| Literature DB >> 33786847 |
Meng Wang1, Yu Fan2, Ping Liu1, Yehua Liu1, Jianlei Zhang1, Yan Jiang1, Chunlei Zhou1, Lei Yang1, Ce Wang1, Chengqian Qian2, Chao Yuan3, Si Zhang2, Xiaohang Zhang4, Zhiqiu Yin5, Hong Mu1, Yuhui Du6.
Abstract
Raoultella ornithinolytica is a poorly understood opportunistic pathogen, and the underlying mechanisms of its multidrug resistance and pathogenicity have not yet been comprehensively investigated. The multidrug-resistant (MDR) strain WM1 was isolated from the blood of a male patient in Tianjin, China, in 2018. Here, we describe the complete genome and provide a genomic analysis of R. ornithinolytica WM1. The isolate was resistant to all tested antimicrobials except amikacin, tobramycin, and tigecycline. Two plasmids, pWM1-1 (IncHI5) and pWM1-2 (IncR), carried multidrug-resistance regions. A large antimicrobial resistance island region resided on pWM1-1 and exhibited mosaic structures resulting from the acquisition of complex integrations of variable regions, including genes conferring resistance to multiple classes of antimicrobials. Moreover, WM1 possessed virulence-related elements that encode several virulence factors, including type I fimbriae, Escherichia coli common pilus, type II and VI secretion systems, yersiniabactin, enterobactin, and surface polysaccharide, indicating pathogenic potential. Furthermore, the core genome phylogeny and pan-genome analyses revealed extensive genetic diversity. Our analysis indicates the need for stringent infection control, antimicrobial stewardship, periodic resistance monitoring, and rational medication to address potential threats posed by MDR R. ornithinolytica strains.Entities:
Keywords: Raoultella ornithinolytica; comparative genomics; multidrug resistance; pathogenicity; whole-genome sequencing
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Year: 2021 PMID: 33786847 DOI: 10.1111/nyas.14595
Source DB: PubMed Journal: Ann N Y Acad Sci ISSN: 0077-8923 Impact factor: 5.691