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Spatial metagenomic characterization of microbial biogeography in the gut.


ABSTRACT: Spatial structuring is important for the maintenance of natural ecological systems1,2. Many microbial communities, including the gut microbiome, display intricate spatial organization3-9. Mapping the biogeography of bacteria can shed light on interactions that underlie community functions10-12, but existing methods cannot accommodate the hundreds of species that are found in natural microbiomes13-17. Here we describe metagenomic plot sampling by sequencing (MaPS-seq), a culture-independent method to characterize the spatial organization of a microbiome at micrometer-scale resolution. Intact microbiome samples are immobilized in a gel matrix and cryofractured into particles. Neighboring microbial taxa in the particles are then identified by droplet-based encapsulation, barcoded 16S rRNA amplification and deep sequencing. Analysis of three regions of the mouse intestine revealed heterogeneous microbial distributions with positive and negative co-associations between specific taxa. We identified robust associations between Bacteroidales taxa in all gut compartments and showed that phylogenetically clustered local regions of bacteria were associated with a dietary perturbation. Spatial metagenomics could be used to study microbial biogeography in complex habitats.

SUBMITTER: Sheth RU 

PROVIDER: S-EPMC6679743 | biostudies-literature | 2019 Aug

REPOSITORIES: biostudies-literature

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Spatial metagenomic characterization of microbial biogeography in the gut.

Sheth Ravi U RU   Li Mingqiang M   Jiang Weiqian W   Sims Peter A PA   Leong Kam W KW   Wang Harris H HH  

Nature biotechnology 20190722 8


Spatial structuring is important for the maintenance of natural ecological systems<sup>1,2</sup>. Many microbial communities, including the gut microbiome, display intricate spatial organization<sup>3-9</sup>. Mapping the biogeography of bacteria can shed light on interactions that underlie community functions<sup>10-12</sup>, but existing methods cannot accommodate the hundreds of species that are found in natural microbiomes<sup>13-17</sup>. Here we describe metagenomic plot sampling by sequen  ...[more]

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