Slezak Kathleen, Krupova Zuzana, Rabot Sylvie, Loh Gunnar, Levenez Florence, Descamps Amandine, Lepage Patricia, Doré Joël, Bellier Sylvain, Blaut Michael
Department of Gastrointestinal Microbiology; German Institute of Human Nutrition Potsdam-Rehbruecke; Nuthetal, Germany.
NRA; GABI UMR1313; Jouy-en-Josas, France.
Gut Microbes. 2014 Mar-Apr;5(2):176-82. doi: 10.4161/gmic.28203. Epub 2014 Feb 13.
Genetic, nutritional, and gut microbiota-derived factors have been proposed to play a role in the development of the whole intestine that is around 40% longer in PRM/Alf mice compared with other mouse strains. The PRM/Alf genotype explains 60% of this length difference. The remaining 40% are due to a maternal effect that could depend on the gut microbiota transmitted by the mother to their pups. Germ-free PRM/Alf mice and C3H/He mice were associated with a simplified human microbiota (SIHUMI) to study its impact on gut length. The small intestines of the SIHUMI-associated mice were 16.4% (PRM/Alf) and 9.7% (C3H/He) shorter than those of the corresponding germ-free counterparts. Temporal temperature gradient gel electrophoresis and quantitative real-time PCR revealed differences in microbiota composition between both SIHUMI-associated mouse strains. Anaerostipes caccae was one log lower in PRM/Alf mice than in C3H/He mice. Since polyamines and short-chain fatty acids (SCFAs) are important intestinal growth factors, their concentrations were explored. Cecal concentrations of putrescine, spermine, spermidine, and N-acetylspermine were 1.5-fold, 3.7-fold, 2.2-fold, and 1.4-fold higher, respectively, in the SIHUMI-C3H/He mice compared with the SIHUMI-PRM/Alf mice. In addition, cecal acetate, propionate, and butyrate concentrations in SIHUMI-C3H/He mice were 1.4-fold, 1.1-fold, and 2.1-fold higher, respectively, than in SIHUMI-PRM/Alf mice. These results indicate that polyamines and SCFAs did not promote gut lengthening in any of the two mouse strains. This suggests that as yet unknown factors provided by the SIHUMI prevented gut lengthening in the SIHUMI-associated mice compared with the germfree mice.
遗传、营养和源自肠道微生物群的因素被认为在整个肠道的发育中发挥作用,PRM/Alf小鼠的整个肠道长度比其他小鼠品系长约40%。PRM/Alf基因型解释了这种长度差异的60%。其余40%归因于母体效应,这可能取决于母亲传给幼崽的肠道微生物群。无菌PRM/Alf小鼠和C3H/He小鼠与简化的人类微生物群(SIHUMI)相关联,以研究其对肠道长度的影响。与相应的无菌小鼠相比,与SIHUMI相关的小鼠的小肠长度分别缩短了16.4%(PRM/Alf)和9.7%(C3H/He)。时间温度梯度凝胶电泳和定量实时PCR揭示了两种与SIHUMI相关的小鼠品系之间微生物群组成的差异。PRM/Alf小鼠中的粪厌氧棒状菌比C3H/He小鼠低一个数量级。由于多胺和短链脂肪酸(SCFA)是重要的肠道生长因子,因此对它们的浓度进行了研究。与SIHUMI-PRM/Alf小鼠相比,SIHUMI-C3H/He小鼠盲肠中腐胺、精胺、亚精胺和N-乙酰精胺的浓度分别高1.5倍、3.7倍、2.2倍和1.4倍。此外,SIHUMI-C3H/He小鼠盲肠中乙酸盐、丙酸盐和丁酸盐的浓度分别比SIHUMI-PRM/Alf小鼠高1.4倍、1.1倍和2.1倍。这些结果表明,多胺和SCFA在两种小鼠品系中均未促进肠道延长。这表明,与无菌小鼠相比,SIHUMI提供的未知因素阻止了与SIHUMI相关的小鼠的肠道延长。