Clinical evolution of ST11 carbapenem resistant and hypervirulent Klebsiella pneumoniae.
Miaomiao XieXuemei YangQi XuLianwei YeKaichao ChenZhiwei ZhengNing DongQiaoling SunLingbin ShuDanxia GuEdward Wai-Chi ChanRong ZhangSheng ChenPublished in: Communications biology (2021)
Carbapenem-resistant and hypervirulent K. pneumoniae (CR-HvKP) strains that have emerged recently have caused infections of extremely high mortality in various countries. In this study, we discovered a conjugative plasmid that encodes carbapenem resistance and hypervirulence in a clinical ST86 K2 CR-HvKP, namely 17ZR-91. The conjugative plasmid (p17ZR-91-Vir-KPC) was formed by fusion of a non-conjugative pLVPK-like plasmid and a conjugative blaKPC-2-bearing plasmid and is present dynamically with two other non-fusion plasmids. Conjugation of p17ZR-91-Vir-KPC to other K. pneumoniae enabled them to rapidly express the carbapenem resistance and hypervirulence phenotypes. More importantly, genome analysis provided direct evidence that p17ZR-91-Vir-KPC could be directly transmitted from K2 CR-HvKP strain, 17ZR-91, to ST11 clinical K. pneumoniae strains to convert them into ST11 CR-HvKP strains, which explains the evolutionary mechanisms of recently emerged ST11 CR-HvKP strains.
Keyphrases
- klebsiella pneumoniae
- escherichia coli
- pet imaging
- multidrug resistant
- antibiotic resistance genes
- crispr cas
- genome wide
- drug resistant
- type diabetes
- cardiovascular disease
- microbial community
- dna methylation
- computed tomography
- cystic fibrosis
- pseudomonas aeruginosa
- coronary artery disease
- acinetobacter baumannii
- respiratory tract
- data analysis