Department of Biotechnology and Food Engineering, Technion-Israel Institute of Technology, Haifa, Israel.
Department of Statistics, The University of Connecticut (UConn), Storrs, Connecticut, USA.
Appl Environ Microbiol. 2019 Aug 29;85(18). doi: 10.1128/AEM.00826-19. Print 2019 Sep 15.
The gut microbiota is a complex ecosystem, affected by both environmental factors and host genetics. Here, we aim at uncovering the bacterial taxa whose gut persistence is controlled by host genetic variation. We used a murine model based on inbred lines BALB/c and C57BL/6J and their F reciprocal hybrids (♀C57BL/6J × ♂BALB/c; ♀BALB/c × ♂C57BL/6J). To guarantee genetic similarity of F offspring, including the sex chromosomes, we used only female mice. Based on 16S rRNA gene sequencing, we found that the genetically different inbred lines present different microbiota, whereas their genetically identical F reciprocal hybrids presented similar microbiota. Moreover, the F microbial composition differed from that of both parental lines. Twelve taxa were shown to have genetically controlled gut persistence, while none were found to show maternal effects. Nine of these taxa were dominantly inherited by the C57BL/6J line. Cohousing of the parental inbred lines resulted in a temporary and minor shift in microbiota composition, which returned back to the former microbial composition following separation, indicating that each line tends to maintain a unique bacterial signature reflecting the line. Taken together, our findings indicate that mouse genetics has an effect on the microbial composition in the gut, which is greater than maternal effect and continuous exposure to different microbiota of the alternative line. Uncovering the bacterial taxa associated with host genetics and understanding their role in the gut ecosystem could lead to the development of genetically oriented probiotic products, as part of the personalized medicine approach. The gut microbiota play important roles for their host. The link between host genetics and their microbial composition has received increasing interest. Using a unique reciprocal cross model, generating genetically similar F hybrids with different maternal inoculation, we demonstrate the inheritance of gut persistence of 12 bacterial taxa. No taxa identified as maternally transmitted. Moreover, cohabitation of two genetically different inbred lines did not dramatically affect the microbiota composition. Taken together, our results demonstrate the importance of the genetic effect over maternal inoculation or effect of exposure to unlike exogenous microbiota. These findings may lead to the development of personalized probiotic products, specifically designed according to the genetic makeup.
肠道微生物群是一个复杂的生态系统,受到环境因素和宿主遗传的影响。在这里,我们旨在揭示肠道持久性受宿主遗传变异控制的细菌分类群。我们使用基于近交系 BALB/c 和 C57BL/6J 及其 F 回交杂种(♀C57BL/6J ×♂BALB/c;♀BALB/c ×♂C57BL/6J)的鼠模型。为了保证 F 代后代(包括性染色体)的遗传相似性,我们只使用雌性小鼠。基于 16S rRNA 基因测序,我们发现遗传不同的近交系具有不同的微生物群,而遗传相同的 F 回交杂种具有相似的微生物群。此外,F 微生物组成与两种亲本系不同。有 12 个分类群被证明具有遗传控制的肠道持久性,而没有一个被发现具有母体效应。其中 9 个分类群主要由 C57BL/6J 系遗传。将亲本近交系共饲养会导致微生物群组成的暂时和轻微变化,分离后会恢复到以前的微生物组成,表明每条线都倾向于维持反映该线的独特细菌特征。总之,我们的研究结果表明,小鼠遗传学对肠道微生物组成有影响,这种影响大于母体效应和持续接触替代线的不同微生物群。揭示与宿主遗传相关的细菌分类群及其在肠道生态系统中的作用,可能导致开发基于遗传的益生菌产品,作为个性化医学方法的一部分。肠道微生物对其宿主具有重要作用。宿主遗传学与其微生物组成之间的联系引起了越来越多的关注。使用独特的回交模型,生成具有不同母体接种的遗传相似的 F 杂种,我们证明了 12 个细菌分类群的肠道持久性遗传。没有鉴定出与母体传播相关的分类群。此外,两种遗传不同的近交系的共饲养并没有显著影响微生物群组成。总之,我们的研究结果表明,遗传效应比母体接种或暴露于不同外源微生物群的影响更为重要。这些发现可能导致开发个性化益生菌产品,根据遗传构成专门设计。