Search tips
Search criteria 


Logo of rsobThe Royal Society PublishingOpen BiologyAboutBrowse by SubjectAlertsEditorial Board
Open Biol. 2017 December; 7(12): 170094.
Published online 2017 December 20. doi:  10.1098/rsob.170094
PMCID: PMC5746543

Deciphering pathogenicity and antibiotic resistance islands in methicillin-resistant Staphylococcus aureus genomes


Staphylococcus aureus is a versatile pathogen that is capable of causing infections in both humans and animals. It can cause furuncles, septicaemia, pneumonia and endocarditis. Adaptation of S. aureus to the modern hospital environment has been facilitated, in part, by the horizontal acquisition of drug resistance genes, such as mecA gene that imparts resistance to methicillin. Horizontal acquisitions of islands of genes harbouring virulence and antibiotic resistance genes have made S. aureus resistant to commonly used antibiotics. To decipher genomic islands (GIs) in 22 hospital- and 9 community-associated methicillin-resistant S. aureus strains and classify a subset of GIs carrying virulence and resistance genes as pathogenicity and resistance islands respectively, we applied a host of methods for localizing genomic islands in prokaryotic genomes. Surprisingly, none of the frequently used GI prediction methods could perform well in delineating the resistance islands in the S. aureus genomes. Rather, a gene clustering procedure exploiting biases in codon usage for identifying horizontally transferred genes outperformed the current methods for GI detection, in particular in identifying the known islands in S. aureus including the SCCmec island that harbours the mecA resistance gene. The gene clustering approach also identified novel, as yet unreported islands, with many of these found to harbour virulence and/or resistance genes. These as yet unexplored islands may provide valuable information on the evolution of drug resistance in S. aureus.

Keywords: Staphylococcus aureus, antibiotic resistance, genomic islands, MRSA, pathogenicity

1. Introduction

Staphylococcus aureus is a Gram-positive coccus and an important human pathogen responsible for nosocomial and community-acquired infections. It colonizes mucous membranes and skin, and can survive even in harsh environmental conditions. Earlier treatment options for S. aureus infections included penicillin G. However, an increase in the emergence of strains resistant to methicillin made treatment very difficult for S. aureus infections [16]. These methicillin-resistant S. aureus (MRSA) strains have since become resistant to other antibiotics including macrolides, lincosamides and all beta-lactams. More recently, multi-drug-resistant MRSA strains have acquired resistance against vancomycin [7,8].

Acquisitions of drug resistance factors are facilitated by horizontal transfer of plasmids, transposons and other mobile genetic elements. For example, the resistance to methicillin was gained by the acquisition of an ‘island’ of genes, namely the staphylococcal chromosome cassette methicillin-resistance (SCCmec) island. SCCmec carries the PBP2a-encoding mecA gene, which is responsible for methicillin resistance. Several studies have, therefore, focused on identifying these genomic islands (GIs) to understand the underlying mechanisms of the emergence of complex antibiotic resistance patterns mediated by horizontal gene transfer (HGT) [3]. These islands and the other mobile genetic elements such as phages, transposons and chromosomal cassettes together constitute the auxiliary or accessory genome of S. aureus. The core genome has previously been reported to be composed of approximately 95% or more of all S. aureus genes [9]; recent studies have revealed recombination hotspots for mobile elements even within the S. aureus core genome [10]. The S. aureus genome backbone is composed of genes present in all or most S. aureus strains, whereas the accessory genome harbours genes that are unique to a strain or are present in only a few strains and are likely a consequence of acquisitions from distantly related or unrelated organisms through HGT. Besides helping gain resistance to antibiotics, foreign genes have also aided S. aureus in causing infections and proliferating in a community setting. For example, the acquisition of Panton–Valentine leucocidin gene by MRSA has given rise to community-acquired MRSA (CA-MRSA) [1,2]. Although S. aureus has traditionally been classified as a nosocomial agent and was believed to cause only hospital-associated infections, the cases of CA-MRSA infection have been increasing owing to the emergence of new CA-MRSA strains as a consequence of HGT [7,11].

Quantifying resistance and virulence-associated GIs is central to understanding the emergence and evolution of hospital-associated (HA) and CA-MRSA strains. In our quest for a robust method for GI detection in MRSA among the currently available GI detection methods, we first assessed their ability to detect known islands in MRSA. The methods displayed varying levels of sensitivity in identifying the known GIs in MRSA, with none found satisfactory in localizing the SCCmec resistance island. We therefore explored an information-entropy-based gene clustering method that uses codon usage bias to identify genes originating from different sources [12]. Although a bottom-up approach (i.e. gene-by-gene analysis) and not usually recommended for detecting large acquisitions, it displayed remarkable success in localizing resistance and other known islands in MRSA in comparison with the existing methods. This is a significant development as more robust detection of MRSA GIs is a precursor to an effective downstream analysis for understanding the emergence and evolution of MRSA strains through GI acquisition. In what follows, we briefly describe the methods used in this study, discuss their performance on localization of known GIs in a representative set of HA- and CA-MRSA genomes, highlight our novel predictions, and conclude with remarks on the impact of this study and future directions.

2. Material and methods

2.1. Methicillin-resistant Staphylococcus aureus genomes

The complete genome sequences and gene coordinates for 22 HA- and 9 CA-MRSA strains were obtained from GenBank ( We referred to the previous studies to compile a high confidence set of known MRSA GIs [5,13,14]. The coordinates of known MRSA GIs, their codon and GC features, and supporting evidence from the corresponding studies are given in table 1 and the electronic supplementary material, tables S1 and S2.

Table 1.
Coordinates of known GIs in the genomes of the five MRSA strains and the corresponding JS-CB predicted GI coordinates. Coordinates of known GIs in MRSA strains [5,13,14] and coordinates of the corresponding JS-CB predicted GIs in the MRSA genomes are ...

2.2. Genomic island detection methods

We used the following GI prediction methods at their default parameter setting unless mentioned otherwise (see §3.2).

2.2.1. Alien_Hunter

Interpolated variable order motifs (IVOM) [15] or Alien_Hunter uses an interpolated Markov model accounting for variable order motifs to assess the compositional difference between a region within a moving window and the genome. Compositionally atypical regions are identified as GIs.

2.2.2. PredictBias

PredictBias examines genomic regions within a moving window and annotates successive ORFs with atypical codon usage bias and either atypical GC composition or dinucleotide composition as GIs [16]. PredictBias also examines the presence of virulence-associated genes within clusters of eight contiguous ORFs; if four of these genes have significant BLAST hits in the virulence factor database (VFDB), the cluster is an annotated GI even if it does not display atypicality in dinucleotide or codon usage bias.

2.2.3. SeqWord

SeqWord uses oligonucleotide usage (OU) patterns to assess compositional differences in the genome [17]. Genomic islands are identified as compositionally divergent regions based on local and global OU patterns.

2.2.4. IslandViewer

This integrated visualization tool provides predictions from three programs, IslandPath-DIMOB, SIGI-HMM, and IslandPick along with the visualization of GIs.

2.2.5. Zisland Explorer

This program uses cumulative GC profile to segment the genome first, assesses the GC heterogeneity to exclude the core (vertically inherited) segments, and finally uses the codon usage bias to identify putative GIs [18].

2.2.6. GIHunter

Genomic Island Hunter (GIHunter) [19] uses a decision tree to identify GIs. It builds a GI/non-GI gene classifier using the dataset of known GIs and non-GIs. GI features, such as sequence composition, presence of mobility genes and integration sites, are used as classification features.

2.2.7. MSGIP

Mean Shift Genomic Island Predictor (MSGIP) is a clustering method based on mean shift algorithm, a non-parametric method that calculates mean shift vector and moves the density estimation window in the direction of local density maxima, until the convergence is reached [20]. Following clustering, MSGIP identifies GIs as clusters of atypical windows with length not exceeding 200 kbp.

2.2.8. GEMINI

GEMINI is a genome-mining tool based on a recursive segmentation and clustering procedure [21]. GEMINI segments a genome recursively into compositionally homogeneous segments within a statistical hypothesis testing framework and then groups similar segments within the same framework. Additionally, GEMINI exploits segment context information to achieve more robust clustering. Potentially, vertically inherited or native segments representing the genome backbone are identified by the largest cluster harbouring segments of ‘typical’ composition. Segments of ‘atypical’ composition, representing putative horizontally acquired DNAs, are assigned to the numerous smaller clusters each representing a likely donor source. Large atypical segments, 8 kbp or more in size, are predicted as GIs.

2.2.9. Gene clustering (JS-CB)

JS-CB is a gene clustering method for identifying putative horizontally acquired genes [12]. Although not designed specifically to detect GIs, we tested its ability to identify GI-borne genes in MRSA genomes [12]. Briefly, JS-CB uses Jensen–Shannon (JS) divergence measure [22,23] to assess the difference in codon usage bias between two genes. Genes with similar codon usage bias are grouped together using an agglomerative hierarchical clustering. JS-CB begins with all individual genes as single-gene clusters, followed by pairwise comparison of the clusters. The two most similar gene clusters (in terms of JS divergence) are merged iteratively within a statistical hypothesis framework. If the p-value, computed based on an analytic approximation of the probability distribution of JS divergence, is less than a preset significance level (default: 0.005), the gene classes are deemed different, otherwise they are merged. The process is performed recursively resulting in clusters of genes with similar codon usage bias. The largest cluster represents the native genes, while the numerous smaller clusters harbour putative alien genes, each representing a potential donor. The clusters of highly expressed genes, e.g. the ribosomal protein genes, are identified and merged with the native cluster. Eight or more contiguous alien genes are annotated GIs.

2.3. Assessment of genomic island prediction methods

To assess the performance of GI prediction tools, we obtained the recall (sensitivity), precision, F-measure (harmonic mean of recall and precision), and performance coefficient (PC) in identifying GIs for each method, as defined below.

equation image

Here, TP [equivalent] true positive, FN [equivalent] false negative, FP [equivalent] false positive.

A predicted GI is deemed a match or true positive if it overlaps with a known GI (see also §3.1 for further details), otherwise it is called a false positive. A misclassified known GI is annotated false negative.

3. Results and discussion

3.1. Comparison of genomic island prediction tools

To understand the contributions of GIs in the evolution of drug-resistant MRSA, we first assessed the published GI detection methods for their ability to identify the well-characterized GIs in the MRSA genomes. These methods were applied to a representative set of MRSA genomes that included three HA-MRSA and two CA-MRSA genomes with known GIs (table 2). Results from the application of current methods, namely JS-CB (gene clustering based on codon usage bias) [12], GIHunter (DGI-database of GIs of 2000 bacterial genomes) [19], IslandPick (automated comparative genomics approach) [24], Zisland Explorer (based on a segmentation algorithm) [18], IslandViewer (database of predicted GIs from three methods) [25], PredictBias (based on G + C content, dinucleotide composition, codon usage bias, and the presence of virulence genes) [16], SeqWord (based on oligonucleotide usage) [17], Alien_Hunter (based on an interpolated Markov model accounting for variable length k-mers and a hidden Markov model) [15], SIGI-HMM (based on a hidden Markov model of codon usage) [26] and MSGIP (clustering using a mean shift algorithm) [20], to MRSA strains MW2, USA300_ FPR3757, COL, Mu50 and N315 are shown in figure 1ae. The known GIs are shown in red on the innermost track in figure 1ae. The number of predicted GIs overlapping the known GIs, with overlap spanning over half of the known GI and the predicted GI not greater than twice the size of the known GI, is listed in the electronic supplementary material, table S3 for each method. PredictBias identified 27 GIs and JS-CB detected 23 GIs, while GIHunter, SeqWord, Zisland Explorer, IslandViewer and Alien_Hunter identified much fewer known GIs. MSGIP did not identify any known GIs. Although PredictBias identified more islands compared to JS-CB, this was achieved at the expense of potentially many false positives (PredictBias predicted 260 GIs, while JS-CB predicted only 66). We quantified a method's ability to identify maximum known GIs with fewer predictions by computing the recall and precision in identifying known islands in the five selected MRSA strains (table 2). If a method generated numerous segments spanning parts of a known GI, the largest segment, i.e. the segment with largest overlap with the GI, was considered the predicted GI corresponding to the known GI. If a prediction overlapped more than one known GI, then each overlap of the predicted segment with the known GIs was considered. In addition to the 50% overlap cut-off for GI identification, the recall and precision were also obtained at cut-offs 75% and 95% (table 2, cut-off N% means that at least N% of a known GI needs to be identified as an alien segment for the prediction to be deemed a success). We thus assessed the ability of a method in identifying GIs as singular units that are mobilized across genomes in single evolutionary events through HGT. The mean values of the performance metrics (averaged over the five strains) are given in table 3. At the cut-off of 50%, JS-CB outperformed the next best performing tools PredictBias, GIHunter and IslandViewer by at least approximately 4% each in the mean accuracy. At the cut-off of 75%, JS-CB performed marginally better than the next best performing tools. At the stringent cut-off of 95%, JS-CB outperformed PredictBias, GIHunter and IslandViewer by approximately 10%, approximately 17%, and approximately 5% respectively in the mean accuracy. We observed similar trend with F-measure and performance coefficient (table 3). Apparently, JS-CB balances recall and precision better than any other methods resulting in overall higher accuracy (tables 2 and and3).3). JS-CB and PredictBias performed much better in identifying the known GIs than the other methods, as indicated by higher recall values; however, PredictBias predicts substantially more GIs than JS-CB and hence suffers from the low precision values (tables 2 and and33).

Figure 1.
GIs predicted in five Staphylococcus aureus MRSA strains by different methods. From the outside inward: first seven circles show the GIs predicted by MSGIP (blank as no island identified), PredictBias, Alien_Hunter, GIHunter, Zisland Explorer, IslandViewer, ...
Table 2.
Assessment of GI prediction tools: Recall and precision in identifying known GIs in five MRSA strains are shown for GI prediction methods. Highest values of recall and precision among all methods are shown in red; recall N%: (number of known GIs with ...
Table 3.
Performance metrics of GI prediction tools: recall, precision, mean accuracy, F-measure, and performance coefficient of GI prediction methods averaged over the five MRSA strains are shown for different overlap cut-offs, with highest values among all methods ...

As many methods often over-segment (i.e. predict more than one segment spanning parts of a GI) or under-segment (i.e. predict a segment that spans whole or parts of more than one GI), we also evaluated their performance through a different assessment criterion—now considering all spanning segments not just the segment having the largest overlap with the GI for the former, and similarly considering all GIs that are spanned wholly or partially by a predicted segment with the restriction that the size of the predicted segment is not more than twice the GI size now removed for the latter. This allowed a known GI to be deemed identified by a method at N% cut-off if the overlaps together exceeded N% threshold for the former, and similarly multiple known GIs were deemed identified if the predicted segment overlapped each of these GIs by over N% of their size. While this raised the recall of these methods, the over-segmentation (identifying a GI as many fragments) was penalized by considering all predicted segments and the under-segmentation (identifying many GIs as one segment) by considering both GI and non-GI regions spanned by the predicted segment in computing the precision of the methods (Case A in the electronic supplementary material, table S4). Alternatively, for under-segmentation, only one GI with the highest per cent overlap among all GIs spanned by a predicted segment was considered in obtaining the recall and precision of a method (Case B in the electronic supplementary material, table S4). This is a reasonable approach that ensures that over-segmenting or under-segmenting methods never reach perfect accuracy (100% recall and 100% precision) as one would expect them not to. JS-CB outperformed other methods for these evaluation criteria. JS-CB yielded the best overall performance, with highest mean accuracy, F-measure, and performance coefficient for all five reference strains at all three cut-offs. The next best performing methods were GIHunter (at 50% cut-off), IslandViewer (at 75% cut-off) and Zisland Explorer (at 95% cut-off) (electronic supplementary material, table S4). Because the complete set of actual GIs in any strain is yet to be determined, these results should be interpreted with caution; in fact, some of the ‘false positives’ could indeed be true positives. However, the relative performance of the methods could still be assessed based on their ability to identify the already-known GIs with fewer predictions; a method balancing this trade-off well, reflected in terms of highest accuracy among the compared methods, could be deemed most successful among the methods.

We performed an additional assessment of the methods by constructing artificial MRSA genomes as described below. The artificial genomes enabled a more objective assessment as the evolutionary history of the segments in these genomes is already known. To construct an artificial recipient MRSA genome, we selected the S. aureus subsp. aureus MW2 genome and purged it of all known GIs as well as sequences that were predicted GIs by any of the nine methods considered in this study. We thus obtained the backbone S. aureus MW2 genome that was identified as core genome by all methods. Artificial donor genomes were similarly constructed, using the genomes of Alkaliphilus metalliredigens QYMF (NC_009633.1), Erysipelothrix rhusiopathiae str. Fujisawa (NC_015601.1), Macrococcus caseolyticus JCSC5402 (NC_011999.1) and Salinicoccus halodurans H3B36 (CP011366.1), which were chosen to represent a broad range of phylogenetically related donors. M. caseolyticus and S. halodurans represent the genera Macrococcus and Salinicoccus respectively within the family Staphylococcaceae that S. aureus belongs to. A. metalliredigens and E. rhusiopathiae represent the classes Clostridia and Erysipelotrichi respectively within the phylum Firmicutes that S. aureus belongs to. We then simulated the transfer of islands into this conservative core of the MW2 genome. Six DNA segments, between 40 and 50 kbp in size, were sampled from the donor genomes and inserted into the artificial MW2 genome, yielding approximately 82% native and approximately 18% alien composition. Ten random trials of this experiment yielded ten artificial genomes on which to assess the methods. Among the assessed methods, JS-CB yielded the highest values for all performance metrics, e.g. the values of F-measure (averaged over 10 artificial genomes) for JS-CB were 0.85, 0.81 and 0.55 at 50%, 75% and 95% cut-offs, whereas those for the next best performing methods were 0.4, 0.31 and 0.29 (Alien_Hunter), 0.37, 0.27 and 0.25 (SeqWord), and 0.29, 0.27 and 0.23 (IslandViewer), respectively (electronic supplementary material, table S5). Similarly, JS-CB outperformed other methods when the methods were evaluated through a different assessment criterion as discussed above (for both Case A and Case B, electronic supplementary material, table S6). The next best performing methods were IslandViewer, Alien_Hunter and SeqWord. We were unable to run PredictBias and GIHunter on artificial genomes; GIHunter returned errors for both artificial and the five reference strains (GI predictions for the reference strains were earlier retrieved from GIHunter's pre-computed database), and PredictBias could not recognize the GenBank annotation files of the artificial genomes). It should be noted that methods such as JS-CB have previously been assessed on simulated genomes of varying complexity [12]. GIs predicted by each method are shown in figure 1, and the performance of the methods on each representative MRSA genome and their ability to identify SCCmec are summarized below.

3.1.1. Staphylococcus aureus strain MW2

Both Alien_Hunter and PredictBias predicted over 50 islands (including both pathogenicity islands and other GIs). By contrast, IslandViewer and GIHunter predicted only five islands in this strain. SCCmec was identified by JS-CB, IslandViewer, Alien_Hunter and PredictBias, but was completely missed by Zisland Explorer and SeqWord. JS-CB predicted 13 GIs identifying seven out of the eight known islands (SCCmecA, νSaα, νSa3, [var phi]Sa2, νSaβ, [var phi]Sa3 and νSa4). Of the seven known islands that overlapped with JS-CB predictions, six could be identified at the 50% cut-off, whereas at this cut-off GIHunter could identify only two known islands, and IslandViewer and Alien_Hunter could detect only one known island. Although PredictBias has the highest recall in identifying the known islands, JS-CB outperformed other methods in terms of precision as is also obvious from the comparison of coordinates of known and predicted islands (table 1 and figure 1).

3.1.2. Staphylococcus aureus strain USA300_FPR3757

The number of predicted islands varied between three (Zisland Explorer) and 50 (PredictBias). SCCmec was identified by JS-CB, Zisland Explorer, GIHunter and PredictBias at the 50% cut-off. JS-CB predicted 15 islands, overlapping with eight of the nine known islands (SCCmec, ACME, νSaα, SaPI-5, [var phi]Sa2, νSaβ, [var phi]Sa3 and νSa4). At the 50% overlap cut-off, JS-CB was most successful, identifying seven of the nine known GIs. PredictBias and GIHunter were the next best, each identifying five of the nine known GIs.

3.1.3. Staphylococcus aureus strain COL

Of the seven known islands, JS-CB's predictions overlapped with six (SCCmec, νSaα, νSaβ, νSa4 (remnant), [var phi]COL, νSa1); however, only four (SCCmec, νSa4, [var phi]COL, νSa1) had over 50% overlap with the predictions. JS-CB predicted an additional 11 GIs in this strain. SCCmec island was also identified by PredictBias and SeqWord. At the 50% overlap cut-off, PredictBias had higher recall than JS-CB but at the cost of many false positives; Zisland Explorer and MGSIP failed to identify any known islands at this cut-off.

3.1.4. Staphylococcus aureus strain Mu50

JS-CB could identify six of the eight known GIs in Staphylococcus aureus strain Mu50, with five overlapping the respective predicted GIs by over 50%. SCCmec was identified by JS-CB and PredictBias at the 50% cut-off. At the 50% cut-off, Alien_Hunter and MGSIP failed to identify any known GIs in this strain.

3.1.5. Staphylococcus aureus strain N315

Of the six known islands in this strain, JS-CB identified four islands at the 50% cut-off. SCCmec was identified by JS-CB, IslandViewer, GIHunter, Alien_Hunter and PredictBias. Zisland Explorer was able to detect only one of the known islands. Alien_Hunter could not identify any GI at the 50% cut-off. MGSIP failed to localize any of the known islands.

Our analysis shows that JS-CB has the highest recall for Mu50 and N315 strains at all cut-offs. PredictBias has highest recall for USA300, MW2 and COL (table 2). JS-CB outperforms all other GI prediction methods by approximately 5% or more in mean recall at the 95% cut-offs, and is outperformed by PredictBias by approximately 11% in mean recall at the lower cut-offs (table 3). PredictBias incurs false positives at much higher rate (mean precision ranges from approximately 4% to 10%, table 3) than JS-CB (mean precision ranges from approximately 18% to 32%, table 3). IslandViewer displays lower recall but higher precision in comparison with JS-CB. GIHunter and Seqword have much lower recall, with a mean recall of 34% and 21% respectively at the cut-off of 50% (table 3); If an island lacks mobility genes or genes required for integration, e.g. [var phi]Sa1, νSaα, νSaβ, νSaγ, GIHunter does not perform well in identifying such islands. By contrast, JS-CB solely relies on codon usage bias for GI identification, and is, therefore, able to identify islands which might have lost their mobility or integration genes. However, the long-term resident islands such as νSaβ, which are likely to have their composition ameliorated to that of the host, were difficult to detect using JS-CB. Compared with JS-CB, PredictBias uses two criteria, namely dinucleotide bias and codon usage bias to delineate GIs; atypicality in either is considered a GI signature. Thus, clusters of ORFs showing atypical dinucleotide bias but not atypical codon usage bias were also annotated as GIs. Furthermore, JS-CB identifies atypical genes by assessing the similarities of the genes against each other rather than assessing the disparities against the genome background, thus identifying even clusters of weakly atypical genes. This may explain the better performance of JS-CB in comparison with the other methods of GI detection. Notably, JS-CB achieves overall highest accuracies by considering only codon usage bias as the discriminant criterion, outperforming the methods that use multiple criteria, such as PredictBias that uses pathogenicity-related gene information in addition to dinucleotide bias and codon usage bias to identify islands.

3.2. Comparison of JS-CB and GEMINI

We further compared JS-CB with a just-published genome mining tool, GEMINI, that performed well in delineating GIs in the Liverpool epidemic strain of Pseudomonas aeruginosa [21]. In application to the P. aeruginosa LESB58 genome, JS-CB identified wholly or partially all four verified islands at its default parameter setting (table 4). By contrast, GEMINI robustly identified three out of the four verified islands (VI-1, VI-2, VI-4) but missed completely VI-3 [21]. This level of performance was achieved by JS-CB by predicting 35.5% of the LESB58 genome as alien, while that by GEMINI by predicting approximately 13% of the genome as alien. When we readjusted the threshold of JS-CB (clustering threshold now set to 1E-28, see [12]) to obtain a conservative estimate of alien DNAs, same as that observed with GEMINI, JS-CB could still detect all four verified islands, with approximately 54% of the total nucleotides from the four verified islands classified as alien, while GEMINI classified approximately 84% of the nucleotides of the verified islands as alien. Both JS-CB and GEMINI identified three of four verified islands at the 50% overlap cut-off. The overall higher sensitivity of GEMINI could be attributed to its segmentation approach that enables detection of large islands with high precision; VI-4 is a large GI with 101 genes, approximately 98% of this island was detected by GEMINI, while JS-CB could detect only approximately 44%. By contrast, the application of GEMINI to MRSA genomes revealed its inability to localize the SCCmec island in N315, Mu50 and COL strains. GEMINI could identify only approximately 500 nucleotides of the SCCmec island for USA300 and MW2 at its default parameter setting. GEMINI predicted approximately 7% of the genome as alien for the five MRSA strains (table 4). When we readjusted the algorithm parameters for GEMINI (segmentation threshold and two-step clustering thresholds now set to 1E-11, 1E-13 and 1E-4 respectively; the default thresholds were earlier set based on P. aeruginosa genome analysis, see [21]), so that GEMINI predicts a similar proportion of a MRSA genome as alien as does JS-CB (approx. 27%). GEMINI was still not able to robustly identify the SCCmec island in all strains; only approximately 23%, approximately 50%, approximately 76%, approximately 92% and approximately 26% of SCCmec were identified in USA300, MW2, N315, Mu50 and COL strains respectively, while these numbers were approximately 99%, approximately 99%, 100%, approximately 99%, approximately 51% for JS-CB (tables 1 and and44).

Table 4.
Comparison of JS-CB and GEMINI: Performance of JS-CB and GEMINI in identifying four verified islands in P. aeruginosa LESB58 strain (a) and SCCmec island in five MRSA strains (b) respectively was assessed at the default parameter setting and at two other ...

SCCmec is characterized by several ORFs with atypical codon usage and GC content at the third codon position [4,28,29]. As JS-CB clusters genes based on codon usage bias, it is better able to exploit codon-specific information and therefore was able to localize SCCmec in the MRSA genomes. By contrast, GEMINI identifies GIs independent of codon information, by examining higher order oligonucleotide compositional biases, and therefore it may miss islands with atypical codon usage biases that are not reflected as atypicality in oligonucleotide composition. GEMINI, by virtue of its ability to analyse multiple genes simultaneously through a recursive segmentation process, localizes large islands more efficiently, which may appear fragmented in the predictions by bottom-up, gene-by-gene analysis methods such as JS-CB that may misclassify weakly atypical genes or compositionally ambiguous genes. Our results from the application of JS-CB and GEMINI to MRSA genomes reveal the complementary strengths of these two methods, which provides a basis for further future research towards the integration of complementary methods for attaining still better accuracy in GI prediction. We also noted that the performance of the GI prediction methods varies genomewise, reinforcing the need to develop methodologies for exploiting the complementary strengths of the prediction methods. An integrative approach to GI detection holds the promise to raise the accuracy bar across all genomes.

3.3. Identification of novel islands in HA- and CA-MRSA strains

JS-CB was able to identify many of the known islands, namely SCCmec, ACME, νSaα, SaPI-5, [var phi]Sa1, [var phi]Sa2, [var phi]Sa3, νSa4, νSa1, νSa3 and [var phi]COL, in the five strains we studied (table 1). However, the compositionally similar islands, such as SCCmec and ACME, and [var phi]Sa3 and νSa4 (electronic supplementary material, table S1), were identified as one combined island instead of two separate islands (table 1). JS-CB missed νSaβ island in N315 and MU50, and νSaγ island in all five strains we examined. This may likely be a consequence of the amelioration process [30], whereby an island loses its inherent evolutionary signatures, after being subjected to the mutational processes of the host genome, over the passage of time since its acquisition. As JS-CB performed comparably or outperformed the current methods in localizing known GIs in five MRSA strains, we applied JS-CB to completely sequenced 22 HA-MRSA and nine CA-MRSA genomes to decipher yet unknown GIs in the MRSA strains. We discuss below our analysis of the JS-CB's novel predictions for the five reference strains, followed by the analysis of novel predictions for the remaining 26 strains.

JS-CB's ability to more robustly identify the known islands in the MRSA strains motivated us to further explore and analyse the novel islands predicted by it. In the five strains that, we examined, JS-CB-identified 42 novel islands (electronic supplementary material, table S7). Several previous studies have enlisted features that typify GIs, e.g. atypical composition, presence of tRNA genes, direct repeats, integrase and transposase genes, and genes that may be imparting novel traits such as those encoding virulence or antibiotic resistance or other novel metabolic traits. To buttress our novel GI predictions, we collected further evidence in support of our predictions (electronic supplementary material, table S7). Of these, seven islands had either transposase or integrase genes, including N315_GI1, N315_GI7, Mu50_GI1 and Mu50_GI6 (figure 2ad, electronic supplementary material, table S7). Fifteen islands harboured genes encoding virulence or antibiotic resistance factors (electronic supplementary material, table S7), including N315_GI3, N315_GI10 and US300_GI7 (figure 3ac). Several islands included repeat regions, e.g. N315_GI1, N315_GI7, Mu50_GI1 and Mu50_GI6. While Mu50_GI1 has a repeat region in an internal site preceding a transposase gene, MU50_GI6 has repeat regions upstream of the island and at an internal site prior to a transposase gene. Likewise, N315_GI1 has a repeat region at an internal site before the transposase genes, while N315_GI7 has a repeat region just upstream of the island. The presence of transposase genes and repeat regions that are often associated with GI integration provides further evidence in support of our novel predictions. Some novel GIs predicted by JS-CB also harboured genes encoding virulence factors (electronic supplementary material, table S7). N315_GI3 (figure 3a) carries genes encoding fibrinogen-binding protein and coagulase, which were previously reported to be involved in virulence [31,32]; this island also harbours a transposase gene. While fibrinogen-binding protein helps S. aureus to colonize its hosts by facilitating attachment to a surface [33], coagulase, also a surface determinant involved in adherence, helps in converting fibrinogen to fibrin [34]. Both N315_GI10 (figure 3b) and USA300_GI7 (figure 3c) have genes encoding intracellular adhesion proteins. These proteins are critical in biofilm formation and adhering to surfaces [35]. USA300_GI7 also harboured an integrase/recombinase gene.

Figure 2.
Gene maps of: (a) N315_GI1: transposase gene imparting mobility to the island has been highlighted in red; (b) N315_GI7: the presence of a transposase gene in the GI is indicated; (c) Mu50_GI1: the presence of a gene encoding transposase of insertion ...
Figure 3.
Gene map of: (a) N315_GI3: this GI possesses multiple copies of transposase genes (shown in red) and genes required for adhesion (i.e. virulence genes), namely fibrinogen-binding protein A and coagulase encoding genes (shown in blue); (b) N315_GI10: the ...

In addition to these five reference strains, we analysed novel predictions by JS-CB for the remaining 26 strains. The full list of putative GIs localized by JS-CB in the completely sequenced HA-MRSA and CA-MRSA genomes is given in the electronic supplementary material, table S8. JS-CB predicted 338 GIs across these 26 genomes. As little information is available about the locations of GIs including SCCmec in these strains, we first attempted to identify SCCmec in the 26 genomes. If a predicted island harboured SCCmec marker genes, namely the mecA and ccr genes, we annotated the predicted island as SCCmec. JS-CB could localize SCCmec in all 26 strains. The approximate location and size of these islands are conserved across all 26 strains, similar to the conservation observed in the five reference strains. If the marker genes were not found in the predicted islands, the sequence alignment program BLAST [36] was used to characterize the islands. Pairwise nucleotide sequence alignment of the predicted islands in 26 strains and the known islands (as in the five reference strains, table 1) was performed using BLAST. νSaα, νSaβ, [var phi]Sa1, [var phi]Sa2 and [var phi]Sa3 were identified based on significantly high similarity of the predicted islands with these islands (query coverage greater than 60% and nucleotide identity greater than 80%). We thus identified 57 known islands across the 26 strains (electronic supplementary material, table S8). Among the remaining 281 predicted islands, 111 contain GI-specific features such as transposase, integrase or phage genes. Among these, 62 islands harbour either virulence or antibiotic resistance genes or both. To identify GIs shared among strains, we grouped the 281 GIs based on sequence similarity using CD-HIT [37]. GIs with high similarity (nucleotide identity greater than 80%) were grouped in a cluster. This yielded in total 22 clusters, each with five or more GIs (electronic supplementary material, table S8).

Several previous studies have reported GIs in MRSA strains [3,4,6,13,14], which were identified based on typical features of GIs, such as mobility genes, transposase, flanking tRNA genes which act as insertion sites, phage genes, insertion sequence elements and direct repeats flanking the GIs. However, with this approach we may miss GIs that lack these features yet have been mobilized through HGT or several long-time resident islands that may have lost some or all of such features. A comprehensive analysis of genomes for the presence of GIs thus requires a combination of complementary methods, including phylogenetic and composition-based or parametric methods. The novel MRSA GIs lacking typical GI-associated features therefore require further investigation.

3.4. Mosaicism of SSCmec

The SCCmec island carries a mec gene complex and chromosome recombinase (ccr) gene complex, and is integrated at integration site sequence (ISS) for SCC [38]. The mec gene complex includes mecA gene, its regulatory genes and insertion sequences [38]. The ccr gene complex includes ccrA, ccB, ccrC genes, and the flanking regions [38]. Depending on the allotype of the genes in the mec and ccr gene complexes, eight types of SCCmec islands have been identified. Of the five reference strains analysed, genes within the SCCmec island were segregated into two or more clusters by JS-CB (electronic supplementary material, table S9), revealing the mosaic structure of SCCmec and the likely distinct ancestries of the disparate segments composing the SCCmec island. Interestingly, methicillin resistance gene mecA and recombinase gene ccr (ccrA, ccrB, ccrC) were assigned to different clusters for N315 and Mu50 strains. GIs structurally similar to SCCmec, carrying ccr genes but lacking mecA gene have been reported previously in Staphylococcus hominis [39]; these islands were also shown to spontaneously excise [39], thus suggesting that the SCCmec like islands lacking mecA gene might have originated earlier and later acquired the mecA gene to form a functional SCCmec island. An alternative explanation for the absence of mecA genes in SCCmec like islands could be the loss of mecA genes from the original SCCmec islands, resulting in the SCCmec like islands lacking mecA in some Staphylococcus genomes. Mosaic islands were not observed in the strains USA300 and COL, but a bipartite SCCmec island was observed in MW2. Of the remaining 26 strains, mosaic SCCmec was observed in 14 strains. Six of these 14 strains with mosaic SCCmec had mecA and ccr genes assigned to different clusters. A tripartite structure of SCCmec was observed in eight strains, and bipartite, quadripartite and pentapartite structures were observed in two strains each in the remaining 26 strains (electronic supplementary material, table S9). The differential mosaicism of SCCmec as observed in our study of course needs further investigation.

4. Conclusion

A gene clustering-based method, JS-CB, outperformed several GI prediction methods in identifying GIs in MRSA genomes. Evidence gathered from the literature and sequence comparison supported many of the novel GIs predicted by JS-CB. The putative functional role of the GIs identified by JS-CB indicates the proclivity of S. aureus to acquire foreign DNAs to become multidrug-resistant or metabolically distinct organisms. JS-CB further revealed the mosaic structures of many GIs including the SCCmec island, which calls for further studies to understand their significance and plausible role in the adaptation of S. aureus to the changing environment. Our study also revealed the complementary strengths of the methods, e.g. JS-CB and GEMINI, which can be exploited in future studies to further improve GI identification in bacterial genomes.

Supplementary Material

Supplementary Tables:


We acknowledge the support by the University of North Texas for accomplishing this project.

Data accessibility

The genome data used are available at NCBI ftp site ( and the software programs used are publicly available from the program websites (JS-CB to be provided on request).

Authors' contributions

R.K.A. initiated and coordinated the project. M.J. and R.K.A. designed the experiments. M.J., S.S. and K.H. performed the experiments. M.J., S.S. and R.K.A. analysed and interpreted the results. M.J., S.S. and R.K.A. wrote the manuscript.

Competing interests

We have no competing interests.


The authors have not received any specific grant from any funding agency for this project.


1. Herold BC, Immergluck LC, Maranan MC, Lauderdale DS, Gaskin RE, Boyle-Vavra S, Leitch CD, Daum RS 1998. Community-acquired methicillin-resistant Staphylococcus aureus in children with no identified predisposing risk. JAMA 279, 593–598. (doi:10.1001/jama.279.8.593) [PubMed]
2. Dufour P, Gillet Y, Bes M, Lina G, Vandenesch F, Floret D, Etienne J, Richet H 2002. Community-acquired methicillin-resistant Staphylococcus aureus infections in France: emergence of a single clone that produces Panton-Valentine leukocidin. Clin. Infect. Dis. 35, 819–824. (doi:10.1086/342576) [PubMed]
3. Holden MTG, et al. 2004. Complete genomes of two clinical Staphylococcus aureus strains: evidence for the rapid evolution of virulence and drug resistance. Proc. Natl Acad. Sci. USA 101, 9786–9791. (doi:10.1073/pnas.0402521101) [PubMed]
4. Baba T, et al. 2002. Genome and virulence determinants of high virulence community-acquired MRSA. Lancet 359, 1819–1827. (doi:10.1016/S0140-6736(02)08713-5) [PubMed]
5. Hiramatsu K. et al 2013. Genomic basis for methicillin resistance in Staphylococcus aureus. Infect. Chemother. 45, 117–136. (doi:10.3947/ic.2013.45.2.117) [PMC free article] [PubMed]
6. Holden MTG, et al. 2010. Genome sequence of a recently emerged, highly transmissible, multi-antibiotic- and antiseptic-resistant variant of methicillin-resistant Staphylococcus aureus, sequence type 239 (TW). J. Bacteriol. 192, 888–892. (doi:10.1128/JB.01255-09) [PMC free article] [PubMed]
7. Centers for Disease Control and Prevention. 1999. Four pediatric deaths from community-acquired methicillin-resistant Staphylococcus aureus—Minnesota and North Dakota, 1997–1999. MMWR Morb. Mortal. Wkly Rep. 48, 707–710. [PubMed]
8. Hiramatsu K. 2001. Vancomycin-resistant Staphylococcus aureus: a new model of antibiotic resistance. Lancet Infect. Dis. 1, 147–155. (doi:10.1016/S1473-3099(01)00091-3) [PubMed]
9. Lan R, Reeves PR 2000. Intraspecies variation in bacterial genomes: the need for a species genome concept. Trends Microbiol. 8, 396–401. (doi:10.1016/S0966-842X(00)01791-1) [PubMed]
10. Everitt RG, et al. 2014. Mobile elements drive recombination hotspots in the core genome of Staphylococcus aureus. Nat. Commun. 5, 3956 (doi:10.1038/ncomms4956) [PMC free article] [PubMed]
11. Huang H, Flynn NM, King JH, Monchaud C, Morita M, Cohen SH 2006. Comparisons of community-associated methicillin-resistant Staphylococcus aureus (MRSA) and hospital-associated MSRA infections in Sacramento, California. J. Clin. Microbiol. 44, 2423–2427. (doi:10.1128/JCM.00254-06) [PMC free article] [PubMed]
12. Azad RK, Lawrence JG 2007. Detecting laterally transferred genes: use of entropic clustering methods and genome position. Nucleic Acids Res. 35, 4629–4639. (doi:10.1093/nar/gkm204) [PMC free article] [PubMed]
13. Diep BA, et al. 2006. Complete genome sequence of USA300, an epidemic clone of community-acquired meticillin-resistant Staphylococcus aureus. Lancet 367, 731–739. (doi:10.1016/S0140-6736(06)68231-7) [PubMed]
14. Gill SR, et al. 2005. Insights on evolution of virulence and resistance from the complete genome analysis of an early methicillin-resistant Staphylococcus aureus strain and a biofilm-producing methicillin-resistant Staphylococcus epidermidis strain. J. Bacteriol. 187, 2426–2438. (doi:10.1128/JB.187.7.2426-2438.2005) [PMC free article] [PubMed]
15. Vernikos GS, Parkhill J 2006. Interpolated variable order motifs for identification of horizontally acquired DNA: revisiting the Salmonella pathogenicity islands. Bioinformatics 22, 2196–2203. (doi:10.1093/bioinformatics/btl369) [PubMed]
16. Pundhir S, Vijayvargiya H, Kumar A 2008. PredictBias: a server for the identification of genomic and pathogenicity islands in prokaryotes. In Silico Biol. 8, 223–234. [PubMed]
17. Ganesan H, Rakitianskaia AS, Davenport CF, Tummler B, Reva ON 2008. The SeqWord genome browser: an online tool for the identification and visualization of atypical regions of bacterial genomes through oligonucleotide usage. BMC Bioinformatics 9, 333 (doi:10.1186/1471-2105-9-333) [PMC free article] [PubMed]
18. Wei W, Gao F, Du M-Z, Hua H-L, Wang J, Guo F-B 2016. Zisland explorer: detect genomic islands by combining homogeneity and heterogeneity properties. Brief. Bioinform. 18, 357–366. (doi:10.1093/bib/bbw019) [PMC free article] [PubMed]
19. Che D, Wang H, Fazekas J, Chen B 2014. An accurate genomic island prediction method for sequenced bacterial and archaeal genomes. J. Proteomics Bioinform. 7, 214–221.
20. de Brito DM, Maracaja-Coutinho V, de Farias ST, Batista LV, do Rêgo TG 2016. A novel method to predict genomic islands based on mean shift clustering algorithm. PLoS ONE 11, e0146352 (doi:10.1371/journal.pone.0146352) [PMC free article] [PubMed]
21. Jani M, Mathee K, Azad RK 2016. Identification of novel genomic islands in Liverpool epidemic strain of Pseudomonas aeruginosa using segmentation and clustering. Front. Microbiol. 7, 1210 (doi:10.3389/fmicb.2016.01210) [PMC free article] [PubMed]
22. Lin J. 1991. Divergence measures based on the Shannon entropy. IEEE Trans. Inf. Theory 37, 145–151. (doi:10.1109/18.61115)
23. Grosse I, Bernaola-Galván P, Carpena P, Román-Roldán R, Oliver J, Stanley HE 2001. Analysis of symbolic sequences using the Jensen-Shannon divergence. Phys. Rev. E 65, 041905 (doi:10.1103/PhysRevE.65.041905) [PubMed]
24. Langille MGI, Brinkman FSL 2009. IslandViewer: an integrated interface for computational identification and visualization of genomic islands. Bioinformatics 25, 664–665. (doi:10.1093/bioinformatics/btp030) [PMC free article] [PubMed]
25. Dhillon BK, et al. 2015. IslandViewer 3: more flexible, interactive genomic island discovery, visualization and analysis. Nucleic Acids Res. 43, W104–W108. (doi:10.1093/nar/gkv401) [PMC free article] [PubMed]
26. Waack S, Keller O, Asper R, Brodag T, Damm C, Fricke WF, Surovcik K, Meinicke P, Merkl R 2006. Score-based prediction of genomic islands in prokaryotic genomes using hidden Markov models. BMC Bioinformatics 7, 142 (doi:10.1186/1471-2105-7-142) [PMC free article] [PubMed]
27. Stothard P, Wishart DS 2005. Circular genome visualization and exploration using CGView. Bioinformatics 21, 537–539. (doi:10.1093/bioinformatics/bti054) [PubMed]
28. Hiramatsu K, Cui L, Kuroda M, Ito T 2001. The emergence and evolution of methicillin-resistant Staphylococcus aureus. Trends Microbiol. 9, 486–493. (doi:10.1016/S0966-842X(01)02175-8) [PubMed]
29. Kuroda M, et al. 2001. Whole genome sequencing of methicillin-resistant Staphylococcus aureus. Lancet 357, 1225–1240. (doi:10.1016/S0140-6736(00)04403-2) [PubMed]
30. Lawrence JG, Ochman H 1997. Amelioration of bacterial genomes: rates of change and exchange. J. Mol. Evol. 44, 383–397. (doi:10.1007/PL00006158) [PubMed]
31. Foster TJ. 2005. Immune evasion by staphylococci. Nat. Rev. Microbiol. 3, 948–958. (doi:10.1038/nrmicro1289) [PubMed]
32. Jonsson P, Lindberg M, Haraldsson I, Wadstrom T 1985. Virulence of Staphylococcus aureus in a mouse mastitis model: studies of alpha hemolysin, coagulase, and protein A as possible virulence determinants with protoplast fusion and gene cloning. Infect. Immun. 49, 765–769. [PMC free article] [PubMed]
33. Foster TJ, Höök M 1998. Surface protein adhesins of Staphylococcus aureus. Trends Microbiol. 6, 484–488. (doi:10.1016/S0966-842X(98)01400-0) [PubMed]
34. Boden MK, Flock JI 1989. Fibrinogen-binding protein/clumping factor from Staphylococcus aureus. Infect. Immun. 57, 2358–2363. [PMC free article] [PubMed]
35. Heilmann C, Schweitzer O, Gerke C, Vanittanakom N, Mack D, Götz F 1996. Molecular basis of intercellular adhesion in the biofilm-forming Staphylococcus epidermidis. Mol. Microbiol. 20, 1083–1091. (doi:10.1111/j.1365-2958.1996.tb02548.x) [PubMed]
36. Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ 1990. Basic local alignment search tool. J. Mol. Biol. 215, 403–410. (doi:10.1016/S0022-2836(05)80360-2) [PubMed]
37. Huang Y, Niu B, Gao Y, Fu L, Li W 2010. CD-HIT Suite: a web server for clustering and comparing biological sequences. Bioinformatics 26, 680–682. (doi:10.1093/bioinformatics/btq003) [PMC free article] [PubMed]
38. Elements IWG-SCC. 2009. Classification of staphylococcal cassette chromosome mec (SCCmec): guidelines for reporting novel SCCmec elements. Antimicrob. Agents Chemother. 53, 4961–4967. (doi:10.1128/AAC.00579-09) [PMC free article] [PubMed]
39. Katayama Y, Takeuchi F, Ito T, Ma XX, Ui-Mizutani Y, Kobayashi I, Hiramatsu K 2003. Identification in methicillin-susceptible Staphylococcus hominis of an active primordial mobile genetic element for the Staphylococcal Cassette Chromosome mec of methicillin-resistant Staphylococcus aureus. J. Bacteriol. 185, 2711–2722. (doi:10.1128/JB.185.9.2711-2722.2003) [PMC free article] [PubMed]

Articles from Open Biology are provided here courtesy of The Royal Society