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经抗生素处理后,单次口服灌胃即可使人类微生物群稳定定植于小鼠体内。

Stable engraftment of human microbiota into mice with a single oral gavage following antibiotic conditioning.

机构信息

BioTechnology Institute, University of Minnesota, St. Paul, MN, USA.

Center for Immunology, University of Minnesota, 2101 6th St. S.E., Room 3-184, Wallin Medical Biosciences Building, Minneapolis, MN, 55414, USA.

出版信息

Microbiome. 2017 Aug 1;5(1):87. doi: 10.1186/s40168-017-0306-2.

DOI:10.1186/s40168-017-0306-2
PMID:28760163
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5537947/
Abstract

BACKGROUND

Human microbiota-associated (HMA) animal models relying on germ-free recipient mice are being used to study the relationship between intestinal microbiota and human disease. However, transfer of microbiota into germ-free animals also triggers global developmental changes in the recipient intestine, which can mask disease-specific attributes of the donor material. Therefore, a simple model of replacing microbiota into a developmentally mature intestinal environment remains highly desirable.

RESULTS

Here we report on the development of a sequential, three-course antibiotic conditioning regimen that allows sustained engraftment of intestinal microorganisms following a single oral gavage with human donor microbiota. SourceTracker, a Bayesian, OTU-based algorithm, indicated that 59.3 ± 3.0% of the fecal bacterial communities in treated mice were attributable to the donor source. This overall degree of microbiota engraftment was similar in mice conditioned with antibiotics and germ-free mice. Limited surveys of systemic and mucosal immune sites did not show evidence of immune activation following introduction of human microbiota.

CONCLUSIONS

The antibiotic treatment protocol described here followed by a single gavage of human microbiota may provide a useful, complimentary HMA model to that established in germ-free facilities. The model has the potential for further in-depth translational investigations of microbiota in a variety of human disease states.

摘要

背景

依赖于无菌受体小鼠的人类微生物群相关(HMA)动物模型被用于研究肠道微生物群与人类疾病之间的关系。然而,将微生物群转移到无菌动物中也会引发受体肠道的全球性发育变化,这可能掩盖供体材料的特定疾病属性。因此,仍然非常需要一种将微生物群替换到发育成熟的肠道环境中的简单模型。

结果

在这里,我们报告了一种序贯的、三疗程抗生素调理方案的开发,该方案允许在单次口服给予人类供体微生物群后,持续定植肠道微生物群。SourceTracker,一种基于 OTU 的贝叶斯算法,表明处理过的小鼠粪便中 59.3±3.0%的细菌群落归因于供体来源。用抗生素调理的小鼠和无菌小鼠的这种总体微生物群定植程度相似。对全身和粘膜免疫部位的有限调查没有显示在引入人类微生物群后出现免疫激活的证据。

结论

这里描述的抗生素处理方案,随后进行单次人类微生物群灌胃,可能为在无菌设施中建立的 HMA 模型提供有用的补充。该模型有可能进一步深入研究各种人类疾病状态下的微生物群。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b79/5537947/de9874fe6ab2/40168_2017_306_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b79/5537947/6cca162d2140/40168_2017_306_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b79/5537947/840c3280ee1b/40168_2017_306_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b79/5537947/7042bd07dd1f/40168_2017_306_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b79/5537947/de9874fe6ab2/40168_2017_306_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b79/5537947/6cca162d2140/40168_2017_306_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b79/5537947/840c3280ee1b/40168_2017_306_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b79/5537947/7042bd07dd1f/40168_2017_306_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b79/5537947/de9874fe6ab2/40168_2017_306_Fig4_HTML.jpg

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