期刊
THERANOSTICS
卷 9, 期 15, 页码 4542-4557出版社
IVYSPRING INT PUBL
DOI: 10.7150/thno.35282
关键词
miRNA; microbiota; inflammation; feces; colitis
资金
- National Institutes of Health of Diabetes and Digestive and Kidney [R01DK116306, R01DK071594, R01DK107739, R01DK099071]
- Department of Veterans Affairs [BX002526, BX004476]
- Crohn's and Colitis Foundation
- Kenneth Rainin Foundation
Disruption of intestine-microbiota symbiosis can result in chronic gut inflammation. We hypothesize that assessing the initial inflammatory potential of the microbiota in patients is essential and that host-derived miRNAs, which can be found in feces, could fulfill this function. We investigated whether the gut microbiota composition impacts the fecal miRNA profile and thereby indicates its ability to influence intestinal inflammation. Methods: We used high-throughput qPCR to compare fecal miRNA profile between germ-free and conventional mice. Conventionalization of germfree mice by various colitogenic and non-colitogenic microbiotas (IL10(-/-) and TLR5(-/-) associated microbiota) was performed. Results: We identified 12 fecal miRNAs impacted by the presence of a microbiota. Conventionalization of germfree mice by various colitogenic and non-colitogenic microbiotas associated with the development of intestinal inflammation (IL10(-/-) and TLR5(-/-) associated microbiota) yielded distinctively altered fecal miRNA profiles compared to that of mice receiving a healthy microbiota. Correlation analysis revealed the existence of interactions between the 12 abovementioned miRNAs and specific microbiota members. Conclusion: These results showed that fecal miRNA profile can be differentially and specifically impacted by microbiota composition, and that miRNA could importantly serve as markers of the colitogenic potential of the microbiota. This is particularly relevant to assess individual state of the microbiota in patients with dysbiosis-related disorders, such as IBD and potentially determine their ability to respond to therapeutics.
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