Culture-independent analyses of temporal variation of the dominant fecal microbiota and targeted bacterial subgroups in Crohn's disease

被引:248
作者
Scanlan, Pauline D.
Shanahan, Fergus
O'Mahony, Caitlin
Marchesi, Julian R. [1 ]
机构
[1] Natl Univ Ireland Univ Coll Cork, Alimentary Pharmabiot Ctr, Cork, Ireland
[2] Natl Univ Ireland Univ Coll Cork, Dept Microbiol, Cork, Ireland
关键词
D O I
10.1128/JCM.00312-06
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Gut microbiota shows host-specific diversity and temporal stability and significantly contributes to maintenance of a healthy gut. However, in inflammatory bowel disease, this microbiota has been implicated as a contributory factor to the illness. This study compared bacterial dynamics in Crohn's disease patients to those in a control group using a culture-independent method to assess the temporal stability, relative diversity, and similarity of the dominant fecal microbiota, Clostridium spp., Bacteroides spp., Bifidobacterium spp., and lactic acid bacteria spp. (LAB) for all individuals. Fecal samples were collected over several time points from individuals with Crohn's disease who were in remission (n = 11), from Crohn's disease patients who relapsed into an active Crohn's disease state (n = 5), and from a control group (n = 18). Denaturing gradient gel electrophoresis profiles were generated for the different microbial groups by specifically targeting different regions of the 16S rRNA gene and were compared on the basis of similarity and diversity. The temporal stability of dominant species for all Crohn's disease patients was significantly lower (P < 0.005) than that for the control group. Analysis of group-specific profiles for Bifidobacterium spp. found that they were similar in all samples, while the diversity of the LAB varied significantly between the groups, but temporal stability was not significantly altered. We observed significant changes in two functionally important mutualistic groups of bacteria, viz., Clostridium and Bacteroides spp., which may have implications for the host's gut health, since some genera are involved in production of short-chain fatty acid, e.g., butyrate.
引用
收藏
页码:3980 / 3988
页数:9
相关论文
共 68 条
[11]   Diversity of the human intestinal microbial flora [J].
Eckburg, PB ;
Bik, EM ;
Bernstein, CN ;
Purdom, E ;
Dethlefsen, L ;
Sargent, M ;
Gill, SR ;
Nelson, KE ;
Relman, DA .
SCIENCE, 2005, 308 (5728) :1635-1638
[12]   Fecal beta-D-galactosidase production and Bifidobacteria are decreased in Crohn's disease [J].
Favier, C ;
Neut, C ;
Mizon, C ;
Cortot, A ;
Colombel, JF ;
Mizon, J .
DIGESTIVE DISEASES AND SCIENCES, 1997, 42 (04) :817-822
[13]   The relation between the number of species and the number of individuals in a random sample of an animal population [J].
Fisher, RA ;
Corbet, AS ;
Williams, CB .
JOURNAL OF ANIMAL ECOLOGY, 1943, 12 :42-58
[14]  
Franks AH, 1998, APPL ENVIRON MICROB, V64, P3336
[15]  
GARRY P, 1998, ECOSYSTEMS, V1, P6
[16]   Linking genetic identity and function in communities of uncultured bacteria [J].
Gray, ND ;
Head, IM .
ENVIRONMENTAL MICROBIOLOGY, 2001, 3 (08) :481-492
[17]   Role of bacteria in experimental colitis [J].
Guarner, F ;
Malagelada, JR .
BEST PRACTICE & RESEARCH CLINICAL GASTROENTEROLOGY, 2003, 17 (05) :793-804
[18]   Clinical aspects and pathophysiology of inflammatory bowel disease [J].
Hendrickson, BA ;
Gokhale, R ;
Cho, JH .
CLINICAL MICROBIOLOGY REVIEWS, 2002, 15 (01) :79-+
[19]   Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease [J].
Hugot, JP ;
Chamaillard, M ;
Zouali, H ;
Lesage, S ;
Cézard, JP ;
Belaiche, J ;
Almer, S ;
Tysk, C ;
O'Morain, CA ;
Gassull, M ;
Binder, V ;
Finkel, Y ;
Cortot, A ;
Modigliani, R ;
Laurent-Puig, P ;
Gower-Rousseau, C ;
Macry, J ;
Colombel, JF ;
Sahbatou, M ;
Thomas, G .
NATURE, 2001, 411 (6837) :599-603
[20]   Regulation of microglial inflammatory response by sodium butyrate and short-chain fatty acids [J].
Huuskonen, J ;
Suuronen, T ;
Nuutinen, T ;
Kyrylenko, S ;
Salminen, A .
BRITISH JOURNAL OF PHARMACOLOGY, 2004, 141 (05) :874-880