) corresponds to high mobility of the beads under magnetic action (no biofilm), while a low value (<2) corresponds to full immobilisation of the beads due to the sessile cells. Three experiments with two repeats were performed per strain and per incubation time.
4.4. Growth Curves Evaluation
Growth profiles were performed in Trypticase Soy Broth (TSB). Then, bacterial suspensions were calibrated to obtain an optical density of around 0.1 at 600 nm. Each bacterial suspension was added to a 96-well plate incubated at 37 °C for 48 h. The absorbance at 600 nm of each well was determined by the Infinite M Mano automatic absorbance reader (Tecan, Männedorf, Switzerland). Each experiment was performed in triplicate. The nonlinear regression model of Gompertz [63] was used with GraphPadPrism 9.2 software (San Diego, CA, USA) to acquire the equations of each growth curve, as well as various notable points (Ym, Y0, K and 1/K). The Gompertz equation can be written as follows:
where Y(t) corresponds to the absorbance at a time t, Ym corresponds to the maximum absorbance (stationary phase), Y0 corresponds to the absorbance at t = 0 h, K determines the lag time (1/h), and 1/K (h) is the inflection point of the exponential phase. Inflection points enabled us to determine the beginning of the exponential phase and to calculate the slope of the linear trend line of this phase.
4.5. Infection of Danio Rerio Embryos
Following the previous protocol [27], S. pettenkoferi strains were cultured in TSB overnight at 37 °C. The cultures were diluted 1:20 and allowed to grow in TSB medium until they reached the mid-exponential growth phase (OD600 = 0.7–0.9). Then, the bacteria were centrifuged for 10 min at 4000 rpm, and the pellets were resuspended in fish water with 60 µg/mL of sea salt (Instant Ocean) in distilled water with 4 × 10−4 N sodium hydroxide at a concentration of 8 × 107 bacteria/mL. After diluting the inoculum in phosphate-buffered saline (PBS), the samples were plated onto TSB agar plates to determine the number of bacteria present. Experiments were conducted with the GAB zebrafish line in fish water at a temperature of 28 °C. The wounded embryos were placed on a Petri plate, given 0.28 mg/mL tricaine as anaesthesia, and a small tail fin injury was caused prior to infection using a 26-gauge needle under a stereomicroscope (Motic). After tail transection, groups of 24 damaged embryos were placed in Petri dishes with the appropriate bacterial solution (or fish water as a control), and then they were distributed individually into 96-well Falcon plates containing 200 µL of the bacterial suspension (or fish water). Throughout the incubation procedure, the plates were maintained at a constant temperature of 28 °C (bacteria were kept throughout the experiment in fish water, which does not support S. pettenkoferi growth). The number of dead embryos could be counted visually based on the absence of a heartbeat.
4.6. Ethical Statement
The animal experiments were carried out at the University of Montpellier in accordance with European Union recommendations for the care and use of laboratory animals (https://ec.europa.eu/environment/chemicals/lab_animals/index_en.htm (accessed on 15 March 2021)) and were authorised by the Direction Sanitaire et Vétérinaire de l’Hérault and Comité d’Ethique pour l’Expérimentation Animale under reference CEEALR-B4-172-37 and APAFIS#5737-2016061511212601 v3. Adult zebrafish were not killed for this study, and breeding of adult fish followed the international norms set out by the EU Animal Protection Directive 2010/63/EU. According to the EU Animal Protection Directive 2010/63/EU, all studies were conducted prior to the embryos’ free feeding stage and did not constitute animal experimentation. The cardiac rhythm was used as a clinical criterion for survival graphs. At the end of the survival monitoring, the plates were parafilmed and quickly frozen, stored at −20 °C for 48 h to ensure embryos’ death, and then autoclaved with the bacterially contaminated waste.
4.7. Statistical Analysis
Statistical analyses were performed using GraphPad Prism version 9.2 and R software version 4.1.0. Tests used for the p-value determination are mentioned in each table and figure legend. A p-value < 0.05 was considered to reflect a statistically significant difference.
5. Conclusions
This study highlights that S. pettenkoferi possesses an important virulence potential as demonstrated in vivo with the zebrafish model of infection, is able to form biofilm and contains a large panel of virulence determinants. Therefore, the genomic analysis of S. pettenkoferi constitutes a valuable resource to study molecular mechanisms involved in its pathogenicity.
Supplementary Materials
The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/ijms232415476/s1
Author Contributions
Conceptualization, J.-P.L. and V.M.; methodology, C.M., N.A.-M., C.P., V.M. and J.-P.L.; software, C.M., M.M. and C.P.; validation, A.S., V.M. and J.-P.L.; formal analysis, C.M., N.A.-M., M.M., S.H.-B. and A.P.; investigation, C.M., N.A.-M. and A.P.; resources, C.M., A.P. and J.-P.L.; writing—original draft preparation, C.M. and J.-P.L.; writing—review and editing, N.A.-M., S.H.-B., M.M., A.P., C.P., C.D.-R., A.S. and V.M.; supervision, C.D.-R., A.S. and V.M.; project administration, V.M. and J.-P.L.; funding acquisition, V.M. and J.-P.L. All authors have read and agreed to the published version of the manuscript.
Funding
This research was funded by CHU Nîmes, grant number Thematique Phare 1. N.A.M. received a PhD grant from InfectioPôle Sud Mediterranée 2020, grant number AO-IHU-2020-3. The funder had no role in study design, data collection and analysis; the decision to publish; or preparation of the manuscript.
Institutional Review Board Statement
The study was conducted in accordance with the Declaration of Helsinki and approved by the Institutional Review Board of Nîmes University Hospital (protocol code 22.07.02 and 2 September 2022).
Informed Consent Statement
Informed consent was obtained from all subjects involved in the study.
Data Availability Statement
Data supporting reported results can be found in the file “S. pettenkoferi project” contained in the computer of the VBIC unit.
Acknowledgments
We thank the Nîmes University Hospital for its structural, human and financial support through the award obtained by our team during the internal call for tenders “Thématiques phares”. We thank Sarah Kabani for her editing assistance.
Conflicts of Interest
The authors declare no conflict of interest.
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Figure 1.
Whole-genome phylogenetic tree of 29 S. pettenkoferi clinical isolates aligned with five available S. pettenkoferi draft genomes and the CIP 107711 reference strain. Neighbour-joining tree was generated using CLC Genomics Workbench 22.0.2 (QIAGEN Bioinformatics). Numbers at nodes indicate the percentage of bootstrap based on analysis of 100 resampled datasets. The scale bar represents 2.2% sequence divergence. Strains are coloured according to their phylogenetic group (clade). Clade I includes subclade I-a (light blue) and I-b (dark blue). Clade II, green. *, denotes the isolates investigated in depth in this paper.
Figure 1.
Whole-genome phylogenetic tree of 29 S. pettenkoferi clinical isolates aligned with five available S. pettenkoferi draft genomes and the CIP 107711 reference strain. Neighbour-joining tree was generated using CLC Genomics Workbench 22.0.2 (QIAGEN Bioinformatics). Numbers at nodes indicate the percentage of bootstrap based on analysis of 100 resampled datasets. The scale bar represents 2.2% sequence divergence. Strains are coloured according to their phylogenetic group (clade). Clade I includes subclade I-a (light blue) and I-b (dark blue). Clade II, green. *, denotes the isolates investigated in depth in this paper.
Figure 2.
Ability of 29 S. pettenkoferi strains to form early biofilm in BHI using BRT® (Biofilm Control). K-means clustering led to three groups: in red, strains with early low biofilm index (BFI) values; in green, low adherent strains; in orange, strains with intermediate BFI values; and in blue, the S. pettenkoferi CIP 107711 reference strain with no biofilm production. Dotted horizontal lines: >7, no biofilm; <2, fixed biofilm. Means ± standard errors of the mean of BFIs for at least three independent replicates per group are presented. Statistical differences between BFI values of the three groups at 3, 4 and 5 h of incubation were obtained using Mann-Whitney tests. ***, p < 0.001.
Figure 2.
Ability of 29 S. pettenkoferi strains to form early biofilm in BHI using BRT® (Biofilm Control). K-means clustering led to three groups: in red, strains with early low biofilm index (BFI) values; in green, low adherent strains; in orange, strains with intermediate BFI values; and in blue, the S. pettenkoferi CIP 107711 reference strain with no biofilm production. Dotted horizontal lines: >7, no biofilm; <2, fixed biofilm. Means ± standard errors of the mean of BFIs for at least three independent replicates per group are presented. Statistical differences between BFI values of the three groups at 3, 4 and 5 h of incubation were obtained using Mann-Whitney tests. ***, p < 0.001.
Figure 3.
Growth curves of four S. pettenkoferi strains compared to S. aureus Newman strain using the Gompertz equation. A Wilcoxon test was used to compare the slopes of all S. pettenkoferi strains vs. S. aureus Newman; significant difference was at ** p < 0.01. A Dunn test was used to compare growth rates between the S. pettenkoferi strains; significant difference was observed between NSP004H and NSP003P at * p < 0.05.
Figure 3.
Growth curves of four S. pettenkoferi strains compared to S. aureus Newman strain using the Gompertz equation. A Wilcoxon test was used to compare the slopes of all S. pettenkoferi strains vs. S. aureus Newman; significant difference was at ** p < 0.01. A Dunn test was used to compare growth rates between the S. pettenkoferi strains; significant difference was observed between NSP004H and NSP003P at * p < 0.05.
Figure 4.
Virulence of S. pettenkoferi strains in zebrafish embryos. Kaplan–Meier representation of the survival of zebrafish embryos injured in the tail fin at 48 h post-fertilization (hpf) in a bath infected with S. pettenkoferi strains at 8 × 107 CFU/mL grown in exponential phase or “fish water” (negative control). Results are presented as the proportion of surviving embryos (n = 24 for each, indicative of four separate experiments). Significant difference at *** p < 0.001, **** p < 0.0001 or no significant difference (ns).
Figure 4.
Virulence of S. pettenkoferi strains in zebrafish embryos. Kaplan–Meier representation of the survival of zebrafish embryos injured in the tail fin at 48 h post-fertilization (hpf) in a bath infected with S. pettenkoferi strains at 8 × 107 CFU/mL grown in exponential phase or “fish water” (negative control). Results are presented as the proportion of surviving embryos (n = 24 for each, indicative of four separate experiments). Significant difference at *** p < 0.001, **** p < 0.0001 or no significant difference (ns).
Figure 5.
Sequences comparison of S. pettenkoferi genomes. The NSP009P strain was compared against SP165 (a virulent strain) and the NSP003P, NSP023P and NSP004H genomes. The inner light red ring represents the NSP009P genome; the middle red one shows the SP165 genome after BLASTn match; while the outer green, light blue and dark blue rings correspond to NSP023P, NSP003P and NSP004H, respectively. Missing regions identified by the BLAST analysis on the CGView server’s PROKSEE software are shown as ‘gaps’ on each of the circular genomes. Arrows represent regions shared between SP165 and NSP009P but not present in the NSP023P, NSP003P and NSP004H genomes. The inner ring corresponds to the GC skew of S. pettenkoferi NSP009P isolate. Light grey profile indicates overabundance of GC nucleotides, whereas dark grey shows the opposite. The inner black ring represents the GC%.
Figure 5.
Sequences comparison of S. pettenkoferi genomes. The NSP009P strain was compared against SP165 (a virulent strain) and the NSP003P, NSP023P and NSP004H genomes. The inner light red ring represents the NSP009P genome; the middle red one shows the SP165 genome after BLASTn match; while the outer green, light blue and dark blue rings correspond to NSP023P, NSP003P and NSP004H, respectively. Missing regions identified by the BLAST analysis on the CGView server’s PROKSEE software are shown as ‘gaps’ on each of the circular genomes. Arrows represent regions shared between SP165 and NSP009P but not present in the NSP023P, NSP003P and NSP004H genomes. The inner ring corresponds to the GC skew of S. pettenkoferi NSP009P isolate. Light grey profile indicates overabundance of GC nucleotides, whereas dark grey shows the opposite. The inner black ring represents the GC%.
Table 1.
Characteristics and resistance profiles of the studied S. pettenkoferi strains (n = 29).
| Isolate ID | Year | Type of Sampling | Hospital Department | Patients | Resistance Profile | |
|---|---|---|---|---|---|---|
| Age | Sex | |||||
| SP165 | 2018 | Tissue biopsy | Diabetic foot clinic | 60 | M | PEN, OXA, ERY, CMN, L, OFX, RIF, FOS |
| NSP003P | 2020 | Tissue biopsy | Diabetic foot clinic | 58 | M | / |
| NSP004P | 2020 | Tissue biopsy | Diabetic foot clinic | 89 | M | OFX, FA, FOS |
| NSP007P | 2020 | Bone biopsy | Diabetic foot clinic | 69 | M | PEN, FA |
| NSP008P | 2020 | Bone biopsy | Vascular surgery | 90 | M | FOS |
| NSP009P | 2020 | Bone biopsy | Diabetic foot clinic | 62 | M | PEN, ERY, CMN, L, PT, SYN, TET, OFX, FA, FOS |
| NSP010P | 2020 | Bone biopsy | Orthopaedic surgery | 61 | F | FOS |
| NSP011P | 2020 | Tissue biopsy | Diabetic foot clinic | 89 | M | / |
| NSP012P | 2021 | Bone biopsy | Orthopaedic surgery | 67 | M | PEN, OFX, FA |
| NSP013P | 2021 | Tissue biopsy | Diabetic foot clinic | 94 | M | PEN, OFX |
| NSP015P | 2021 | Bone biopsy | Orthopaedic surgery | 64 | M | FOS |
| NSP016P | 2021 | Bone biopsy | Diabetic foot clinic | 56 | M | FA |
| NSP017P | 2021 | Tissue biopsy | Diabetic foot clinic | 84 | M | / |
| NSP018P | 2021 | Bone biopsy | Vascular surgery | 76 | M | / |
| NSP019P | 2021 | Bone biopsy | Vascular surgery | 71 | M | FOS |
| NSP020P | 2021 | Tissue biopsy | Orthopaedic surgery | 63 | M | / |
| NSP021P | 2021 | Bone biopsy | Diabetic foot clinic | 60 | M | PEN, FOS |
| NSP022P | 2021 | Tissue biopsy | Diabetic foot clinic | 66 | F | FA |
| NSP023P | 2021 | Bone biopsy | Orthopaedic surgery | 94 | F | PEN |
| NSP024P | 2021 | Tissue biopsy | Diabetic foot clinic | 78 | F | PEN |
| NSP025P | 2022 | Tissue biopsy | Diabetic foot clinic | 93 | M | / |
| NSP026P | 2022 | Tissue biopsy | Diabetic foot clinic | 63 | M | PEN |
| NSP001H | 2020 | Blood culture | Geriatric | 83 | M | PEN, OFX, FA, FOS |
| NSP002H | 2020 | Blood culture | Emergency | 59 | F | ERY, FOS |
| NSP003H | 2020 | Blood culture | Emergency | 65 | M | FA, FOS |
| NSP004H | 2021 | Blood culture | Polyvalent medicine | 44 | F | PEN |
| NSP005H | 2021 | Blood culture | Intensive care unit | 58 | M | FOS |
| NSP007H | 2022 | Blood culture | Neurology | 72 | M | PEN, FOS |
| NSP008H | 2022 | Blood culture | Intensive care unit | 62 | M | FOS |
F, female; M, male; PEN, penicillin G; OXA, oxacillin; ERY, erythromycin; CMN, clindamycin; L, lincomycin; PT, pristinamycin; SYN, synergystin; TET, tetracyclin; OFX, ofloxacin; FA, fusidic acid; RIF, rifampicin; FOS, fosfomycin.
Table 2.
Comparison of resistomes between blood culture and DFU S. pettenkoferi strains.
| Resistance Genes | Blood Culture Strains (n = 7) | DFU Strains (n = 22) | Total (n = 29) | p-Value |
|---|---|---|---|---|
| Blood vs. DFU | ||||
| blaZ | 3 (42.9%) | 9 (40.9%) | 12 (41.4%) | 1 |
| mecA | 0 (0%) | 1 (4.5%) | 1 (3.4%) | 1 |
| ermA | 0 (0%) | 3 (13.6%) | 3 (10.3%) | 0.56 |
| vgaA | 3 (42.9%) | 3 (13.6%) | 6 (20.7%) | 0.13 |
| gyrA | 1 (14.3%) | 5 (22.7%) | 6 (20.7%) | 1 |
| grlA | 6 (87.5%) | 17 (77.2%) | 23 (79.3%) | 1 |
| grlB | 1 (14.3%) | 13 (59%) | 14 (48.3%) | 0.08 |
| tetk | 0 (0%) | 1 (4.5%) | 1 (3.4%) | 1 |
| rpoB | 0 (0%) | 1 (4.5%) | 1 (3.4%) | 1 |
| fusB | 1 (14.3%) | 7 (31.8%) | 8 (27.6%) | 0.63 |
| ant(9)-Ia | 0 (0%) | 3 (13.6%) | 3 (10.3%) | 0.56 |
| fosB | 4 (57.1%) | 6 (27.3%) | 11 (37.9%) | 0.19 |
Fisher’s exact test was used to establish statistical significance.
Table 3.
Comparison of biofilm-related genes between the S. pettenkoferi blood culture and DFU strains groups and biofilm groups.
Table 3.
Comparison of biofilm-related genes between the S. pettenkoferi blood culture and DFU strains groups and biofilm groups.
| Biofilm Steps | Putative Genetic Determinants of Virulence | Blood Culture (n = 7) | DFU (n = 22) | p-Value B vs. D | Biofilm Group 1 (n = 17) | Biofilm Group 2 (n = 9) | Biofilm Group 3 (n = 3) | p-Value G1 vs. G2 vs. G3 | Total (n = 29) | ||
|---|---|---|---|---|---|---|---|---|---|---|---|
| INITIAL ADHESION | To abiotic surfaces | bhp | Biofilm associated protein | 0 (0%) | 2 (9%) | 1 | 0 (0%) | 1 (11%) | 1 (33%) | 0.07 | 2 (6.9%) |
| atlE | Autolysin E | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | ||
| sesC, sasC, sasG | Surface proteins | 0 (0%) | 0 (0%) | - | 0 (0%) | 0 (0%) | 0 (0%) | - | 0 (0%) | ||
| embp | Extracellular matrix binding protein Embp | 0 (0%) | 0 (0%) | - | 0 (0%) | 0 (0%) | 0 (0%) | - | 0 (0%) | ||
| To biotic surfaces | fnbpA, fnbpB | Fibronectin binding protein A and B | 0 (0%) | 0 (0%) | - | 0 (0%) | 0 (0%) | 0 (0%) | - | 0 (0%) | |
| fbl, fib | Fibrinogen binding protein | 0 (0%) | 0 (0%) | - | 0 (0%) | 0 (0%) | 0 (0%) | - | 0 (0%) | ||
| clfA, clfB | Clumping factors A and B | 0 (0%) | 0 (0%) | - | 0 (0%) | 0 (0%) | 0 (0%) | - | 0 (0%) | ||
| sdrCDEFH | Serine-aspartate repeat-containing protein C,D,E,F,H | 0 (0%) | 0 (0%) | - | 0 (0%) | 0 (0%) | 0 (0%) | - | 0 (0%) | ||
| sdrD B-like domain | B-like domain from the SdrD protein | 4 (57.1%) | 5 (22.7%) | 0.15 | 7 (41.2%) | 1 (11%) | 1 (33%) | 0.24 | 9 (31%) | ||
| MATURATION | Intercellular aggregation | icaA, icaB, icaC | Polysaccharide Intercellular Adhesion (PIA) | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) |
| icaD | Polysaccharide Intercellular Adhesion (PIA) | 0 (0%) | 0 (0%) | - | 0 (0%) | 0 (0%) | 0 (0%) | - | 0 (0%) | ||
| isdA, isdB | Iron-regulated surface determinant protein A,B | 0 (0%) | 0 (0%) | - | 0 (0%) | 0 (0%) | 0 (0%) | - | 0 (0%) | ||
| aap | Accumulation associated protein | 0 (0%) | 0 (0%) | - | 0 (0%) | 0 (0%) | 0 (0%) | - | 0 (0%) | ||
| sbp | S. epidermidis biofilm accumulation | 0 (0%) | 0 (0%) | - | 0 (0%) | 0 (0%) | 0 (0%) | - | 0 (0%) | ||
| Biofilm structuration | splABCDE | Serine proteases SplA, SplB, SplC, SplD, SplE | 0 (0%) | 0 (0%) | - | 0 (0%) | 0 (0%) | 0 (0%) | - | 0 (0%) | |
| splF | Serine protease SplF | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | ||
| clpP | ClpP protease | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | ||
| SSP1763 | Serine protease HtrA-like | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | ||
| HMPREF2802_03390 | Serine protease | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | ||
| REGULATION | icaR | Biofilm operon icaADBC regulator | 0 (0%) | 0 (0%) | - | 0 (0%) | 0 (0%) | 0 (0%) | - | 0 (0%) | |
| agrA, agrC | Accessory genes regulators A and C | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | ||
| agrB, agrD | Accessory gene sregulators B and D | 0 (0%) | 0 (0%) | - | 0 (0%) | 0 (0%) | 0 (0%) | - | 0 (0%) | ||
| sigB | Sigma B | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | ||
| rsbUVW | / | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | ||
| lytSR | LytSR two component regulatory system | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | ||
| arlRS | ArlRS two-component system | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | ||
| mgrA | HTH-type transcription regulator MgrA | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | ||
| cidA | Holin-like protein CidA | 6 (85.7%) | 17 (77.3%) | 1 | 12 (70.6%) | 9 (100%) | 2 (67%) | 0.22 | 23 (79.3%) | ||
| lrgA | Antiholin-like protein LrgA | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | ||
| sarA | Transcriptional regulator SarA | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | ||
| luxS | S-ribosylhomocysteine lyase | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | ||
| DISPERSION | BUY34_08050 | Hemolysin H3C: Phenol soluble modulin beta protein | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | |
Fisher’s exact test was used to establish statistical significance.
Table 4.
Comparison of virulence-related genes between S. pettenkoferi isolated from blood cultures and infected DFUs and their biofilm group profiles.
Table 4.
Comparison of virulence-related genes between S. pettenkoferi isolated from blood cultures and infected DFUs and their biofilm group profiles.
| Putative Genetic Determinants of Virulence | Blood Culture (n = 7) | DFU (n = 22) | p-Value B vs. D | Biofilm Group 1 (n = 17) | Biofilm Group 2 (n = 9) | Biofilm Group 3 (n = 3) | p-Value G1 vs. G2 vs. G3 | Total (n = 29) | ||
|---|---|---|---|---|---|---|---|---|---|---|
| Toxins | yqfA | Hemolysin III | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) |
| hld | Delta hemolysin | 5 (71.4%) | 18 (81.8%) | 0.61 | 14 (82.4%) | 6 (66.7%) | 3 (100%) | 0.53 | 23 (79.3%) | |
| ERS010499_02103 | Hemolysin H1U | 6 (85.7%) | 9 (40.9%) | 0.0801 | 11 (65.7%) | 4 (44.4%) | 0 (0%) | 0.1218 | 15 (51.7%) | |
| hly (hla), hlb, hlg | α- β- γ-hemolysins | 0 (0%) | 0 (0%) | - | 0 (0%) | 0 (0%) | 0 (0%) | - | 0 (0%) | |
| sea, sel, seg, sed | Enterotoxins | 0 (0%) | 0 (0%) | - | 0 (0%) | 0 (0%) | 0 (0%) | - | 0 (0%) | |
| tst-1 | Toxic shock syndrome toxin | 0 (0%) | 0 (0%) | - | 0 (0%) | 0 (0%) | 0 (0%) | - | 0 (0%) | |
| etA, etB, etD | Exfoliatin | 0 (0%) | 0 (0%) | - | 0 (0%) | 0 (0%) | 0 (0%) | - | 0 (0%) | |
| lukDE | Leukotoxin LukD and LukE | 0 (0%) | 0 (0%) | - | 0 (0%) | 0 (0%) | 0 (0%) | - | 0 (0%) | |
| Avoid Host Immune Response and Invasiveness | capA | Capsule biosynthesis protein CapA | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) |
| eno | Enolase | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | |
| katA | Catalase | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | |
| / | esXA: Type VII secretion system (T7SS) substrate | 2 (28.6%) | 4 (18.2%) | 0.61 | 4 (23.5%) | 1 (11.1%) | 1 (33%) | 0.67 | 6 (20.7%) | |
| T7SSB apparatus encoding genes | T7SSb apparatus: EsaA, EsaB, EssA, EssB and EssC | 1 (14.3%) | 1 (4.5%) | 0.43 | 1 (5.9%) | 1 (11.1%) | 0 (0%) | 1 | 2 (6.9%) | |
| tuf | Elongation factor tu | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | |
| lspA | Lipoprotein signal peptidase | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | |
| lgt | Lipoprotein diacylglycerol transferase | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | |
| nucH | Thermonuclease H | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | |
| coA | Coagulase | 0 (0%) | 0 (0%) | - | 0 (0%) | 0 (0%) | 0 (0%) | - | 0 (0%) | |
| spA | Staphylococcus protein A | 0 (0%) | 0 (0%) | - | 0 (0%) | 0 (0%) | 0 (0%) | - | 0 (0%) | |
| vwb | Von Willebrand factor binding protein Vwb | 0 (0%) | 0 (0%) | - | 0 (0%) | 0 (0%) | 0 (0%) | - | 0 (0%) | |
| saK | Staphylokinase | 0 (0%) | 0 (0%) | - | 0 (0%) | 0 (0%) | 0 (0%) | - | 0 (0%) | |
| Protease activity or implicated in proteolysis | clpC, clpX, clpXP | Clp protases | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) |
| mecA | Adapter protein MecA | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | |
| aur | Aureolysin | 0 (0%) | 0 (0%) | - | 0 (0%) | 0 (0%) | 0 (0%) | - | 0 (0%) | |
| Regulation | nsaS | Sensor histidine kinase | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) |
| nsaR | DNA-binding response regulator | 0 (0%) | 0 (0%) | - | 0 (0%) | 0 (0%) | 0 (0%) | - | 0 (0%) | |
| srrB | Sensor protein SrrB | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | |
| srrA | Transcriptional regulatory protein SrrA | 0 (0%) | 0 (0%) | - | 0 (0%) | 0 (0%) | 0 (0%) | - | 0 (0%) | |
| vraSR | Sensor Pt VraS/ Response regulator pt VraR | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | |
| saeSR | Histidine protein kinase SaeS/ Response regulator SaeR | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | |
| Others | virE | Virulence-associated protein E | 0 (0%) | 2 (9.1%) | 1 | 0 (0%) | 1 (11%) | 1 (33%) | 0.07 | 2 (6.9%) |
| cvfB, cvfC | Conserved virulence factor B and C | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | |
| CJ235_09000 | α- β- hydrolase | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | |
| isdF | Iron-regulated surface determinant protein F | 7 (100%) | 22 (100%) | - | 17 (100%) | 9 (100%) | 3 (100%) | - | 29 (100%) | |
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Magnan, C.; Ahmad-Mansour, N.; Pouget, C.; Morsli, M.; Huc-Brandt, S.; Pantel, A.; Dunyach-Remy, C.; Sotto, A.; Molle, V.; Lavigne, J.-P. Phenotypic and Genotypic Virulence Characterisation of Staphylococcus pettenkoferi Strains Isolated from Human Bloodstream and Diabetic Foot Infections. Int. J. Mol. Sci. 2022, 23, 15476. https://doi.org/10.3390/ijms232415476
AMA Style
Magnan C, Ahmad-Mansour N, Pouget C, Morsli M, Huc-Brandt S, Pantel A, Dunyach-Remy C, Sotto A, Molle V, Lavigne J-P. Phenotypic and Genotypic Virulence Characterisation of Staphylococcus pettenkoferi Strains Isolated from Human Bloodstream and Diabetic Foot Infections. International Journal of Molecular Sciences. 2022; 23(24):15476. https://doi.org/10.3390/ijms232415476
Chicago/Turabian StyleMagnan, Chloé, Nour Ahmad-Mansour, Cassandra Pouget, Madjid Morsli, Sylvaine Huc-Brandt, Alix Pantel, Catherine Dunyach-Remy, Albert Sotto, Virginie Molle, and Jean-Philippe Lavigne. 2022. "Phenotypic and Genotypic Virulence Characterisation of Staphylococcus pettenkoferi Strains Isolated from Human Bloodstream and Diabetic Foot Infections" International Journal of Molecular Sciences 23, no. 24: 15476. https://doi.org/10.3390/ijms232415476
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