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From the CoverPNAS Plus: Spatial organization of a model 15-member human gut microbiota established in gnotobiotic mice

机译:来自CoverPNAS Plus:在gnotobiotic小鼠中建立的15人模型肠道菌群的空间组织

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摘要

Knowledge of the spatial organization of the gut microbiota is important for understanding the physical and molecular interactions among its members. These interactions are thought to influence microbial succession, community stability, syntrophic relationships, and resiliency in the face of perturbations. The complexity and dynamism of the gut microbiota pose considerable challenges for quantitative analysis of its spatial organization. Here, we illustrate an approach for addressing this challenge, using (i) a model, defined 15-member consortium of phylogenetically diverse, sequenced human gut bacterial strains introduced into adult gnotobiotic mice fed a polysaccharide-rich diet, and (ii) in situ hybridization and spectral imaging analysis methods that allow simultaneous detection of multiple bacterial strains at multiple spatial scales. Differences in the binding affinities of strains for substrates such as mucus or food particles, combined with more rapid replication in a preferred microhabitat, could, in principle, lead to localized clonally expanded aggregates composed of one or a few taxa. However, our results reveal a colonic community that is mixed at micrometer scales, with distinct spatial distributions of some taxa relative to one another, notably at the border between the mucosa and the lumen. Our data suggest that lumen and mucosa in the proximal colon should be conceptualized not as stratified compartments but as components of an incompletely mixed bioreactor. Employing the experimental approaches described should allow direct tests of whether and how specified host and microbial factors influence the nature and functional contributions of “microscale” mixing to the dynamic operations of the microbiota in health and disease.
机译:肠道菌群的空间组织知识对于理解其成员之间的物理和分子相互作用非常重要。这些相互作用被认为会影响微生物的演替,群落的稳定性,营养关系以及在面对干扰时的适应力。肠道菌群的复杂性和动态性对其空间组织的定量分析提出了相当大的挑战。在这里,我们举例说明了一种解决此挑战的方法,该方法是使用(i)建立模型的15个成员组成的系统发育多样性,序列化的人类肠道细菌菌株,该物种引入到富含多糖饮食的成年gnotobiotic小鼠体内,以及(ii)原位杂交和光谱成像分析方法,可以在多个空间尺度上同时检测多种细菌菌株。菌株对底物(如粘液或食物颗粒)的结合亲和力的差异,再加上在优选的微生境中更快的复制,原则上可以导致局部克隆扩展的聚集体,该聚集体由一种或几种分类群组成。但是,我们的结果显示了一个以微米尺度混合的结肠群落,其中某些分类单元相对于彼此具有明显的空间分布,特别是在粘膜和内腔之间的边界。我们的数据表明,近端结肠的内腔和粘膜不应概念化为分层隔室,而应作为不完全混合的生物反应器的组成部分。采用所述的实验方法应该可以直接测试特定的宿主和微生物因素是否以及如何影响“微量”混合对微生物在健康和疾病中的动态运行的性质和功能的贡献。

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