Carriage of Clostridium difficile in outpatients with irritable bowel syndrome

被引:16
作者
Clayton, Evelyn M. [1 ,2 ]
Rea, Mary C. [1 ,2 ]
Shanahan, Fergus [2 ,3 ]
Quigley, Eamonn M. M. [2 ,3 ]
Kiely, Barry [4 ]
Ross, R. Paul [1 ,2 ]
Hill, Colin [2 ,5 ]
机构
[1] Moorepark, Teagasc Food Res Ctr, Cork, Ireland
[2] Natl Univ Ireland Univ Coll Cork, Alimentary Pharmabiot Ctr, Cork, Ireland
[3] Natl Univ Ireland Univ Coll Cork, Dept Med, Cork, Ireland
[4] Cork Airport Business Pk, Alimentary Hlth, Cork, Ireland
[5] Natl Univ Ireland Univ Coll Cork, Dept Microbiol, Cork, Ireland
关键词
GASTROINTESTINAL MICROBIOTA; PATHOGENICITY LOCUS; FECAL MICROBIOTA; TOXIN PRODUCTION; BINARY TOXIN; PCR; REGULATOR; RIFAXIMIN; INFECTION; STRAINS;
D O I
10.1099/jmm.0.040568-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Irritable bowel syndrome (IBS) is a common, typically chronic and sometimes disabling gastrointestinal condition of uncertain aetiology. Recently, a variety of links to gastrointestinal infections have been described including the onset of IBS following exposure to enteric pathogens and an apparent predisposition to gastrointestinal infection. The prevalence of Clostridium difficile in a population of IBS outpatients (n=87) in the absence of established risk factors for the acquisition of C. difficile infection was examined. Overall, 5.7% of patients (n=5) carried culturable C. difficile and 4.6% (n=4) of isolates were toxigenic, belonging to toxinotype group 0, compared with 1.1% (n=1) for the healthy control group (n=88). These isolates were members of toxigenic PCR ribotype groups 005 and 050 (IBS group) and 062 (control group) and were identified further as three individual strains by PFGE. Although no significant difference was observed between IBS patients and healthy volunteers, these findings support the concept that a subpopulation of IBS patients may be susceptible to gastrointestinal infection.
引用
收藏
页码:1290 / 1294
页数:5
相关论文
共 28 条
[21]   A randomized double-blind placebo-controlled trial of rifaximin in patients with abdominal bloating and flatulence [J].
Sharara, AI ;
Aoun, E ;
Abdul-Baki, H ;
Mounzer, R ;
Sidani, S ;
ElHajj, I .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2006, 101 (02) :326-333
[22]   Genomic diversity and relatedness of bifidobacteria isolated from a porcine cecum [J].
Simpson, PJ ;
Stanton, C ;
Fitzgerald, GF ;
Ross, RP .
JOURNAL OF BACTERIOLOGY, 2003, 185 (08) :2571-2581
[23]   Molecular analysis of the pathogenicity locus and polymorphism in the putative negative regulator of toxin production (TcdC) among Clostridium difficile clinical isolates [J].
Spigaglia, P ;
Mastrantonio, P .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (09) :3470-3475
[24]  
Spiller RC, 2003, AM J GASTROENTEROL, V98, P238
[25]   Role of infection in irritable bowel syndrome [J].
Spiller, Robin C. .
JOURNAL OF GASTROENTEROLOGY, 2007, 42 (Suppl 17) :41-47
[26]   Production of actin-specific ADP-ribosyltransferase (binary toxin) by strains of Clostridium difficile [J].
Stubbs, S ;
Rupnik, M ;
Gibert, M ;
Brazier, J ;
Duerden, B ;
Popoff, M .
FEMS MICROBIOLOGY LETTERS, 2000, 186 (02) :307-312
[27]   PCR targeted to the 16S-23S rRNA gene intergenic spacer region of Clostridium difficile and construction of a library consisting of 116 different PCR ribotypes [J].
Stubbs, SLJ ;
Brazier, JS ;
O'Neill, GL ;
Duerden, BI .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (02) :461-463
[28]  
Wilcox M., 2010, CLOSTRIDIUM DIFFICIL