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Wild Mouse Gut Microbiota Promotes Host Fitness and Improves Disease Resistance
- Source :
- Cell. 171:1015-1028.e13
- Publication Year :
- 2017
- Publisher :
- Elsevier BV, 2017.
-
Abstract
- Summary Laboratory mice, while paramount for understanding basic biological phenomena, are limited in modeling complex diseases of humans and other free-living mammals. Because the microbiome is a major factor in mammalian physiology, we aimed to identify a naturally evolved reference microbiome to better recapitulate physiological phenomena relevant in the natural world outside the laboratory. Among 21 distinct mouse populations worldwide, we identified a closely related wild relative to standard laboratory mouse strains. Its bacterial gut microbiome differed significantly from its laboratory mouse counterpart and was transferred to and maintained in laboratory mice over several generations. Laboratory mice reconstituted with natural microbiota exhibited reduced inflammation and increased survival following influenza virus infection and improved resistance against mutagen/inflammation-induced colorectal tumorigenesis. By demonstrating the host fitness-promoting traits of natural microbiota, our findings should enable the discovery of protective mechanisms relevant in the natural world and improve the modeling of complex diseases of free-living mammals. Video Abstract
- Subjects :
- Male
0301 basic medicine
Carcinogenesis
Animals, Wild
Inflammation
Gut flora
Plant disease resistance
Article
General Biochemistry, Genetics and Molecular Biology
Virus
Microbiology
Mice
03 medical and health sciences
Peromyscus
0302 clinical medicine
Animals, Laboratory
medicine
Animals
Microbiome
Physiological Phenomenon
Disease Resistance
Maryland
biology
Host (biology)
Laboratory mouse
biology.organism_classification
Gastrointestinal Microbiome
Mice, Inbred C57BL
030104 developmental biology
Virus Diseases
030220 oncology & carcinogenesis
Female
medicine.symptom
Subjects
Details
- ISSN :
- 00928674
- Volume :
- 171
- Database :
- OpenAIRE
- Journal :
- Cell
- Accession number :
- edsair.doi.dedup.....37245b1eb67c611859da3b01cb815438