Department of Clinical Laboratory, Peking University People's Hospital, Beijing.
Department of Clinical Laboratory, Hunan Provincial People's Hospital, Changsha, Hunan.
Clin Infect Dis. 2018 Nov 13;67(suppl_2):S196-S205. doi: 10.1093/cid/ciy660.
Carbapenem-resistant Enterobacteriaceae (CRE) strains are a major threat to global health. The development of effective control measures requires more detailed phenotypic and genotypic characterization of CRE.
CRE isolates were collected from 65 hospitals in 25 provinces across China between January 1, 2012, and December 31, 2016. The isolates were characterized by antimicrobial susceptibility testing and multilocus sequence typing. Genes encoding carbapenemases, mobilized colistin resistance (mcr-1), and β-lactamases were detected by polymerase chain reaction and DNA sequencing.
A total of 1801 independent CRE isolates (1201 Klebsiella pneumoniae, 282 Escherichia coli, and 179 Enterobacter cloacae) were collected during the study period. Overall, 96.9%, 89.7%, 54.5%, 49.9%, and 40% of CRE strains were susceptible to colistin, tigecycline, amikacin, minocycline, and fosfomycin, respectively. Notably, 1091/1201 (91%) K. pneumoniae, 225/282 (80%) E. coli, and 129/179 (72%) E. cloacae harbored carbapenemase gene. K. pneumoniae carbapenemase (KPC) was predominant in K. pneumoniae (77%), whereas New Delhi metallo-β-lactamase (NDM) was predominant in E. coli (75%) and E. cloacae (53%). The mcr-1 gene was detected in 13 NDM-carrying E. coli isolates (4.6%). Sequence type (ST)11 and ST167 were predominant among the 100 K. pneumoniae and 47 E. coli STs, respectively. KPC-ST11, which accounted for 64% of K. pneumoniae isolates, had higher levels of resistance than non-ST11 strains to aztreonam, fosfomycin, and amikacin (P < .001). The proportions of KPC and NDM enzymes in CRE increased from 2012 to 2016 (54%-59% and 12%-28%, respectively).
The number of CRE strains harboring carbapenemase is increasing. KPC-ST11 K. pneumoniae, the predominant strain, shows a reduced susceptibility to most available antibiotics.
耐碳青霉烯肠杆菌科(CRE)菌株对全球健康构成重大威胁。开发有效的控制措施需要更详细的 CRE 表型和基因型特征。
2012 年 1 月 1 日至 2016 年 12 月 31 日期间,从中国 25 个省的 65 家医院采集 CRE 分离株。通过药敏试验和多位点序列分型对分离株进行特征描述。通过聚合酶链反应和 DNA 测序检测碳青霉烯酶、移动性粘菌素耐药(mcr-1)和β-内酰胺酶基因。
研究期间共采集 1801 株独立的 CRE 分离株(1201 株肺炎克雷伯菌、282 株大肠埃希菌和 179 株阴沟肠杆菌)。总体而言,CRE 菌株对粘菌素、替加环素、阿米卡星、米诺环素和磷霉素的敏感性分别为 96.9%、89.7%、54.5%、49.9%和 40%。值得注意的是,1091/1201(91%)肺炎克雷伯菌、225/282(80%)大肠埃希菌和 129/179(72%)阴沟肠杆菌携带碳青霉烯酶基因。肺炎克雷伯菌碳青霉烯酶(KPC)在肺炎克雷伯菌中占优势(77%),而新德里金属β-内酰胺酶(NDM)在大肠埃希菌(75%)和阴沟肠杆菌(53%)中占优势。在 13 株携带 NDM 的大肠埃希菌分离株中检测到 mcr-1 基因(4.6%)。100 株肺炎克雷伯菌和 47 株大肠埃希菌 ST 中,ST11 和 ST167 分别占优势。产 KPC-ST11 的肺炎克雷伯菌占肺炎克雷伯菌分离株的 64%,对氨曲南、磷霉素和阿米卡星的耐药性高于非 ST11 株(P<0.001)。2012 年至 2016 年期间,CRE 菌株中 KPC 和 NDM 酶的比例分别从 54%-59%和 12%-28%增加。
携带碳青霉烯酶的 CRE 菌株数量不断增加。产 KPC-ST11 的肺炎克雷伯菌是主要流行株,对大多数现有抗生素的敏感性降低。