Original Research ARTICLE
The Staphylococcus aureus Two-Component System AgrAC Displays Four Distinct Genomic Arrangements That Delineate Genomic Virulence Factor Signatures
- 1Systems Biology Research Group, Department of Bioengineering, University of California, San Diego, San Diego, CA, United States
- 2Bioinformatics and Systems Biology Program, University of California, San Diego, San Diego, CA, United States
- 3Department of Pediatrics, University of California, San Diego, San Diego, CA, United States
Two-component systems (TCSs) consist of a histidine kinase and a response regulator. Here, we evaluated the conservation of the AgrAC TCS among 149 completely sequenced Staphylococcus aureus strains. It is composed of four genes: agrBDCA. We found that: (i) AgrAC system (agr) was found in all but one of the 149 strains, (ii) the agr positive strains were further classified into four agr types based on AgrD protein sequences, (iii) the four agr types not only specified the chromosomal arrangement of the agr genes but also the sequence divergence of AgrC histidine kinase protein, which confers signal specificity, (iv) the sequence divergence was reflected in distinct structural properties especially in the transmembrane region and second extracellular binding domain, and (v) there was a strong correlation between the agr type and the virulence genomic profile of the organism. Taken together, these results demonstrate that bioinformatic analysis of the agr locus leads to a classification system that correlates with the presence of virulence factors and protein structural properties.
Staphylococcus aureus is a gram positive human pathogen that has evolved considerable antimicrobial resistance during the clinical antibiotic era. It can cause a wide spectrum of infection types and severity, including soft tissue infection, bloodstream infections, pneumonia, osteomyelitis, and nosocomial device related infections (Lowy, 1998; Yarwood and Schlievert, 2003; Tong et al., 2015). The wide range of pathogenicity of S. aureus can be attributed to its ability to produce various secreted virulence factors, such as enterotoxin, hemolysin (hla), serine proteases (SspA), and TSST-1 (toxic shock syndrome toxin-1), as well as those mediating cell adhesion and host evasion (Nizet, 2007). Most of the virulence factors are regulated by a two-component system (TCS), AgrAC. AgrAC TCS is encoded by the agr locus and acts as a quorum sensing (QS) system in S. aureus. This QS mechanism modulates gene expression based on population density in response to environmental stimuli.
The agr locus of S. aureus contains four genes: agrB, agrD, agrC, and agrA. agrD encodes for pre-peptide signal AgrD, which is modified to mature QS autoinducing peptide (AIP) and secreted to the extracellular space by the protein AgrB. agrC and agrA encode for histidine kinase and its cognate response regulator, respectively, and form the TCS. The agr operon can classify S. aureus strains into four variants or agr types (Novick et al., 1995; Jarraud et al., 2000; Dufour et al., 2002). These four variants (agr types) produce different AIPs that are characterized by different motifs of varying length. The AIP of one group has been identified to cross-inhibit the agr expression in the other groups (Jarraud et al., 2000; Shopsin et al., 2003; Geisinger et al., 2009). While much is known about the divergence of the agr variants (Dufour et al., 2002), most studies have focused on host proclivity (e.g., humans, bovine, etc.) (Jarraud et al., 2002; Lim et al., 2012; Wan et al., 2013; Schmidt et al., 2017) or on geographical location (Zaraket et al., 2007; Xie et al., 2011; Liu et al., 2012).
In this study, we predicted the agr type of all the completely sequenced S. aureus strains, irrespective of the host type or geographical location, and analyzed the divergence amongst the four agr types. We also proposed the evolutionary implications of these divergences.
Materials and Methods
S. aureus Genomic Data
The genomic sequences of 149 completely sequenced S. aureus strains were downloaded from the PATRIC database (sequenced until December 2016) (Gillespie et al., 2011) and re-annotated them with the Prokka v1.12 (Seemann, 2014) annotation tool to identify protein coding genes. The re-annotation was performed to standardize annotations across all genomes. Draft genomes were excluded from the analysis because of their incompleteness.
In Silico Prediction of the agr Locus
The protein concatenated FASTA files of all the acquired 149 strains of S. aureus obtained from Prokka were searched for the presence of the domains of histidine kinases and response regulators using HMMsearch from HMMER package (Eddy, 1998). Hidden Markov Model (HMM) profiles of the histidine kinases and response regulators from Pfam database were utilized to scan the protein sequences. An e-value of 0.01 and score ≥ 0.25 was taken as a threshold to filter the hits from HMMsearch. For identifying the agr operon, neighborhood genes were scanned for the presence of agrB and agrD genes from the protein feature table obtained from Prokka.
Classification of Strains Based on AgrD and Detection of Chromosomal Arrangement in agr Types
Based on the four types of AIPs in S. aureus, we classified S. aureus strains into four agr types. Protein sequences of AgrD for all the S. aureus strains were scanned for the presence of the conserved motifs that are present in each AIP by a custom python script. The corresponding strain was accordingly grouped into agr types. Further, the differences in the chromosomal arrangement of genes in the agr locus for each agr type were investigated. The chromosomal arrangement was identified in the form of “gene context,” defined by conserved intergenic distances between the genes in the agr locus.
AgrC Sequence Variations Among the agr Types
To analyze sequence variation in AgrC across types, we utilized the ssbio package to inspect the biochemical properties of all sequences as well as mutations when aligned to a reference sequence (Mih et al., 2018). All strain sequences were loaded and those of non-standard length (∼430 residues) were ignored for this analysis. For the principal component analysis (PCA), we calculated general biochemical properties of the full sequences using the Biopython ProtParam and EMBOSS pepstats tools (Rice et al., 2000; Cock et al., 2009). These gave general descriptors such as the percentage of polar, non-polar, aromatic, small amino acids, etc. We used these descriptors to create a feature matrix which was then normalized with the Python scikit-learn package (Pedregosa et al., 2011). This feature matrix was then used for PCA, and the largest contributors to the first three principal components were then analyzed.
We conducted pairwise sequence alignments using the EMBOSS needle tool with default parameters (Rice et al., 2000) of all AgrC types to the reference AgrC sequence, set to the available crystallized protein of the cytoplasmic domain (UniProt: A0A0H2WWL2, PDB: 4BXI) (Srivastava et al., 2014). The reference sequence is a type I AgrC protein of S. aureus strain COL. We then analyzed the sequence diversity among types with respect to the reference sequence in terms of amino acid variations at each residue. Variations were scored by the Grantham score, which is a simple measure of biochemical and biophysical property differences of amino acids (Grantham, 1974). These scores of variations for each AgrC type, along with the frequencies of variations observed in each strain types, were plotted on the six transmembrane model of AgrC-I (Lina et al., 1998), using the Protter web service (Omasits et al., 2014). Variation within the cytoplasmic domain was additionally mapped to a homology model from SWISS-MODEL (template PDB: 4JAU) as well as the crystal structure (PDB: 4BXI). Stability changes incurred from these mutations were predicted using FoldX and the included BuildModel function (Guerois et al., 2002; Schymkowitz et al., 2005).
Virulence Genes Prediction and Decision Tree
We downloaded experimentally studied virulence genes in S. aureus from virulence factor database (VFDB) (Chen et al., 2005) and did a BLAST search on the protein FASTA sequences of all the studied S. aureus strains (Altschul et al., 1990) to predict potential virulence genes in S. aureus strains. A threshold of 85% identity and e-value 0.001 was set to only identity significant hits. A decision tree was constructed using rpart package in R based on presence/absence of virulence genes in strains (Therneau et al., 2017).
Classification of agr Types Based on Virulence Genes
We built random forest predictive model using virulence factors as features to classify samples by agr type using the “randomForest” package in R (Liaw et al., 2015). Random forest classifier was built by growing 5,000 trees. For detecting important virulence genes, we used variable importance measure in “randomForest” algorithm.
The aim of this study was to compare the divergence of the four agr types in the strains of S. aureus. Therefore, we first predicted the agr types of the available completely sequenced strains and then subsequently set out to determine the agr type specific differences in (i) the arrangement of genes in the agr locus, (ii) sequence variation in the histidine kinase AgrC, and (iii) the presence of different virulence genes.
agr Types and MLST Typing
We analyzed 149 completely sequenced S. aureus strains from PATRIC database (Wattam et al., 2014) for the presence of agr locus. Of these, 148 strains were predicted to be positive for agr locus, based on the domain search of histidine kinase and response regulator proteins and querying the neighborhood genes for the presence of agrB and agrD (section “Materials and Methods”). Out of these 148 Agr positive strains, 85, 42, 16, and 4 strains were predicted as strains belonging to types I, II, III, and IV, respectively. This prediction was made by scanning the AgrD protein sequences by a custom python script for the presence of conserved motif that are present in each AIP type (Hawver et al., 2016). There was one exception to the type classification we observed. S. aureus strain TCH 959 did not have any conserved cysteine residue for AgrD and therefore could not be classified into any of the four types, thus, we classified it as “type_undefined.”
In addition to the agr typing, Multilocus Sequence Typing (MLST) is used as a tool to further delineate strains according to the sequence similarity (Robinson et al., 2005). Although a specific agr type has been linked to specific MLST groups (Wright et al., 2005), MLST groups within a specific agr type may show clonal divergence (Wright et al., 2005). Hence, we further classified strains within a agr type based on MLST grouping.
MLST grouping of these 148 S. aureus strains were analyzed from the PATRIC database (Wattam et al., 2014; Supplementary Data Sheet 1). This analysis was unable to identify MLST for all the strains in our study. Hence, a manual literature curation was conducted to assign MLST groups to these unclassified S. aureus strains. The names of the strains and their types (agr and MLST) are provided in the Supplementary Data Sheet 1. The MLST grouping which we curated through manual literature search is highlighted in red in Supplementary Data Sheet 1.
Orientation of agr Genes Classifies S. aureus Strains Into Four Specificity Groups
Comparing the differences in the core gene arrangements within the agr locus would allow us to identify if the genomic features of the agr locus could contribute to the agr type specificity. To identify these differences, we analyzed the orientation of genes in the agr locus for each agr type. We found that the intergenic distances between genes in the agr locus differed among the four agr types (Figure 1) and were highly conserved within a specific agr type. For example, over 90% (77/85) of type I strains have a precise overlap of 3 bp between agrB and agrD, whereas genes are separated by 3, 4, and 2 bp in types II, III, and IV, respectively. Similarly, the intergenic distance between agrD and agrC in type II was 30 bp, while the same distance was 25 bp in the other three agr types. The intergenic distance between agrC and agrA was conserved and separated by 19 bp in all the four types.
FIGURE 1. agr locus in different agr types. The intergenic distances between agrB, agrD, agrC, and agrD genes are conserved with agr types. The arrangement is true for 77 out of 85 strains in type I, 37 out of 42 for type II, and all the strains of type III and IV. The direction of arrows in the agr locus is the representation of those present in the positive strand. A similar arrangement occurs in the negative strand. The length of the arrows representing genes is not to scale. The black dotted line highlights the variable region in the agr locus.
However, we did observe a few non-canonical arrangements in types I (8/85) and II (5/42) which did not follow these same trends of intergenic distances indicated. Two of the type I strains (S. aureus strain T0131 and S. aureus strain HC1335) were found to contain a transposase gene between the hypothetical gene adjacent to agrD and agrC (Supplementary Figure 1). A previous study from Botelho et al. (2016) identified IS256 transposase in these two strains and suggested that this transposase truncated agrC into two, which inhibited the gene and subsequently the regulation of agr locus. While we were unable to identify any conserved motifs in the hypothetical gene between agrD and agrC to define it as a histidine kinase, we did observe five transmembrane helices. Further, to test the hypothesis whether transposase truncated agrC into two, we conducted a sequence alignment of the protein coding regions of the hypothetical gene between agrD and agrC, transposase, and agrC of these two strains with the rest of the canonical type I AgrC using Clustal Omega (Sievers and Higgins, 2014; Supplementary Figure 9). We observed that the protein coding region of the hypothetical gene between agrD and agrC and the agrC of S. aureus strain T0131 and S. aureus strain HC1335 aligned perfectly with the rest of the canonical type I AgrC, but there was a clear separation within the region of the transposase (these two strains are highlighted in Supplementary Figure 9). This observation may suggest that the transposase cleaved agrC in a manner that separated the transmembrane domain from its catalytic domain, disrupting the regulation of agr locus. Nevertheless, even with the insertion of transposase or a hypothetical gene, type I maintained its canonical intergenic distances of -3, 25, and 19 bp between agrB, agrD, agrC, and agrA, respectively. The type II variants seem to deviate from the canonical intergenic distances of 3, 30, and 19 bp distance between agrB, agrD, agrC, and agrA, respectively, due to the insertion of hypothetical genes in the agr locus (Supplementary Figure 1). These variations identify sets that may be pseudo non-functional agr locus, as opposed to the canonical fully functional agr locus.
Thus, it was clear that the gene arrangements in the agr locus are specific to the agr types which may contribute to the type specificity of the AIP recognition and allow selective advantage over the niche selection.
AgrC Sequence Variations Among the agr Types
In the previous section, we identified that the gene arrangements in the agr locus is specific to the agr types, suggesting that the AgrC protein sequences may show divergence according to the type of AIP it senses (Ji et al., 1997; Dufour et al., 2002; Goerke et al., 2005; Robinson et al., 2005; Geisinger et al., 2008). Thus, we further wanted to identify specific differences in all the AgrC protein sequences among the four agr types. The variance in AgrC proteins amongst agr types was identified in two ways: (A) by investigating the overall differences in the biochemical content of the AgrC sequences among the four agr types and (B) by scoping out individual amino acid variations between the types.
Overall Differences in the Biochemical Properties of AgrC Proteins
We first looked at characterizing differences in the basic biochemical properties of AgrC among the four agr types, to give us a general idea of the changes occurring at the level of the entire protein sequence. For this, we wanted to see if AgrC protein sequences clustered together as described by these biochemical properties in a PCA. The first two components (PC1-55 and PC2-34%) explained much of the variance seen. The first principal component (PC1) distinguishes between types I/IV, II, and III (Figure 2A). Type II proteins are enriched with a higher percentage of alanine, glycines, and leucines, with an overall greater molar percentage of small and basic residues and a higher isoelectric point (Figure 2B). In correspondence with these properties, type II proteins will also have a lower percentage of tryptophans, serines, glutamic acids, and isoleucines, with an overall lower molar percentage of acidic residues.
FIGURE 2. PCA of AgrC protein sequences across the agr types. (A) A total of 89% of variance is explained with the first two components. Visually, the types cluster well together. A group of six type I strains (purple triangles) cluster close to type IV strains (dark green diamonds) and are commented upon in the main text. The biochemical properties of some strains within the same agr type are very similar to each other and they overlap in the plot, for example: six type I strains which cluster close to type IV strains are represented by a single symbol. (B) Properties that contribute most to principal component 1. A positive sign (blue bar) indicates that this property increases with PC1, while a negative sign (red bar) indicates that this property decreases with PC1. Properties shown are those with a contribution score greater than 1/(total number of properties). (C) Properties that contribute most to principal component 2.
Six type I AgrC proteins (purple triangles in Figure 2A) four of which belong to ST59 type strains clustered near the type IV AgrC proteins (dark green diamonds), potentially suggesting that type IV may have diverged from these type I strains during evolution. Goerke et al. (2005) have also noted a subgroup of type I which was related to type IV. The third principal component (Supplementary Figure 2) explains an additional 5% of variance, and interestingly clusters these six strains alongside the type IV strains. Thus, from this component, these strains are characterized by an enrichment of polar residues, particularly histidine, with a lower molar percentage of non-polar residues. Finally, the second principal component (PC2) (Figure 2C) distinguished type III (cyan circles) very well from the other types and is characterized by higher molar percentage of aliphatic amino acids, charged amino acids, and valines, along with a lower percentage of methionines, lysine, prolines, phenylalanines, and a lower instability index (predicted to be more stable). We also attempted PCA on each of the domains of AgrC (extracellular or intracellular loops, transmembrane helices, or cytoplasmic domain), with the results presented in Supplementary Figure 3. Interestingly, we saw the same clustering of the types for most of the sub-domains.
Amino Acid Variants in AgrC Proteins
From the previous section, it was clear that the biochemical properties of the AgrC protein were specific to the agr type except for a few strains of type I that may form a subgroup closer to type IV. We further looked at the specific amino acid variations in the AgrC protein that may have contributed to the distinctive variations in the biochemical properties among the four agr types. For this analysis, we compared the protein sequences of AgrC for each agr type against a type I AgrC (AgrC-I) from S. aureus (strain COL) as a reference sequence (UniProt: A0A0H2WWL2) (Srivastava et al., 2014). This comparison was limited to AgrC proteins forming canonical gene arrangements, as those in non-canonical arrangements were mostly truncated by insertion sequences and hence amino acid variations would not be correctly identified. Furthermore, the amino acid variations observed in each agr type were mapped onto the predicted six transmembrane domain model (Lina et al., 1998) of the reference AgrC-I sequence A0A0H2WWL2 and were classified using Grantham scores to rate their changes on a scale of “conservative” to “radical” (see section “Materials and Methods”).
Only a few strains of type I deviated from the reference AgrC-I sequence and, moreover, these variations were mostly conservative in nature, demonstrating that the change in the amino acids within the type I would hypothetically not affect the AgrC structure (Figure 3 and Supplementary Figure 4). The variations observed within type I strains were seen to be dictated by the MLST typing of the strains (Supplementary Data Sheet 2), e.g., the mutation L3T occurred in six strains of type I, four of which belong to the ST59 group. A few notable changes included a mutation of V42G which appeared in 22 strains of type I (ST7, ST72, ST398, ST25, ST464) in the first extracellular loop, and F114S which appeared in only two related strains (ST25) near the predicted second extracellular loop (Figure 3D and Supplementary Figure 4). The AgrC sequences for types II and III strains were found to be the most divergent from the reference AgrC-I (Figure 3A). The amino acid variations were mainly concentrated on the first 200 residues, which comprise the N-terminal transmembrane region responsible for sensing AIPs (Figure 3B). We determined that in types II and III, the majority of amino acid variations were from non-polar to non-polar residues (Figure 3C), likely to preserve the helical transmembrane structure as they were mostly found in these regions. Some of the amino acid variations observed in type II were classified as radical changes (Figure 3E and Supplementary Figure 5). Specifically, a few biochemically divergent residues (e.g., G29F, S64F, F65S, C91L, marked in red in Figure 3E) were observed, all of which may rearrange the three-dimensional orientation of the transmembrane helices and consequently their helix–helix contacts in type II strains. In type III strains, none of variations were classified as radical changes (Supplementary Figure 6). Type IV showed very little divergence compared to type I (Supplementary Figure 7).
FIGURE 3. Sequence divergence in AgrC of four agr types. (A) The number of amino acid variations in each protein of agr types. Type I shows the least variation, as the reference strain used for the analysis is of type I. AgrC sequence of type II and type III have the highest number of amino acid variations. (B) The percent of strains having a variation in that residue number. Around 92 and 100% of strains of type II and type III, respectively, have variations mostly in the first 200 residues of AgrC protein. (C) Properties of amino acid variations in each type show that the majority of variations are between non-polar amino acids in type II and type III, meaning there is a much higher divergence in the transmembrane region. Abbreviations: NP, non-polar; P, Polar. (D,E): specific amino acid divergence between type I and type II. The predicted transmembrane topology of AgrC-I reference sequence from CCTOP with highlighted amino acid residues that tend to diverge in (D) type I strains and (E) type II strains, from this study. The color coding is per biochemical and biophysical property of the amino acid residue mutated. Radical, moderate, and conservative is the nomenclature given in the order of amino acid divergence. Radical is a vast difference between amino acid properties and could change the properties of the protein. Conservative is an amino acid substitution which can be tolerated by the protein. Moderate is a biochemically moderate change in the amino acid substitution. Low frequency: amino acid variations that occurred only in very few strains.
Finally, we inspected variations which occurred together (referred to as co-occurring mutations) in the cytoplasmic domain, of which the CA domain has been crystallized (Srivastava et al., 2014) to understand the stability of the AgrC proteins for each type. The mutation of P247 to a threonine corresponds to a phosphotransfer specificity residue (A268) found in a previous study of a similar TCS (Podgornaia et al., 2013) and does not seem to be a type specific mutation itself. This mutation was found to commonly co-occur with additional mutations at S320 and S321 which are located distal to the ATP-binding domain (Supplementary Figure 8). However, we were able to observe various combinations of co-occurring variations that were type specific, e.g., a set of seven type I AgrC proteins had the co-occurring mutations of P247T, Y251F, S320T, S321R, and T345S. The downstream effects of these mutations remain difficult to elucidate even with experimental data (Capra et al., 2010; Podgornaia et al., 2013) but likely have impacts on both the specificity and strength of binding to cognate receptors. We inspected the impact of these co-occurring mutations on the stability of the AgrC protein by using a homology model of the dimeric cytoplasmic domain, and each set of the co-occurring mutation was predicted to be significantly destabilizing (Supplementary Table 1). This destabilization suggests that these mutations may increase the propensity of the kinase to seek out its binding partners (ATP or a response regulator), then induce additional phosphotransfer reactions and lower response times to environmental stimuli. Another potential consequence would be an increase in the likelihood of non-cognate receptors to bind (Studer et al., 2013; Srivastava et al., 2014).
Comparison of Presence of Virulence Genes in the Four Specificity agr Types
To further determine whether there is a correlation between the agr types and the presence/absence of the virulence factors, we evaluated the presence of virulence genes in all the 148 agr positive strains.
We predicted 216 virulence genes in total to be present in the 148 agr positive strains. Of those predicted, 104 were present in all 148 strains (Figure 4A). Some of the conserved virulence genes were capsular polysaccharide genes (cap5A-G genes), aureolysin, autolysin, gamma, and beta hemolysin (hlg, hlb), genes encoding iron regulated proteins (isd genes), and staphylococcal protein A (spa). S. aureus strain SA564 was predicted to have the highest number of virulence genes (189 out of 216) and a mecA negative strain of S. aureus strain SA17_S6 was found to have the least number of virulence genes (131 out of 216) (Supplementary Data Sheet 3). Although most of the virulence genes seemed to be conserved in all the strains of S. aureus (Figure 4A), a classification tree of presence and absence of virulence genes suggested a few differences among the types (Figure 4B). For example, strains in which set15 exotoxin is absent and set30 exotoxin and hld are present may be characterized as type I strains. Similarly, type III can be characterized by the absence of set15, set30, and the presence of cap8H.
FIGURE 4. Virulence factors in Staphylococcus aureus strains. (A) Heat map showing presence and absence of virulence genes in each strain of S. aureus. Red depicts absence and green depicts the presence of a virulence genes. White line demarcates the heatmap into agr types. (B) Classification tree reveals differential regulation of various virulence genes in S. aureus dictated by agr types. (C) Accuracy of the random forest model in predicting agr types. (D) The variable importance computed by random forest algorithm.
Next, we built a predictive model using random forest classifier to classify agr type based on the virulence phenotype. Random forest is a machine learning technique which builds an ensemble of classification trees and then takes the average of all the predictions to determine the class. The model showed an accuracy of 94.5% with an error rate of 5.44% in predicting the agr types. Of 85 type I strains, 97.6% were correctly predicted. Similarly, 92.8% of type II, 87.5% of type III, and 75% of type IV were correctly predicted by this model (Figure 4C). The high accuracy of the model to correctly predict the agr type of the strains based on virulence genes demonstrates that virulence genes can be used to discriminate agr types. Similar to the decision tree shown in Figure 4B, we identified virulence genes that are important for accurate prediction of the agr types (Figure 4D). Random forest algorithm allows two types of importance measurements: “mean decrease in accuracy” and “mean decrease in gini coefficient.” The “mean decrease in accuracy” measures how the accuracy of the model decreases if a variable is dropped. The higher the decrease in accuracy due to exclusion of a variable, the more important that variable is considered. The “mean decrease in gini coefficient” measures the contribution of the variable toward the homogeneity of the nodes in the random forest tree. We utilized the variable importance measure in random forest algorithm to identify important virulence genes.
With these results it was evident that the presence or absence of virulence factors are dependent on the agr type of the S. aureus strains.
In this study, we analyzed the divergence among the agr types of S. aureus with respect to the genomic features and the virulence capacity and found that the genomic features of the agr locus and the virulence capacity of the S. aureus are strongly correlated to the agr types.
We identified that the gene arrangement of the agr locus is specific to the particular agr types. However, we also identified some strains of type I and type II which may have incorporated a “self-destruct” mechanism of the agr inactivation by incorporating transposase or additional hypothetical genes in the agr locus. Inactivation of agr appears to confer a fitness advantage under the conditions of antibiotic selection, in vivo environment, and biofilm formation (Paulander et al., 2012; Tan et al., 2015; Botelho et al., 2016). Loss of agr function has been associated with resistance to host cationic antimicrobial peptides, tolerance to vancomycin, and development of intermediate resistance to vancomycin, a phenotype that is associated with treatment failure in bloodstream infections (Sakoulas et al., 2002, 2003, 2005; Mwangi et al., 2007; Tsuji et al., 2007; Fischer et al., 2011). Therefore, the subsequent study of agr function from isolates derived from healthcare settings as compared to those from the community, as well as agr function with respect to site of infection, may shed further insights on the role of agr inactivation in the pathogenesis of different infections.
We also identified the specific biochemical properties and the amino acid variations that distinguished AgrC proteins among the four agr types. The biochemical properties of the overall protein as well as the sub-domains were found to be type specific, highlighting the fact that individual domains contribute to the structure-function relationship of AgrC. We also observed that the variant agr alleles may form within the same agr types depending on the MLST typing, however, this phenomenon was more evident in AgrC type I strains. Strains belonging to ST59 had different biochemical properties and amino acid variations than the canonical agr type I strains. We observed that ST59 strains were more related to type IV strains; however, they had not attained a full transformation to type IV strains. A similar evolutionary model was proposed by Robinson et al. (2005) where they hypothesized that amino acid variations may occur in the agr locus which may affect agr activity beyond the specificity of the four agr types. The amino acid variations did seem to be concentrated in the transmembrane domain of the AgrC protein, but we could also identify specific co-occurring mutations in the catalytic domain that were type specific. We predicted that these mutations can lead to protein destabilization and change the function of the protein either by increasing the catalytic activity or by decreasing the substrate specificity (Studer et al., 2013; Srivastava et al., 2014).
Finally, we predicted agr type specific production of virulence genes in S. aureus strains (Figure 4). This distinction may be because different agr type strains secrete and recognize different AIP signals and this inherent variability to sense diverse signals correlates with pathogenesis (Yarwood and Schlievert, 2003). In addition, random forest classifier enabled us to correctly predict the agr type with an accuracy of 94.5%. The accuracy of the model confirmed our hypothesis that the virulence capacity is indeed correlated with the agr type of the strain which may give them a more competitive advantage over others. It is important to note that although ST59 strains (type I strains) have diverged from the rest of the type I strains, as seen from the amino acid variations in the AgrC sequence, the divergence is not enough to differentiate the virulence capacity of these strains.
Our study suggests that during evolution, agr typing and the gene arrangements of the agr locus may have evolved together, giving rise to differential virulence capacity. The AgrC sequences subsequently diverged, giving rise to variant agr alleles among the same agr types owing to environmental pressure and competitive advantage.
KC and BP designed the research. KC, NM, and JM performed the research. KC, NM, JM, EK, JY, and GS performed analyses. KC, NM, JM, EK, JY, GS, and BP wrote the manuscript. All the authors have read and approved the manuscript.
This work was supported by grant U01AI124316 from the NIH NIAID.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
We would like to thank Dr. Ke Chen for helpful discussion. We would also like to thank Marc Abrams for proofreading and editing of the manuscript.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmicb.2018.01082/full#supplementary-material
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Keywords: Staphylococcus, AgrAC, agr types, genomic arrangements, virulence, bioinformatics, microbiology
Citation: Choudhary KS, Mih N, Monk J, Kavvas E, Yurkovich JT, Sakoulas G and Palsson BO (2018) The Staphylococcus aureus Two-Component System AgrAC Displays Four Distinct Genomic Arrangements That Delineate Genomic Virulence Factor Signatures. Front. Microbiol. 9:1082. doi: 10.3389/fmicb.2018.01082
Received: 09 March 2018; Accepted: 07 May 2018;
Published: 25 May 2018.
Edited by:Dimitris G. Hatzinikolaou, National and Kapodistrian University of Athens, Greece
Reviewed by:William Schwan, University of Wisconsin–La Crosse, United States
Christian U. Riedel, Universität Ulm, Germany
Copyright © 2018 Choudhary, Mih, Monk, Kavvas, Yurkovich, Sakoulas and Palsson. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.