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Effects of Myeloid Hif-1β Deletion on the Intestinal Microbiota in Mice under Environmental Hypoxia.

Authors :
Han N
Pan Z
Huang Z
Chang Y
Hou F
Liu G
Yang R
Bi Y
Source :
Infection and immunity [Infect Immun] 2020 Dec 15; Vol. 89 (1). Date of Electronic Publication: 2020 Dec 15 (Print Publication: 2020).
Publication Year :
2020

Abstract

External environmental factors can cause an imbalance in intestinal flora. For people living in the extremes of a plateau climate, lack of oxygen is a primary health challenge that leads to a series of reactions. We wondered how intestinal microorganisms might change in a simulated plateau environment and what changes might occur in the host organism and intestinal microorganisms in the absence of hypoxia-related factors. In this study, mice carrying a knockout of hypoxia-inducible factor 1β ( Hif-1β ) in myeloid cells and wild-type mice were raised in a composite hypoxic chamber to simulate a plateau environment at 5,000 m of elevation for 14 days. The mice carrying the myeloid Hif-1β deletion displayed aggravated hypoxic phenotypes in comparison to and significantly greater weight loss and significantly higher cardiac index values than the wild-type group. The levels of some cytokines increased in the hypoxic environment. Analysis of 16S rRNA sequencing results showed that hypoxia had a significant effect on the gut microbiota in both wild-type and Hif-1β -deficient mice, especially on the first day. The levels of members of the Bacteroidaceae family increased continuously from day 1 to day 14 in Hif-1β deletion mice, and they represented an obviously different group of bacteria at day 14 compared with the wild-type mice. Butyrate-producing bacteria, such as Butyricicoccus , were found in wild-type mice only after 14 days in the hypoxic environment. In conclusion, hypoxia caused heart enlargement, greater weight loss, and obvious microbial imbalance in myeloid Hif-1β -deficient mice. This study revealed genetic and microecological pathways for research on mechanisms of hypoxia.<br /> (Copyright © 2020 American Society for Microbiology.)

Details

Language :
English
ISSN :
1098-5522
Volume :
89
Issue :
1
Database :
MEDLINE
Journal :
Infection and immunity
Publication Type :
Academic Journal
Accession number :
33106294
Full Text :
https://doi.org/10.1128/IAI.00474-20