Fecal beta-D-galactosidase production and Bifidobacteria are decreased in Crohn's disease

被引:170
作者
Favier, C
Neut, C
Mizon, C
Cortot, A
Colombel, JF
Mizon, J
机构
[1] FAC PHARMACEUT & BIOL, BIOCHIM LAB, F-59006 LILLE, FRANCE
[2] CTR HOSP REG & UNIV LILLE, HOP HURIEZ, SERV MALAD APPAREIL DIGEST & NUTR, F-59037 LILLE, FRANCE
关键词
Crohn's disease; Bifidobacteria; beta-D-galactosidase;
D O I
10.1023/A:1018876400528
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Digestive bacterial microflora play a major role in the pathogenesis of Crohn's disease (CD). Bacterial enzyme activities, especially beta-D-galactosidase, are decreased in fecal extracts from CD patients. We hypothesized that an alteration of the colonic flora might be responsible for this decrease. Indeed, we demonstrate that beta-D-galactosidase production in supernates of anaerobic cultures was significantly (P < 0.01) reduced in feces from patients with active Crohn's disease (N = 7), when compared to healthy controls (N = 8). Therefore using X-gal and selective media, we enumerated bacteria able to release beta-D-galactosidase in feces from patients with active (N = 16) or quiescent disease (N = 5) and healthy controls (N = 14). Bifidobacteria numbers were significantly reduced in patients (P < 0.01 for active; P < 0.02 for quiescent disease) whereas Bacteroides and Lactobacilli counts remained unchanged. beta-D-Galactosidase activity and Bifidobacteria counts were significantly correlated (P < 0.03). Bifidobacteria are regarded as beneficial for the host. The reduction in Bifidobacteria is responsible for decreased beta-D-galactosidase activity. Thus oral administration of prebiotics that promote their growth might have potential therapeutic interest.
引用
收藏
页码:817 / 822
页数:6
相关论文
共 26 条
[1]   AN ELECTIVE AND SELECTIVE ISOLATION MEDIUM FOR BIFIDOBACTERIUM SPP [J].
BEERENS, H .
LETTERS IN APPLIED MICROBIOLOGY, 1990, 11 (03) :155-157
[2]  
BEST WR, 1976, GASTROENTEROLOGY, V70, P439
[3]   Bacterial enzymes used for colon-specific drug delivery are decreased in active Crohn's disease [J].
Carrette, O ;
Favier, C ;
Mizon, C ;
Neut, C ;
Cortot, A ;
Colombel, JF ;
Mizon, J .
DIGESTIVE DISEASES AND SCIENCES, 1995, 40 (12) :2641-2646
[4]  
DELCAMBRE VC, 1993, GASTROENTEROL CLIN B, V17, P718
[5]  
ELYAMANI J, 1992, CLIN SCI, V83, P409
[6]   Differentiation and identification of human faecal anaerobic bacteria producing beta-galactosidase (a new methodology) [J].
Favier, C ;
Neut, C ;
Mizon, C ;
Cortot, A ;
Colombel, JF ;
Mizon, J .
JOURNAL OF MICROBIOLOGICAL METHODS, 1996, 27 (01) :25-31
[7]   THE ASSESSMENT OF FECAL FLORA IN PATIENTS WITH INFLAMMATORY BOWEL-DISEASE BY A SIMPLIFIED BACTERIOLOGICAL TECHNIQUE [J].
GIAFFER, MH ;
HOLDSWORTH, CD ;
DUERDEN, BI .
JOURNAL OF MEDICAL MICROBIOLOGY, 1991, 35 (04) :238-243
[8]   REGULATORY EFFECTS OF BIFIDOBACTERIA ON THE GROWTH OF OTHER COLONIC BACTERIA [J].
GIBSON, GR ;
WANG, X .
JOURNAL OF APPLIED BACTERIOLOGY, 1994, 77 (04) :412-420
[9]   DIETARY MODULATION OF THE HUMAN COLONIC MICROBIOTA - INTRODUCING THE CONCEPT OF PREBIOTICS [J].
GIBSON, GR ;
ROBERFROID, MB .
JOURNAL OF NUTRITION, 1995, 125 (06) :1401-1412
[10]   MOLECULAR EVIDENCE FOR 2 FORMS OF CROHN-DISEASE [J].
GILBERTS, ECAM ;
GREENSTEIN, AJ ;
KATSEL, P ;
HARPAZ, N ;
GREENSTEIN, RJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (26) :12721-12724