Lactate has the potential to promote hydrogen sulphide formation in the human colon

被引:109
作者
Marquet, Perrine [2 ]
Duncan, Sylvia H. [1 ]
Chassard, Christophe [2 ]
Bernalier-Donadille, Annick [2 ]
Flint, Harry J. [1 ]
机构
[1] Univ Aberdeen, Rowett Inst Nutr & Hlth, Microbial Ecol Grp, Aberdeen AB21 9SB, Scotland
[2] INRA, Microbiol UR454, CR Clermont Ferrand Theix, F-63122 St Genes Champanelle, France
关键词
lactate; butyrate; sulphide; Eubacterium hallii; Desulfovibrio piger; BUTYRATE-PRODUCING BACTERIA; SULFATE-REDUCING BACTERIA; HUMAN LARGE-INTESTINE; CHAIN FATTY-ACIDS; ULCERATIVE-COLITIS; HUMAN FECES; FERMENTATION PRODUCTS; MICROBIAL COMMUNITIES; HUMAN GUT; IN-VITRO;
D O I
10.1111/j.1574-6968.2009.01750.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
High concentrations of sulphide are toxic for the gut epithelium and may contribute to bowel disease. Lactate is a favoured cosubstrate for the sulphate-reducing colonic bacterium Desulfovibrio piger, as shown here by the stimulation of sulphide formation by D. piger DSM749 by lactate in the presence of sulphate. Sulphide formation by D. piger was also stimulated in cocultures with the lactate-producing bacterium Bifidobacterium adolescentis L2-32. Other lactate-utilizing bacteria such as the butyrate-producing species Eubacterium hallii and Anaerostipes caccae are, however, expected to be in competition with the sulphate-reducing bacteria (SRB) for the lactate formed in the human colon. Strains of E. hallii and A. caccae produced 65% and 96% less butyrate from lactate, respectively, in a coculture with D. piger DSM749 than in a pure culture. In triculture experiments involving B. adolescentis L2-32, up to 50% inhibition of butyrate formation by E. hallii and A. caccae was observed in the presence of D. piger DSM749. On the other hand, sulphide formation by D. piger was unaffected by E. hallii or A. caccae in these cocultures and tricultures. These experiments strongly suggest that lactate can stimulate sulphide formation by SRB present in the colon, with possible consequences for conditions such as colitis.
引用
收藏
页码:128 / 134
页数:7
相关论文
共 51 条
[1]   Hydrogen sulfide induces direct radical-associated DNA damage [J].
Attene-Ramos, Matias S. ;
Wagner, Elizabeth D. ;
Gaskins, H. Rex ;
Plewa, Michael J. .
MOLECULAR CANCER RESEARCH, 2007, 5 (05) :455-459
[2]   Phylogenetic relationships of butyrate-producing bacteria from the human gut [J].
Barcenilla, A ;
Pryde, SE ;
Martin, JC ;
Duncan, SH ;
Stewart, CS ;
Henderson, C ;
Flint, HJ .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (04) :1654-1661
[3]   Impact of pH on lactate formation and utilization by human fecal microbial communities [J].
Belenguer, Alvaro ;
Duncan, Sylvia H. ;
Holtrop, Grietje ;
Anderson, Susan E. ;
Lobley, Gerald E. ;
Flint, Harry J. .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2007, 73 (20) :6526-6533
[4]   Quantitative Analysis of Microbial Metabolism in the Human Large Intestine [J].
Belenguer, Alvaro ;
Duncan, Sylvia H. ;
Holtrop, Grietje ;
Flint, Harry J. ;
Lobley, Gerald E. .
CURRENT NUTRITION & FOOD SCIENCE, 2008, 4 (02) :109-126
[5]   Two routes of metabolic cross-feeding between Bifidobacterium adolescentis and butyrate-producing anaerobes from the human gut [J].
Belenguer, Alvaro ;
Duncan, Sylvia H. ;
Calder, A. Graham ;
Holtrop, Grietje ;
Louis, Petra ;
Lobley, Gerald E. ;
Flint, Harry J. .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2006, 72 (05) :3593-3599
[6]   Treatment of ulcerative colitis using fecal bacteriotherapy [J].
Borody, TJ ;
Warren, EF ;
Leis, S ;
Surace, R ;
Ashman, O .
JOURNAL OF CLINICAL GASTROENTEROLOGY, 2003, 37 (01) :42-47
[7]   Lactate is mainly fermented to butyrate by human intestinal microfloras but inter-individual variation is evident [J].
Bourriaud, C ;
Robins, RJ ;
Martin, L ;
Kozlowski, F ;
Tenailleau, E ;
Cherbut, C ;
Michel, C .
JOURNAL OF APPLIED MICROBIOLOGY, 2005, 99 (01) :201-212
[8]   BUTYRATE OXIDATION IS IMPAIRED IN THE COLONIC MUCOSA OF SUFFERERS OF QUIESCENT ULCERATIVE-COLITIS [J].
CHAPMAN, MAS ;
GRAHN, MF ;
BOYLE, MA ;
HUTTON, M ;
ROGERS, J ;
WILLIAMS, NS .
GUT, 1994, 35 (01) :73-76
[9]   SHORT CHAIN FATTY-ACIDS IN HUMAN LARGE-INTESTINE, PORTAL, HEPATIC AND VENOUS-BLOOD [J].
CUMMINGS, JH ;
POMARE, EW ;
BRANCH, WJ ;
NAYLOR, CPE ;
MACFARLANE, GT .
GUT, 1987, 28 (10) :1221-1227
[10]   ENUMERATION OF H-2-UTILIZING METHANOGENIC ARCHAEA, ACETOGENIC AND SULFATE-REDUCING BACTERIA FROM HUMAN FECES [J].
DORE, J ;
POCHART, P ;
BERNALIER, A ;
GODEREL, I ;
MORVAN, B ;
RAMBAUD, JC .
FEMS MICROBIOLOGY ECOLOGY, 1995, 17 (04) :279-284