Genetic Diversity of Carbapenem-Resistant Enterobacteriaceae (CRE) Clinical Isolates From a Tertiary Hospital in Eastern China

被引:51
作者
Miao, Minhui [1 ,2 ]
Wen, Huiyan [1 ]
Xu, Ping [3 ]
Niu, Siqiang [4 ]
Lv, Jingnan [1 ]
Xie, Xiaofang [1 ]
Mediavilla, Jose R. [5 ]
Tang, Yi-Wei [6 ]
Kreiswirth, Barry N. [5 ]
Zhang, Xia [7 ]
Zhang, Haifang [1 ]
Du, Hong [1 ]
Chen, Liang [5 ]
机构
[1] Soochow Univ, Affiliated Hosp 2, Dept Clin Lab, Suzhou, Peoples R China
[2] Jiangyin Hosp Tradit Chinese Med, Dept Clin Lab, Jiangyin, Peoples R China
[3] Fifth Peoples Hosp Suzhou, Dept Clin Lab, Suzhou, Peoples R China
[4] Chongqing Med Univ, Affiliated Hosp 1, Dept Lab Med, Chongqing, Peoples R China
[5] Rutgers State Univ, Publ Hlth Res Inst, TB Ctr, New Jersey Med Sch, Newark, NJ USA
[6] Mem Sloan Kettering Canc Ctr, 1275 York Ave, New York, NY 10021 USA
[7] Nanjing Med Univ, North Dist Affiliated Suzhou Hosp, Dept Clin Lab, Suzhou, Peoples R China
基金
美国国家卫生研究院; 中国国家自然科学基金;
关键词
carbapenem-resistant Enterobacteriaceae; carbapenemase; resistance mechanism; genetic diversity; plasmid; ESCHERICHIA-COLI; BETA-LACTAMASES; SEQUENCE; PLASMID; EPIDEMIOLOGY; SURVEILLANCE; VIRULENCE; DISTINCT; STRAINS; IMPACT;
D O I
10.3389/fmicb.2018.03341
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The prevalence of carbapenem-resistant Enterobacteriaceae (CRE) is increasing globally, with different molecular mechanisms described. Here we studied the molecular mechanisms of carbapenem resistance, including clonal and plasmid dissemination, of 67 CRE isolates collected between 2012 and 2016 from a tertiary hospital in Eastern China, an CRE endemic region. Species identification and susceptibility testing were performed using the BD Phoenix Automated Microbiology System. Isolates were characterized by PCR (for carbapenemases, ESBLs, AmpC and porin genes), multilocus sequence typing (MLST), pulsed-field gel electrophoresis (PFGE), and conjugation transfer experiments. Selected bla(KPC-2) -harboring plasmids were subjected to next-generation sequencing using the Illumina Miseq platform. Among the 67 CRE isolates, 42 Klebsiella pneumoniae, 10 Serratia marcescens, 6 Enterobacter cloacae, 2 Raoultella ornithinolytica, 2 K. oxytoca, 1 K. aerogenes, and 4 Escherichia coli isolates were identified. Six different carbapenemases were detected, including bla(KPC-2) (n = 45), bla(KPC-3) (n = 1), bla(NDM-1) (n = 6), bla(NDM-5) (n = 1), bla(IMP-4) = 2), and bla(VIM -1 )(n= 2); bla(OXA-48) -like genes were not detected. One E. cloacae strain possessed both bIa(NDM-1) and bla(KPC-3), while two E. cloacae isolates harbored bla(NDM-1) and bla(VIM-1). ESBLs (CTX-M, SHV, and TEM) and/or AmpC (CMY, DHA, and ACT/MIR) genes were also identified in 59 isolates, including 13 strains that lacked carbapenemases. Several insertions or stop codon mutations were found within porin genes of K. pneumoniae, E. coli and S. marcescens isolates, both with and without carbapenemases. The 42 K. pneumoniae isolates belonged to 12 different sequence types (ST), with ST11 being the most common, while the 6 E. cloacae isolates comprised 4 different STs. The 10 S. marcescens all shared the same PFGE pulsotype, suggestive of clonal spread. Complete plasmid sequencing and PCR screening revealed both intra-strain and inter-species spread of a common bla(KPC-2 )-harboring plasmid in our hospital. Taken together, our study revealed extensive genetic diversity among CRE isolates form a single Chinese hospital. CRE isolates circulating in the hospital differ significantly in their species, STs, porin genes, carbapenemase genes, and their plasmid content, highlighting the complex dissemination of CRE in this endemic region.
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