Complex carbohydrate utilization by the healthy human microbiome.
Complex carbohydrate utilization by the healthy human microbiome.
复制标题
DOI:
10.1371/journal.pone.0028742
复制
发表时间:
2012
期刊:
影响因子:
3.7
通讯作者:
Henrissat B
中科院分区:
文献类型:
--
作者:
Cantarel BL;Lombard V;Henrissat B
The various ecological habitats in the human body provide microbes a wide array of nutrient sources and survival challenges. Advances in technology such as DNA sequencing have allowed a deeper perspective into the molecular function of the human microbiota than has been achievable in the past. Here we aimed to examine the enzymes that cleave complex carbohydrates (CAZymes) in the human microbiome in order to determine (i) whether the CAZyme profiles of bacterial genomes are more similar within body sites or bacterial families and (ii) the sugar degradation and utilization capabilities of microbial communities inhabiting various human habitats. Upon examination of 493 bacterial references genomes from 12 human habitats, we found that sugar degradation capabilities of taxa are more similar to others in the same bacterial family than to those inhabiting the same habitat. Yet, the analysis of 520 metagenomic samples from five major body sites show that even when the community composition varies the CAZyme profiles are very similar within a body site, suggesting that the observed functional profile and microbial habitation have adapted to the local carbohydrate composition. When broad sugar utilization was compared within the five major body sites, the gastrointestinal track contained the highest potential for total sugar degradation, while dextran and peptidoglycan degradation were highest in oral and vaginal sites respectively. Our analysis suggests that the carbohydrate composition of each body site has a profound influence and probably constitutes one of the major driving forces that shapes the community composition and therefore the CAZyme profile of the local microbial communities, which in turn reflects the microbiome fitness to a body site.
登录
查看更多内容
DOI:
10.1126/science.1183605
发表时间:
2010-05-21
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Human Microbiome Jumpstart Reference Strains Consortium;Nelson KE;Weinstock GM;Highlander SK;Worley KC;Creasy HH;Wortman JR;Rusch DB;Mitreva M;Sodergren E;Chinwalla AT;Feldgarden M;Gevers D;Haas BJ;Madupu R;Ward DV;Birren BW;Gibbs RA;Methe B;Petrosino JF;Strausberg RL;Sutton GG;White OR;Wilson RK;Durkin S;Giglio MG;Gujja S;Howarth C;Kodira CD;Kyrpides N;Mehta T;Muzny DM;Pearson M;Pepin K;Pati A;Qin X;Yandava C;Zeng Q;Zhang L;Berlin AM;Chen L;Hepburn TA;Johnson J;McCorrison J;Miller J;Minx P;Nusbaum C;Russ C;Sykes SM;Tomlinson CM;Young S;Warren WC;Badger J;Crabtree J;Markowitz VM;Orvis J;Cree A;Ferriera S;Fulton LL;Fulton RS;Gillis M;Hemphill LD;Joshi V;Kovar C;Torralba M;Wetterstrand KA;Abouellleil A;Wollam AM;Buhay CJ;Ding Y;Dugan S;FitzGerald MG;Holder M;Hostetler J;Clifton SW;Allen-Vercoe E;Earl AM;Farmer CN;Liolios K;Surette MG;Xu Q;Pohl C;Wilczek-Boney K;Zhu D
通讯作者:
Zhu D
DOI:
10.1073/pnas.0806191105
发表时间:
2009-02-10
影响因子:
11.1
作者:
Brulc, Jennifer M.;Antonopoulos, Dionysios A.;White, Bryan A.
通讯作者:
White, Bryan A.
DOI:
10.1038/nbt0885-722
发表时间:
1985-01-01
期刊:
BIO-TECHNOLOGY
影响因子:
--
作者:
HENRISSAT, B;DRIGUEZ, H;SCHULEIN, M
通讯作者:
SCHULEIN, M
影响因子:
6.8
作者:
Henrissat, B;Davies, G
通讯作者:
Davies, G
影响因子:
4.3
作者:
LAINE, RA
通讯作者:
LAINE, RA