Han Mei, Liu Chang, Xie Hui, Zheng Jie, Zhang Yan, Li Chuchu, Shen Han, Cao Xiaoli
Department of Laboratory Medicine, Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School, Nanjing, Jiangsu, China.
Department of Acute Infectious Disease Control and Prevention, Jiangsu Provincial Center for Disease Control and Prevention, Nanjing, Jiangsu, China.
Front Microbiol. 2023 Feb 21;14:1127948. doi: 10.3389/fmicb.2023.1127948. eCollection 2023.
To analyze the molecular epidemiology of carbapenem-resistant complex (CREC) by whole-genome sequencing and to explore its clinical characteristics.
complex isolates collected in a tertiary hospital during 2013-2021 were subjected to whole-genome sequencing to determine the distribution of antimicrobial resistance genes (ARGs), sequence types (STs), and plasmid replicons. A phylogenetic tree of the CREC strains was constructed based on the whole-genome sequences to analyze their relationships. Clinical patient information was collected for risk factor analysis.
Among the 51 CREC strains collected, NDM-1 ( = 42, 82.4%) was the main carbapenem-hydrolyzing β-lactamase (CHβL), followed by IMP-4 ( = 11, 21.6%). Several other extended-spectrum β-lactamase-encoding genes were also identified, with SHV-12 ( = 30, 58.8%) and TEM-1B ( = 24, 47.1%) being the predominant ones. Multi-locus sequence typing revealed 25 distinct STs, and ST418 ( = 12, 23.5%) was the predominant clone. Plasmid analysis identified 15 types of plasmid replicons, among which IncHI2 ( = 33, 64.7%) and IncHI2A ( = 33, 64.7%) were the main ones. Risk factor analysis showed that intensive care unit (ICU) admission, autoimmune disease, pulmonary infection, and previous corticosteroid use within 1 month were major risk factors for acquiring CREC. Logistic regression analysis showed that ICU admission was an independent risk factor for CREC acquisition and was closely related with acquiring infection by CREC with ST418.
NDM-1 and IMP-4 were the predominant carbapenem resistance genes. ST418 carrying NDM-1 not only was the main clone, but also circulated in the ICU of our hospital during 2019-2021, which highlights the necessity for surveillance of this strain in the ICU. Furthermore, patients with risk factors for CREC acquisition, including ICU admission, autoimmune disease, pulmonary infection, and previous corticosteroid use within 1 month, need to be closely monitored for CREC infection.
通过全基因组测序分析耐碳青霉烯类肠杆菌科细菌(CREC)的分子流行病学特征,并探讨其临床特点。
对2013年至2021年期间在一家三级医院收集的CREC分离株进行全基因组测序,以确定抗菌药物耐药基因(ARGs)、序列类型(STs)和质粒复制子的分布。基于全基因组序列构建CREC菌株的系统发育树,以分析它们之间的关系。收集临床患者信息进行危险因素分析。
在收集的51株CREC菌株中,NDM-1(n = 42,82.4%)是主要的碳青霉烯水解β-内酰胺酶(CHβL),其次是IMP-4(n = 11,21.6%)。还鉴定出了其他几种超广谱β-内酰胺酶编码基因,其中SHV-12(n = 30,58.8%)和TEM-1B(n = 24,47.1%)最为常见。多位点序列分型显示有25种不同的STs,其中ST418(n = 12,23.5%)是主要克隆。质粒分析鉴定出15种质粒复制子类型,其中IncHI2(n = 33,64.7%)和IncHI2A(n = 33,64.7%)是主要类型。危险因素分析表明,入住重症监护病房(ICU)、自身免疫性疾病、肺部感染以及1个月内曾使用皮质类固醇是获得CREC的主要危险因素。逻辑回归分析显示,入住ICU是获得CREC的独立危险因素,且与感染携带ST418的CREC密切相关。
NDM-1和IMP-4是主要的碳青霉烯耐药基因。携带NDM-1的ST418不仅是主要克隆,还在2019年至2021年期间在我院ICU中传播,这凸显了在ICU中监测该菌株的必要性。此外,对于有获得CREC危险因素的患者,包括入住ICU、自身免疫性疾病、肺部感染以及1个月内曾使用皮质类固醇,需要密切监测CREC感染。