Department of Infection Control and Prevention, The University of Tokyo Hospital, Tokyo, Japan.
Department of Microbiology and Infectious Diseases, Toho University School of Medicine, Tokyo, Japan.
J Glob Antimicrob Resist. 2024 Sep;38:309-316. doi: 10.1016/j.jgar.2024.06.020. Epub 2024 Jul 14.
The aim of this study is to characterise the molecular characteristics of NDM-producing Enterobacterales, which have been on the increase in recent years in Japan, where IMP-producing bacteria are dominant among carbapenemase-producing Enterobacterales.
We collected 21 strains of NDM-producing Enterobacterales detected between 2015 and 2022 at five hospitals in Tokyo and performed illumina whole genome sequencing. For the seven selected strains, nanopore long-read sequencing was also performed to characterise the plasmids harbouring bla.
Fourteen strains were Escherichia coli and all carried bla. Among these strains, eight and three were sequence type (ST) 410 and ST167, respectively, and both groups of strains were spread clonally in different hospitals. Two strains of Klebsiella pneumoniae ST147 carrying bla were detected in a hospital, and these strains had also spread clonally. The remainder included Enterobacter hormaechei, Klebsiella quasipneumoniae, Citrobacter amalonaticus, and Klebsiella michiganensis. Plasmid analysis revealed that an identical IncX3 plasmid harbouring bla was shared among four strains of different bacterial species (E. coli, C. amalonaticus, K. michiganensis, and E. hormaechei) detected at the same hospital. In addition, a Klebsiella quasipneumoniae strain detected at a different hospital also carried an IncX3 plasmid with a similar genetic structure.
Nosocomial spread of multiple multidrug-resistant global clones and transmission of IncX3 plasmids harbouring bla among multiple species were detected as the major pathways of spread of NDM-producing Enterobacterales in Tokyo. Early detection of carriers and measures to prevent nosocomial spread are important to prevent further spread of NDM-producing organisms.
本研究旨在对近年来日本产碳青霉烯酶肠杆菌科中 NDM 产生菌的分子特征进行分析,在这些产碳青霉烯酶肠杆菌科中,IMP 产生菌占主导地位。
我们收集了 2015 年至 2022 年在东京的五家医院检测到的 21 株 NDM 产生肠杆菌科细菌,并进行了 illumina 全基因组测序。对于选定的 7 株菌,还进行了纳米孔长读测序,以分析携带 bla 的质粒。
14 株为大肠埃希菌,均携带 bla。在这些菌株中,8 株和 3 株分别为 ST410 和 ST167,两组菌株均在不同医院呈克隆传播。在一家医院检测到两株携带 bla 的肺炎克雷伯菌 ST147,这些菌株也呈克隆传播。其余包括阴沟肠杆菌、产酸克雷伯菌、阿氏柠檬酸杆菌和密歇根克雷伯菌。质粒分析显示,在同一医院检测到的不同细菌物种(大肠埃希菌、阿氏柠檬酸杆菌、密歇根克雷伯菌和阴沟肠杆菌)的 4 株菌中,共享一个携带 bla 的相同 IncX3 质粒。此外,在另一家医院检测到的一株产酸克雷伯菌也携带一个具有相似遗传结构的 IncX3 质粒。
在东京,发现了多重多药耐药全球克隆的医院内传播以及携带 bla 的 IncX3 质粒在多种物种之间的传播,这是 NDM 产生肠杆菌科传播的主要途径。早期发现携带者并采取措施防止医院内传播,对于防止 NDM 产生菌的进一步传播非常重要。