Increase in antioxidant capacity associated with the successful subclone of hypervirulent carbapenem-resistant Klebsiella pneumoniae ST11-KL64

被引:0
|
作者
Wang, Ruobing [1 ]
Zhang, Anru [1 ]
Sun, Shijun [1 ]
Yin, Guankun [1 ]
Wu, Xingyu [1 ]
Ding, Qi [1 ]
Wang, Qi [1 ]
Chen, Fengning [1 ]
Wang, Shuyi [1 ]
van Dorp, Lucy [2 ]
Zhang, Yawei [1 ]
Jin, Longyang [1 ]
Wang, Xiaojuan [1 ]
Balloux, Francois [2 ]
Wang, Hui [1 ]
机构
[1] Peking Univ Peoples Hosp, Dept Clin Lab, Beijing, Peoples R China
[2] UCL, UCL Genet Inst, Dept Genet Evolut & Environm, London, England
基金
中国国家自然科学基金;
关键词
ANNOTATION; CHINA; ENTEROBACTERIACEAE; VISUALIZATION; CONVERGENCE; INFECTIONS; EMERGENCE; ST11;
D O I
暂无
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The acquisition of exogenous mobile genetic material imposes an adaptive burden on bacteria, whereas the adaptational evolution of virulence plasmids upon entry into carbapenem-resistant Klebsiella pneumoniae (CRKP) and its impact remains unclear. To better understand the virulence in CRKP, we characterize virulence plasmids utilizing a large genomic data containing 1219 K. pneumoniae from our long-term surveillance and publicly accessible databases. Phylogenetic evaluation unveils associations between distinct virulence plasmids and serotypes. The sub-lineage ST11-KL64 CRKP acquires a pK2044-like virulence plasmid from ST23-KL1 hypervirulent K. pneumoniae, with a 2698 bp region deletion in all ST11-KL64. The deletion is observed to regulate methionine metabolism, enhance antioxidant capacity, and further improve survival of hypervirulent CRKP in macrophages. The pK2044-like virulence plasmid discards certain sequences to enhance survival of ST11KL64, thereby conferring an evolutionary advantage. This work contributes to multifaceted understanding of virulence and provides insight into potential causes behind low fitness costs observed in bacteria.
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页数:14
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