SAMPL-seq reveals micron-scale spatial hubs in the human gut microbiome

作者：Miles Richardson, Shijie Zhao, Ravi U. Sheth, Liyuan Lin, Yiming Qu, Jeungchan Lee, Thomas Moody, Deirdre Ricaurte, Yiming Huang, Florencia Velez‐Cortes, Guillaume Urtecho, Harris H. Wang · 发表于：bioRxiv (Cold Spring Harbor Laboratory) · 年份：2024 · DOI：10.1101/2024.10.08.617108 · 被引用次数：4 · 研究领域：Gut microbiota and health、Clostridium difficile and Clostridium perfringens research、Probiotics and Fermented Foods

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 Summary High throughput micron-scale subcommunity sampling and sequencing identifies distinct spatial associations of gut bacteria within and across individuals.