Shenzhen Institute of Respiratory Diseases, Second Clinical Medical College (Shenzhen People's Hospital), Jinan University; the First Affiliated Hospital (Shenzhen People's Hospital), Southern University of Science and Technology, Shenzhen, People's Republic of China.
Department of Laboratory Medicine, Nanjing Drum Tower Hospital Clinical College of Jiangsu University, Nanjing, People's Republic of China.
Emerg Microbes Infect. 2022 Dec;11(1):1959-1972. doi: 10.1080/22221751.2022.2103456.
Convergence of and carbapenemase genes has been sporadically detected in complex (ECC) with an upward trend. However, the state of the epidemic and underlying mechanism of such convergence has been poorly understood. In this study, the co-occurrence of MCR and carbapenemases was systematically analyzed in 230 clinical ECC isolates collected between 2000 and 2018 together with a global dataset consisting of 3,559 ECC genomes compiled from GenBank. We identified 48 /-positive isolates (MCR-ECC) (20.9%) in our collection, and a comparable ratio of MCR-ECC (720/3559, 20.2%) was detected in the global dataset. A high prevalence of carbapenemase-producing MCR-ECC (MCR-CREC) was further identified in the MCR-ECC of both datasets (16/48, 33.3%; 388/720, 53.9%), demonstrating a frequent convergence of and carbapenemase genes in ECC worldwide. An epidemic IncHI2/2A plasmid with a highly conserved backbone was identified and largely contributed to the dissemination of in ECC worldwide. A highly conserved IncX3-type NDM-1-carrying plasmid and IncN-type IMP-4-carrying plasmid were additionally detected in MCR-CREC isolated in China. Our surveillance data showed that MCR-CREC emerged (in 2013) much later than MCR-ECC (in 2000), indicating that MCR-CREC could be derived from MCR-ECC by additional captures of carbapenemase-encoding plasmids. Tests of plasmid stability and incompatibility showed that the -encoding plasmids with the NDM-1-encoding plasmids stably remained in ECC but incompatible in , suggesting that the convergence was host-dependent. The findings extend our concern on the convergence of resistance to the last resort antibiotics and highlight the necessity of continued surveillance in the future.
在肠杆菌科复合体(ECC)中, 和碳青霉烯酶基因的融合已零星检出,且呈上升趋势。然而,这种融合的流行状态和潜在机制仍知之甚少。在这项研究中,我们系统分析了 2000 年至 2018 年间收集的 230 株临床 ECC 分离株中 MCR 和碳青霉烯酶的共现情况,并结合来自 GenBank 的 3559 株 ECC 基因组的全球数据集进行分析。我们在收集的样本中发现了 48 株 MCR-阳性分离株(MCR-ECC)(20.9%),在全球数据集中也检测到了相当比例的 MCR-ECC(720/3559,20.2%)。在两个数据集的 MCR-ECC 中,还进一步鉴定出了高流行率的产碳青霉烯酶的 MCR-ECC(MCR-CREC)(16/48,33.3%;388/720,53.9%),这表明 在全球范围内 ECC 中, 和碳青霉烯酶基因经常融合。鉴定出一种流行的高度保守的 IncHI2/2A 质粒,它在全球范围内对 ECC 中 的传播起了重要作用。此外,在中国分离的 MCR-CREC 中还检测到了高度保守的 IncX3 型 NDM-1 携带质粒和 IncN 型 IMP-4 携带质粒。我们的监测数据显示,MCR-CREC 的出现(2013 年)远晚于 MCR-ECC(2000 年),这表明 MCR-CREC 可能是通过额外捕获碳青霉烯酶编码质粒从 MCR-ECC 衍生而来。质粒稳定性和不相容性测试表明,NDM-1 编码质粒与 编码质粒稳定地保留在 ECC 中,但在 中不相容,这表明融合具有宿主依赖性。这些发现扩展了我们对最后一道抗生素耐药性融合的关注,并强调了未来持续监测的必要性。