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关键发育窗口期的定殖揭示了营养不良期间微生物群依赖性的生长和免疫变化。

Colonization during a key developmental window reveals microbiota-dependent shifts in growth and immunity during undernutrition.

作者信息

Serrano Matos Yadeliz A, Cano Jasmine, Shafiq Hamna, Williams Claire, Sunny Julee, Cowardin Carrie A

机构信息

Division of Pediatric Gastroenterology & Hepatology, Department of Pediatrics, University of Virginia School of Medicine, Charlottesville, Virginia 22908, USA.

Department of Microbiology, Immunology and Cancer Biology, University of Virginia School of Medicine, Charlottesville, Virginia 22908, USA.

出版信息

bioRxiv. 2023 Jul 7:2023.07.07.547849. doi: 10.1101/2023.07.07.547849.

Abstract

Childhood undernutrition is a major global health challenge with devastating lifelong consequences. Linear growth stunting due to undernutrition has been linked to poor outcomes, and mothers who experience stunting are more likely to give birth to stunted children. Murine models that capture the intergenerational and multifactorial nature of undernutrition are critical to understanding the underlying biology of this disorder. Here we report a gnotobiotic mouse model of undernutrition using microbiota from human infants with healthy or stunted growth trajectories. Intergenerational transmission of microbiota from parents to offspring leads to the development of growth and immune features of undernutrition and enteropathy, including reduced linear growth, intestinal villus blunting and accumulation of intraepithelial lymphocytes. In contrast, colonization after weaning reduces sensitivity to detect changes driven by distinct microbial communities. Overall, these results suggest intergenerational colonization is a useful approach with which to investigate microbiota-dependent growth and immunity in early life.

摘要

儿童期营养不良是一项重大的全球健康挑战,会造成具有毁灭性的终身后果。营养不良导致的线性生长迟缓与不良后果有关,而经历过生长迟缓的母亲更有可能生下发育迟缓的孩子。能够体现营养不良的代际和多因素性质的小鼠模型对于理解这种疾病的潜在生物学机制至关重要。在此,我们报告了一种无菌小鼠营养不良模型,该模型使用了具有健康或发育迟缓生长轨迹的人类婴儿的微生物群。微生物群从亲代到子代的代际传递导致了营养不良和肠病的生长及免疫特征的发展,包括线性生长减少、肠绒毛变钝和上皮内淋巴细胞积聚。相比之下,断奶后进行定殖会降低检测由不同微生物群落驱动的变化的敏感性。总体而言,这些结果表明代际定殖是一种用于研究生命早期微生物群依赖性生长和免疫的有用方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee29/10350093/05818ea9bc47/nihpp-2023.07.07.547849v1-f0001.jpg

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