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细菌的离散作用作为一种肠道细菌的相互作用机制。

Disaggregation as an interaction mechanism among intestinal bacteria.

机构信息

Department of Physics and Materials Science Institute, University of Oregon, Eugene, Oregon.

Institute of Molecular Biology, University of Oregon, Eugene, Oregon.

出版信息

Biophys J. 2022 Sep 20;121(18):3458-3473. doi: 10.1016/j.bpj.2022.08.010. Epub 2022 Aug 18.

Abstract

The gut microbiome contains hundreds of interacting species that together influence host health and development. The mechanisms by which intestinal microbes can interact, however, remain poorly mapped and are often modeled as spatially unstructured competitions for chemical resources. Recent imaging studies examining the zebrafish gut have shown that patterns of aggregation are central to bacterial population dynamics. In this study, we focus on bacterial species of genera Aeromonas and Enterobacter. Two zebrafish gut-derived isolates, Aeromonas ZOR0001 (AE) and Enterobacter ZOR0014 (EN), when mono-associated with the host, are highly aggregated and located primarily in the intestinal midgut. An Aeromonas isolate derived from the commensal strain, Aeromonas-MB4 (AE-MB4), differs from the parental strain in that it is composed mostly of planktonic cells localized to the anterior gut. When challenged by AE-MB4, clusters of EN rapidly fragment into non-motile, slow-growing, dispersed individual cells with overall abundance two orders of magnitude lower than the mono-association value. In the presence of a certain set of additional gut bacterial species, these effects on EN are dampened. In particular, if AE-MB4 invades an already established multi-species community, EN persists in the form of large aggregates. These observations reveal an unanticipated competition mechanism based on manipulation of bacterial spatial organization, namely dissolution of aggregates, and provide evidence that multi-species communities may facilitate stable intestinal co-existence.

摘要

肠道微生物组包含数百种相互作用的物种,这些物种共同影响宿主的健康和发育。然而,肠道微生物相互作用的机制仍未得到很好的描绘,并且通常被建模为对化学资源的无空间结构竞争。最近研究斑马鱼肠道的成像研究表明,聚集模式是细菌种群动态的核心。在这项研究中,我们专注于气单胞菌属和肠杆菌属的细菌物种。两种从斑马鱼肠道中分离出来的细菌,气单胞菌 ZOR0001(AE)和肠杆菌 ZOR0014(EN),当与宿主单关联时,高度聚集并主要位于肠道中肠。从共生菌株气单胞菌-MB4(AE-MB4)中分离出来的气单胞菌菌株与亲本菌株不同,因为它主要由定殖在前肠的浮游细胞组成。当受到 AE-MB4 的挑战时,EN 的集群迅速分裂成非运动的、生长缓慢的、分散的单个细胞,其总丰度比单关联值低两个数量级。在存在一组额外的肠道细菌物种的情况下,这些对 EN 的影响会减弱。特别是,如果 AE-MB4 入侵已经建立的多物种群落,EN 则以大聚集的形式存在。这些观察结果揭示了一种基于操纵细菌空间组织的意想不到的竞争机制,即聚集物的溶解,并提供了多物种群落可能促进稳定肠道共存的证据。

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