婴儿肠道微生物群有助于提高小鼠的认知能力

Cell host & microbe Pub Date : 2023-12-13 Epub Date: 2023-12-04 DOI:10.1016/j.chom.2023.11.004
Tomás Cerdó, Alicia Ruiz-Rodríguez, Inmaculada Acuña, Francisco José Torres-Espínola, Sergio Menchén-Márquez, Fernando Gámiz, Milagros Gallo, Nico Jehmlich, Sven-Bastiaan Haange, Martin von Bergen, Cristina Campoy, Antonio Suárez
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引用次数: 0

摘要

肠道微生物群与婴儿神经发育有关。在本研究中,婴儿综合认知能力与肠道微生物群组成之间的联系在婴儿6个月时就已确立。综合认知能力高于中位值(Inf-aboveCC)和低于中位值(Inf-belowCC)的婴儿的微生物群落具有更高的多样性和均匀性。元蛋白组和代谢组分析确定了微生物组氨酸氨裂解酶和婴儿组氨酸代谢组与认知能力之间的联系。将Inf-aboveCC和Inf-belowCC供体的粪便移植到无菌小鼠体内表明,通过新物体识别测试评估的记忆力是一种可传递的性状。此外,Inf-aboveCC小鼠富含属于Phocaeicola以及Bacteroides和Bifidobacterium的物种,这些物种以前与认知能力有关。最后,与Inf-belowCC小鼠相比,Inf-aboveCC小鼠粪便中的组氨酸、尿氨酸:组氨酸和尿氨酸:谷氨酸比率较低。总之,这些发现揭示了肠道微生物群对婴儿认知的致病作用,并指出组氨酸代谢物水平的调节是潜在的内在机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Infant gut microbiota contributes to cognitive performance in mice.

Infant gut microbiota contributes to cognitive performance in mice.

Gut microbiota has been linked to infant neurodevelopment. Here, an association between infant composite cognition and gut microbiota composition is established as soon as 6 months. Higher diversity and evenness characterize microbial communities of infants with composite cognition above (Inf-aboveCC) versus below (Inf-belowCC) median values. Metaproteomic and metabolomic analyses establish an association between microbial histidine ammonia lyase and infant histidine metabolome with cognition. Fecal transplantation from Inf-aboveCC versus Inf-belowCC donors into germ-free mice shows that memory, assessed by a novel object recognition test, is a transmissible trait. Furthermore, Inf-aboveCC mice are enriched in species belonging to Phocaeicola, as well as Bacteroides and Bifidobacterium, previously linked to cognition. Finally, Inf-aboveCC mice show lower fecal histidine and urocanate:histidine and urocanate:glutamate ratios in the perirhinal cortex compared to Inf-belowCC mice. Overall, these findings reveal a causative role of gut microbiota on infant cognition, pointing at the modulation of histidine metabolite levels as a potential underlying mechanism.

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