Relative abundance of the Prevotella genus within the human gut microbiota of elderly volunteers determines the inter-individual responses to dietary supplementation with wheat bran arabinoxylan-oligosaccharides

被引:43
|
作者
Chung, Wing Sun Faith [1 ]
Walker, Alan W. [1 ]
Bosscher, Douwina [2 ]
Garcia-Campayo, Vicenta [3 ]
Wagner, Josef [4 ]
Parkhill, Julian [5 ]
Duncan, Sylvia H. [1 ]
Flint, Harry J. [1 ]
机构
[1] Univ Aberdeen, Rowett Inst, Gut Hlth Grp, Foresterhill, Aberdeen AB25 2ZD, Scotland
[2] Cargill R&D Ctr Europe BVBA, Havenstr 84, B-1800 Vilvoorde, Belgium
[3] Cargill Inc, POB 9300, Minneapolis, MN 55440 USA
[4] Wellcome Sanger Inst, Pathogen Genom Grp, Hinxton CB10 1SA, Cambs, England
[5] Univ Cambridge, Dept Vet Med, Madingley Rd, Cambridge CB3 0ES, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
Gut microbiota; Diversity; Bacteroides; Prevotella; Bifidobacteria; Wheatbran extract; Arabinoxylan oligosaccharides (AXOS); Short chain fatty acids; Propionate; Butyrate; FOOD-FREQUENCY QUESTIONNAIRE; RANDOMIZED CONTROLLED-TRIAL; CEREAL ARABINOXYLANS; FERMENTATION; ENTEROTYPES; POPULATION; DIVERSITY; NUTRITION; EXTRACT; PROBIOTICS;
D O I
10.1186/s12866-020-01968-4
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background The human colon is colonised by a dense microbial community whose species composition and metabolism are linked to health and disease. The main energy sources for colonic bacteria are dietary polysaccharides and oligosaccharides. These play a major role in modulating gut microbial composition and metabolism, which in turn can impact on health outcomes. Results We investigated the influence of wheat bran arabinoxylan oligosaccharides (AXOS) and maltodextrin supplements in modulating the composition of the colonic microbiota and metabolites in healthy adults over the age of 60. Male and female volunteers, (n = 21, mean BMI 25.2 +/- 0.7 kg/m(2)) participated in the double-blind, cross over supplement study. Faecal samples were collected for analysis of microbiota, short chain fatty acids levels and calprotectin. Blood samples were collected to measure glucose, cholesterol and triglycerides levels. There was no change in these markers nor in calprotectin levels in response to the supplements. Both supplements were well-tolerated by the volunteers. Microbiota analysis across the whole volunteer cohort revealed a significant increase in the proportional abundance of faecalBifidobacteriumspecies (P <= 0.01) in response to AXOS, but not maltodextrin, supplementation. There was considerable inter-individual variation in the other bacterial taxa that responded, with a clear stratification of volunteers as eitherPrevotella-plus (n = 8; > 0.1% proportional abundance) orPrevotella-minus (n = 13; <= 0.1% proportional abundance) subjects founded on baseline sample profiles. There was a significant increase in the proportional abundance of both faecalBifidobacterium(P <= 0.01) andPrevotellaspecies (P <= 0.01) inPrevotella-plus volunteers during AXOS supplementation, whilePrevotellaandBacteroidesrelative abundances showed an inverse relationship. Proportional abundance of 26 OTUs, including bifidobacteria andAnaerostipes hadrus,differed significantly between baseline samples ofPrevotella-plus compared toPrevotella-minus individuals. Conclusions The wheat bran AXOS supplementation was bifidogenic and resulted in changes in human gut microbiota composition that depended on the initial microbiota profile, specifically the presence or absence ofPrevotellaspp. as a major component of the microbiota. Our data therefore suggest that initial profiling of individuals through gut microbiota analysis should be considered important when contemplating nutritional interventions that rely on prebiotics.
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  • [1] Relative abundance of the Prevotella genus within the human gut microbiota of elderly volunteers determines the inter-individual responses to dietary supplementation with wheat bran arabinoxylan-oligosaccharides
    Wing Sun Faith Chung
    Alan W. Walker
    Douwina Bosscher
    Vicenta Garcia-Campayo
    Josef Wagner
    Julian Parkhill
    Sylvia H. Duncan
    Harry J. Flint
    [J]. BMC Microbiology, 20