Huertas-Díaz Lucía, Vestergaard Louise Guldager, Marietou Angeliki, Irla Marta, Behr Jürgen, Somoza Mark M, Feilberg Anders, Schwab Clarissa
Department of Biological and Chemical Engineering, Aarhus University, Aarhus, Denmark.
Leibniz Institute for Food Systems Biology at the Technical University of Munich, Freising, Germany.
Gut Pathog. 2025 Apr 11;17(1):23. doi: 10.1186/s13099-025-00689-1.
Breastfeeding is a major determinant of gut microbiota composition and fermentation activity during the first months of life. Breastmilk delivers human milk oligosaccharides (HMO) as substrates for microbial intestinal fermentation. One of the main metabolites that accumulates in feces of breastfed infants is 1,2-propanediol (1,2PD) resulting from the metabolism of fucosylated HMO. 1,2PD is used in microbial cross-feeding to produce propionate, but 1,2PD is also an alcohol that can impact the state of the microbial cell envelope. To shed further light on an understudied compound in the infant gut, we investigated the genetic and metabolic potential of the early gut colonizer Clostridium perfringens to utilise 1,2PD, and the interactions of 1,2PD with the cell envelope.
Based on genome analysis, C. perfringens FMT 1006 isolated from infant feces possessed most genes of the pdu operon related to 1,2PD metabolism. C. perfringens consumed 1,2PD (78%) and produced 1-propanol as the main metabolite, while propionate was not detected. In agreement, genes responsible for 1,2PD utilisation and propanol formation (pduCDE, dhaT) were highly expressed. When cultivated in the presence of 1,2PD and glucose, a higher proportion of 1,2PD carbon (87%) was recovered as compared to incubation with only 1,2PD (34%). At the same time, lactate and acetate were formed in a ratio of 2.16:1.0 with 1,2PD and glucose compared to a ratio 9.0:1.0 during growth with only glucose possibly due to reallocation of the NAD/NADH pool in favor of 1-propanol formation. The presence of 1,2PD slightly increased membrane fluidity and modified the composition of the membrane to a higher content of elongated glycerophosphoethanolamines.
We provide here new knowledge on the metabolism of 1,2PD by a microbial species that is present during breastfeeding and observed that C. perfringens metabolised 1,2PD mainly to propanol. The presence of 1,2PD had little impact on membrane fluidity and let to modifications of membrane lipid composition. Collectively, these findings advance our understanding of on intestinal metabolite-microbe interactions during breastfeeding.
母乳喂养是生命最初几个月肠道微生物群组成和发酵活性的主要决定因素。母乳提供人乳寡糖(HMO)作为微生物肠道发酵的底物。母乳喂养婴儿粪便中积累的主要代谢产物之一是岩藻糖基化HMO代谢产生的1,2 - 丙二醇(1,2PD)。1,2PD用于微生物互养以产生丙酸盐,但1,2PD也是一种可影响微生物细胞膜状态的醇类。为了进一步阐明婴儿肠道中一种研究较少的化合物,我们研究了早期肠道定植菌产气荚膜梭菌利用1,2PD的遗传和代谢潜力,以及1,2PD与细胞膜的相互作用。
基于基因组分析,从婴儿粪便中分离出的产气荚膜梭菌FMT 1006拥有与1,2PD代谢相关的pdu操纵子的大多数基因。产气荚膜梭菌消耗1,2PD(78%)并产生1 - 丙醇作为主要代谢产物,未检测到丙酸盐。与此一致,负责1,2PD利用和丙醇形成的基因(pduCDE、dhaT)高度表达。当在1,2PD和葡萄糖存在下培养时,与仅用1,2PD培养(34%)相比,回收的1,2PD碳比例更高(87%)。同时,乳酸和乙酸盐的形成比例在1,2PD和葡萄糖存在下为2.16:1.0,而仅用葡萄糖生长时为9.0:1.0,这可能是由于NAD/NADH库重新分配有利于1 - 丙醇的形成。1,2PD的存在略微增加了膜流动性,并使膜的组成发生改变,使伸长的甘油磷酸乙醇胺含量更高。
我们在此提供了关于母乳喂养期间存在的一种微生物对1,2PD代谢的新知识,并观察到产气荚膜梭菌将1,2PD主要代谢为丙醇。1,2PD的存在对膜流动性影响不大,但导致膜脂质组成发生改变。总体而言,这些发现推进了我们对母乳喂养期间肠道代谢物 - 微生物相互作用的理解。