Nature MicrobiologySystems BiologyPeer-reviewed journal article
SAMPL-seq reveals micron-scale spatial hubs in the human gut microbiome
Miles RichardsoniD, Shijie ZhaoiD, Liyuan LiniD, Ravi U. ShethiD, Yiming QuiD, Jeongchan Lee, Thomas U. Moody, Deirdre RicaurteiD, Yiming HuangiD, Florencia Velez‐CortesiD, Guillaume UrtechoiD, Harris H. WangiD
Abstract
The local arrangement of microbes can profoundly impact community assembly, function, and stability. To date, little is known about the spatial organization of the human gut microbiome. Here, we describe a high-throughput and streamlined method, dubbed SAMPL-seq, that samples microbial composition of micron-scale sub-communities with split-and-pool barcoding to capture spatial colocalization in a complex consortium. SAMPL-seq analysis of the gut microbiome of healthy humans identified bacterial taxa pairs that consistently co-occurred both over time and across multiple individuals. These colocalized microbes organize into spatially distinct groups or "spatial hubs" dominated by Bacteroideceae, Ruminococceae, and Lachnospiraceae families. From a dietary perturbation using inulin, we observed reversible spatial rearrangement of the gut microbiome, where specific taxa form new local partnerships. Spatial metagenomics using SAMPL-seq can unlock new insights to improve the study of microbial communities. One Sentence SummaryHigh throughput micron-scale subcommunity sampling and sequencing identifies distinct spatial associations of gut bacteria within and across individuals.
- organism: human
- assay: metagenomics
- research focus: spatial domain detection
- approach: experimental assay
- Citations
- 24
- FWCI
- 7.17
- Field percentile
- top 2%
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