Comparative Genomics and Drug Resistance of a Geographic Variant of St239 Methicillin-resistant Staphylococcus Aureus Emerged in Russia

Two distinct classes of methicillin-resistant Staphylococcus aureus (MRSA) are spreading in hospitals (as hospital-acquired MRSA, HA-MRSA) and in the community (as community-acquired MRSA, CA-MRSA). Multilocus sequence type (ST) 239 MRSA, one of the most worldwide-disseminated lineages, has been noted as a representative HA-MRSA. Here, we isolated ST239 MRSA (spa type 3 [t037] and staphylococcal cassette chromosome mec [SCCmec] type III.1.1.1) and its novel variant with ST239/spa351 (t030)/SCCmecIII.1.1.4 (SCCmecIII R) not only from hospitals but also from patients with urethritis in the community in Russia. The Russian variant (strain 16K) possessed a hybrid genome consisting of CC8 and CC30, similar to the ST239/spa3/SCCmecIII.1.1.1 HA-MRSA (TW20) genome, but with marked diversity. The 16K9 CC30 section had SCCmecIII R carrying the dcs-carrying unit (which corresponded to the SCCmecIVc J3 joining region of ST30 CA-MRSA), lacked SCCmercury, and possessed a novel mobile element structure (MES16K) carrying the ccrC-carrying unit (with the recombinase gene ccrC1 allele 3) and drug resistance tranposons. The Russian variant included strains with a high ability to transfer its multiple drug resistance by conjugation; e.g., for strain 16K, the transfer frequency of a chloramphenicol resistance plasmid (p16K-1 with 2.9 kb in size) reached 1.4610 22 , followed by Tn554 conjugative transfer at 3.66l0 24. The Russian variant, which has been increasing recently, included divergent strains with different plasmid patterns and pulsed field gel electrophoresis profiles. The data demonstrate the alternative nature of ST239 MRSA as CA-MRSA and also as a drug resistance disseminator, and its micro but dynamic evolution in Russia. Copyright: ß 2012 Yamamoto et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.


Introduction
Methicillin-resistant Staphylococcus aureus (MRSA) was isolated in the early 1960s and has continued to be a life-threatening multiple drug-resistant bacterium in hospitals [1,2]. MRSA is generated from methicillin-susceptible S. aureus (MSSA) by the acquisition of staphylococcal cassette chromosome mec (SCCmec) at the 39 end of orfX (SCCmec insertion site, att) [3]. It is considered that this has occurred only a limited number of times, resulting in the current epidemics in hospital settings [3][4][5].
Of those, the Brazilian clone (first ST239 MRSA) spread among hospitals in Brazil in 1992 [18], and then caused intercontinental spread to hospitals in Portugal, possibly linked to Brazil-to-Portugal migration of human populations since 1992-1993 [11,19]. The Hungarian clone emerged in hospitals in Hungary in 1993, became predominant in hospitals until 1998, and then almost disappeared in 2003-2004 from Hungary [12][13][14]; however, there is no single reference addressing the molecular typing or characteristics of MRSA strains (Hungarian clone) isolated in Hungary. SCCmec types were SCCmecIIIA for the Brazilian clone (e.g., strain HU25) while SCCmecIII for the Hungarian clone (e.g., strain HU106) [19].
Moreover, the ST239 TW clone (strain TW20) was noted as intensive care unit (ICU)-associated MRSA in London between 2002 and 2004 [20], and the complete genome of TW20 was described [8]. Harris et al. [6] have recently described the comparative genomics of globally-collected ST239 strains using Illumina genome analysis and the TW20 genome as a reference, demonstrating the global geographic structure within ST239 MRSA, based on genome-wide single nucleotide polymorohisms (SNPs). The ST239 lineage consisted of more than five MRSA clades reflecting the continental origin, such as Asia, North America, South America, Europe (with marked divergence), and Australia, albeit with some intercontinental transmission cases. According to the study of Harris et al. [6], TW20 clustered within the Thai clade (most probably suggesting transmission from southeast Asia to London), the Brazilian clone (e.g., strain HU25) clustered within the South America clade, and Hungarian isolates (during 1993-1996) exhibited divergent European phylogeny in SNPs.
The term, hospital-acquired MRSA (HA-MRSA), which includes MRSA isolated in the nosocomial environment, has been used since the description of CA-MRSA. In this study, we isolated MRSA, including ST239 MRSA, from patients in hospitals and also from patients with nongonococcal urethritis in the community in Russia, and examined the molecular characteristics of these MRSA strains. We also investigated the comparative genomics of an ST239 variant (strain 16K) with unique features in terms of evolution and drug resistance using the TW20 genome as a reference.

Patients and bacterial strains
Thirteen outpatients were enrolled in this study, all of whom were male outpatients (age range, 19-40 years; mean age, 29 years) of two hospitals in Vladivostok, Russia, through the period from 2006 to 2008. All outpatients had discharge (pus) from the urethra, discomfort inside the urethra, and discomfort while passing urine. Examination of swabs (discharge) from the urethra revealed the presence of polymorphonuclear neutrophils and MRSA in all cases; no other pathogens, such as Neisseria gonorrhea, Chlamydia, Ureaplasma, Mycoplasma, Candia, Trichomonas and STDassociated viruses, were detected; therefore, outpatients were diagnosed with nongonococcal urethritis due to MRSA. No nosocomial or familial transmissions were observed. The 13 MRSA (including strain 16K) were epidemiologically diagnosed as CA-MRSA; in this study, CA-MRSA was defined as MRSA isolated from outpatients who had no history of hospitalization within at least the past year and presented with no other established risk factors for MRSA infections, such as surgery, residence in a long-term care facility, dialysis, or indwelling percutaneous medical devices and catheters; and HA-MRSA was defined as MRSA isolated from inpatients 48 h after hospitalization [2,22].
In this study, 18 HA-MRSA strains, isolated from inpatients (age, 34-71 years; mean age, 51.8 years) in four hospitals in Vladivostok between 2004 and 2008, were also examined; they were isolated from surgical wound infections, pneumonia, and blood stream infection (including sepsis). Five HA-MRSA strains were isolated from inpatients (age, 3-64 years; mean age, 26.6 years) in two hospitals in Vladivostok in 2011 from surgical wound infections and burn infections. This study was complied with the ethics review board Niigata University School of Medicine, Niigata, Japan. Written informed consent was obtained from patients.

PFGE analysis
Bacterial DNA was digested with SmaI and the digested DNA was applied to PFGE (1.2% agarose), as described previously [34]. A lambda ladder (Bio-Rad Laboratories, Tokyo, Japan) was used as the molecular size standard.

Plasmid analysis
Plasmid DNA of MRSA strains was prepared using a Plasmid Midi Kit (QIAGEN Sciences, Tokyo). Plasmid DNA was introduced into MRSA by electroporation using a Gene Pulser II electroporator (Bio-Rad).

Conjugative transfer
Donor strains were mated with S. aureus RN2677 (recipient strain, which is restriction-negative and resistant to rifampicin and novobiocin) on membrane filters on tryptic soy agar (Difco, Sparks, MD, USA) (filter mating), as previously described [25]; RN2677 was used as a recipient because it carried no plasmids and had non-transmissible drug resistance (recipient) markers. In some experiments, donor and recipient cultures were mixed at 1:2, centrifuged, and spotted on tryptic soy agar without filters (nonfilter mating). Alternatively, donor and recipient cultures were mixed in tryptic soy broth (Difco) (liquid mating). The resistance genes of donor strains and transconjugants were examined by PCR as previously described [27].

Susceptibility testing
Bacterial susceptibility testing was carried out according to previous procedures [35]. Breakpoints for drug resistance were those described by the CLSI [35].
Therefore, around 2006, the ST239/spa3/SCCmecIII.1.1.1 type was the most prevalent and the variant (ST239/spa351/SCCme-cIII R ) type was the second most prevalent, not only in the community but also in hospitals.
Of the five MRSA strains epidemiologically diagnosed as HA-MRSA in 2011, one strain (group C1) corresponded to group A1 or B1. Four strains (group C2) exhibited the same genotype as group A2 or B2, indicating the increase of the ST239 variant type in 2011; however, of four C2 strains, three strains exhibited slightly distinct PFGE profiles and plasmid patterns (containing 2.9-kb chloramphenicol resistance and 38-kb cadmium resistance plasmids) ( Table 1 and Figure 1).

Comparative genomics of the ST239 Russian variant (strain 16K)
The 16K genome sequence was compared with the TW20 genome ( Figure 2). The 16K genome was estimated to be at least 2.8 Mb in size, showing approximately 99.9% homology with the TW20 region (in green), excluding four large non-or less homologous regions (283.6-Kb, in yellow). The CC30 and CC8 hybrid regions on the genome were assigned according to Holden et al. [8].
There were several phage deletions in16K: WSa1 and WSPb-like were absent; and a part of WSa3 was lacking ( Figure S2A). Moreover, marked divergence was observed with SaPI1 ( Figure S2B).
In 16K, the blaz gene (encoding ampicillin resistance) was located in ICE6013 (Figure 2), and the tetM gene (encoding tetracycline and minocycline resistance) was in a smaller Tn5801like structure, which lacked dfrG (encoding trimethoprim resistance) ( Figure S2C). Rifampicin resistance (MIC, 256 mg/ml) was due to Leu 466Ser and His481Asn mutations in rpoB, and levofloxacin resistance (MIC, 4 mg/ml) was due to mutations Ser80Phe in grlA and Glu88Lys in gyrA (Figure 2).

MES16K structure of strain 16K
The complete sequence of MES16K was determined ( Figure 4A). It was 30,818 bp in size and flanked by 16-bp inverted repeats (IRs). MES16K was inserted into the orf on the 16K genome, corresponding to SATW20_27600 of TW20; the att (target) sequence was 8-bp long, and was duplicated at both ends of MES16K. The 8-bp att and 16-bp IR sequences showed no homology to the 15-bp att sequences for SCCmecIII or SCCmercury. MES16K shared a similar ccrC-carrying unit with SCCmercury, albeit with ccrC1 allele 3 for 16K and ccrC1 novel allele 10 for TW20 ( Figure 4B) and also with IS insertion in ccrC1 in TW20 (but not in 16K). Tn554 was present in both MES16K and SCCmercury, but in MES16K, Tn4001 was inserted into the ermA gene of Tn554.

Conjugative transfer of drug resistance
The ST239/spa351/SCCmecIII R variant (especially group A2) transferred its drug resistance to S. aureus RN2677 by bacterial mating on agar plates, in the order of chloramphenicol, erythromycin, gentamicin, cadmium, and tetracycline resistance ( Table 2).
Plasmids were detected only in chloramphenicol-resistant transconjugants (Tables 1 and 2). For group A2 MRSA (isolated from the community during 2006-2008), the size of chloramphenicol-resistance plasmids was 2.9-kb. The sequence of the chloramphenicol-resistance plasmid (GenBank accession number, AB539725), donated from strain 16K (group A2), was consistent with p16K-1 in Figure 2. In contrast, for MRSA strains from P4) for SCCmecIII R and two bands (PM1 and PM2, marked with arrows) for MES16K. PCR band P4 was shared by SCCmecIII R and SCCmecIVc (and SCCmecIVa, SCCmecII, and SCCmecI). The combination of P1, P2, P4, PM1, and PM2 was unique to the Russian variant (strain 16K). doi:10.1371/journal.pone.0029187.g003 Figure 4. MES16K structure and phylogenetic tree analysis for the ccrC genes. The SCCmercury data for strain TW20 are from GenBank accession number FN433596. The GenBank accession number of MES16K is AB666466. Homologous regions are shaded. In A, for strain TW20, the ccrC-carrying unit was located within SCCmercury; the ccrC gene (marked in yellow) was split by the insertion of IS (IS200 family). For strain 16K, the ccrC-carrying unit was located within a mobile element structure MES16K, which was inserted into the orf (corresponding to SATW20_27600 of TW20) on the 16K genome, as shown in Fig. 2; the ccrC gene (marked in yellow) was intact. The attachment sequence (att) of MES16K showed no homology to that (att) of the orfX, SCCmecIII.1.1.1 or SCCmercury. Arrowheads PM1 and PM2 represent PCR targets for detection of SCCmercury of ST239/ SCCmecIII.1.1.1 MRSA and MES16K of the Russian variant (strain 16K) by multiplex PCR (Fig. 3). In B, the ccrC gene sequence of strain 16K and that of strain TW20 (expected intact ccrC gene sequence, obtained by excluding the inserted IS200-family sequence) were analyzed for phylogenetic diversity, as described previously [36]. The ccrC gene of strain TW20 was a novel ccrC1 allele (named ccrC1 allele 10) and that of strain 16K was assigned as ccrC1 allele 3, unambiguously demonstrating evolutionary diversity between them; moreover, the ccrC1 gene of ST398 MRSA strain S0385 was also a novel allele (named ccrC1 allele 11). doi:10.1371/journal.pone.0029187.g004 hospitals during 2004-2008 (one B1 strain [strain 2H] and B2 strains), the plasmid size was 41-kb or 30-kb. And, for MRSA from hospitals in 2011, the plasmid size in one strain (strain 105H) was 41-kb, while the plasmid size in three strains (strains 102H, 103H, and 104H) was 2.9-kb, indicating periodical changes of chloramphenicol-resistance plasmids. No transfer or low-level transfer was observed for ST239/spa3/ SCCmecIII.1.1.1 strains (groups A1, B1, and C1), except for strain 2H (group B1) which donated a 41-kb chlorampenicol resistance plasmid (Table 2). Moreover, group A1 strain 6K carrying p16K-1, which was constructed by introduction of p16K-1 DNA into strain 6K by electroporation, gave no transconjugants, indicating that p16K-1 transfer occurred in a host (strain 16K)-dependent manner.
In mating between 16K and RN2677, erythromycin-resistant transconjugants (including RN2677-16KEmA2) possessed Tn554 (GenBank accession number, AB539726) inserted into the radC gene (Figures 2 and 5A). There were no repeats at either terminus of Tn554 and no repeats of the ''target'' sequence, unlike other transposons (as reported previously [37][38][39]). The hexanucleotide sequence at the left end of Tn554 in RN2677-16KEmA2  Transconjugant RN2677-16KEmA2 was obtained by mating between strain 16K (donor) and S. aureus RN2677 (recipient). The data for strain TW20 are from GenBank accession number FN433596. In A, Tn554 was integrated into the radC gene in RN2677, at exactly the same site as the Tn554 integration site in radC for strain TW20; the radC right-side hexanucleotide sequence, immediately adjacent to Tn554, is marked in blue. The Tn554 left-side hexanucleotide sequence (marked in red) was distinct between the two Tn554 sequences of strains RN2677-16KEmA2 and TW20, reflecting (59-GACATC) was distinct from that of Tn554 within the TW20 radC gene (59-CAAGCT) ( Figure 5A; sequence in red), reflecting the former target site sequence [37][38][39] in each case. The free circular intermediate of Tn554 was present for both donor strain 16K and transconjugant RN2677-16KEmA2 ( Figure 5B-D). For Tn554 in the transconjugant, there was a deletion in spc ( Figure 5A), although it still conferred spectinomycin resistance. Conjugative transfer of erythromycin resistance was also observed for group A3, group B2, group C2, and ST239 reference strains ANS46 and HU25 ( Table 2); these transconjugants also carried spectinomycin resistance gene (spc) and were positive for a Tn554 circular intermediate by PCR (data not shown).

Discussion
The ST239 MRSA lineage is a representative multiple drugresistant HA-MRSA circulating worldwide [2,[4][5][6]8]; for example, it includes TW20, which emerged in an ICU in London [20]. Harris et al. [6] recently demonstrated, based on genome-wide SNPs, that the ST239 lineage consisted of more than five MRSA clades, such as Asia, North America, South America, Europe, and Australia. In this study, we isolated two divergent ST239 MRSA groups with spa3/SCCmecIII.1.1.1 and spa351/SCCmecIII R from Russia; the latter has tended to increase recently. According to Harris et al. [6], spa3 (t037) represents the ancestral (most prevalent) ST239 spa type, and the spa3 type is distributed worldwide, including North and South America, Australia, Europe, and Asia. In contrast, the spa351 (t030) type has been found only in areas of Europe. Based on this, together with the deletion patterns of genomic islands and mobile genetic elements by Harris et al. [6], the Russian ST239/spa351/SCCmecIII R variant may belong to the European clade, suggesting possible transmission from Europe to Far Eastern Russia (although SCCmecIII subtypes or sequences have not been described by Harris et al. [6]).
The two ST239 MRSA groups in Russia were isolated not only from patients in hospitals but also from patients with nongonococcal urethritis in the community; therefore, MRSA may be an agent of sexually transmitted disease in Russia, which would cause great concern about the potential to spread in the community. When the Russian ST239 MRSA strains (spa3/ SCCmecIII.1.1.1 or spa351/SCCmecIII R ) from hospitals and the community were compared, there was a marked divergence in plasmid patterns; e.g., a 2.9-kb chloramphenicol-resistance plasmid in group A2 vs. a 41-kb chloramphenicol-resistance plasmid in group B2. Moreover, the ST239/spa351/SCCmecIII R variant isolated recently (in 2011) showed a slightly divergent PFGE pattern, suggesting micro but dynamic evolution in Russia.
The CC30 genome section of the ST239 hybrid genome (16K) carried two mobile elements, SCCmecIII R and MES16K, and three potential virulence genes, spa [40,41], cna [26,42], and psmmec (encoding a peptide cytolysin [43]). SCCmecIII R was a mosaic SCCmec, consisting of the SCCmecIII core and dcs-carrying unit (as a J3 region). An identical dcs-carrying unit was found in SCCmecIVc of ST30 CA-MRSA (strains NN1 and 80s-2 in Japan [25,44] and also strain RS08 in Russia [45]), indicating that the dcs-carrying unit of the Russian variant could originate in ST30 CA-MRSA. The dcs-carrying unit corresponds to a region with the ccrC-carrying unit in SCCmecVII [36] (now renamed SCCmecV [33]). This region flanked by orfX(attL) and IS431 seems to be a hot spot for recombination.
In strain 16K, the ccrC-carrying unit, found in SCCmecV and SCCmercury [36], was located in MES16K, which carried a composite transposon. MES16K is markedly distinguished from SCCmer or SCCmercury, even in terms of the attachment sequence (att). The ccrC gene is highly variable; for example, it is ccrC1 allele 3 for strain 16K, ccrC1 allele 8 for ST59 CA-MRSA strain PM1 [36], and ccrC1 allele 10 (novel allele type) for ST239 HA-MRSA strain TW20.
One of the most striking features of the Russian variant is its behavior as a multiple drug resistance disseminator. To our knowledge, this is the first demonstration of multiple drug resistance transfer in the ST239 MRSA lineage. For mating, close contact of donor and recipient cells on agar plates is needed, but the use of filters is not essential. There is a possibility that during close-contact mating, plasmids in donor (16K) cells are preferably transferred into recipient bacterial cells, as in the case of p16K-1. For Tn554, which transposes through the circular intermediate [38,39], the circular intermediate may be transferred, followed by subsequent integration into the recipient genome, thus exhibiting lower transfer frequency than a chloramphenicol plasmid (p16K-1).
In conclusion, the ST239/spa3/SCCmecIII.1.1.1 MRSA and its variant (ST239/spa351/SCCmecIII R ) have emerged not only in hospitals but also in the community, associated with nongonococcal urethritis, in Russia. The Russian variant showed high similarity to TW20 in terms of the bulk of the hybrid genome, but was markedly divergent from TW20, such as spa351 vs. spa3, novel mosaic SCCmecIII R vs. SCCmecIII.1.1.1, MES16K vs. SCCmercury, and the presence vs. absence of small chloramphenicol-resistance plasmids. The Russian variant behaved as a drug resistance disseminator, mediating chloramphenicol-resistance plasmid transfer and conjugative Tn554 transposition. Micro but dynamic evolution of ST239 MRSA is proceeding in Russia. Figure S1 The agr subtyping for the Russian variant strain 49K. In A, PCR primers for agr typing are shown as an arrow. Strains: agr1, agr1 type strain; agr2, agr2 type strain; 49K, the Russian variant strain 49K. Strain 49K produced a product only for primer sets (Pan and agr1), and not for (Pan and agr2), assigning strain 49K as agr1. However, in the other PCR assay, strain 49K produced a product both for primer sets (agr1 forward and agr1 reverse) and for agr2 forward and agr2 reverse, resulting in no precise assignment. In B, the agr subtypes were examined by phylogenetic tree analysis, based on the nucleotide sequences of the agr variable region, as described previously [30]. GenBank previous target site sequences for each Tn554 (note that the orientation of the Tn554 structure in the figure is opposite, when compared with previously described Tn554 structures [37][38][39]). The spc gene on Tn554 in a transconjugant (RN2677-16KEmA2) had a single base substitution, resulting in a truncated gene product (lacking 27-aa at the 39-end); the mutated spc gene still conferred spectinomycin resistance. In B, since Tn554 transposes through a circular intermediate [38][39], PCR primers to detect a Tn554 circular intermediate were designed for Tn554 originated in strain 16K. In C, the PCR primer set (CI/F and CI/R, shown in B) exactly detected a Tn554 circular intermediate in strains 16K and RN2677-16KEmA2 (PCR product size, 772 bp) in PCR assay; there were no such bands for strain RN2677. In D, when the sequence of the PCR product, obtained in C, was determined, the Tn554 circular intermediate in RN2677-16KEmA2 possessed the radC hexanucleotide (59-TACATC; marked in blue), but not the Tn554 hexanucleotide sequence (59-GACATC; marked in red). doi:10.1371/journal.pone.0029187.g005 accession number for the variable region sequence of strain 49K is AB592345. Based on the data, strain 49K was assigned as agr19. (TIF) Figure S2 Deletions in drug resistance or virulence genetic traits in 16K, in comparison with TW20. The data of strain TW20 are from GenBank accession number FN433596. Homologous regions are shaded. In A, contigs 41, 14, 85, and 63 (and probably 77) of strain 16K constituted the bulk of the WSa3 phage sequence, showing the presence of the sea gene (encoding superantigen SEA, a virulence factor associated with severe invasive infections) in strain 16K; no right side sequence of WSa3 was present. In B, contigs 4 and 13 of strain 16K constituted the left and right side regions of the SaPI1 superantigen-associated pathogenicity island, showing the presence of the superantigen genes sek and seq in strain 16K. In C, contigs of 42 and 28 of strain 16K constituted the Tn5801-like sequence (including 20-bp direct repeat at both ends), but with deletion of the dfrG gene sequence (encoding trimethoprim resistance) in contig 28. Strain 16 was also negative for dfrG by PCR assay. (TIF)