Department of Molecular and Cellular Medicine, Texas A&M Health Science Center, College Station, TX, 77843, USA.
Department of Nutrition, Texas A&M University, College Station, TX, 77843, USA.
Microbiome. 2023 Oct 3;11(1):220. doi: 10.1186/s40168-023-01588-w.
The gut microbiota is modulated by a combination of diet, host genetics, and sex effects. The magnitude of these effects and interactions among them is important to understanding inter-individual variability in gut microbiota. In a previous study, mouse strain-specific responses to American and ketogenic diets were observed along with several QTLs for metabolic traits. In the current study, we searched for genetic variants underlying differences in the gut microbiota in response to American and ketogenic diets, which are high in fat and vary in carbohydrate composition, between C57BL/6 J (B6) and FVB/NJ (FVB) mouse strains.
Genetic mapping of microbial features revealed 18 loci under the QTL model (i.e., marginal effects that are not specific to diet or sex), 12 loci under the QTL by diet model, and 1 locus under the QTL by sex model. Multiple metabolic and microbial features map to the distal part of Chr 1 and Chr 16 along with eigenvectors extracted from principal coordinate analysis of measures of β-diversity. Bilophila, Ruminiclostridium 9, and Rikenella (Chr 1) were identified as sex- and diet-independent QTL candidate keystone organisms, and Parabacteroides (Chr 16) was identified as a diet-specific, candidate keystone organism in confirmatory factor analyses of traits mapping to these regions. For many microbial features, irrespective of which QTL model was used, diet or the interaction between diet and a genotype were the strongest predictors of the abundance of each microbial trait. Sex, while important to the analyses, was not as strong of a predictor for microbial abundances.
These results demonstrate that sex, diet, and genetic background have different magnitudes of effects on inter-individual differences in gut microbiota. Therefore, Precision Nutrition through the integration of genetic variation, microbiota, and sex affecting microbiota variation will be important to predict response to diets varying in carbohydrate composition. Video Abstract.
肠道微生物群受饮食、宿主遗传和性别效应的共同调节。了解这些因素的作用大小及其相互作用对于理解肠道微生物群个体间的差异非常重要。在之前的研究中,观察到了不同小鼠品系对美式和生酮饮食的特异性反应,以及几个与代谢特征相关的 QTL。在本研究中,我们在 C57BL/6J(B6)和 FVB/NJ(FVB)两种小鼠品系之间,搜索了对高脂肪、碳水化合物组成不同的美式和生酮饮食的肠道微生物群反应存在差异的遗传变异。
微生物特征的遗传图谱显示了 18 个 QTL 模型下的基因座(即不是特定于饮食或性别的边缘效应)、12 个饮食模型下的 QTL 基因座和 1 个性别模型下的 QTL 基因座。多个代谢和微生物特征映射到 Chr 1 和 Chr 16 的远端,以及主坐标分析中提取的测量β多样性的特征向量。Bilophila、Ruminiclostridium 9 和 Rikenella(Chr 1)被确定为性别和饮食独立的 QTL 候选关键生物,而 Parabacteroides(Chr 16)则被确定为在映射到这些区域的特征的验证性因子分析中,饮食特异性的候选关键生物。对于许多微生物特征,无论使用哪个 QTL 模型,饮食或饮食与基因型的相互作用都是预测每个微生物特征丰度的最强因素。尽管性别对分析很重要,但它不是微生物丰度的主要预测因素。
这些结果表明,性别、饮食和遗传背景对肠道微生物群个体间差异的影响程度不同。因此,通过整合影响肠道微生物群变化的遗传变异、微生物群和性别来实现精准营养,对于预测对碳水化合物组成不同的饮食的反应将非常重要。