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    Genomic and Phenotypic Diversity of Carbapenemase-Producing Enterobacteriaceae Isolates from Bacteremia in China: A Multicenter Epidemiological, Microbiological, and Genetic Study

    2022-08-17 07:18:32BeiwenZhengHoXuLihuGuoXioYuJinruJiChoqunYingYunoChenPingShenHuimingHnChenHungShuntinZhngToLvYonghongXio
    Engineering 2022年5期

    Beiwen Zheng, Ho Xu, Lihu Guo, Xio Yu, Jinru Ji, Choqun Ying, Yuno Chen, Ping Shen,Huiming Hn, Chen Hung,c, Shuntin Zhng, To Lv, Yonghong Xio,*

    a State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou 310003, China

    b Medical College of Beihua University, Jilin 132013, China

    c Department of Infectious Diseases, Ningbo Medical Center Li Huili Hospital, Ningbo 315040, China

    Keywords:Carbapenemase Carbapenemase-producing Enterobacteriaceae Plasmid-mediated China Extended-spectrum β-lactamase

    ABSTRACT

    1. Introduction

    The emergence and spread of carbapenem resistance,especially in extended-spectrum β-lactamase (ESBL)-producing bacteria, are of particular clinical relevance [1,2]. Recently, carbapenemresistant Enterobacteriaceae (CRE) were listed as the most critical group of pathogens by the World Health Organization[3], indicating that they have emerged as a global threat to the antibiotic era[4]. Among these microorganisms, carbapenemase-producing Enterobacteriaceae (CPE) are recognized as the most worrying threat due to the limited therapeutic options against these pathogens and their mobility[5,6].As per the literature,concomitant use of antimicrobial agents and proton pump inhibitors prolongs the duration of the gastrointestinal colonization by CPE[7].Our recent work also revealed that antibiotic exposure, surgical history, and CPE positivity are correlated [8].

    Bloodstream infections(BSIs)are major causes of infectious diseases worldwide and have become one of the leading causes of death in developed countries [9,10]. Approximately 9300 healthcareassociated infections are caused by CPE each year in the United States,and almost half of the hospitalized patients with BSIs due to CPE die from the infection[11].Therefore,it is particularly important to understand how resistance elements spread between strains and the extent of transmission that goes undetected between cases[11].However, only a few large-scale resistance surveillance programs have targeted the testing of BSI isolates[12].

    In China, an increasing incidence of CPE-mediated infections has been observed over the past decade [13]. To date, only a few studies have reported the national surveillance of CPE isolates[13-15]. A high prevalence of ESBL-producing Enterobacteriaceae in BSIs in China was reported recently; however, the detection of CPE was not described in that study [16]. In our previous study,we also reported the preliminary data of BSIs caused by Enterobacteriaceae in China [17]. The vast majority of these studies were based on epidemiological data or Sanger sequencing data; thus,those studies were not able to perform comparative genomics analysis to track the dissemination and transmission of such strains or antimicrobial resistance genes (ARGs).

    Thus far,the population structure and genetic characteristics of CPE isolates among BSIs remain largely unknown. To address this knowledge gap, we recruited patients with clinically significant BSIs caused by Enterobacteriaceae isolates from China. Moreover,a comprehensive phenotypic characterization was conducted on Enterobacteriaceae isolates causing BSIs. We further employed the whole genome sequencing (WGS) and plasmid analysis methods in an effort to obtain a snapshot of the epidemiology of CPE among and within hospitals. Our findings help in understanding the implications of the dissemination of resistance within and between species and geographical areas in China.

    2. Materials and methods

    2.1. Study design, setting, and bacterial isolates

    The Consortium of Blood Bacterial Resistant Investigation Collaborative Systems (BRICS) is a prospective, multicenter, and observational consortium for tracking antimicrobial resistance among BSI-causing isolates in China since 2014[17].Patients with BSI judged to be clinically significant were identified by the responsible clinical microbiologist of the sentinel hospital. As part of this program, all nonduplicate BSI isolates were collected from 26 sentinel hospitals located in 21 cities (Fig. 1) between January 2014 and December 2015 in this study. Outpatients or patients with incomplete data were excluded. All isolates were sent to the central laboratory of the First Affiliated Hospital of Zhejiang University to be tested and analyzed. Clinical data were extracted using centralized queries from clinical and medical record systems used for patients with CPE infections.Ethical approval was granted by the Ethics Committee of the First Affiliated Hospital of Zhejiang University. Individual consent was obtained from all patients either face-to-face or by phone.

    2.2. Identification, antimicrobial susceptibility testing, and molecular biology

    Bacterial species were identified using matrix-assisted laser desorption ionization(MALDI)time-of-flight(TOF)mass spectrometry (MS) (Bruker Daltonics, Germany). Antimicrobial susceptibility testing (AST) was done using the agar dilution method according to the Clinical and Laboratory Standards Institute (CLSI)standards[18].AST of colistin and tigecycline was performed using the microbroth dilution method as described by the European Committee on Antimicrobial Susceptibility Testing (EUCAST)?? http://www.eucast.org/.. The ESBL production of Escherichia coli (E. coli), Klebsiella pneumoniae(K.pneumoniae),Proteus mirabilis(P.mirabilis),and Klebsiella oxytoca(K.oxytoca)isolates was phenotypically performed using the doubledisk dilution method following CLSI recommendations.Carbapenem non-susceptible isolates were screened for the presence of carbapenemase-encoding genes of imipenemase (blaIMP), Verona integrin-encoded metallo-β-lactamase (blaVIM), K. pneumoniae carbapenemase (blaKPC), oxacillinase (blaOXA-48), and New Delhi metallo-β-lactamase (blaNDM) as described previously [19].

    2.3. WGS and genomics analysis

    To characterize the genetic features of the CPE strains,WGS was performed on all CPE isolates. Total DNA was extracted using the Gentra Puregene Yeast/Bact. Kit (Qiagen, Germany) and then subjected to WGS using an Illumina Hiseq 2500 platform (Novogene Co.,China).Paired reads were assembled into a number of scaffolds using Velvet 1.1 [20]. Multilocus sequence typing (MLST) analysis was performed on E. coli, K. pneumoniae, Enterobacter cloacae (E.cloacae), and K. oxytoca isolates as described previously [4]. ARGs were identified using the ResFinder 2.1 database [21]. Genome alignments of all CPE isolates were performed with progressiveMauve [22] based on an estimate of the shared gene content among each pair of input genomes with a multiple whole genome alignment algorithm. The putative coding sequences of the flanking region of carbapenemase-encoding genes and rmpA/rmpA2 genes were manually inspected using open reading frame (ORF)finder programs?? https://www.ncbi.nlm.nih.gov/orffinder/.? http://brig.sourceforge.net/.?? https://itol.embl.de/.?? http://bigsdb.web.pasteur.fr..

    Fig. 1. Study flowchart. MLST: multilocus sequence typing.

    2.4. Plasmid analysis

    Nuclease digestion, pulsed-field gel electrophoresis (S1-PFGE),and Southern blot were performed to estimate the size of the blaNDM/blaKPC/blaIMP/rmpA/rmpA2-carrying plasmids [23]. The sequence of the target plasmids was assembled using plasmidSPAdes [24]. To identify the targeted plasmids, a similarity search against the GenBank nucleotide (NT) database was performed by a basic local alignment search tool(BLAST)for each scaffold. Plasmid sequences were defined when >70% of the scaffold length matched the plasmid sequences and < 30% matched either the mobile element or chromosomal sequences based on MUMmer alignment [25]. The best BLAST hit to each scaffold was manually inspected using the plasmid database (PLSDB), a resource of complete bacterial plasmids[26].The estimated length of each plasmid was calculated as the sum of the length of all scaffolds associated with a specific reference plasmid.Reference plasmids having ≥99%identity with ≥70% overall coverage by scaffolds of one isolate were considered as present in that isolate. Plasmid Finder 1.3 was used to identify the incompatibility type of the plasmids[27]. The sequences of representative plasmids were compared against other plasmid sequences accessed from US National Center for Biotechnology Information (NCBI) using BLAST and plotted using the BLAST Ring Image Generator (BRIG)?? https://www.ncbi.nlm.nih.gov/orffinder/.? http://brig.sourceforge.net/.?? https://itol.embl.de/.?? http://bigsdb.web.pasteur.fr..

    2.5. Phylogenetic analysis of K. pneumoniae isolates

    To further characterize the phylogenetic structure of K.pneumoniae carbapenemase(KPC)-2-producing K.pneumoniae isolates,we created a core single-nucleotide polymorphism(SNP)-based phylogenetic tree and identified SNPs via mapping of Illumina reads to a reference genome(K.pneumoniae strain HS11268,CP003200).Core genes were defined as previously described [28]. The maximum likelihood-based phylogenetic reconstruction was performed with RAxML version 8.2.10 using the generalized time reversible (GTR)evolutionary model after the removal of recombination sites [29].Phylogenetic tree visualizations were produced using the Interactive Tree of Life??? https://www.ncbi.nlm.nih.gov/orffinder/.? http://brig.sourceforge.net/.?? https://itol.embl.de/.?? http://bigsdb.web.pasteur.fr..

    2.6. Characterization of the known virulence and capsule genes of K.pneumoniae isolates

    To identify the virulence and capsule genes in the 27 K.pneumoniae isolates,we further screened all short-read sets for the known alleles of virulence genes and wzi gene allele sequences using the K.pneumoniae Bacterial Isolate Genome Sequence database (BIGSdb)at Institute Pasteur??? https://www.ncbi.nlm.nih.gov/orffinder/.? http://brig.sourceforge.net/.?? https://itol.embl.de/.?? http://bigsdb.web.pasteur.fr..

    3. Results

    3.1. High prevalence of ESBLs in BSI isolates

    During the two-year study period, a total of 4801 unique cases of bacteremia were reported in 26 hospitals in 21 cities.Nonduplicate 2569 Enterobacterales isolates were prospectively collected,accounting for 53.5% (2569/4801) of all the Gram-negative bacteremia cases. Among the Enterobacteriaceae isolates, E. coli(n = 1617) was the predominant species, followed by K. pneumoniae (n = 570). Among the 2242 investigated isolates, 1111(49.6%) isolates were confirmed as ESBL-producing isolates. The overall proportions of ESBL-producing E.coli,K.pneumoniae,K.oxytoca, and P. mirabilis were 57.0% (922/1617), 30.0% (171/570),33.3% (8/24), and 35.7% (10/28), respectively. Although most of the isolates were susceptible to trimethoprim/sulfamethoxazole(50.3%), polymyxin B (98.0%), meropenem (96.8%), and imipenem(95.9%), high-level resistances to amoxicillin (88.6%), cefazolin(60.6%), and cefuroxime (53.7%) were also observed.

    3.2. Identification and distribution of CPE isolates

    In total, 66 meropenem non-susceptible isolates and 73 imipenem non-susceptible isolates were identified, including 42 carbapenemase-positive isolates confirmed using polymerase chain reaction (PCR) and sequencing. Among these isolates, 27 were K.pneumoniae,followed by E.coli(n=5),Serratia marcescens(S.marcescens)(n=3),E.cloacae(n=3),Klebsiella michiganensis(K.michiganensis)(n=1),Klebsiella variicola(K.variicola)(n=1),K.oxytoca(n=1),and Raoultella planticola(R.planticola)(n=1).All CPE isolates were non-susceptible to carbapenems and resistant to a broad array of antimicrobials.Among these isolates,total resistance to cefotaxime and piperacillin-tazobactam was observed (100.0%), followed by very high incidences of resistance to aztreonam (95.2%) and ceftazidime(92.9%).As a result,the most active antimicrobials against CPE isolates were tigecycline,polymyxin B,and trimethoprim/sulfa methoxazole.All isolates were susceptible to tigecycline,while only one S.marcescens isolate was resistant to polymyxin B.

    Sanger sequencing further revealed that blaKPC-2was the most prevalent variant found in 31 (91.3%) isolates, followed by bla-NDM-5(n = 5), blaNDM-1(n = 4), blaIMP-4(n = 1), and blaIMP-8(n = 1).Interestingly, carbapenemase genes were present in 27 (4.7%) of 570 K.pneumoniae isolates and 5(0.3%)of 1617 E.coli strains.Additionally, these CPE isolates were collected from 14 hospitals located in 12 cities, and the highest CPE ratio was observed in the First Affiliated Hospital of Wannan Medical College,with a rate of 17.4%.

    3.3. Clinical description of CPE-positive patients

    All patients with CPE infections were hospitalized. The mean age of the 42 patients was 61.1 years with a range of 1-90 years,and 66.7% (28/42) were males. Twenty-one (50.0%) patients were admitted to the intensive care unit(ICU)(including the emergency ICU (EICU) and neonatal ICU (NICU)). As a result, 15 of 42 (35.7%)patients died in this study. It is worth noting that 5 of 6 (83.3%)patients infected with rmpA/rmpA2-producing K. pneumoniae isolates died,suggesting the high risk of infection with such hypervirulent pathogens.

    3.4. Clonal spread of K. pneumoniae ST11 and E. coli ST167 isolates

    All genome assemblies of the 42 CPE isolates were deposited in GenBank and are registered under BioProject accession No.PRJNA393804. The results of the WGS data are summarized in Table 1. Through comparative genomic analyses within each species and sequence type (ST), we identified eight CPE clades(Fig. 2), which is in line with the species identification. It is worth noting that KPC-2-producing K. pneumonia ST11 and New Delhi metallo-β-lactamase (NDM)-5-producing E. coli ST167 isolates were detected in ten and four sentinel hospitals, respectively.These data suggest the clonal spread of KPC-2-producing K. pneumoniae ST11 and NDM-5-producing E. coli ST167 in our study.

    Table 1 Overview of CPE assembly statistics and genome coverage based on the assembly data.

    3.5. Characterization of ARGs

    Using the WGS data, we identified a broad array of ARGs associated with a broad array of antimicrobials: aminoglycosides, βlactams, fosfomycin, carbapenems, quinolones, sulfonamide,trimethoprim,and phenicol(Fig.2).Moreover,33 of 42(78.6%)isolates carrying carbapenemases also harbored a predicted ESBL.Interestingly, among these ESBLs, cefotaxime hydrolyzing βlactamase (CTX-M)-65 was the most predominant cluster (47.6%,20/42), followed by CTX-M-14 (23.8%, 10/42). Seven isolates produced two blaCTX-Malleles. As expected, at least one variant of the sulfhydryl reagent variable (SHV) enzyme was found in 30 Klebsiella isolates. Among these isolates, 22 harbored blaSHV-11and 11 harbored blaSHV-178.

    3.6. Genetic context of carbapenemase-encoding genes

    S1-PFGE, Southern hybridization, and replicon typing analysis revealed that all carbapenemase-encoding genes were plasmidmediated (Table 2 and Fig. S1 in Appendix A). Plasmids harboring blaKPC-2(n = 31) were genetically divergent and could be categorized into the following groups: IncFII plasmid with a size of ~79 to ~260 kilobase (kb), IncR plasmid with a size of ~55 kb, and IncP-6 plasmid with a size of ~38 kb (Fig. S1). Although blaKPCwas mainly associated with the Tn3 transposon with three main structures,they were found to share a similar conserved structure,ISKpn27-blaKPC-2-ISKpn6-korC-hp-klcA, implying that this mobile element played a key role in the transmission of the blaKPC-2gene in China (Fig. 3(a)).

    In addition, blaIMP-4and blaIMP-8were located on ~55 kb IncN and ~73 kb non-typeable plasmids, respectively (Table 2 and Fig. S1(e)). In silico analysis revealed that blaIMP-4was carried by a class I integron in the blaIMP-4-ltrA-qacED1-sul1 cassette array on pEN987-imipenemase (IMP), which shows sequence similarity with plasmid p19501-IMP from K. pneumoniae (MF344565)(Fig. 3(b)). In contrast, blaIMP-8was harbored by a class I integron in the blaIMP-8-aac(6′)-Ib-blaOXA-1-catB3-arr-3-qacEdelta1-sul1 cassette array on pEN3600-IMP. Interestingly, this structure exhibits high similarity with the sequence of the blaKPC-2plasmid p112298-KPC, although blaIMP-8is absent from that plasmid(Fig. 3(c)).

    Plasmids harboring blaNDMfrom E. coli (n = 5) and E. cloacae(n = 1) all belonged to IncX3 with a size of ~46 kb; however, two Klebsiella isolates carried blaNDMgenes encoded by the IncFI plasmid with a size of ~55 kb and a non-typeable plasmid with a size of ~220 kb(Table 2 and Fig.S1(d)).Although a fragment consisting of dsbC-trpF-bleMBL-blaNDMwas observed in all the blaNDM-bearing plasmids,eight plasmids exhibited three different types of blaNDM-1gene contexts (Figs. 3(d) and (e)). The absence of insertion sequence Aba125 (ISAba125) was identified in three plasmids(pK950-NDM, pK3287-NDM, and E4219-NDM), and pK3287-NDM showed low similarity with other plasmids,except for the blaNDMcontaining region.

    Fig.2. Alignment of genome sequences of 42 CPE isolates and ARGs identified via WGS.The figure was generated using progressiveMauve based on an estimate of the shared gene content among each pair of input genomes with a multiple whole genome alignment algorithm.ARGs are shown on the right side(presence represented by blue shapes).

    Table 2 Features of 42 carbapenemase-encoding plasmids identified from BSIs.

    3.7. The genetic diversity of K. pneumoniae ST11 isolates

    Fig. 3. Genetic environment of carbapenemase-encoding genes in 42 CPE isolates. (a) Colinear genome alignment among 31 blaKCP-2-harboring plasmids. (b) Genetic environment of the blaIMP-4 gene in isolate EN987. (c) Genetic environment of the blaIMP-8 gene in isolate EN3600. (d) Genomic map of the blaNDM-1-carrying plasmids.(e) Comparative genomics of five blaNDM-5-harboring plasmids. The Easyfig program was applied in comparative genomics. Colored arrows indicate ORFs, and the shaded region reflects sequence similarity.Arrows indicate the directions of transcription of the genes, and different genes are shown in different colors. The ARGs are indicated in red. Isolates with different sizes of the core region of carbapenemase-encoding genes are indicated by vertical lines as well as numbers. IS: insertion sequence.

    Phylogenetic analysis of K. pneumoniae isolates was further investigated given that K. pneumoniae was the most prevalent organism identified in the 42 carbapenemase-positive isolates.We identified a total of 21 711 core genome SNPs among 27 K.pneumoniae genomes(Fig.4(a)).Then,these genomes were divided into four distinct phylogenetic clades based on analysis of the core gene maximum likelihood tree using RAxML. Additionally, SNP analysis identified three pairs of closely related isolates (K4314 &K4324,K666&K559,and K3871&K3902)shared by two patients,which indicates likely hospital transmission of these isolates.Analysis of the capsular polysaccharide (cps) locus showed that 27 K.pneumoniae isolates contained six different wzi alleles (Fig. 4(b)).According to the Klebsiella PasteurMLST database,these wzi alleles corresponded to different K types: KL47 (n = 16), KL64 (n = 6), K1(n=2),K20(n=1),K19(n=1),and KL13(n=1).Interestingly,five K types were detected among ST11 isolates (n = 23), and the analysis of the K. pneumoniae ST11 clone also indicated that the median pairwise SNP distance was 15 (range: 0-42) (Fig. 4(b)).These data suggest a genetic diversity among the ST11 lineage.

    Fig.4. Comparative genomics of 27 KPC-2-producing K.pneumoniae isolates.(a)Maximum likelihood-based phylogenetic tree built from 21 711 core genome SNPs of 27 BSI isolates mapped to the reference genome of K. pneumoniae strain HS11268 (CP003200). Isolates were grouped with a threshold of the maximum 1000 SNPs to the nearest group member,and the four resulting groups are shown.The origins of the isolates containing different STs are indicated in pie charts,and the different origins are shown in different colors. (b) Distribution of capsular types among 27 KPC-2-producing K. pneumoniae isolates. The origins of the isolates containing different capsular types are indicated in circles, and the different origins are shown in different colors.

    3.8. Distribution of virulence factors among K. pneumoniae isolates

    A total of 76 known virulence factors were detected in K.pneumoniae isolates(Fig.5).A high prevalence of biofilm-encoding mrk gene clusters and ybt genes was observed in these isolates.All 27 K.pneumoniae isolates encoded mrk genes, and 26 isolates harbored ybt genes. Moreover, aerobactin, allantoinase, colibactin, the ferric uptake operon, microcin, KP1_1364 and KP1_1371, and salmochelin-associated genes were detected in seven, two, three,three, two, two, and two isolates, respectively. Surprisingly, the isolate K950 possessed the highest number of virulence genes and encoded 74 virulence factors,all except for the ybbW and mceJ genes.

    3.9. Plasmid analysis of rmpA/rmpA2-harboring plasmids

    Fig.5. Distribution of virulence-associated genes in K.pneumoniae strains.Heatmaps were generated by aligning the draft genome sequence of each isolate to the BIGSdb-Kp database. The presence of virulence genes in a specific genome is represented by a blue box, and the absence of virulence genes is represented by a cream-colored box.Virulence factors are shown on the left side. iucABCD: aerobactin-related genes; iutA: ferric aerobactin receptor gene; allABCDRS/arcC/fdrA/gcl/ylbEF/ybbWY/hyi/glxKR:allantoniase-related genes;kfuABC:ferric uptake operon-associated genes;clbABCDEFGHILMNOPQR:colibactin-associated genes;mceABCDEGHIJ:microcin-associated genes;mrkABCDFHIJ: type 3 fimbriae-associated genes; rmpA/rmpA2: cps transcriptional activator genes; iroBCDN: salmochelin-associated genes; ybtAEPQSTUX/fyuA/irp1/irp2:yersiniabactin-associated genes.

    We additionally identified the ‘‘regulators of mucoid phenotype”rmpA and rmpA2 genes in three and six isolates,respectively(Fig. S2 in Appendix A). S1-PFGE and Southern hybridization revealed that rmpA was carried by ~200 kb IncHIB and ~260 kb IncHIB plasmids (Fig. S2(a)). Compared to rmpA, the rmpA2-bearing plasmids were structurally more divergent, as the rmpA2 gene was located on IncHIB plasmids with sizes of ~370, ~260,~218, ~200, and ~150 kb (Fig. S2(b)). Notably, rmpA and rmpA2 coexisted on the plasmids from isolates K950, K3175, and K4803(Fig. S2 and Table 3). Comparative sequence analysis showed that K950 and K3175 shared the conserved genetic context of the rmpA gene, with a difference from that of K4803 (Fig. S2(c)). Further analysis identified chromosome-encoded salmochelin-associated genes iroBCDN in K950 and K3175, but it was absent in K4803(Fig. 5). In silico analysis also found a similar core structure of the rmpA2 gene (Fig. S2(d)). These data indicated that rmpA2-bearing plasmids were genetically divergent, although these plasmids shared a similar structure surrounding rmpA2, indicating that this structure played a key role in the transmission of the rmpA2 gene.

    4. Discussion

    Over the past decade, China has witnessed the emergence and rapid increase of CRE in some regions [13,15]. In light of the increasing burden of CRE infections, there is an urgent need to update our knowledge on the genomic characteristics of CRE isolates in China, which is pivotal for monitoring carbapenem resistance as well as for formulating relevant policies for the control and management of CRE infections. Moreover, bacteremia due to CRE is usually associated with increased rates of treatment failure,high mortality, and high hospitalization costs, and is gradually becoming a real clinical challenge [30,31]. Previous investigations of BSIs caused by CPE in China were mainly based on the epidemiological results of retrospective studies [14] and case series using small sample sizes [32,33]. Thus far, the genomic characteristics of CPE isolates from individuals with bacteremia are largely unknown.Here,we provide the first high-resolution genomic analysis of CPE isolates from a multicenter BSI surveillance in China.

    This report documents that CPE are widespread in BSIs in China,accounting for 1.6% of the Enterobacteriaceae isolates, and were identified in 54.0%of the hospitals screened in this study.The combined results of this work and those of previous studies suggest that carbapenemase producers have disseminated throughout China. The dissemination of CPE among BSI isolates, as observed in our collection,raises concerns for the treatment of patients with Gram-negative sepsis and suggests a need to reduce selective pressure and control the spread of resistant organisms [34].

    In this work, blaKPC-2and blaNDM-5were found to be the major carbapenemase genes responsible for mediating the carbapenem resistance phenotypes in CPE. In China, the majority of CRE infections are due to K. pneumoniae ST11 that harbor the blaKPC-2carbapenemase, which is closely related to the international epidemic clone ST258[35].A previous national survey of CRE identified KPC-2-producing K. pneumoniae strains as the predominant CRE isolates [13], which is consistent with our identified 80%-KPC-2-producing rate among CPE isolates. Moreover, the rapid spread of blaKPC-2is mainly due to the clonal dissemination of K.pneumoniae ST11 strains. Previous investigations have described the high prevalence and mortality rates of ST11-KL47 and ST11-KL64 in China[36,37].We detected that ST11 was partitioned into five clades, with ST11-KL47 being the predominant subclone. We also noted that rmpA and rmpA2 coexisted on ST11-KL64 isolates,which is consistent with recent observations [8,37].

    In contrast, a previous national survey revealed that CRE infections due to E. coli harboring carbapenemase are associated with the globally distributed ST131 lineage, which accounted for 33.0%of the isolates in that study,thus being the most dominant in China[13]. However, in recent years, there have been increasing reports of the detection of the NDM-5-producing E. coli ST167 lineage in clinical infections in China [13,38,39]. The observation of ST167 being the most common type of E. coli in our collection is in line with this trend. In addition to the wide spread of E. coli ST167 in China,some reports from European countries hint toward an emergence of a blaNDMcarrying E. coli ST167 [40-43], with epidemic potential. Appropriate measures to effectively control the spread of KPC-2-producing K. pneumoniae ST11 and NDM-5-producing E.coli ST167 are needed to prevent further spread in China as well as serious public health consequences.

    Most of the blaKPC-2/blaNDM/blaIMPgenes detected in Enterobacteriaceae were located on transmissible plasmids [13]. Consistent with these data, characterization of the carbapenemaseharboring plasmids recovered in this study indicated that all carbapenemase-encoding genes among clinical CPE strains were plasmid-mediated.Here,we found KPC genes in four bacterial species and in ≥33 different STs,carried by 11 plasmid replicon types,suggesting that both plasmid spread and the mobility between plasmids play important roles in the dissemination of KPC enzymes in China.Even within ST11,we found at least eight different KPC plasmid replicon types, indicative of the success of this clone as a host of KPC plasmids. In contrast to blaKPC, the blaNDMgenes (blaNDM-1and blaNDM-5) have frequently been reported to be located on IncX3 plasmids among multiple enterobacterial species,implying that IncX3 plasmids may provide an efficient vehicle for blaNDMdissemination within bacterial strains and interspecies from humans[13,44]. Our observations further illustrate the clinical significance of IncX plasmids in the transmission of carbapenem resistance.

    Notably, most K. pneumoniae isolates were found to be significantly prevalent with siderophore yersiniabactin, which is the most common K. pneumoniae high-virulence determinant and closely associated with the virulence of Enterobacteriaceae strains that cause invasive human infections [45,46]. Furthermore, it is well documented that the rmpA and rmpA2 genes are significantly associated with invasive human infection compared with noninvasive or carriage isolates [28]. Therefore, the coexistence of these genes in K. pneumoniae ST11 KPC producers in BSIs is worrisome because they are simultaneously multidrug resistant, highly transmissible,and hypervirulent[47].In addition,the combination of virulence factor genes such as aerobactin, allantoinase, colibactin, ferric uptake operon, microcin, salmochelin, rmpA2, and yersiniabactin was detected in the same isolate in this work. This finding may explain the high mortality rate associated with K.pneumoniae infections in this study and suggests that these isolatesmay potentially be hypervirulent in BSIs, although future experimental studies are needed for confirmation.

    Table 3 An overview of rmpA/rmpA2-encoding plasmids.

    This study had several limitations.First,although hospitals in a broad geographic distribution of China were enrolled in this study,only a limited number of CPE strains were obtained and investigated. Therefore, these data may not be truly representative of the prevalence and characterization of CPE for the entirety of China. Second, our findings of carbapenemase-harboring plasmids should be explained with caution; thus, further studies are required to increase confidence in the findings of this work since only BSI-causing isolates were included in the collection.

    5. Conclusions

    In conclusion, our study reported the wide dissemination of ESBL and CPE isolates from individuals with bacteremia in China.Importantly, this work indicated that K. pneumoniae ST11 and E. coli ST167 have become serious clinical problems in China. The study also reveals a genomic picture of invasive CPE infections in China, which highlights the significance of country-level surveillance of BSIs. Plasmid analysis revealed that plasmids played important roles in the process of carbapenemase-encoding gene dissemination. The prevalence of CPE in BSIs should be continuously and closely monitored in China. Furthermore, large-scale detailed microbiological and genomic investigations into the epidemic clone K. pneumoniae ST11 with potential hypervirulence are also particularly needed to understand the transmission of the blaKPC-2gene and virulence genes so that effective strategies for national control of CPE infections can be developed.

    Acknowledgments

    We gratefully acknowledge the financial support of the National Key Research and Development Program of China(2017YFC1200203 and 2016YFD0501105), the Mega-projects of Science Research of China (2018ZX10733402-004 and 2018ZX10712001-005), the National Natural Science Foundation of China (81741098 and 81711530049), the Zhejiang Provincial Key Research and Development Program (2015C03032), and the Zhejiang Provincial Natural Science Foundation of China(LY17H190003).

    Compliance with ethics guidelines

    Beiwen Zheng, Hao Xu, Lihua Guo, Xiao Yu, Jinru Ji, Chaoqun Ying,Yunbo Chen,Ping Shen,Huiming Han,Chen Huang,Shuntian Zhang, Tao Lv, and Yonghong Xiao declare that they have no conflict of interest or financial conflicts to disclose.

    Appendix A. Supplementary data

    Supplementary data to this article can be found online at https://doi.org/10.1016/j.eng.2020.10.015.

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