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. 2016 Aug 3;7:1200. doi: 10.3389/fmicb.2016.01200

Typing of Panton-Valentine Leukocidin-Encoding Phages and lukSF-PV Gene Sequence Variation in Staphylococcus aureus from China

Huanqiang Zhao 1,†, Fupin Hu 2,†, Shu Jin 3, Xiaogang Xu 2, Yuhan Zou 3, Baixing Ding 2, Chunyan He 1, Fang Gong 4, Qingzhong Liu 1,*
PMCID: PMC4971802  PMID: 27536288

Abstract

Panton-Valentine leukocidin (PVL, encoded by lukSF-PV genes), a bi-component and pore-forming toxin, is carried by different staphylococcal bacteriophages. The prevalence of PVL in Staphylococcus aureus has been reported around the globe. However, the data on PVL-encoding phage types, lukSF-PV gene variation and chromosomal phage insertion sites for PVL-positive S. aureus are limited, especially in China. In order to obtain a more complete understanding of the molecular epidemiology of PVL-positive S. aureus, an integrated and modified PCR-based scheme was applied to detect the PVL-encoding phage types. Phage insertion locus and the lukSF-PV variant were determined by PCR and sequencing. Meanwhile, the genetic background was characterized by staphylococcal cassette chromosome mec (SCCmec) typing, staphylococcal protein A (spa) gene polymorphisms typing, pulsed-field gel electrophoresis (PFGE) typing, accessory gene regulator (agr) locus typing and multilocus sequence typing (MLST). Seventy eight (78/1175, 6.6%) isolates possessed the lukSF-PV genes and 59.0% (46/78) of PVL-positive strains belonged to CC59 lineage. Eight known different PVL-encoding phage types were detected, and Φ7247PVL/ΦST5967PVL (n = 13) and ΦPVL (n = 12) were the most prevalent among them. While 25 (25/78, 32.1%) isolates, belonging to ST30, and ST59 clones, were unable to be typed by the modified PCR-based scheme. Single nucleotide polymorphisms (SNPs) were identified at five locations in the lukSF-PV genes, two of which were non-synonymous. Maximum-likelihood tree analysis of attachment sites sequences detected six SNP profiles for attR and eight for attL, respectively. In conclusion, the PVL-positive S. aureus mainly harbored Φ7247PVL/ΦST5967PVL and ΦPVL in the regions studied. lukSF-PV gene sequences, PVL-encoding phages, and phage insertion locus generally varied with lineages. Moreover, PVL-positive clones that have emerged worldwide likely carry distinct phages.

Keywords: Staphylococcus aureus, Panton-Valentine leukocidin, sequence variation, phage typing, genetic background

Introduction

Staphylococcus aureus causes a spectrum of diseases from minor skin and soft tissue infections (SSTIs) to life-threatening conditions due to its potential to produce many toxins and efficiency at overcoming antibiotics (David and Daum, 2010; Uhlemann et al., 2014). Panton-Valentine leukocidin (PVL), found in some strains of S. aureus, plays a key role in the leukocytolysis and tissue necrosis (Shallcross et al., 2013). The genes (lukSF-PV) encoding PVL are composed of two co-transcribed open reading frames (lukS-PV and lukF-PV), and located on lysogenized bacteriophages integrated into S. aureus chromosome (Boyle-Vavra and Daum, 2007; Shallcross et al., 2013).

To date, all known S. aureus phages belong to the order Caudovirales, which can be separated into three major families (Podoviridae, Siphoviridae, and Myoviridae) depending on the tail morphology (Xia and Wolz, 2014). At least 10 PVL phages have been described and sequenced, and all of them belong to the Siphoviridae family characterized by double-stranded DNA and a long non-contractile tail (Zhang et al., 2011; Xia and Wolz, 2014). As the mobile genetic elements, phages can be mobilized and transferred among S. aureus strains. Hence, investigating the typing of PVL-encoding phages among S. aureus may help to better understand the evolution of these pathogens. The PCR-based scheme targeting a small part of the phage genome is a cursory means of predicting phages types inexpensively. However, there is no unified pattern for this scheme. To identify as many PVL-encoding phages as possible, this article summarized a strategy by integrating and modifying the expanded PCR-based scheme described previously (Ma et al., 2008; Boakes et al., 2011; Chen et al., 2013; Sanchini et al., 2014). Subsequently, by the usage of this strategy, fifteen-reaction PCR assay was carried out to detect 10 of the PVL-encoding phages (ΦPVL, Φ108PVL, Φtp310-1, ΦSa2958, ΦSa2mw, ΦSLT, ΦSa2USA, ΦTCH60, Φ7247PVL/ ΦST5967PVL, and ΦSa119) in S. aureus from China.

At least 22 single-nucleotide polymorphisms (SNPs) have been identified in the lukSF-PV genes (Wolter et al., 2007; O'Hara et al., 2008; Boakes et al., 2011; Li et al., 2012; Chen et al., 2013; Sanchini et al., 2014). And several PVL protein isoforms carrying non-synonymous mutations have recently been revealed (O'Hara et al., 2008; Li et al., 2012), which may implicate functional significance. As we all know, phages lysogenize into the bacterial chromosome through the integrative pathway. Boakes et al. (2011) analyzed the sequence diversity at the insertion site for the different PVL-encoding phages and found two lineage-specific insertion sites within the S. aureus chromosome: Ins1 and Ins2. Of note, site-specific attachment sequences (attL and attR) are also conserved across lineages of PVL-carrying strains although some variations were found (Boakes et al., 2011; Chen et al., 2013).

Due to the absence of a uniform detection method, complete data on Chinese epidemiology of PVL-encoding phages are limited (Li et al., 2012; Hu et al., 2015). In addition, no details yet about chromosomal PVL-encoding phage insertion sites for S. aureus in China are reported. In the present study, we aimed to obtain a more complete description of the molecular epidemiology of PVL-positive S. aureus from China by detecting PVL-encoding phage types, analyzing PVL variant alleles and the chromosomal phage insertion junctions, and determining the genetic background. Moreover, the relationships among them were also elucidated.

Materials and methods

Bacterial isolates

During January 2010 to May 2015, a total of 1175 consecutive, non-duplicate clinical S. aureus isolates were collected from seven hospitals in China, namely, Shanghai General Hospital, Shanghai sixth People's Hospital, Tongren Hospital, Ruijin hospital, Shanghai People's Hospital of Putuo District, Zhejiang Xiaoshan Hospital, and The Central Hospital of Lishui City, Zhejiang province (Figure 1). All the isolates, including 924 methicillin-resistant S. aureus (MRSA) strains and 251 methicillin-susceptible S. aureus (MSSA) strains, were identified by VITEK Systems (BioMérieux, Marcy l′ Etoile, France), the susceptibility of cefoxitin (30 μg, Oxoid, Basingstoke, UK), and the presence of mecA and mecC genes (Bignardi et al., 1996; Ganesan et al., 2013; Clinical Laboratory Standards Institute, 2014). The presence of lukSF-PV genes was determined by PCR according to previously published method (Lina et al., 1999).

Figure 1.

Figure 1

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The geographic distribution of 1175 S. aureus isolates.

Single-nucleotide polymorphisms of the lukSF-PV genes

All isolates were cultured on blood agar and incubated overnight at 37°C. Genomic DNA was extracted by TIANamp Bacterial DNA Kit (TIANGEN BIOTECH Co., Ltd., Beijing, China). Three primer pairs were designed to amplify three fragments (654, 718, and 680 nucleotides in length, respectively) of lukSF-PV genes as described by Boakes et al. (2011). All the products of PCR were sequenced in both directions by Shanghai Sangon Biotech.

Characterization of PVL-positive isolates

PVL-positive S. aureus were characterized by staphylococcal cassette chromosome mec (SCCmec) typing (Zhang et al., 2005), staphylococcal protein A (spa) gene polymorphisms typing (Koreen et al., 2004), pulsed-field gel electrophoresis (PFGE) typing (Mulvey et al., 2001), accessory gene regulator (agr) locus typing (Lina et al., 2003) and multilocus sequence typing (MLST; Enright et al., 2000). The spa type for each isolate was obtained based on a website (http://www.ridom.de/spaserver/). Sequence types (STs) were determined by allelic profile according to the MLST database (http://saureus.mlst.net/). And clustering of related STs into clonal complexes (CCs) was analyzed using eBURST (http://www.mlst.net).

PVL-encoding phage typing

Integrating the expanded PCR-based scheme described by previous studies (Ma et al., 2008; Boakes et al., 2011; Chen et al., 2013; Sanchini et al., 2014) with a little modification, three sets of PCRs including 15 PCR reactions (Set 1: PCR-1, -4 -7, and -8, Set 2: PCR-2, -5, and -9 to -13, and Set 3: PCR-3, -6, -14, and -15), were carried out to detect 10 of the PVL-encoding phages (ΦPVL, Φ108PVL, Φtp310-1, ΦSa2958, ΦSa2mw, ΦSLT, ΦSa2USA, ΦTCH60, Φ7247PVL/ ΦST5967PVL, and ΦSa119) (Table 1). PCR-1 to -3 (step-1) targeting genes encoding icosahedral or elongated head shape allowed classification of elongated-head group, icosahedral-head group I and icosahedral-head group II phages; PCR-4 to -6 (step-2) were used to link these morphologically specific tail genes to the lukSF-PV genes with primer pairs commonly conserved among each of the groups; PCR-7 to -15 (step-3) were designed to detect 10 specific PVL-encoding phages. All the PVL-positive isolates were detected by PCR-1 to -3 (step-1). Only when a positive result was obtained from step-1, were step-2, and step-3 performed. Phages which were positive by icosahedral/elongated head classification assays (PCR-1 to -3) and characterization assays (PCR-7 to -15) but negative for linkage assays (PCR-4 and -6), were defined as “phage-like” depending on the existence of known individual phage type (Chen et al., 2013). The workflow and the detailed PCR-based scheme for PVL-encoding phage typing were summarized in Figure 2 and Table 1, respectively.

Table 1.

PCR-based scheme for PVL-phage typing.

Step 1 Step 2 Step 3
Primer use Primer name Target locus Size of PCR product (bp) References PCR's order number Primer use Primer name Target locus Size of PCR product (bp) References PCR's order number PVL phage(s) Primer use Primer (pair) name Target locus Size of PCR product (bp) GenBank accession no. References PCR's order number
Set 1 Icosahedral-head group I portal-1F por 569 Ma et al., 2008 PCR-1 To link icosahedral-head group I specific tail genes to the PVL genes. tail-ico-F mtp 8570 Ma et al., 2008 PCR-4 ΦPVL To Classify individual PVL phages by detecting the gene lineage between the integrase gene and the genes located downstream of the gene. intF-2/PVL-aR int/JP030 1411 AB009866 Ma et al., 2008 PCR-7
portal-1R por Ma et al., 2008 10,497 Φ108PVL intF-2/108-aR int/ant 4340 AB243556 Ma et al., 2008 PCR-8
tail-1F mtp 489 Ma et al., 2008 lukSR1 lukS-PV 8574 Ma et al., 2008 Φtp310-1* intF-2/PVL-aR /108-aR* int/JP030/ ant 1411/4579* EF462197 Ma et al., 2008; Chen et al., 2013 PCR-7, -8
tail-1R mtp Ma et al., 2008
Set 2 Elongated-head group portal-2F por 656 Ma et al., 2008 PCR-2 To link elongated-head group specific tail genes to the PVL genes. tailE-F2 mtp 9483 Otter et al., 2010 PCR-5 ΦSa2958 To Classify individual PVL phages by detecting the gene lineage between the integrase gene and the genes located downstream of the gene. intF-2/2958-aR int/JP004 2238 AP009363 Ma et al., 2008 PCR-9
portal-2R por Ma et al., 2008 9484 ΦSa2mw intF-2/MW2-aR int/ cro 4065 BA000033 Ma et al., 2008 PCR-10
tail-2F mtp 468 Ma et al., 2008 lukSR1 lukS-PV 9486 Ma et al., 2008 ΦSLT intF-2/SLT-aR int/ ssb 8770 AB045978 Ma et al., 2008 PCR-11
tail-2R mtp Ma et al., 2008 9484 ΦSa2USA Sa2USA-F /Sa2USA-R2 phiSLT ORF484-like/lukS-PV 679 CP000255 Boakes et al., 2011; Sanchini et al., 2014 PCR-12
9482 ΦTCH60 intF-2/ TCH60-aR int/HMPREF0772-11656 2675 NC-017342 Ma et al., 2008; Chen et al., 2013 PCR-13
Set 3 Icosahedral-head group II portal-3F por 535 Sanchini et al., 2014 PCR-3 To link icosahedral-head group II specific tail genes to the PVL genes. TAIL-5 mtp 9164 Sanchini et al., 2014 PCR-6 Φ7247PVL/ΦST5967PVL To Classify individual PVL phages by detecting the gene lineage between the integrase gene and the genes located downstream of the gene. intF-2/repR int/rep 2965 AP011956 /AP011955 Ma et al., 2008; Chen et al., 2013; Sanchini et al., 2014 PCR-14
portal-3R por
tail-3F mtp 842 Sanchini et al., 2014 lukSR1 lukS-PV 10.728 Ma et al., 2008 ΦSa119 intF-2/SA119Ant1 int/ant 4918 KJ596420 Ma et al., 2008; Sanchini et al., 2014 PCR-15
tail-3R mtp
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*

Φtp310-1 harbors an icosahedral head and can be identified by the presence of PCR products specific both for ΦPVL and Φ108PVL (positive both for PCR-7 and -8).

Figure 2.

Figure 2

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Work flow for PVL-encoding phage typing. The structure of ΦSLT (GenBank accession no. AB045978) (Xia and Wolz, 2014) and three steps of set-2 PCRs are taken as examples for illustrating the workflow for determination of PVL-encoding phages. The red rectangular boxes indicate target loci of phage typing primers, and the positions of primers are indicated by black arrowheads. Horizontal braces indicate the PCR or PCR groups for 3 steps of PCR-based scheme. The dotted arrows represent the correspondence between assays and steps. Figures in the circle represent several possibilities for PCR results or conclusions. “+” indicates positive result, while “–” indicates negative result.

In case of the fragments amplified >3000 nucleotides, the PCRs were carried out using PrimeSTAR® Max DNA Polymerase (TaKaRa, Dalian, China) adhering to the protocols recommended by manufacturer.

Phage insertion locus sequencing

PCR designed to detect the proximal and distal junctions of PVL-encoding phage insertion sites were performed by the method described previously (Boakes et al., 2011). Sequences were aligned using CLUSTA L X 2.0. Phylip3.6 was used to construct a maximum-likelihood phylogenetic tree with 500 bootstrap replicates for the junction region sequences.

Results

Frequency and characterization of S. aureus harboring lukSF-PV genes

Of 1175 S. aureus isolates, 78 (6.6%) isolates were lukSF-PV genes positive, including 62 MRSA and 16 MSSA. Among the 78 lukSF-PV genes positive strains, 66 (55 MRSA and 11 MSSA) were agr1, 9 (6 MRSA and 3 MSSA) were agr3, and 2 (MSSA) were agr4. One isolate was unable to be classified in any of the established agr groups, which may be an agr-negative variant associated with the extensive use of antibiotics (Paulander et al., 2013). Of course, point mutation occurring in primer binding sequence may be another reason. MLST results showed 15 ST types were produced in isolates studied, namely ST1 (CC1), ST9 (CC9), ST22 (CC22), ST25 (CC25), ST30 (CC30), ST59 (CC59), ST88 (CC88), ST188 (CC1), ST149 (CC5), ST217 (CC22), ST338 (CC59), ST398 (CC398), ST1301 (CC121), ST160 (CC121), and ST172 (singleton). ST59 (64.5%, 40/62) was the most frequent ST in MRSA isolates, while ST398 (25%, 4/16) was the most prevalent type in MSSA strains. Two STs identified in this study have not found matching profiles in the MLST database, and subsequently were designated ST160 and ST172 after we uploaded the data to the website (http://pubmlst.org/saureus/). By sequence analysis of PCR products of the spa gene, 23 spa types were yielded in 78 PVL-positive isolates. The most common spa type identified was t437 (48.7%, 38/78). Two spa types determined in this study were not found in Ridom SpaServer, which were subsequently designated t15796 and t15797 after our submission. It is notable that 94.7% (36/38) of t437 isolates were associated with CC59. In addition, most of t034 strains (75%, 3/4) related to CC398. PFGE typing showed that 78 PVL-positive isolates were divided into 17 patterns. Most of isolates were clustered into PFGE type A (subtypes A1 to A7), type B (subtypes B1 to B3), and type C (subtypes C1 to C7) together accounting for 44.9% (35/78). In 62 PVL-positive MRSA isolates, 57 could be typed (SCCmec I-V) by SCCmec typing method, and 5 (8.1%) were non-typeable. The SCCmec type most commonly found was type III (53.2%, 33/62), followed by type IVa (32.3%, 20/62), type II (3.2%, 2/62), type IVb, and type V (1.6%, 1/62 each). The detailed molecular characterization of PVL-positive isolates by SCCmec, agr, spa, PFGE, and MLST typing was shown in Table 2.

Table 2.

Characteristics and PVL-phage typing of 78 PVL-positive S. aureus isolates.

Isolate ID location ST CC SCCmec spa type agr type PFGE attL cluster attR cluster Phage morphology PVL-phage type Isoform of PVL
MRSA (n = 62)
7 Zhejinag ST1 CC1 V t114 I K I I Icosahedral II Φ7247PVL/
ΦST5967PVL		 H2
LS2183 Zhejinag ST59 CC59 NT t437 I B1 I I Icosahedral II NT H1
161 Zhejinag ST188 CC1 NT t189 I M NS NS Icosahedral II NT H2
SH12 Shanghai ST88 CC88 NT t12147 III A1 IV III Icosahedral I ΦPVL H2
244 Zhejinag ST88 CC88 NT t7637 III C7 IV III Elongated ΦTCH60 H2
104 Zhejinag ST88 CC88 NT t5269 III N IV III Elongated ΦTCH60* R2
148 Zhejinag ST9 CC9 IVb t309 I O VI II Icosahedral I ΦPVL H2
203 Zhejinag ST1 CC1 IVa t127 III H3 I NS Icosahedral I Φ108PVL* H1
SH9 Shanghai ST59 CC59 IVa t441 I I1 I I Icosahedral I ΦPVL H1
209 Zhejinag ST59 CC59 IVa t437 I E3 II I Elongated ΦSa2958 H1
LS373 Zhejinag ST59 CC59 IVa t1751 I B3 I I Icosahedral II NT H2
60 Zhejinag ST59 CC59 IVa t437 I D3 NS I Icosahedral II NT H2
34 Zhejinag ST59 CC59 IVa t437 I J I I Icosahedral II NT H2
65 Zhejinag ST59 CC59 IVa t437 I D1 I I Icosahedral II NT H2
79 Zhejinag ST59 CC59 IVa t437 I F2 I I Icosahedral II ΦSa119 H2
186 Zhejinag ST59 CC59 IVa t437 I I1 I I Icosahedral II ΦSa119 H2
238 Zhejinag ST59 CC59 IVa t437 I C3 II I Icosahedral II ΦSa119* H2
212 Zhejinag ST59 CC59 IVa t437 I E1 II I Elongated ΦSa2958 H2
226 Zhejinag ST59 CC59 IVa t437 I C3 II I Elongated ΦSa2958 H2
246 Zhejinag ST338 CC59 IVa t437 I C5 II III Elongated ΦTCH60 H2
202 Zhejinag ST88 CC88 IVa t7637 III H1 IV III Elongated ΦTCH60 H2
213 Zhejinag ST59 CC59 IVa t1451 I H1 NS NS Icosahedral II NT H2
LS1939 Zhejinag ST59 CC59 Iva t437 I B3 I I Icosahedral II NT H2
SH6 Shanghai ST59 CC59 IVa t441 I A3 I I Icosahedral I ΦPVL H2
40 Zhejinag ST59 CC59 IVa t437 I J II I Icosahedral II ΦSa119 R1
218 Zhejinag ST59 CC59 IVa t437 NT E2 II NS Icosahedral II NT R2
206 Zhejinag ST59 CC59 IVa t437 I H2 II I Icosahedral I ΦPVL R2
LS2032 Zhejinag ST59 CC59 III t437 I A2 I I Icosahedral II NT H1
130 Zhejinag ST59 CC59 III t441 I F2 I I Icosahedral II ΦSa119 H1
242 Zhejinag ST338 CC59 III t441 I C2 I I Icosahedral II Φ7247PVL/
ΦST5967PVL		 H1
256 Zhejinag ST59 CC59 III t5983 I D2 I I Icosahedral II Φ7247PVL/
ΦST5967PVL		 H1
211 Zhejinag ST22 CC22 III t5983 I G1 VI II Icosahedral I Φtp310-1 H1
LS1268 Zhejinag ST59 CC59 III t437 I B3 I I Icosahedral II NT H1
233 Zhejinag ST30 CC30 III t1749 III L VII V Icosahedral II NT H2
219 Zhejinag ST338 CC59 III t437 I C1 I I Icosahedral II NT H2
82 Zhejinag ST59 CC59 III t437 I F1 I I Icosahedral II NT H2
253 Zhejinag ST59 CC59 III t437 I D1 I I Icosahedral II NT H2
8 Zhejinag ST59 CC59 III t437 I D1 I NS Icosahedral II NT H2
204 Zhejinag ST59 CC59 III t437 I E3 I I Icosahedral II NT H2
210 Zhejinag ST59 CC59 III t437 I E4 I I Icosahedral II NT H2
214 Zhejinag ST22 CC22 III t5983 I G1 IV II Icosahedral I ΦPVL H2
221 Zhejinag ST338 CC59 III t437 I C1 I I Icosahedral I ΦPVL H2
69 Zhejinag ST217 CC22 III t309 I G3 III II Icosahedral I ΦPVL* H2
195 Zhejinag ST59 CC59 III t437 I P I I Icosahedral II ΦSa119 H2
51 Zhejinag ST59 CC59 III t441 I D2 I I Elongated ΦSa2958 H2
220 Zhejinag ST338 CC59 III t437 I C1 I I Icosahedral II Φ7247PVL/
ΦST5967PVL		 H2
74 Zhejinag ST59 CC59 III t437 I F1 I I Icosahedral II Φ7247PVL/
ΦST5967PVL		 H2
170 Zhejinag ST59 CC59 III t437 I F2 I I Icosahedral II Φ7247PVL/
ΦST5967PVL		 H2
254 Zhejinag ST59 CC59 III t437 I D1 I I Icosahedral II Φ7247PVL/
ΦST5967PVL		 H2
237 Zhejinag ST59 CC59 III t437 I C4 I I Icosahedral II Φ7247PVL/
ΦST5967PVL		 H2
236 Zhejinag ST59 CC59 III t437 I C4 I I Icosahedral II Φ7247PVL/
ΦST5967PVL		 H2
108 Zhejinag ST59 CC59 III t437 I F2 I I Icosahedral II Φ7247PVL/
ΦST5967PVL		 H2
145 Zhejinag ST59 CC59 III t437 I D2 I I Icosahedral II Φ7247PVL/
ΦST5967PVL		 H2
217 Zhejinag ST59 CC59 III t437 I E1 I I Icosahedral II Φ7247PVL/
ΦST5967PVL		 H2
16 Zhejinag ST59 CC59 III t437 I D3 I I Icosahedral II Φ7247PVL/
ΦST5967PVL		 H2
205 Zhejinag ST22 CC22 III t5983 I G1 I II Icosahedral I Φtp310-1 H2
239 Zhejinag ST22 CC22 III t5983 I G2 I II Icosahedral I Φtp310-1 H2
RJ117 Shanghai ST338 CC59 III t437 I A4 I I Icosahedral II NT H2
LS2137 Zhejinag ST59 CC59 III t2755 I A6 I I Icosahedral II NT H2
3 Zhejinag ST59 CC59 III t034 I Q III III Elongated ΦSa2USA H2
222 Zhejinag ST149 CC5 II t437 I C6 I I Elongated ΦSa2USA H2
255 Zhejinag ST149 CC5 II t437 I K II III Icosahedral I Φtp310-1 H2
MSSA (n = 16)
LS126 Zhejinag ST30 CC30 – t318 I B2 I I Icosahedral II NT H1
SH14 Shanghai ST398 CC398 – t034 I A5 III III Elongated NT H1
LS1985 Zhejinag ST22 CC22 – t309 I B1 IV II Icosahedral I ΦPVL H1
LS2074 Zhejinag ST25 CC25 – t227 I B1 NS IV Icosahedral I ΦPVL H1
SH26 Shanghai ST25 CC25 – t078 I A2 NS NS Elongated ΦSa2958 H1
SH135 Shanghai ST1301 CC121 – t12145 IV A1 V VI Icosahedral I NT H1
LS1940 Zhejinag ST30 CC30 – t318 III A7 I VI Icosahedral II NT H1
LS2078 Zhejinag ST172 singleton – t078 I B1 NS VI Icosahedral I ΦPVL H1
LS1004 Zhejinag ST160 CC121 – t15797 IV B3 V VI Icosahedral I NT H2
LS1966 Zhejinag ST88 CC88 – t15796 III B2 IV III Icosahedral I ΦPVL H2
SH13 Shanghai ST88 CC88 – t2310 III A3 IV III Elongated ΦTCH60 H2
SH25 Shanghai ST217 CC22 – t309 I A4 VIII II Elongated ΦSa2958 H2
SH19 Shanghai ST217 CC22 – t309 I A4 VIII II Elongated ΦSa2958 H3
SJ1775 Shanghai ST398 CC398 – t034 I I2 III III Elongated ΦSa2USA R1
SH3 Shanghai ST398 CC398 – t1255 I A3 III NS Elongated ΦSa2USA R1
LS1911 Zhejinag ST398 CC398 – t034 I B3 III III Elongated ΦSa2USA R1
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*

Phages-like, positive by icosahedral/elongated head classification assays (PCR-1 to -3) and characterization assays (PCR-7 to -15) but negative for linkage assays (PCR-4 and -6). –, no SCCmec elements was detected (MSSA).

NT, non-typeable.

NS, could not be sequenced.

Typing of PVL-encoding phages

Applying the expanded PCR-based scheme described above, it was possible to identify 10 of known phages carrying lukSF-PV genes. Our results showed that 67.9% (53/78, 42 MRSA and 11 MSSA) of PVL-positive isolates could be divided into 8 phage types [ΦPVL (n = 12, including one ΦPVL-like), Φ108PVL-like (n = 1), Φtp310-1 (n = 4), ΦSa2958 (n = 7), ΦSa2USA (n = 5), ΦTCH60 (n = 5, including one ΦTCH60-like), Φ7247PVL/ΦST5967PVL (n = 13), and ΦSa119 (n = 6, including one ΦSa119-like)], which were almost equally split among elongated-head group (n = 17), icosahedral-head group I (n = 17), and II (n = 19). Phage typeability was 68.8% in MSSA (11 out of 16) and 67.7% in MRSA (42 out of 62). Unfortunately, 25 isolates (32.1%) could not be typed by the present scheme. Four MRSA isolates were considered to be “phage-like,” named ΦPVL-like, Φ108PVL-like, ΦTCH60-like and ΦSa119-like, according to the definition from materials and methods. The details of PVL-encoding phages types were shown in Table 2.

Variation of lukSF-PV genes

The amplification products of the lukSF-PV genes from 78 isolates were sequenced, and nucleotide variations were seen at five sites (position 527 and 663 located in the lukS locus and position 1022, 1396, 1729 located in the lukF locus) using the lukSF-PV genes of ΦSLT as a reference. Of 78 PVL-positive isolates, 71 (91.0%, 71/78) were of H variant as defined by O'Hara et al. (2008), which can be further separated into H1 (Genbank Accession no. EF571669) (23.1%, 18/78), H2 (Genbank Accession no. EF571668) (66.7%, 52/78), and H3 (Genbank Accession no. EF571713) (1.3%, 1/78) groups differed at nucleotide position 1396 and 663 (Table 2). The rest of seven isolates were identified as R variant displaying non-synonymous nucleotide 527 A to G mutation, and further divided into R1 (Genbank Accession no. EF571829) (5.1%, 4/78), and R2 (Genbank Accession no. EF571830) (3.8%, 3/78) groups according to the distinction of nucleotide site 1729 (Table 2).

DNA sequencing of phage/chromosome junctions

To investigate the chromosomal insertion site of phage in the present study, we performed PCR based on the known phage/chromosome junctions in the other strains (Boakes et al., 2011; Li et al., 2011). Seventy two (92.3%) isolates showed positive amplification for attL sequences, and 71 (91.0%) for attR sequences. This indicated a relatively conserved PVL-encoding phage integration site regardless of difference among genetic features of strains, PVL-encoding phage types, and lukSF-PV genes variants. Maximum-likelihood phylogenetic tree analysis of the attR and attL attachment sites showed four clusters (I, II, III, and VI) and two singletons (IV and V) for attR and seven clusters (I, II, III, IV, V, VI, and VIII) and one singleton (VII) for attL (Figure 3, Table 2).

Figure 3.

Figure 3

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ML analysis trees for (A) attR attachment site (71 isolates) and (B) attL attachment site (72 isolates). Among 78 PVL-positive isolates, the attR and attL attachment site sequences cannot be identified in 7 and 6 strains, respectively. Branching numbers represent bootstrap values.

Discussion

PVL-positive S. aureus, strongly associated with SSTI and necrotizing pneumonia, has gained great attention in recent years (David and Daum, 2010; Shallcross et al., 2013). In China, the PVL positive rate ranged from 5.5 to 28.6% in HA-MRSA isolates (Yu et al., 2008; Fan et al., 2009; Li et al., 2012; Xiao et al., 2013; Hu et al., 2015). The major clone with lukSF-PV genes was ST59 in MRSA, while ST398, and ST88 in MSSA according to the previous studies (Yu et al., 2008; Fan et al., 2009; Li et al., 2012; Xiao et al., 2013; Hu et al., 2015). In the current study, we also revealed a high percentage of PVL-positive ST59 clones associated with MRSA and ST398 with MSSA strains.

A previously published eight-reaction PCR assay was performed to identify five (ΦSa2958, ΦSa2mw, ΦPVL, Φ108PVL, and ΦSLT) of the PVL-encoding phages in S. aureus (Ma et al., 2008). Subsequently, this scheme was improved to include the detection of ΦSa2USA (Boakes et al., 2011), ΦTCH60, Φtp310-1, and Φ7247PVL (Chen et al., 2013). Recently, Sanchini et al. (2014) divided PVL-encoding phages into three groups including the elongated-head group, icosahedral-head group I, and icosahedral-head group II, and incorporated ΦSa119 and ΦST5967PVL belonging to icosahedral-head group II into the scheme. However, this PCR-based scheme could not discriminate ΦST5967PVL from Φ7247PVL (Chen et al., 2013; Sanchini et al., 2014), because the genomes of both phages showed more than 99% identity (Zhang et al., 2011). Therefore, these two phages were marked as “Φ7247PVL/Φ5967PVL” in this study.

Applying the PCR-based strategy, the distribution of PVL-encoding phages was investigated all over the world. Two morphologically distinct phages (ΦPVL and ΦSa2958) were found to be predominant among Japanese PVL-positive MRSA (Ma et al., 2008), and ΦSa2USA was the most prevalent phage in Italy (Sanchini et al., 2014), while in United Kingdom, the most common phage types were ΦSa2USA and ΦSa2mw (Otter et al., 2010; Boakes et al., 2011). In this study, the results revealed that Φ7247PVL/ΦST5967PVL, and ΦPVL were the major PVL phage types in the isolates studied. Notably, all the untypeable isolates were positive for PCR-3 and belonged to ST30 and ST59 strains, indicating that both the clones may harbor novel unknown icosahedral-head group II phage type(s) in China. In line with the previous observations (Ma et al., 2008; Otter et al., 2010; Boakes et al., 2011; Chen et al., 2013; Sanchini et al., 2014), lineage-specificity of PVL-encoding phages were noted in this study. For instance, 92.3% of Φ7247PVL/ΦST5967PVL-carrying isolates belonged to CC59 lineage, harboring cluster I attR, and attL, and 60% of ΦSa2USA-hosting isolates pertained to ST398. However, the ΦPVL-carrying isolates showed more variability of genetic characterization, with CC22, CC25, CC59, CC88, and CC9 detected within this group. ΦSa119, recently identified in CC5 lineage by Sanchini et al. (2014), was detected in CC59 lineage. ΦSa2958, associated with MRSA belonging to CC30 (Ma et al., 2008), was related to CC22 and CC59 in the present study.

These findings are similar with those reported in China previously (Li et al., 2012; Hu et al., 2015). However, Φ108PVL, which was the predominant phage type in CA-MRSA from children in mainland China (Li et al., 2012), and ΦSLT, which was prevalent in 74 health care-associated PVL-positive MRSA strains (Hu et al., 2015), are not common in the present study. The difference of regions across China and sources of isolates may account for the dissimilarity of the predominant PVL-encoding phages among these studies.

The correlation between the presence of PVL in S. aureus infections and the clinical outcome has been controversial because of some conflicting data from epidemiological study or in vivo animal models (Hermos et al., 2010; Otto, 2011). Corresponding protein models of two lukSF-PV sequence variants, named R and H variant, may indicate certain functional significance (Wolter et al., 2007; John and Lindsay, 2008; O'Hara et al., 2008). In our study, the H- and R-PVL isoforms could be identified in three morphological phage groups. Of note, the R1 isoform was mainly associated with ΦSa2USA, similar to the previous study (Chen et al., 2013). Of the five SNPs in the present study, two were non-synonymous, including a previously described arginine to histidine replacement at amino acid residue 176 (nucleotide 527) and a valine to isoleucine replacement at amino acid 340 (nucleotide 1022). The latter amino acid change presented in only one sequence (LS2074) and decreased the predicted molecular size of LukF from 36962Da to 36948Da, but did not influence the theoretical isoelectric point (9.1). The nucleotide sequence of the lukSF-PV genes has been deposited in GenBank under the Accession no. KX443594. Further work is required to confirm whether this non-synonymous replacement results in clinical significance.

Another interesting finding was that all the attR cluster I-harboring isolates possessed the same agr type (agr I) and were mostly observed within CC59 lineage. With the exception of one strain (strain 148), all of the attR sequences of cluster II strains were identified in CC22 lineage. The CC88 isolates were completely associated with attR cluster III and attL cluster IV. The main variations in attL were located in the phage binding sites (P1 and P2) and those in attR were located in the phage binding site P3 and chromosome binding sites B2. These indicated that the diversity of junction sequences was mainly due to differences in the phage DNA, which was different from the previous report that the main variations in attR were located in the 29-bp chromosome binding sites (B2) (Chen et al., 2013).

There were two limitations in this study. First, the identification of PVL-encoding phages was on the basis of PCR assays targeting only a part of the phage genome. Since phages tend to have recombination events, positivity by PCR should be supposed to be a family of PVL-encoding phages with variable genomic portions, instead of being taken as a specific phage (Sanchini et al., 2014; Xia and Wolz, 2014). Second, the proportion of phage-untypable PVL-positive isolates is a little high (32.1%), although the rate is within the range of 16.4–77.6% reported previously (Ma et al., 2008; Boakes et al., 2011; Li et al., 2012; Hu et al., 2015) by the PCR-based scheme. This could be because some unknown or newly published PVL-encoding phages such as Φ7401PVL (Mariem et al., 2013) have not being included in the scheme. Therefore, unknown PVL-encoding phages remain to be discovered and new primer pairs are expected to be designed to further expand this scheme. Whatever, next-generation sequencing may provide us with a way to achieve perfect epidemiological picture of diversity of PVL-encoding phages, which seems to represent a trend in the future.

Conclusion

This study characterized PVL-encoding phages, the chromosomal phage insertion sites, the polymorphism of lukSF-PV genes, and the genetic background of PVL-positive S. aureus clinical isolates from China, and found the existence of some correlation among them. Our findings may contribute to the understanding of the epidemiology and evolution of PVL-positive S. aureus, and add the evidence that PVL-positive strains disseminating worldwide likely carry distinct PVL phages.

Author contributions

HZ, FH performed the experiments; QL designed and conceived the study; HZ, QL, CH analyzed the clinical data and wrote this manuscript; QL, SJ, XX, YZ, BD, and FG collected the clinical samples. All authors read and approved the final manuscript.

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.

Acknowledgments

The authors thank Jinwei Huang, Jianmin Ren, Chuanling Zhang, Lizhong Han, Zhengyin Zhang, and Jin Tang to provide the clinical S. aureus isolates from Zhejiang Province and Shanghai. This work was supported by grants from Natural Science Foundation, Science and Technology Commission of Shanghai (No. 12ZR1425000), the National Natural Science Foundation of China (No. 81371872), and Putuo District, Major Scientific and Technological Research Projects (No. KW15101).

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