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人类肠道中拟杆菌目物种的流行、维持和 IgA 反应的纵向分析。

Longitudinal analysis of the prevalence, maintenance, and IgA response to species of the order Bacteroidales in the human gut.

机构信息

Department of Gastroenterology, Children's Hospital, Boston, Massachusetts 02115, USA.

出版信息

Infect Immun. 2011 May;79(5):2012-20. doi: 10.1128/IAI.01348-10. Epub 2011 Mar 14.

Abstract

Bacteroidales species are the most abundant Gram-negative bacteria of the human intestinal microbiota. These bacteria evolved to synthesize numerous capsular polysaccharides (PS) that are subject to phase variation. In Bacteroides fragilis, PS synthesis is regulated so that only one of the eight PS biosynthesis loci is transcribed at a time in each bacterium. To determine if the bacteria evolved this unusual property to evade a host IgA response, we directly studied the human fecal ecosystem. We performed a longitudinal analysis of the abundant Bacteroidales species from 15 healthy adults at four intervals over a year. For this study, we used bacterial culture to perform analyses not accurate with DNA-based methods, including quantification of total viable Bacteroidales bacteria, strain maintenance, and IgA responses. Abundant Bacteroidales isolates were identified to the species level using multiplex PCR and 16S rRNA gene sequencing. Arbitrarily primed PCR was used for strain typing. IgA responses to endogenous strains carried over the year were analyzed, and the orientations of the invertible PS locus promoters from the ecosystem were quantified. Subjects consistently harbored from 5 × 10(8) to 8 × 10(10) Bacteroidales bacteria/g of feces. Within the cohort, 20 different Bacteroidales species were detected at high concentrations. Bacteroides uniformis was the most prevalent; however, abundant Bacteroidales species varied between subjects. Strains could be maintained over the year within the ecosystem at high density. IgA responses were often not induced and did not correlate with the elimination of a strain or major changes in the orientations of the capsular PS locus promoters.

摘要

拟杆菌门物种是人类肠道微生物群中最丰富的革兰氏阴性细菌。这些细菌进化出了合成大量荚膜多糖 (PS) 的能力,这些多糖会发生相变异。在脆弱拟杆菌中,PS 的合成受到调控,使得每个细菌一次只能转录八个 PS 生物合成基因座中的一个。为了确定这些细菌是否为了逃避宿主 IgA 反应而进化出这种不寻常的特性,我们直接研究了人类粪便生态系统。我们对 15 名健康成年人的丰富拟杆菌门物种进行了为期一年四个时间点的纵向分析。在这项研究中,我们使用细菌培养来进行分析,这些分析与基于 DNA 的方法不同,包括定量总可培养拟杆菌门细菌、菌株维持和 IgA 反应。使用多重 PCR 和 16S rRNA 基因测序对丰富的拟杆菌属分离株进行种水平鉴定。使用任意引物 PCR 进行菌株分型。分析了全年携带的内源性菌株的 IgA 反应,并对来自生态系统的可反转 PS 基因座启动子的取向进行了定量。受检者粪便中始终含有 5×10(8)到 8×10(10)个拟杆菌门细菌/g。在队列中,检测到 20 种高浓度的拟杆菌门物种。均匀拟杆菌最为普遍;然而,丰富的拟杆菌门物种在受检者之间存在差异。在生态系统中,菌株可以在一年内保持高密度。IgA 反应通常不会被诱导,并且与菌株的消除或荚膜 PS 基因座启动子取向的重大变化无关。

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