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

被引:131
作者
Staley, Christopher [1 ]
Kaiser, Thomas [1 ]
Beura, Lalit K. [2 ,3 ]
Hamilton, Matthew J. [1 ]
Weingarden, Alexa R. [1 ]
Bobr, Aleh [2 ,4 ]
Kang, Johnthomas [2 ,4 ]
Masopust, David [2 ,3 ]
Sadowsky, Michael J. [1 ,5 ]
Khoruts, Alexander [1 ,2 ,4 ]
机构
[1] Univ Minnesota, BioTechnol Inst, St Paul, MN 55108 USA
[2] Univ Minnesota, Ctr Immunol, 2101 6th St SE,Room 3-184,Wallin Med Biosci Bldg, Minneapolis, MN 55414 USA
[3] Univ Minnesota, Dept Microbiol & Immunol, Minneapolis, MN 55414 USA
[4] Univ Minnesota, Dept Med, Div Gastroenterol, Minneapolis, MN 55414 USA
[5] Univ Minnesota, Dept Soil Water & Climate, St Paul, MN 55108 USA
来源
MICROBIOME | 2017年 / 5卷
关键词
Antibiotics; Fecal microbiota transplantation; Germ-free; Humanization; Mouse model; FECAL MICROBIOTA; IMMUNE-SYSTEM; COMMENSAL BACTERIA; GUT MICROBIOTA; HOST; TRANSPLANTATION; ECOLOGY; MODEL; IMPROVEMENT; METABOLISM;
D O I
10.1186/s40168-017-0306-2
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
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页数:13
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