Gladstone Institutes, San Francisco, CA, USA.
Division of Biostatistics, Institute for Human Genetics, and Institute for Computational Health Sciences, University of California, San Francisco, CA, USA.
Microbiome. 2017 Mar 23;5(1):36. doi: 10.1186/s40168-017-0244-z.
While human gut microbiomes vary significantly in taxonomic composition, biological pathway abundance is surprisingly invariable across hosts. We hypothesized that healthy microbiomes appear functionally redundant due to factors that obscure differences in gene abundance between individuals.
To account for these biases, we developed a powerful test of gene variability called CCoDA, which is applicable to shotgun metagenomes from any environment and can integrate data from multiple studies. Our analysis of healthy human fecal metagenomes from three separate cohorts revealed thousands of genes whose abundance differs significantly and consistently between people, including glycolytic enzymes, lipopolysaccharide biosynthetic genes, and secretion systems. Even housekeeping pathways contain a mix of variable and invariable genes, though most highly conserved genes are significantly invariable. Variable genes tend to be associated with Proteobacteria, as opposed to taxa used to define enterotypes or the dominant phyla Bacteroidetes and Firmicutes.
These results establish limits on functional redundancy and predict specific genes and taxa that may explain physiological differences between gut microbiomes.
尽管人类肠道微生物组在分类组成上存在显著差异,但生物途径的丰度在宿主之间却惊人地不变。我们假设,由于个体间基因丰度差异的因素掩盖,健康的微生物组表现出功能上的冗余。
为了解释这些偏差,我们开发了一种强大的基因可变性测试方法,称为 CCoDA,它适用于来自任何环境的 shotgun 宏基因组,并且可以整合来自多个研究的数据。我们对来自三个独立队列的健康人类粪便宏基因组进行了分析,发现了数千个基因,这些基因在个体之间的丰度存在显著差异且一致,包括糖酵解酶、脂多糖生物合成基因和分泌系统。即使是维持生命所必需的途径也包含了可变和不变的基因的混合,尽管大多数高度保守的基因是不变的。可变基因往往与变形菌门相关,而不是用于定义肠型或优势菌门拟杆菌门和厚壁菌门的分类群。
这些结果确定了功能冗余的限制,并预测了可能解释肠道微生物组之间生理差异的特定基因和分类群。