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在 中,编码aerobactin 和 salmochelin 的毒力质粒的遗传多样性和进化。

Genetic diversity and evolution of the virulence plasmids encoding aerobactin and salmochelin in .

机构信息

Department of Laboratory Medicine, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.

State Key Laboratory of Microbial Metabolism, Joint International Laboratory on Metabolic & Developmental Sciences, School of Life Sciences & Biotechnology, Shanghai Jiao Tong University, Shanghai, China.

出版信息

Virulence. 2021 Dec;12(1):1323-1333. doi: 10.1080/21505594.2021.1924019.

DOI:10.1080/21505594.2021.1924019
PMID:33970792
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8115583/
Abstract

Virulence plasmids of hypervirulent (hvKp) have the potential to transfer to drug-resistant strains or integrate with other plasmids, facilitating the genome evolution of threatening pathogens. We conducted an in-depth analysis of the publicly available 156 complete genome sequences of hvKp together with a multi-region clinical cohort of 171 hvKp strains from China to provide evidence for the virulence plasmid evolution. Virulence plasmids were frequently detected in the ST23 and ST11 strains. Multidrug-resistant hvKp (MDR-hvKp) occupied a large proportion of hvKp, and the coexistence of virulence and resistance plasmids may be the major cause. Virulence plasmids commonly possessed multiple replicons, of which IncFIB was the most prevalent (84.6%). We identified 49 IncFIB alleles among 583 IncFIB plasmids, and they could be divided into Clades I, II, and III. We further observed that conjugative and non-conjugative virulence plasmids could be distinguished by IncFIB genetic diversity, and IncFIB subtyping could also indirectly indicate a chimeric preference of conjugative virulence plasmids. On this basis, we developed an open-access web tool called for IncFIB subtyping. In conclusion, the genetic diversity of IncFIB virulence plasmids could be used for tracking the evolution of virulence plasmids, and further preventing the emergence of MDR-hvKp strains.

摘要

毒力质粒的高毒力 (hvKp) 有可能转移到耐药株或与其他质粒整合,从而促进威胁病原体的基因组进化。我们对公开的 156 株 hvKp 全基因组序列和来自中国的 171 株 hvKp 多区域临床株进行了深入分析,为毒力质粒进化提供了证据。毒力质粒在 ST23 和 ST11 株中经常被检测到。多药耐药性 hvKp (MDR-hvKp) 在 hvKp 中占有很大比例,毒力和耐药质粒的共存可能是主要原因。毒力质粒通常具有多个复制子,其中 IncFIB 最为普遍(84.6%)。在 583 个 IncFIB 质粒中,我们鉴定了 49 个 IncFIB 等位基因,它们可以分为 I、II 和 III 类。我们进一步观察到,可接合和不可接合的毒力质粒可以通过 IncFIB 遗传多样性来区分,IncFIB 亚型也可以间接表明可接合毒力质粒的嵌合偏好。在此基础上,我们开发了一个名为 IncFIB 亚型的开放访问网络工具。总之,IncFIB 毒力质粒的遗传多样性可用于追踪毒力质粒的进化,并进一步防止 MDR-hvKp 菌株的出现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b65/8115583/cd0beb4ca5ea/KVIR_A_1924019_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b65/8115583/65dd0ae90f50/KVIR_A_1924019_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b65/8115583/6f0726134de5/KVIR_A_1924019_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b65/8115583/a0b268ee8b47/KVIR_A_1924019_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b65/8115583/cd0beb4ca5ea/KVIR_A_1924019_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b65/8115583/65dd0ae90f50/KVIR_A_1924019_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b65/8115583/6f0726134de5/KVIR_A_1924019_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b65/8115583/a0b268ee8b47/KVIR_A_1924019_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b65/8115583/cd0beb4ca5ea/KVIR_A_1924019_F0004_OC.jpg

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