基于图谱的变异发现揭示了人类微生物组的新动态

Harihara Subrahmaniam Muralidharan, Jacquelyn S Michaelis, Jay Ghurye, Todd Treangen, Sergey Koren, Marcus Fedarko, Mihai Pop
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摘要

然而,表征微生物群落内菌株级变异的工具范围有限,只关注单核苷酸多态性,或者依赖于基于参考文献的分析,从而错过了复杂的功能和结构变异。在这里,我们展示了装配图分析在人类微生物组计划中生成的近 1000 个基因组中检测和描述结构变异的能力。我们发现了九百多万个变异,包括插入/删除事件、重复拷贝数变化和移动元素(如质粒)。我们强调了这些基因组变化的一些潜在功能作用。我们的分析揭示了不同体位变异率的显著差异,突出了细菌适应的特定机制。我们检测到的结构变异还包括潜在的新型噬菌体整合事件,这凸显了基于图的分析在发现噬菌体方面的潜在用途。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Graph-based variant discovery reveals novel dynamics in the human microbiome
Sequence differences between the strains of bacteria comprising host-associated and environmental microbiota may play a role in community assembly and influence the resilience of microbial communities to disturbances. Tools for characterizing strain-level variation within microbial communities, however, are limited in scope, focusing on just single nucleotide polymorphisms, or relying on reference-based analyses that miss complex functional and structural variants. Here, we demonstrate the power of assembly graph analysis to detect and characterize structural variants in almost 1,000 metagenomes generated as part of the Human Microbiome Project. We identify over nine million variants comprising insertion/deletion events, repeat copy-number changes, and mobile elements such as plasmids. We highlight some of the potential functional roles of these genomic changes. Our analysis revealed striking differences in the rate of variation across body sites, highlighting niche-specific mechanisms of bacterial adaptation. The structural variants we detect also include potentially novel prophage integration events, highlighting the potential use of graph-based analyses for phage discovery.
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