Two routes of metabolic cross-feeding between Bifidobacterium adolescentis and butyrate-producing anaerobes from the human gut

被引:631
作者
Belenguer, Alvaro
Duncan, Sylvia H.
Calder, A. Graham
Holtrop, Grietje
Louis, Petra
Lobley, Gerald E.
Flint, Harry J.
机构
[1] Rowett Res Inst, Bucksburn AB21 9SB, Aberdeen, Scotland
[2] Biomath & Stat Scotland, Bucksburn AB21 9SB, Aberdeen, Scotland
关键词
D O I
10.1128/AEM.72.5.3593-3599.2006
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Dietary carbohydrates have the potential to influence diverse functional groups of bacteria within the human large intestine. Of 12 Bifidobacterium strains of human gut origin from seven species tested, four grew in pure culture on starch and nine on fructo-oligosaccharides. The potential for metabolic cross-feeding between Bifidobacterium adolescentis and lactate-utilizing, butyrate-producing Firmicute bacteria related to Eubacterium hallii and Anaerostipes caccae was investigated in vitro. E. hallii L2-7 and A. caccae L1-92 failed to grow on starch in pure culture, but in coculture with B. adolescentis L2-32 butyrate was formed, indicating cross-feeding of metabolites to the lactate utilizers. Studies with [C-13] lactate confirmed carbon How from lactate, via acetyl coenzyme A, to butyrate both in pure cultures of E. hallii and in cocultures with B. adolescentis. Similar results were obtained in cocultures involving B. adolescentis DSM 20083 with fructo-oligosaccharides as the substrate. Butyrate formation was also stimulated, however, in cocultures of B. adolescentis L2-32 grown on starch or fructo-oligosaccharides with Roseburia sp. strain A2-183, which produces butyrate but does not utilize lactate. This is probably a consequence of the release by B. adolescentis of oligosaccharides that are available to Roseburia sp. strain A2-183. We conclude that two distinct mechanisms of metabolic cross-feeding between B. adolescentis and butyrate-forming bacteria may operate in gut ecosystems, one due to consumption of fermentation end products (lactate and acetate) and the other due to cross-feeding of partial breakdown products from complex substrates.
引用
收藏
页码:3593 / 3599
页数:7
相关论文
共 47 条
[1]   Selective plating underestimates abundance and shows differential recovery of bifidobacterial species from human feces [J].
Apajalahti, JHA ;
Kettunen, A ;
Nurminen, PH ;
Jatila, H ;
Holben, WE .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2003, 69 (09) :5731-5735
[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]   Characterization of bacterial communities in feces from healthy elderly volunteers and hospitalized elderly patients by using real-time PCR and effects of antibiotic treatment on the fecal microbiota [J].
Bartosch, S ;
Fite, A ;
Macfarlane, GT ;
McMurdo, MET .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2004, 70 (06) :3575-3581
[4]   Microbiological effects of consuming a synbiotic containing Bifidobacterium bifidum, Bifidobacterium lactis, and oligofructose in elderly persons, determined by real-time polymerase chain reaction and counting of viable bacteria [J].
Bartosch, S ;
Woodmansey, EJ ;
Paterson, JCM ;
McMurdo, MET ;
Macfarlane, GT .
CLINICAL INFECTIOUS DISEASES, 2005, 40 (01) :28-37
[5]   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
[6]   EFFECTS OF LACTULOSE AND OTHER LAXATIVES ON ILEAL AND COLONIC PH AS MEASURED BY A RADIOTELEMETRY DEVICE [J].
BOWN, RL ;
GIBSON, JA ;
SLADEN, GE ;
HICKS, B ;
DAWSON, AM .
GUT, 1974, 15 (12) :999-1004
[7]  
Calder AG, 1999, RAPID COMMUN MASS SP, V13, P2080, DOI 10.1002/(SICI)1097-0231(19991115)13:21<2080::AID-RCM755>3.0.CO
[8]  
2-O
[9]   The Ribosomal Database Project (RDP-II): sequences and tools for high-throughput rRNA analysis [J].
Cole, JR ;
Chai, B ;
Farris, RJ ;
Wang, Q ;
Kulam, SA ;
McGarrell, DM ;
Garrity, GM ;
Tiedje, JM .
NUCLEIC ACIDS RESEARCH, 2005, 33 :D294-D296
[10]   FERMENTATION IN THE HUMAN LARGE-INTESTINE AND THE AVAILABLE SUBSTRATES [J].
CUMMINGS, JH ;
ENGLYST, HN .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1987, 45 (05) :1243-1255