Human Gut Microbes Use Multiple Transporters to Distinguish Vitamin B12 Analogs and Compete in the Gut

被引:206
作者
Degnan, Patrick H. [1 ,2 ]
Barry, Natasha A. [1 ,2 ]
Mok, Kenny C. [3 ]
Taga, Michiko E. [3 ]
Goodman, Andrew L. [1 ,2 ]
机构
[1] Yale Univ, Dept Microbial Pathogenesis, New Haven, CT 06536 USA
[2] Yale Univ, Microbial Divers Inst, New Haven, CT 06536 USA
[3] Univ Calif Berkeley, Dept Plant & Microbial Biol, Berkeley, CA 94720 USA
基金
美国国家卫生研究院;
关键词
SPOROMUSA-OVATA; METABOLISM; COBALAMIN; IDENTIFICATION; BACTERIA; GROWTH;
D O I
10.1016/j.chom.2013.12.007
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Genomic and metagenomic sequencing efforts, including human microbiome projects, reveal that microbes often encode multiple systems that appear to accomplish the same task. Whether these predictions reflect actual functional redundancies is unclear. We report that the prominent human gut symbiont Bacteroides thetaiotaomicron employs three functional, homologous vitamin B-12 transporters that in at least two cases confer a competitive advantage in the presence of distinct B-12 analogs (corrinoids). In the mammalian gut, microbial fitness can be determined by the presence or absence of a single transporter. The total number of distinct corrinoid transporter families in the human gut microbiome likely exceeds those observed in B. thetaiotaomicron by an order of magnitude. These results demonstrate that human gut microbes use elaborate mechanisms to capture and differentiate corrinoids in vivo and that apparent redundancies observed in these genomes can instead reflect hidden specificities that determine whether a microbe will colonize its host.
引用
收藏
页码:47 / 57
页数:11
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