Systematic genome assessment of B-vitamin biosynthesis suggests co-operation among gut microbes

被引:552
作者
Magnusdottir, Stefania [1 ]
Ravcheev, Dmitry [1 ]
de Crecy-Lagard, Valerie [2 ,3 ]
Thiele, Ines [1 ]
机构
[1] Univ Luxembourg, Luxembourg Ctr Syst Biomed, L-4362 Esch Sur Alzette, Luxembourg
[2] Univ Florida, Dept Microbiol & Cell Sci, Inst Food & Agr Sci, Gainesville, FL 32611 USA
[3] Univ Florida, Genet Inst, Gainesville, FL 32611 USA
关键词
ESCHERICHIA-COLI; FAECALIBACTERIUM-PRAUSNITZII; FUNCTIONAL-CHARACTERIZATION; FOLATE-DEFICIENCY; NAD BIOSYNTHESIS; INTERACTIVE TREE; GROWTH-MEDIUM; GENE-CLUSTER; IDENTIFICATION; RIBOFLAVIN;
D O I
10.3389/fgene.2015.00148
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The human gut microbiota supplies its host with essential nutrients, including B-vitamins. Using the PubSEED platform, we systematically assessed the genomes of 256 common human gut bacteria for the presence of biosynthesis pathways for eight B-vitamins: biotin, cobalamin, folate, niacin, pantothenate, pyridoxine, riboflavin, and thiamin. On the basis of the presence and absence of genome annotations, we predicted that each of the eight vitamins was produced by 40-65% of the 256 human gut microbes. The distribution of synthesis pathways was diverse; some genomes had all eight biosynthesis pathways, whereas others contained no de novo synthesis pathways. We compared our predictions to experimental data from 16 organisms and found 88% of our predictions to be in agreement with published data. In addition, we identified several pairs of organisms whose vitamin synthesis pathway pattern complemented those of other organisms. This analysis suggests that human gut bacteria actively exchange B-vitamins among each other, thereby enabling the survival of organisms that do not synthesize any of these essential cofactors. This result indicates the co-evolution of the gut microbes in the human gut environment. Our work presents the first comprehensive assessment of the B-vitamin synthesis capabilities of the human gut microbiota. We propose that in addition to diet, the gut microbiota is an important source of B-vitamins, and that changes in the gut microbiota composition can severely affect our dietary B-vitamin requirements.
引用
收藏
页数:18
相关论文
共 79 条
[1]   Genetic Control of Biosynthesis and Transport of Riboflavin and Flavin Nucleotides and Construction of Robust Biotechnological Producers [J].
Abbas, Charles A. ;
Sibirny, Andriy A. .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2011, 75 (02) :321-+
[2]   Identification and quantitation of cobalamin and cobalamin analogues in human feces [J].
Allen, Robert H. ;
Stabler, Sally P. .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2008, 87 (05) :1324-1335
[3]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[4]   Role of antibiotic penetration limitation in Klebsiella pneumoniae biofilm resistance to ampicillin and ciprofloxacin [J].
Anderl, JN ;
Franklin, MJ ;
Stewart, PS .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (07) :1818-1824
[5]   Vitamin B12 (cobalamin) deficiency in elderly patients [J].
Andrès, E ;
Loukili, NH ;
Noel, E ;
Kaltenbach, G ;
Ben Abdelgheni, M ;
Perrin, AE ;
Noblet-Dick, M ;
Maloisel, F ;
Schlienger, JL ;
Blicklé, JF .
CANADIAN MEDICAL ASSOCIATION JOURNAL, 2004, 171 (03) :251-259
[6]  
[Anonymous], 1998, Dietary Reference Intakes: A Risk Assessment Model for Establishing Upper Intake Levels for Nutrients
[7]  
Begley TP, 2001, VITAM HORM, V61, P103
[8]   NAD+ metabolism in health and disease [J].
Belenky, Peter ;
Bogan, Katrina L. ;
Brenner, Charles .
TRENDS IN BIOCHEMICAL SCIENCES, 2007, 32 (01) :12-19
[9]   Genetic diversity of viable, injured, and dead fecal bacteria assessed by fluorescence-activated cell sorting and 16S rRNA gene analysis [J].
Ben-Amor, K ;
Heilig, H ;
Smidt, H ;
Vaughan, EE ;
Abee, T ;
de Vos, WM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2005, 71 (08) :4679-4689
[10]   Interaction between H2-producing and non-H2-producing cellulolytic bacteria from the human colon [J].
Chassard, C ;
Gaillard-Martinie, B ;
Bernalier-Donadille, A .
FEMS MICROBIOLOGY LETTERS, 2005, 242 (02) :339-344