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鉴定粘质沙雷氏菌中多重耐药肺炎克雷伯氏菌的毒力决定因子。

Identifying virulence determinants of multidrug-resistant Klebsiella pneumoniae in Galleria mellonella.

机构信息

Department of Veterinary Medicine, University of Cambridge, Madingley Road, Cambridge, CB3 0ES, UK.

Pathogen Genomics, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, CB10 1SA, UK.

出版信息

Pathog Dis. 2021 Mar 20;79(3). doi: 10.1093/femspd/ftab009.

Abstract

Infections caused by Klebsiella pneumoniae are a major public health threat. Extensively drug-resistant and even pan-resistant strains have been reported. Understanding K. pneumoniae pathogenesis is hampered by the fact that murine models of infection offer limited resolution for non-hypervirulent strains which cause the majority of infections. The insect Galleria mellonella larva is a widely used alternative model organism for bacterial pathogens. We have performed genome-scale fitness profiling of a multidrug-resistant K. pneumoniae ST258 strain during infection of G. mellonella, to determine if this model is suitable for large-scale virulence factor discovery in this pathogen. Our results demonstrated a dominant role for surface polysaccharides in infection, with contributions from siderophores, cell envelope proteins, purine biosynthesis genes and additional genes of unknown function. Comparison with a hypervirulent strain, ATCC 43816, revealed substantial overlap in important infection-related genes, as well as additional putative virulence factors specific to ST258, reflecting strain-dependent fitness effects. Our analysis also identified a role for the metalloregulatory protein NfeR (YqjI) in virulence. Overall, this study offers new insight into the infection fitness landscape of K. pneumoniae, and provides a framework for using the highly flexible and easily scalable G. mellonella infection model to dissect molecular virulence mechanisms of bacterial pathogens.

摘要

肺炎克雷伯菌引起的感染是一个主要的公共卫生威胁。已经报道了广泛耐药甚至泛耐药菌株。由于感染的大多数非高毒力菌株的鼠模型提供的分辨率有限,因此了解肺炎克雷伯菌的发病机制受到阻碍。昆虫家蚕幼虫是一种广泛用于细菌病原体的替代模式生物。我们在感染家蚕幼虫时对一株多药耐药肺炎克雷伯菌 ST258 株进行了全基因组适应性分析,以确定该模型是否适合在此病原体中进行大规模毒力因子发现。我们的结果表明,表面多糖在感染中起主导作用,铁载体、细胞包膜蛋白、嘌呤生物合成基因和其他未知功能的基因也有贡献。与高毒力菌株 ATCC 43816 的比较显示,重要的感染相关基因有很大的重叠,以及 ST258 特有的其他潜在毒力因子,反映了菌株依赖性的适应性效应。我们的分析还确定了金属调节蛋白 NfeR(YqjI)在毒力中的作用。总的来说,这项研究提供了对肺炎克雷伯菌感染适应性景观的新见解,并为利用高度灵活和易于扩展的家蚕幼虫感染模型来剖析细菌病原体的分子毒力机制提供了框架。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd36/7981267/55fcb20813d1/ftab009fig1.jpg

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