{"title":"高度简化的微生物群对产后肠道、免疫和大脑发育的影响。","authors":"Hannah Sturgeon , Alexandra Castillo-Ruiz , Emem Ukpong , Lavanika Praveen , Gina Leyva , Benoit Chassaing , Nancy G. Forger","doi":"10.1016/j.bbi.2025.106085","DOIUrl":null,"url":null,"abstract":"<div><div>At birth, the newborn mammal enters a highly microbial world, leading to colonization of the gut by trillions of microorganisms, known as the microbiota. We previously reported that germ-free (GF) mice have altered brain development in the first days of life, suggesting that the arrival of microbes at birth is essential for normal brain development. However, GF mice are a highly artificial model system, with known deficits in immune and intestinal development. To determine the effects of a more realistic curtailment of microbial exposure, we utilized a reduced, defined microbiota. Specifically, GF mouse dams were colonized with the altered Schaedler flora (ASF), a community of eight bacterial species, which supports relatively normal immune and intestinal function in adulthood. Measures in the periphery (colon histology and gene expression, plasma cytokines) and brain (neuronal cell death, microglial density, forebrain expression of cytokine and blood–brain barrier protein genes) were then compared among offspring born to ASF, GF, and conventionally colonized (CC; i.e., control) mice at postnatal day (P)3 or P23, focusing on those measures previously reported to differ between CC and GF conditions. We observed that ASF newborns have a higher bacterial load in the colon than CC mice but are essentially monocolonized. For some measures (e.g., plasma cytokines, neuronal cell death), ASF newborns at P3 are similar to controls, whereas for others they are GF-like or intermediate. The ASF microbiota grows to comprise 5 bacterial species by weaning age, compared to explosive diversification in CC offspring. Analyses at P23 demonstrate that microglia density is like that of controls in ASF weanlings but several peripheral measures remain GF-like. Thus, effects of an absent microbiota are evident within a few days of life, and colonization with a highly simplified, defined microbiota normalizes some, but not all, measures in the developing periphery and brain.</div></div>","PeriodicalId":9199,"journal":{"name":"Brain, Behavior, and Immunity","volume":"130 ","pages":"Article 106085"},"PeriodicalIF":7.6000,"publicationDate":"2025-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effects of a highly simplified microbiota on postnatal intestinal, immune, and brain development\",\"authors\":\"Hannah Sturgeon , Alexandra Castillo-Ruiz , Emem Ukpong , Lavanika Praveen , Gina Leyva , Benoit Chassaing , Nancy G. Forger\",\"doi\":\"10.1016/j.bbi.2025.106085\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>At birth, the newborn mammal enters a highly microbial world, leading to colonization of the gut by trillions of microorganisms, known as the microbiota. We previously reported that germ-free (GF) mice have altered brain development in the first days of life, suggesting that the arrival of microbes at birth is essential for normal brain development. However, GF mice are a highly artificial model system, with known deficits in immune and intestinal development. To determine the effects of a more realistic curtailment of microbial exposure, we utilized a reduced, defined microbiota. Specifically, GF mouse dams were colonized with the altered Schaedler flora (ASF), a community of eight bacterial species, which supports relatively normal immune and intestinal function in adulthood. Measures in the periphery (colon histology and gene expression, plasma cytokines) and brain (neuronal cell death, microglial density, forebrain expression of cytokine and blood–brain barrier protein genes) were then compared among offspring born to ASF, GF, and conventionally colonized (CC; i.e., control) mice at postnatal day (P)3 or P23, focusing on those measures previously reported to differ between CC and GF conditions. We observed that ASF newborns have a higher bacterial load in the colon than CC mice but are essentially monocolonized. For some measures (e.g., plasma cytokines, neuronal cell death), ASF newborns at P3 are similar to controls, whereas for others they are GF-like or intermediate. The ASF microbiota grows to comprise 5 bacterial species by weaning age, compared to explosive diversification in CC offspring. Analyses at P23 demonstrate that microglia density is like that of controls in ASF weanlings but several peripheral measures remain GF-like. Thus, effects of an absent microbiota are evident within a few days of life, and colonization with a highly simplified, defined microbiota normalizes some, but not all, measures in the developing periphery and brain.</div></div>\",\"PeriodicalId\":9199,\"journal\":{\"name\":\"Brain, Behavior, and Immunity\",\"volume\":\"130 \",\"pages\":\"Article 106085\"},\"PeriodicalIF\":7.6000,\"publicationDate\":\"2025-08-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Brain, Behavior, and Immunity\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0889159125003204\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brain, Behavior, and Immunity","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0889159125003204","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
Effects of a highly simplified microbiota on postnatal intestinal, immune, and brain development
At birth, the newborn mammal enters a highly microbial world, leading to colonization of the gut by trillions of microorganisms, known as the microbiota. We previously reported that germ-free (GF) mice have altered brain development in the first days of life, suggesting that the arrival of microbes at birth is essential for normal brain development. However, GF mice are a highly artificial model system, with known deficits in immune and intestinal development. To determine the effects of a more realistic curtailment of microbial exposure, we utilized a reduced, defined microbiota. Specifically, GF mouse dams were colonized with the altered Schaedler flora (ASF), a community of eight bacterial species, which supports relatively normal immune and intestinal function in adulthood. Measures in the periphery (colon histology and gene expression, plasma cytokines) and brain (neuronal cell death, microglial density, forebrain expression of cytokine and blood–brain barrier protein genes) were then compared among offspring born to ASF, GF, and conventionally colonized (CC; i.e., control) mice at postnatal day (P)3 or P23, focusing on those measures previously reported to differ between CC and GF conditions. We observed that ASF newborns have a higher bacterial load in the colon than CC mice but are essentially monocolonized. For some measures (e.g., plasma cytokines, neuronal cell death), ASF newborns at P3 are similar to controls, whereas for others they are GF-like or intermediate. The ASF microbiota grows to comprise 5 bacterial species by weaning age, compared to explosive diversification in CC offspring. Analyses at P23 demonstrate that microglia density is like that of controls in ASF weanlings but several peripheral measures remain GF-like. Thus, effects of an absent microbiota are evident within a few days of life, and colonization with a highly simplified, defined microbiota normalizes some, but not all, measures in the developing periphery and brain.
期刊介绍:
Established in 1987, Brain, Behavior, and Immunity proudly serves as the official journal of the Psychoneuroimmunology Research Society (PNIRS). This pioneering journal is dedicated to publishing peer-reviewed basic, experimental, and clinical studies that explore the intricate interactions among behavioral, neural, endocrine, and immune systems in both humans and animals.
As an international and interdisciplinary platform, Brain, Behavior, and Immunity focuses on original research spanning neuroscience, immunology, integrative physiology, behavioral biology, psychiatry, psychology, and clinical medicine. The journal is inclusive of research conducted at various levels, including molecular, cellular, social, and whole organism perspectives. With a commitment to efficiency, the journal facilitates online submission and review, ensuring timely publication of experimental results. Manuscripts typically undergo peer review and are returned to authors within 30 days of submission. It's worth noting that Brain, Behavior, and Immunity, published eight times a year, does not impose submission fees or page charges, fostering an open and accessible platform for scientific discourse.