Zhou Shaoming, Xu Ruihuan, He Fusheng, Zhou Jiaxiu, Wang Yan, Zhou Jianli, Wang Mingbang, Zhou Wenhao
Division of Gastroenterology, Shenzhen Children's Hospital, Shenzhen, Guangdong, China.
Clinical Laboratory, Longgang Central Hospital of Shenzhen, Guangdong, China.
PLoS One. 2016 Sep 1;11(9):e0161627. doi: 10.1371/journal.pone.0161627. eCollection 2016.
Early colonization of gut microbiota in human gut is a complex process. It remains unclear when gut microbiota colonization occurs and how it proceeds. In order to study gut microbiota composition in human early life, the present study recruited 10 healthy pairs of twins, including five monozygotic (MZ) and five dizygotic (DZ) twin pairs, whose age ranged from 0 to 6 years old. 20 fecal samples from these twins were processed by shotgun metagenomic sequencing, and their averaged data outputs were generated as 2G per sample. We used MEGAN5 to perform taxonomic and functional annotation of the metagenomic data, and systematically analyzed those 20 samples, including Jaccard index similarity, principle component, clustering, and correlation analyses. Our findings indicated that within our study group: 1) MZ-twins share more microbes than DZ twins or non-twin pairs, 2) gut microbiota distribution is relatively stable at metabolic pathways level, 3) age represents the strongest factor that can account for variation in gut microbiota, and 4) a clear metabolic pathway shift can be observed, which speculatively occurs around the age of 1 year old. This research will serve as a base for future studies of gut microbiota-related disease research.
人类肠道微生物群的早期定殖是一个复杂的过程。目前尚不清楚肠道微生物群何时开始定殖以及其如何发展。为了研究人类早期生命中的肠道微生物群组成,本研究招募了10对健康双胞胎,包括5对同卵双胞胎(MZ)和5对异卵双胞胎(DZ),年龄范围为0至6岁。对这些双胞胎的20份粪便样本进行了鸟枪法宏基因组测序,并将每个样本的平均数据产出设定为2G。我们使用MEGAN5对宏基因组数据进行分类和功能注释,并对这20个样本进行了系统分析,包括杰卡德指数相似度、主成分、聚类和相关性分析。我们的研究结果表明,在我们的研究组中:1)同卵双胞胎比异卵双胞胎或非双胞胎对共享更多的微生物;2)肠道微生物群在代谢途径水平上分布相对稳定;3)年龄是解释肠道微生物群变异的最强因素;4)可以观察到明显的代谢途径转变,推测这一转变大约发生在1岁左右。本研究将为未来肠道微生物群相关疾病研究奠定基础。