Olsson Lisa M, Boulund Fredrik, Nilsson Staffan, Khan Muhammad Tanweer, Gummesson Anders, Fagerberg Linn, Engstrand Lars, Perkins Rosie, Uhlén Mathias, Bergström Göran, Tremaroli Valentina, Bäckhed Fredrik
The Wallenberg Laboratory, Department of Molecular and Clinical Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Department of Microbiology, Tumour and Cell Biology, Karolinska Institutet, Stockholm, Sweden.
Cell Host Microbe. 2022 May 11;30(5):726-739.e3. doi: 10.1016/j.chom.2022.03.002. Epub 2022 Mar 28.
Temporal dynamics of the gut microbiota potentially limit the identification of microbial features associated with health status. Here, we used whole-genome metagenomic and 16S rRNA gene sequencing to characterize the intra- and inter-individual variations of gut microbiota composition and functional potential of a disease-free Swedish population (n = 75) over one year. We found that 23% of the total compositional variance was explained by intra-individual variation. The degree of intra-individual compositional variability was negatively associated with the abundance of Faecalibacterium prausnitzii (a butyrate producer) and two Bifidobacterium species. By contrast, the abundance of facultative anaerobes and aerotolerant bacteria such as Escherichia coli and Lactobacillus acidophilus varied extensively, independent of compositional stability. The contribution of intra-individual variance to the total variance was greater for functional pathways than for microbial species. Thus, reliable quantification of microbial features requires repeated samples to address the issue of intra-individual variations of the gut microbiota.
肠道微生物群的时间动态可能会限制与健康状况相关的微生物特征的识别。在此,我们使用全基因组宏基因组测序和16S rRNA基因测序,对瑞典75名无疾病人群在一年时间内肠道微生物群组成和功能潜力的个体内和个体间差异进行了表征。我们发现,个体内差异解释了总组成差异的23%。个体内组成变异性的程度与普拉梭菌(一种丁酸盐产生菌)和两种双歧杆菌的丰度呈负相关。相比之下,兼性厌氧菌和气耐受性细菌(如大肠杆菌和嗜酸乳杆菌)的丰度变化很大,与组成稳定性无关。个体内差异对总差异的贡献在功能途径方面比对微生物物种更大。因此,可靠地量化微生物特征需要重复采样,以解决肠道微生物群个体内差异的问题。