Genome analysis of clinical multilocus sequence Type 11 Klebsiella pneumoniae from China

The increasing prevalence of KPC-producing Klebsiella pneumoniae strains in clinical settings has been largely attributed to dissemination of organisms of specific multilocus sequence types, such as ST258 and ST11. Compared with the ST258 clone, which is prevalent in North America and Europe, ST11 is common in China but information regarding its genetic features remains scarce. In this study, we performed detailed genetic characterization of ST11 K. pneumoniae strains by analyzing whole-genome sequences of 58 clinical strains collected from diverse geographic locations in China. The ST11 genomes were found to be highly heterogeneous and clustered into at least three major lineages based on the patterns of single-nucleotide polymorphisms. Exhibiting five different capsular types, these ST11 strains were found to harbor multiple resistance and virulence determinants such as the blaKPC-2 gene, which encodes carbapenemase, and the yersiniabactin-associated virulence genes irp, ybt and fyu. Moreover, genes encoding the virulence factor aerobactin and the regulator of the mucoid phenotype (rmpA) were detectable in six genomes, whereas genes encoding salmochelin were found in three genomes. In conclusion, our data indicated that carriage of a wide range of resistance and virulence genes constitutes the underlying basis of the high level of prevalence of ST11 in clinical settings. Such findings provide insight into the development of novel strategies for prevention, diagnosis and treatment of K. pneumoniae infections.


INTRODUCTION
Klebsiella pneumoniae has gained notoriety as a major opportunistic pathogen which causes a range of hospitalacquired infections [1]. The emergence of multidrugresistant K. pneumoniae strains, which cause untreatable infections, has resulted in extensive public concern [2]. Notably, K. pneumoniae carbapenemase (KPC)-producing K. pneumoniae, one of the most clinically significant carbapenem-resistant Enterobacteriaceae (CRE) strains, has not only been disseminated globally, but is also associated with high morbidity and mortality rates [3]. To date, 16 different KPC variants (KPC-2-KPC-17), classified on the basis of single-amino-acid mutations, have been identified, among which KPC-2 and KPC-3 are the best-studied enzymes [2,4]. Transmission of the bla KPC gene involves multiple mechanisms ranging from clonal spread to horizontal transfer mediated by plasmids and other transposable genetic elements, notably Tn4401 [5].
The clinical prevalence of KPC-producing K. pneumoniae has been largely attributed to dissemination of strains of the clonal group (CG) 258, with ST258 and ST11 being the dominant multilocus sequence types (ST) [3,[5][6][7][8]. ST258 has disseminated worldwide since its emergence during the early to mid-2000s, especially in North America, Latin America and several countries in Europe [5,8,9]. In Asia and South America, however, the dominant KPC-producing clone is ST11 [8,10], which is a single locus (tonB) variant of ST258, with the tonB4 gene in ST11 differing from tonB79 in ST258 by four single-nucleotide polymorphisms (SNPs) [10]. According to Gaiarsa et al., a putative recombination event (which happened sometime before 1985), during which a donor related to K. pneumoniae ST1628 contributed approximately 1.3 Mbp to an ancestor of ST11 (CG258), gave rise to CG258 [11]. Results from a recent genome-based study indicated that ST258 K. pneumoniae differed significantly from ST11 in terms of genetic composition. ST258 was found to be a hybrid clone, with 80 % of its genome derived from ST11-like strains and 20 % from ST442-like strains [2,5,12]. Strains of the ST258 type were found to comprise at least two distinct lineages, namely clade 1 and clade 2, which differ mainly in a genomic region where the gene encoding capsule polysaccharide (CPS), cps, is located [6]. In contrast, the genetic composition of ST11, which is the dominant carbapneme-resistant K. pneumoniae clone in China, remains poorly understood [10,13]. The complete genomic sequences of two clinical ST11 multidrug-resistant strains, HS11286 and JM45, are publicly available and widely used as references for various genetic studies [5,[14][15][16]. A previous study demonstrated that the ST11 genomes exhibited a relatively high degree of diversity [17]. Jiang et al. tracked the outbreak of ST11 K. pneumoniae in a single Chinese hospital by performing whole-genome sequencing of 12 strains; in this previous work, phylogenetic analysis resulted in partitioning of these strains into three separate clades [16]. However, a comprehensive clonal lineage map of ST11 strains prevailing in China is currently not available. Also, data regarding the pathogenicity and antimicrobial resistance profiles of the ST11 strains is scarce. To address these issues, we performed whole-genome sequencing to obtain the complete genome of one KPC-producing ST11 clinical isolate, followed by phylogenetic analysis and genome mining of a total of 58 ST-11 clinical isolates collected from diverse geographic locations in China. Findings from this work led to the identification of unique genetic traits of the ST11 clone and helped promote better understanding of the genetic basis of virulence of this important clone.

K. pneumoniae isolates and sequencing
Thirty-one carbapenem-resistant K. pneumoniae isolates were collected from blood, sputum and stool specimens of patients at eight hospitals located in different provinces of China. The isolates were non-outbreak-related and randomly selected from various locations in China. Antimicrobial susceptibilities were determined by the agar dilution method according to the Clinical and Laboratory Standards Institute (CLSI) guidelines [18]. Genomic DNA was extracted from overnight cultures by using the PureLink Genomic DNA Mini Kit (Invitrogen). Genomic libraries were prepared with an approximately 350 bp insert size using the NEBNext Ultra DNA Library Prep Kit (New England Biolabs) and sequenced with the Illumina NextSeq 500 sequencing platform. One of these strains, GD4, was simultaneously selected for sequencing with the PacBio RSII single-molecule real-time (SMRT) sequencing platform (Wuhan Institute of Biotechnology). All ST-11 K. pneumoniae genomes that were publicly available in the NCBI Pathogen Detection database (https://www.ncbi.nlm. nih.gov/pathogens/) as of January 2017 (a total of 27 genomes), were also included for analysis in this study. Genetic information for the test isolates is listed in File S1.

Genome assembly and annotation
Raw reads generated in this study and the Illumina reads of 11 strains obtained from the NCBI database were trimmed or filtered to remove low-quality sequences and adaptors. Both Illumina and PacBio reads were de novo assembled with the SPAdes Genome Assembler v3.9.1 [19,20]. Illumina reads of strain GD4 was aligned to the corresponding PacBio contigs to improve the accuracy of the genome sequence data and obtain the complete genome sequence of strain GD4. The 30 draft and 1 complete genome sequences

IMPACT STATEMENT
A comprehensive genomic analysis of 58 clinical strains of ST11 K. pneumoniae, the dominant KPC-producing clinical clone in China, was performed in this study. We found that that these strains, collected from geographically diverse locations in the country, were genetically diverse and could be segregated into three clades, each of which exhibited distinct capsule polysaccharide (cps) loci. Various antimicrobial resistance genes and virulence genes, such as those encoding salmochelin, aerobactin and RmpA, the hallmarks of hypervirulent K. pneumoniae, were detected in the genomes of these strains. This study provides insights for the development of strategies for prevention, diagnosis and treatment of ST11 clinical infections. generated in this study and the 27 genome sequences retrieved from the NCBI database were all annotated with the RAST tool [21] and Prokka [22].

Phylogenetic analysis
The harvest suite, which was designated for analyzing intraspecific microbial genomes and encompasses three modules (Parsnp, Gingr and HarvestTools), was applied to filter recombination (-x), run core genome alignment and variant calling and reconstruct the phylogenetic tree with the 58 assembled genomes using default settings [28]. Interactive tree of life (iTOL) v3 (http://itol.embl.de/) was applied to modify and visualize the reconstructed phylogenetic tree [29]. Genome assemblies for two representative ST258 K. pneumoniae isolates, NJST258_1 (GenBank accession number CP006923) and NJST258_2 (GenBank accession number NZ_CP006918), and one CG258-unrelated isolate, K. pneumoniae MGH78578 (ST38, GenBank accession number AB720665) were retrieved from GenBank and used to reconstruct a phylogenetic tree with three ST11 isolates (each from a different evolutionary clade) using the harvest suite. This tree, as well as the variants, was visualized with gingr [28]. The chromosome sequence of K. pneumoniae strain GD4 was used as a reference for both phylogenetic analyses.
Core genome and pan-genome analysis Conserved core genes among the ST11 isolates were analyzed with Roary [30] with a blastp percentage identity of 95 %. The Prokka [22] annotated files were used as inputs for Roary. The parameter for the percentage of isolates a gene must be in to be classified as core was set to be 99 %.

RESULTS AND DISCUSSION
Genome sequence of carbapenem-resistant ST11 K. pneumoniae clinical isolates ST11 was found to be the dominant sequence type of carbapenem-resistant K. pneumoniae strains in China, accounting for 60 % of such strains [34]. K. pneumoniae has been reported to be highly genetically diverse, with a large accessory genome that comprises 30 000 protein-coding genes [35]. In this study, the complete genome sequence of a multidrug-resistant K. pneumoniae strain GD4 isolated from a sputum specimen in 2015 at Huashan Hospital, Guangdong, PR China (MIC profile in File S1) was obtained. The genome of this strain was found to comprise a chromosome of 5 366 808 bp in size, and a 170 821 bp plasmid designated pKPGD4. The overall DNA G+C content of the chromosome, in which 5215 coding sequences (CDSs) and 80 tRNA molecules were detectable, was 57.5 %. The genetic diversity of K. pneumoniae genomes has been previously demonstrated to be primarily due to elements that migrate frequently by horizontal gene transfer, including plasmids, phages, integrated conjugative elements (ICEs) and insertion sequences (ISs) [36]. Resembling the ST258 strains [6], the chromosome of strain GD4 was found to harbor numerous mobile genetic elements including eight putative prophages (designated prophages 11.1-11.8), two ICEs (designated ICEKpnHS11286-1 and ICEKpnHS11286-2 based on the name of the parent strain HS11286) and 40 insertion sequences (ISs) (Fig. 1). The chromosomal features of three completely sequenced ST11 K. pneumoniae strains, namely GD4, HS11286 and JM45, were compared and are summarized in Table 1. Information on all 58 strains tested in this study is listed in File S1. Apart from the completely assembled sequences, the genomes of other ST11 isolates in this study were found to comprise 74-161 scaffolds. Like other K. pneumoniae genomes [6], the genome sizes of the ST11 strains ranged from approximately 5.4 Mbp to around 5.7 Mbp. Pan-genome analysis identified a total of 8285 genes in the genomes of the 58 ST11 K. pneumoniae isolates, among which 4297 (about 82.4 % of the total genes in isolate GD4) were core to all isolates. The ST11 K. pneumoniae clone harbors a large set of accessory genes to render the clone adaptable to different environments.

Phylogenetic analysis
After filtering the recombination, a 4 205 312 bp conserved core genome was identified among the genomes of the 58 ST11 strains. A total of 6749 SNPs were identified in the core genomes and were used to reconstruct an approximately maximum-likelihood phylogenetic tree (File S2). Similar to the ST258 K. pneumoniae strains, which comprised at least two distinct lineages [6], the 58 ST11 isolates were found to be clustered into three major groups, namely clade 1, clade 2 and clade 3 with respectively 4, 10 and 44 strains in each clade (Fig. 2). Isolates within clade 1 and clade 2 were found to differ from those of clade 3 by an average of 2848 (a range of 2595-3353, around one SNP per 1884 nucleotides) and 1198 (a range of 1181-1244, about one SNP per 4480 nucleotides) SNPs, respectively (File S2). This finding was similar to those of a previous study, in which the 12 ST11 outbreak strains from a single hospital could also be grouped into three clades [16], indicating that the ST11 lineage should not be regarded as a single clone. It should be noted that strains in clades 2 and 3 of the previous study were mostly clustered in clade 3 of this study, whereas, strains in clade 1 of the previous study was clustered into clade 2 in this work (Fig. 2). Importantly, none of strains belonging to clade 1 in this study was detectable in the previous study. The discrepancy between the clustering data from the two studies was probably due to the large sample size and inclusion of more genetically diverse strains in our work. Phylogeographic clustering could not be properly resolved in the current study, owing to the small number of strains and presence of different lineages at a single location.
Using ST38 K. pneumoniae isolate MGH78578 as an outgroup, the CG258 isolates could be grouped into a twobranched clade which shows extensive variations compared with the ST38 clade (Fig. 3). The ST258 lineage harbors an approximately 1.1 Mbp region divergent from the ST11 lineage which have been proposed to have originated from an ST442-like clone [12]. This finding is consistent with the results of a previous study, which indicated that members of CG258 descend from a common ancestor (mostly of ST11) and then diversified into distinct lineages [17]. The ST11 lineage, which was grouped into three clades in this study, were mainly classified by the cps locus it harbors as displayed in the variation regions in Fig. 3.

Comparison of the cps cluster
The genomes of ST258 and ST11 K. pneumoniae strains have been reported to differ mainly in the composition of an approximately 1.1 Mbp region in which the cps locus is located [12]. SNPs analysis showed that the most diversified area in this region was the cps operon, which encoded the capsule polysaccharide (CPS), a known key virulence determinant in K. pneumoniae [2]. Large-scale recombination events and capsule switches are known to contribute to the strain variation within CG258 [17]. Traditional serological typing has been used to identify more than 78 distinct capsular types (K types) in K. pneumoniae [2,6,17,37]. Recently a novel program (Kaptive) for identifying the CPS synthesis loci (K loci) has been developed by using the full locus information extracted from the genome data, the use of which resulted in an increasing in the total number of known K loci to 134 [32]. By adopting the Kaptive program in our study, the K types of 58 ST11 isolates were identified (Fig. 2b). In line with the previous finding that two distinct cps gene clusters were involved in segregating the ST258 clinical isolates into two distinct clades [17], the cps loci of the ST11 strains could also be segregated into phylogenetically defined sublineages. The 10 strains in clade 2 were KL64 and all the 44 strains in clade 3 were found to belong to KL47. On the other hand, the four strains (HS11286, JM45, kp10 and XL-1) within clade 1 were found to belong to different K types, KL103, KL125, KL64 and KL105. This is not surprising as the four strains did not exhibit significant genetic relatedness, even though we manually grouped them into one cluster (Fig. 2a). On the basis of these observations, we speculated that the ST11 'strain' has undergone a number of capsular exchanges since its emergence as a major nosocomial outbreak agent. Notably, the serotype of strain HS11286 has been previously characterized as K74 through wzi typing [17]. However, the 78 different wzi loci could be clustered into four homology groups, indicating that wzi typing has lower discrimination power compared with cps loci typing [37]. By using the complete locus sequence, it is reasonably to redefine HS11286 as the novel type, KL103 based on the genetic sequence of its cps locus. Some novel capsular types have been reported to be predominant among clinical carbapenem-resistant K. pneumoniae strains in Italy and the USA [6,38,39].
The common genetic features of the cps clusters in K. pneumoniae strains have been determined previously [2]. Generally, the cps locus harbored a highly conserved 5¢ end region of six genes (galF, orf2, wzi, wza, wzb and wzc) whose products are responsible for CPS assembly and translocation with sequence variations often observable in the central and 3¢ end regions (from gnd to ugd) [37,40]. The structures of the five distinct loci detected in this study as well as two reference loci types (cps BO-4 and cps ATCC BAA-2146 ) reported in previous studies [41,42] were compared and are shown in Fig. 4 and Table S2. Briefly, the cps loci of the Chinese ST11 strains ranged from approximately 23 kpb to approximately 28 kbp with 18-23 ORFs ( Table 2). Synthesis of the capsular repeat in K. pneumoniae is mediated by the initial glycosyltransferase (GT) WbaP or WcaJ, which catalyze transferal of galactose-1-phosphate or glucose-1-phosphate to undecaprenol phosphate, respectively [37]. The wcaJ gene 5was found only in the clade 2 strains and one strain (kp10) in clade 1, and the initial GTs genes for other ST11 strains were all found to be wbaP, indicating that different saccharides might be present in the repeat unit of the capsule. Addition of sugars in the capsule is catalyzed by specific non-initial GTs [43]. In the case of ST11 K. pneumoniae, strains within distinct clades were found to harbor different combinations of non-initial GT genes (Fig. 4, blue arrows) in the central cps region. For instance, clade 3 strains such as GD4 were found to harbor wcaA, wcqC and wcuT genes in the central region, whereas clade 2 strains such as SH-2 contained wcoV, wcoU, wcoT, wcsF and wbaZ. The 3¢ end gnd-ugd region of the cps locus which harbored the gene clusters manCB or rmlBADC, which are known to be responsible for the synthesis of GDP-D-mannose or dTDP-L-rhamnose in the majority of capsular types [37]. In this work, the finding that the cps types KL107 (cps BO-4 ), KL103 (cps HS11286 ), KL47 (cps GD4 ) and KL105 (cps XL-1 ) harbored the rmlBADC gene cluster, is highly consistent with the phenomenon of the presence of rhamnose in the repeat units of the capsule [37]. On the other hand, the presence of manCB genes does not always correlate with the existence of mannose in the capsule [37]. Both manCB and rmlBADC gene clusters were detected in the KL64 cps type (cps SH-2 ) and neither of the two clusters was found in the KL125 type (cps HS11286 ). Additionally, genes for capsule modification was detected in the cps loci of some strains, such as those encoding carbohydrate lyase in HS11286 and the pectate lyase superfamily protein-encoding gene in XL-1 (Fig. 4), indicating that distinct modifying systems were responsible for production of different capsule structures. It should be ICE, integrative and conjugative elements; IS, insertion sequence.
*Data for this column are from reference [15]. †Data for this column are from reference [12] except for IS numbers which are derived from this study.   [32]. Sequence origins, accession numbers and STs for the respective strains are indicated. Arrows indicate the direction, relative length and function of ORFs. The cps loci of K. pneumoniae strains ATCC BAA-2146 and BO4 were downloaded from the NCBI database and used as references for the comparison. ORFs encoding transposases are colored in red, while those encoding noninitial glycosyltransferases are colored in blue. HP, CL and PLSP are short for hypothetical protein, carbohydrate lyase and pectate lyase superfamily protein, respectively. Homologous regions are connected by areas of different colors reflecting the degree of nucleotide identity (from 64 to 100 %). noted that when T11 and ST258 were compared to each other the region which exhibited the largest degree of genetic variation was the middle section of cps; the presence of three putative ORFs in this region in ST258 strains indicates that the sugar content in the capsule of ST11 might be very different from that of ST258. Such a difference may account for the discrepancy in the level of prevalence of these genetically related strains in different parts of the world. Future studies should focus on investigating the underlying mechanisms governing their adaptability to different environmental conditions. Antimicrobial resistance (AMR) genes in ST11 K. pneumoniae Dissemination of resistance determinants has been recognized as a major challenge in treatment of bacterial infections worldwide [44]. A targeted survey performed within the 58 ST11 genomes revealed a total of 62 known AMR genes (Fig. 5). The bla SHV and fosA3 genes were shown to be the core chromosomal genes that were present in all the ST11 strains, indicating that these two AMR genes were likely to have been present in the ST11 K. pneumoniae ancestor (File S3) [35,45]. The oqxA and oqxB genes were both detected in 34 different strains. Being the core genes in K. pneumoniae, their role in conferring resistance to fluoroquinolones is not well defined [27,35]. Other AMR genes that were found to be present in more than 30 strains included bla KPC-2 (detectable in 57 strains, and only absent in strain kp10), aadA2 (51), bla TEM-1b (45), rmtB (38), bla CTX-M-65 (33) and fosA-14 (31), conferring resistance to carbapenems, aminoglycosides, b-lactams or fosfomycin, respectively. The test strains were also found to harbor different combinations of the following resistance genes arr-3, qnrB, qnrS, sul, tet, str, msr, mph, floR, dfrA, cat, bla VEB , bla-TEM , bla NDM , bla DHA , armA, aph and aac, with the number of such genes harbored by each strain ranging from 4 to 17.
Undoubtedly, the presence of resistance determinants allows the ST11 strains to survive the barrage of antibiotics used in treatment of hospital infections. The distribution of these genes varied dramatically among strains and was not related to lineage (Fig. 5), indicating that the AMR genes were acquired through horizontal transfer. Due to the constraints of using short-read illumina data [35], we were not able to link each resistance locus to a specific plasmid reliably. However, a search against the PlasmidFinder database [24] allowed us to identify 26 plasmid replicons in the 58 strains (File S5), including 6 colicin replicons and 20 associated with large conjugative AMR plasmids. Importantly, two to seven distinct types of plasmid replicon were detectable in each strain. The bla KPC-2 genes were found to be frequently associated with the IncFII/IncR plasmid replicons and to have a similar core structure, ISKpn27-blaKPC-2-ISKpn6, as reported in our previous nationwide surveillance study [46]. The completely sequenced plasmid pKPGD4 was found to be an IncFII/IncR-like plasmid, carrying the bla KPC-2 , bla CTX-M-65 , bla TEM-1b , rmtB, catA2 and fosA14 genes. The sequence organization of pKPGD4 was similar to that of the unnamed plasmid (accession number: CP018455) in strain K. pneumoniae SWU01 (coverage 91 %, identity 99 %) and plasmid pCT-KPC (accession number: KT185451.1, coverage 86 %, identity 99 %) (Fig. 6). This plasmid has been shown to be very common in these ST11 CRKP strains (File S5).
Prevalence of virulence factors in ST11 K. pneumoniae As an opportunistic pathogen, K. pneumoniae relies on an array of virulence factors to colonize and propagate in a host, which include at least (a) surface antigen, especially capsular polysaccharide (CPS, K antigen); (b) siderophores that are responsible for binding ferric iron secreted by the iron-binding proteins of the host; and (c) adherence factors that are responsible for attachment to host cell surfaces, such as type 1 and type 3 fimbriae, and non-fimbrial adhesion proteins [14]. the results of virulence gene analysis of these ST11 strains indicated that some of the virulence genes were commonly present in ST11 strains. The FimA, B, C, D, E, F, G, H, I and K genes encoding type 1 fimbriae, which have been reported to be involved in enhancing bacterial virulence during urinary tract infection, were detected in almost all the ST11 strains and ST258 strains. The mrkA, B, C, D, F, J, H and I genes encoding type 3 fimbriae, which have been shown to mediate biofilm formation on both abiotic and biotic surfaces, as well as kpn (coding for FimHlike adhesins) and ycfM [coding for outer membrane lipoproteins (OMLs)], both of which have been reported to be involved in bacterial adhesion processes, were also detected in almost all the ST11 strains and ST258 strains [47]. Expression of these genes might therefore enhance the adhesive capacity of K. pneumoniae towards respiratory epithelial cells and surfaces of medical devices like ventilators, thus enhancing their ability to cause ventilator-associated infections. Besides, findings of two previous studies revealed a strong relationship between antibiotic resistance and the prevalence of biofilms and OMLs in bacteria, as biofilms and OMLs are known to actively protect bacteria from drug exposure [48,49]. Carriage of all these virulence determinants might be associated with the high level antimicrobial resistance phenotype of ST11 K. pneumoniae. Another outer membrane lipoprotein TraT, encoded by the plasmid-borne transfer gene traT, has been previously demonstrated to be able to mediate resistance to bacterial killing by serum. The traT gene was found to be frequently associated with production of K1 capsule [50]. Interestingly, the results of virulence factor analysis indicated that some of the ST11 strains also harbored this gene.
Several types of siderophores are known to be differently expressed in ST11 K. pneumoniae, with genes encoding enterobactin synthesis, such as entB, being present in the majority of ST11 strains [2]. Genes encoding yersiniabactin (the irp genes) and its transporters (the ybt and fyu genes) were detected in majority of the ST11 K. pneumoniae genomes in this work, with only one exception (strain JM45, Fig. 7, File S4). Interestingly, these genes were not detectable in the ST258 type of K. pneumoniae, constituting a major difference between these two types of strains. The ybt locus has been reported to be located in a self-transmissible ICE in the K. pneumoniae genome and was significantly associated with infections [27,35]. Carriage of yersiniabactin-encoding genes in the ST11 strains may pose a significant threat to public health since multidrug-resistant and virulent K. pneumoniae strains are causing an increasing number of fatal hospital infections in China. Surprisingly, genes encoding salmochelin (iroBCDN), aerobactin (iucABCD) and the rmpA gene were also detected in a few ST11 genomes. Notably, three strains (HN-26, HN34-2 and SH-2) in phylogenetic clade 2, all of the capsular locus type KL64, were found to harbor the iucABCD and rmpA genes, and three strains (SH-16, SH-1 and SH-9) in clade 3 of the capsular locus type KL47 were found to contain the gene cluster iroCDN in addition to iucABCD and rmpA (Fig. 6, File S4). Combined carriage of the iro and iuc gene clusters, as well as the rmpA gene, is frequently, but not always linked to the publicly known K. pneumoniae virulence plasmid pLVPK, which is uniquely associated with hvKP strains [2,35,51]. These strains may belong to the newly emerged ST11 carbapenem-resistant, hypervirulent K. pneumonia (ST11-CR-HvKP) indicating the wide spread of this new superbug in different parts of China [52].
Conclusions ST11 K. pneumoniae has emerged as the dominant KPCproducing clone in PR China [10]. Comprehensive genomic analysis was performed on representative ST11 strains collected from various locations in China. The genomes of these ST11 strains were found to be highly heterogeneous and could be grouped into three major genetic lineages and five different capsular types through phylogenetic analysis. Multiple resistance and virulence determinants were found in the ST11 genomes; such transposable elements are apparently responsible for rendering these strains a severe threat to human health. These data therefore provide insights into the development of prevention, diagnosis and treatment strategies to combat infections caused by ST11 K. pneumoniae strains.

Funding information
This study was funded by the Collaborative Research Fund from the Research Grant Council (C7038-15G and C5026-16G).