Crosstalk between butyrate oxidation in colonocyte and butyrate-producing bacteria

被引:2
|
作者
Park, Bohye [1 ,3 ]
Kim, Ji Yeon [1 ]
Riffey, Olivia F. [2 ]
Walsh, Triston J. [2 ]
Johnson, Jeremiah [2 ]
Donohoe, Dallas R. [1 ,2 ]
机构
[1] Univ Tennessee, Dept Nutr, Knoxville, TN 37996 USA
[2] Univ Tennessee, Dept Microbiol, Knoxville, TN 37996 USA
[3] Univ Alabama Birmingham, Dept Pathol, Birmingham, AL 35233 USA
关键词
CHAIN FATTY-ACIDS; GUT MICROBIOTA; DIETARY FIBER; FAECALIBACTERIUM-PRAUSNITZII; METABOLISM; HEALTH; TRANSFERASE; FERMENTATION; DIVERSITY; BARRIER;
D O I
10.1016/j.isci.2024.110853
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The composition of gut microbiota, including butyrate-producing bacteria (BPB), is influenced by diet and physiological conditions. As such, given the importance of butyrate as an energetic substrate in colonocytes, it is unclear whether utilization of this substrate by the host would enhance BPB levels, thus defining a host-microbiome mutualistic relationship based on cellular metabolism. Here, it is shown through using a mouse model that lacks short-chain acyl dehydrogenase (SCAD), which is the first enzyme in the beta- oxidation pathway for short-chain fatty acids (SCFAs), that there is a significant diminishment in BPB at the phylum, class, species, and genus level compared to mice that have SCAD. Furthermore, SCAD-deficient mice do not show a prebiotic response from dietary fiber. Thus, oxidation of SCFAs by the host, which includes butyrate, is important in promoting BPB. These data help define the functional importance of diet-microbiome-host interactions toward microbiome composition, as it relates to function.
引用
收藏
页数:14
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