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人类微生物组、饮食、肠道病毒与免疫系统之间的相互作用:悉生猪研究的新见解。

Interactions between human microbiome, diet, enteric viruses and immune system: Novel insights from gnotobiotic pig research.

作者信息

Vlasova Anastasia N, Rajashekara Gireesh, Saif Linda J

机构信息

Food Animal Health Research Program, CFAES, Ohio Agricultural Research and Development Center, Department of Veterinary Preventive Medicine, College of Veterinary Medicine, The Ohio State University, Wooster, OH 44691, USA.

出版信息

Drug Discov Today Dis Models. 2018 Summer;28:95-103. doi: 10.1016/j.ddmod.2019.08.006.

DOI:10.1016/j.ddmod.2019.08.006
PMID:33149747
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7594741/
Abstract

Studies over the past few decades demonstrated that gnotobiotic (Gn) pigs provide an unprecedented translational model to study human intestinal health and diseases. Due to the high degree of anatomical, physiological, metabolic, immunological, and developmental similarity, the domestic pig closely mimics the human intestinal microenvironment. Also, Gn piglets can be efficiently transplanted with human microbiota from infants, children and adults with resultant microbial profiles remarkably similar to the original human samples, a feat consistently not achievable in rodent models. Finally, Gn and human microbiota-associated (HMA) piglets are susceptible to human enteric viral pathogens (including human rotavirus, HRV) and can be fed authentic human diets, which further increases the translational potential of these models. In this review, we will focus on recent studies that evaluated the pathophysiology of protein malnutrition and the associated dysbiosis and immunological dysfunction in neonatal HMA piglets. Additionally, we will discuss studies of potential dietary interventions that moderate the effects of malnutrition and dysbiosis on antiviral immunity and HRV vaccines in HMA pigs. Such studies provide novel models and novel mechanistic insights critical for development of drug interventions.

摘要

过去几十年的研究表明,无菌猪为研究人类肠道健康与疾病提供了前所未有的转化模型。由于在解剖学、生理学、代谢、免疫和发育方面具有高度相似性,家猪能紧密模拟人类肠道微环境。此外,无菌仔猪可高效移植来自婴儿、儿童和成人的人类微生物群,其微生物谱与原始人类样本极为相似,这是啮齿动物模型始终无法实现的壮举。最后,无菌和人类微生物群相关(HMA)仔猪易感染人类肠道病毒病原体(包括人类轮状病毒,HRV),并且可以喂食正宗的人类饮食,这进一步提高了这些模型的转化潜力。在这篇综述中,我们将重点关注近期评估新生HMA仔猪蛋白质营养不良的病理生理学以及相关的微生物失调和免疫功能障碍的研究。此外,我们将讨论关于潜在饮食干预措施的研究,这些措施可减轻营养不良和微生物失调对HMA猪抗病毒免疫力和HRV疫苗的影响。此类研究为药物干预的开发提供了关键的新型模型和新的机制见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61a0/7594741/9ed0801ac984/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61a0/7594741/4298f20a309f/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61a0/7594741/4f686514134c/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61a0/7594741/318d977e2a1e/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61a0/7594741/9ed0801ac984/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61a0/7594741/4298f20a309f/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61a0/7594741/4f686514134c/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61a0/7594741/318d977e2a1e/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61a0/7594741/9ed0801ac984/gr3.jpg

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