BGI-Shenzhen, Shenzhen 518083, China.
Nature. 2010 Mar 4;464(7285):59-65. doi: 10.1038/nature08821.
To understand the impact of gut microbes on human health and well-being it is crucial to assess their genetic potential. Here we describe the Illumina-based metagenomic sequencing, assembly and characterization of 3.3 million non-redundant microbial genes, derived from 576.7 gigabases of sequence, from faecal samples of 124 European individuals. The gene set, approximately 150 times larger than the human gene complement, contains an overwhelming majority of the prevalent (more frequent) microbial genes of the cohort and probably includes a large proportion of the prevalent human intestinal microbial genes. The genes are largely shared among individuals of the cohort. Over 99% of the genes are bacterial, indicating that the entire cohort harbours between 1,000 and 1,150 prevalent bacterial species and each individual at least 160 such species, which are also largely shared. We define and describe the minimal gut metagenome and the minimal gut bacterial genome in terms of functions present in all individuals and most bacteria, respectively.
为了了解肠道微生物对人类健康和福祉的影响,评估其遗传潜力至关重要。在这里,我们描述了基于 Illumina 的宏基因组测序、组装和特征分析,共涉及来自 124 位欧洲个体的粪便样本的 576700000 个非冗余微生物基因,这些基因的序列总长为 576700000 个碱基对。该基因集的大小大约是人类基因总数的 150 倍,其中包含了队列中绝大多数流行(更常见)的微生物基因,可能还包含了很大一部分常见的人类肠道微生物基因。这些基因在队列中的个体中大量共享。超过 99%的基因是细菌,这表明整个队列中存在 1000 到 1150 种流行的细菌物种,每个个体至少存在 160 种这样的物种,而且这些物种也在很大程度上是共享的。我们分别根据存在于所有个体和大多数细菌中的功能,定义并描述了最小肠道宏基因组和最小肠道细菌基因组。
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