Suppr超能文献

菱形蛋白酶GlpG促进肠道外致病性大肠杆菌在肠道内的持续存在。

The Rhomboid Protease GlpG Promotes the Persistence of Extraintestinal Pathogenic Escherichia coli within the Gut.

作者信息

Russell Colin W, Richards Amanda C, Chang Alexander S, Mulvey Matthew A

机构信息

Division of Microbiology and Immunology, Department of Pathology, University of Utah, Salt Lake City, Utah, USA.

Division of Microbiology and Immunology, Department of Pathology, University of Utah, Salt Lake City, Utah, USA

出版信息

Infect Immun. 2017 May 23;85(6). doi: 10.1128/IAI.00866-16. Print 2017 Jun.

Abstract

Extraintestinal pathogenic (ExPEC) strains are typically benign within the mammalian gut but can disperse to extraintestinal sites to cause diseases like urinary tract infections and sepsis. As occupation of the intestinal tract is often a prerequisite for ExPEC-mediated pathogenesis, we set out to understand how ExPEC colonizes this niche. A screen using transposon sequencing (Tn-seq) was performed to search for genes within ExPEC isolate F11 that are important for growth in intestinal mucus, which is thought to be a major source of nutrients for in the gut. Multiple genes that contribute to ExPEC fitness in mucus broth were identified, with genes that are directly or indirectly associated with fatty acid beta-oxidation pathways being especially important. One of the identified mucus-specific fitness genes encodes the rhomboid protease GlpG. , we found that the disruption of had polar effects on the downstream gene , which encodes a transcriptional repressor of factors that catalyze glycerol degradation. Mutation of either or impaired ExPEC growth in mucus and on plates containing the long-chain fatty acid oleate as the sole carbon source. In contrast, in a mouse gut colonization model in which the natural microbiota is unperturbed, the disruption of but not significantly reduced ExPEC survival. This work reveals a novel biological role for a rhomboid protease and highlights new avenues for defining mechanisms by which ExPEC strains colonize the mammalian gastrointestinal tract.

摘要

肠外致病性(ExPEC)菌株通常在哺乳动物肠道内无害,但可扩散至肠外部位引发诸如尿路感染和败血症等疾病。由于占据肠道往往是ExPEC介导发病机制的先决条件,我们着手了解ExPEC如何定殖于这一生态位。利用转座子测序(Tn-seq)进行筛选,以寻找ExPEC分离株F11中对在肠黏液中生长至关重要的基因,肠黏液被认为是肠道中主要的营养来源。鉴定出多个对ExPEC在黏液肉汤中适应性有贡献的基因,其中与脂肪酸β-氧化途径直接或间接相关的基因尤为重要。鉴定出的一个黏液特异性适应性基因编码菱形蛋白酶GlpG。我们发现,GlpG的破坏对下游基因glpR产生极性影响,glpR编码催化甘油降解因子的转录阻遏物。GlpG或glpR的突变损害了ExPEC在黏液中和以长链脂肪酸油酸作为唯一碳源的平板上的生长。相比之下,在天然微生物群未受干扰的小鼠肠道定殖模型中,GlpG而非glpR的破坏显著降低了ExPEC的存活率。这项工作揭示了菱形蛋白酶的一种新的生物学作用,并突出了确定ExPEC菌株定殖于哺乳动物胃肠道机制的新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd0b/5442614/afe39f88c438/zii9990920560001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验