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开发一种新型的人类肠道模型,以阐明厌氧共生菌对大肠杆菌感染的影响。

Development of a novel human intestinal model to elucidate the effect of anaerobic commensals on Escherichia coli infection.

机构信息

Department of Clinical Medicine, Norwich Medical School, University of East Anglia, Norwich NR4 7UQ, UK.

Gut Microbes and Health Programme, Quadram Institute Bioscience, Gut Microbes and Health Institute Strategic Programme, Norwich NR4 7UQ, UK.

出版信息

Dis Model Mech. 2022 Apr 1;15(4). doi: 10.1242/dmm.049365. Epub 2022 Apr 28.

Abstract

The gut microbiota plays a crucial role in protecting against enteric infection. However, the underlying mechanisms are largely unknown owing to a lack of suitable experimental models. Although most gut commensals are anaerobic, intestinal epithelial cells require oxygen for survival. In addition, most intestinal cell lines do not produce mucus, which provides a habitat for the microbiota. Here, we have developed a microaerobic, mucus-producing vertical diffusion chamber (VDC) model and determined the influence of Limosilactobacillus reuteri and Ruminococcus gnavus on enteropathogenic Escherichia coli (EPEC) infection. Optimization of the culture medium enabled bacterial growth in the presence of mucus-producing T84/LS174T cells. Whereas L. reuteri diminished EPEC growth and adhesion to T84/LS174T and mucus-deficient T84 epithelia, R. gnavus only demonstrated a protective effect in the presence of LS174T cells. Reduced EPEC adherence was not associated with altered type III secretion pore formation. In addition, co-culture with L. reuteri and R. gnavus dampened EPEC-induced interleukin 8 secretion. The microaerobic mucin-producing VDC system will facilitate investigations into the mechanisms underpinning colonization resistance and aid the development of microbiota-based anti-infection strategies. This article has an associated First Person interview with the first author of the paper.

摘要

肠道微生物群在防止肠道感染方面起着至关重要的作用。然而,由于缺乏合适的实验模型,其潜在机制在很大程度上尚不清楚。尽管大多数肠道共生菌是厌氧的,但肠道上皮细胞的生存需要氧气。此外,大多数肠细胞系不产生黏液,而黏液为微生物群提供了栖息地。在这里,我们开发了一种微需氧、产黏液的垂直扩散室(VDC)模型,并确定了罗伊氏乳杆菌和加氏瘤胃球菌对肠致病性大肠杆菌(EPEC)感染的影响。培养基的优化使在产黏液的 T84/LS174T 细胞存在的情况下能够进行细菌生长。虽然罗伊氏乳杆菌减少了 EPEC 的生长和对 T84/LS174T 和缺乏黏液的 T84 上皮细胞的黏附,但加氏瘤胃球菌仅在 LS174T 细胞存在的情况下表现出保护作用。EPEC 黏附的减少与 III 型分泌孔形成的改变无关。此外,与罗伊氏乳杆菌和加氏瘤胃球菌共培养可抑制 EPEC 诱导的白细胞介素 8 分泌。这种微需氧产黏液的 VDC 系统将有助于研究定植抗性的机制,并有助于开发基于微生物组的抗感染策略。本文有该论文第一作者的相关第一人称采访。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40b2/9066490/b202c21d93e2/dmm-15-049365-g1.jpg

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