A Crypt-Specific Core Microbiota Resides in the Mouse Colon

Author:

Pédron Thierry12,Mulet Céline12,Dauga Catherine3,Frangeul Lionel3,Chervaux Christian4,Grompone Gianfranco45,Sansonetti Philippe J.126

Affiliation:

1. Unité de Pathogénie Microbienne Moléculaire, Institut Pasteur, Paris, France

2. INSERM U 786, Institut Pasteur, Paris, France

3. Groupe Bioinformatique pour l’Analyse Génomique, Institut Pasteur, Paris, France

4. Danone Research, Centre de Recherche Daniel Carasso, Palaiseau, France

5. Institut Pasteur de Montevideo, Montevideo, Uruguay

6. Chaire de Microbiologie et Maladies Infectieuses, Collège de France, Paris, France

Abstract

ABSTRACT In an attempt to explore the microbial content of functionally critical niches of the mouse gastrointestinal tract, we targeted molecular microbial diagnostics of the crypts that contain the intestinal stem cells, which account for epithelial regeneration. As current evidence indicates, the gut microbiota affects epithelial regeneration; bacteria that are likely to primarily participate in this essential step of the gut, microbiota cross talk, have been identified. We show in this article that only the cecal and colonic crypts harbor resident microbiota in the mouse and that regardless of the line and breeding origin of these mice, this bacterial population is unexpectedly dominated by aerobic genera. Interestingly, this microbiota resembles the restricted microbiota found in the midgut of invertebrates; thus, the presence of our so-called “crypt-specific core microbiota” (CSCM) in the mouse colon potentially reflects a coevolutionary process under selective conditions that can now be addressed. We suggest that CSCM could play both a protective and a homeostatic role within the colon. This article is setting the bases for such studies, particularly by providing a bona fide —and essentially cultivable—crypt microbiota of reference. IMPORTANCE Metagenomic typing of the whole-gut luminal microbiome was recently provided, revealing great opportunities for physiological and physiopathological analysis of the host-microbiota interface. On this basis, it appears increasingly important to analyze which niches of the gut exposed to a particular microbiota are of major functional importance, specifically focusing on the crypt, which accounts for permanent epithelial renewal, and to analyze how this microbiota compares to its luminal counterpart in composition and quantity. Crypt-specific core microbiotas may show themselves as important elements regarding crypt protection and homeostasis of its functions.

Publisher

American Society for Microbiology

Subject

Virology,Microbiology

Cited by 172 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. The microbiome compositional and functional differences between rectal mucosa and feces;Microbiology Spectrum;2024-08-06

2. The Impact of Gestational Diabetes Mellitus (GDM) on the Development and Composition of the Neonatal Gut Microbiota: A Systematic Review;Microorganisms;2024-07-31

3. The role of animal hosts in shaping gut microbiome variation;Philosophical Transactions of the Royal Society B: Biological Sciences;2024-03-18

4. The importance of host physical niches for the stability of gut microbiome composition;Philosophical Transactions of the Royal Society B: Biological Sciences;2024-03-18

5. Microbiomes of bats;A Natural History of Bat Foraging;2024

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3