Suppr超能文献

中国 ST2012 临床型肺炎克雷伯菌携带 bla 的基因组和表型特征。

Genomic and phenotypic characterization of ST2012 clinical Klebsiella quasipneumoniae subsp. similipneumoniae harboring bla in China.

机构信息

State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, National Medical Center for Infectious Diseases, Zhejiang University School of Medicine, Hangzhou, China.

Shandong First Medical University, Shandong Academy of Medical Sciences, Jinan, China.

出版信息

BMC Microbiol. 2024 Nov 29;24(1):506. doi: 10.1186/s12866-024-03637-2.

Abstract

BACKGROUND

Klebsiella pneumoniae has emerged as a significant pathogen that causes community and hospital infections due to its high resistance rate and transmissibility. Klebsiella pneumoniae complex is classified into three phylogroups: Klebsiella pneumoniae (KpI), Klebsiella quasipneumoniae (KpII), and Klebsiella variicola (KpIII) in classical taxonomy, but KpII and KpIII are infrequently isolated clinically. Although pathogenic KpII has been reported worldwide, the understanding of this pathogen remains limited.

METHODS

Whole-genome sequencing (WGS) of K. quasipneumoniae subsp. similipneumoniae ACESH00366hy was performed. Plasmid characterization was demonstrated using S1-PFGE, Southern blotting, and conjugation assays. Antimicrobial susceptibility testing was performed and interpreted according to CLSI, EUCAST, and FDA standards. The virulence of the strain was assessed using the Galleria mellonella infection assay, serum-killing assay, and biofilm formation assay. A phylogenetic tree was constructed to explore its biological evolution.

RESULTS

The K. quasipneumoniae subsp. similipneumoniae isolate ACESH00366hy, belonging to ST2012 and KL139, contains several resistance genes including bla, bla, bla, and oqxAB, as well as various virulence genes including iroE, iutA, mrkABCDFHIJ, entABCDEFS, and fepABCDG. The bla and bla genes were present on the 53,624 bp IncX3 plasmid. Virulence assays showed that the virulence of ACESH00366hy was greater than that of the low-toxicity strain ATCC 700,603. Phylogenetic analysis demonstrated the emergence of ST2012 KpII-B in Asia and revealed the spread of K. quasipneumoniae subsp. similipneumoniae in humans, animals, and the environment.

CONCLUSION

This study highlights the emergence of clinical ST2012 KpII strains harbouring bla via the IncX3 plasmid in China. We evaluated its resistance and virulence characteristics and performed phylogenetic analysis, thereby enhancing our understanding of its resistance and pathogenicity and contributing to the clinical surveillance of K. quasipneumoniae.

摘要

背景

由于高耐药率和传染性,肺炎克雷伯菌已成为引起社区和医院感染的重要病原体。在经典分类学中,肺炎克雷伯菌复合体被分为三个进化群:肺炎克雷伯菌(KpI)、产酸克雷伯菌(KpII)和中间克雷伯菌(KpIII),但临床上很少分离到 KpII 和 KpIII。虽然全世界都有致病性 KpII 的报道,但对这种病原体的了解仍然有限。

方法

对肺炎克雷伯菌亚种相似发酵菌 ACESH00366hy 进行全基因组测序(WGS)。通过 S1-PFGE、Southern 印迹和接合试验证明质粒特征。根据 CLSI、EUCAST 和 FDA 标准进行药敏试验和解释。使用金蝇幼虫感染试验、血清杀菌试验和生物膜形成试验评估菌株的毒力。构建系统发育树以探索其生物进化。

结果

肺炎克雷伯菌亚种相似发酵菌分离株 ACESH00366hy,属于 ST2012 和 KL139,含有 bla、bla、bla 和 oqxAB 等多种耐药基因,以及iroE、iutA、mrkABCDFHIJ、entABCDEFS 和 fepABCDG 等多种毒力基因。bla 和 bla 基因位于 53624 bp IncX3 质粒上。毒力试验表明,ACESH00366hy 的毒力大于低毒力菌株 ATCC 700603。系统发育分析表明,亚洲出现了 ST2012 KpII-B,揭示了肺炎克雷伯菌亚种相似发酵菌在人类、动物和环境中的传播。

结论

本研究强调了中国临床 ST2012 KpII 菌株携带 bla 的 IncX3 质粒的出现。我们评估了其耐药性和毒力特征,并进行了系统发育分析,从而提高了我们对其耐药性和致病性的认识,并有助于肺炎克雷伯菌的临床监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1428/11606014/631002b12460/12866_2024_3637_Fig1_HTML.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验