Correlation of disease severity with fecal toxin levels in patients with Clostridium difficile-associated diarrhea and distribution of PCR ribotypes and toxin yields in vitro of corresponding isolates

被引:104
作者
Åkerlund, T [1 ]
Svenungsson, B
Lagergren, Å
Burman, LG
机构
[1] Swedish Inst Infect Dis Control, Dept Bacteriol, S-17182 Solna, Sweden
[2] Karolinska Hosp, Dept Communicable Dis Control & Prevent, S-10401 Stockholm, Sweden
[3] Huddinge Univ Hosp, Karolinska Inst, Dept Med, Div Infect Dis, S-14186 Huddinge, Sweden
关键词
D O I
10.1128/JCM.44.2.353-358.2006
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We investigated in vivo and in vitro yields of toxins A and B from and PCR ribotypes of Clostridium difficile isolates from 164 patients with differing severities of C. difficile-associated diarrhea (CDAD) (patients were grouped as follows: < 3 loose stools per day, n = 45; 3 to 10 per day, n = 97; > 10 per day, n = 22). The median fecal toxin levels in each group were 0.5, 6.8, and 149 U/g feces (P < 0.001), respectively. Patients with severe diarrhea also had more-frequent occurrence of blood in stool and vomiting, but there was no association with fecal toxin levels per se. There was no correlation between fecal toxin level and toxin yield in vitro for the corresponding C. difficile isolate or between its PCR ribotype and disease severity. A broad range of toxin yields among isolates belonging to major PCR ribotypes indicated a presence of many subtypes. We hypothesize that bacterial and host factors that affect C. difficile toxin levels in feces are important determinants of symptoms in CDAD patients. An inverse correlation between toxin yield and spore count (r = 0.66) in stationary-phase cultures supported the notion that toxin production and sporulation represent opposite alternative survival strategies for C. difficile cells facing nutrient shortage.
引用
收藏
页码:353 / 358
页数:6
相关论文
共 39 条
[1]   Comparison of PCR-ribotyping, arbitrarily primed PCR, and pulsed-field gel electrophoresis for typing Clostridium difficile [J].
Bidet, P ;
Lalande, V ;
Salauze, B ;
Burghoffer, B ;
Avesani, V ;
Delmée, M ;
Rossier, A ;
Barbut, F ;
Petit, JC .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (07) :2484-2487
[2]   Immunological detection and cytotoxic properties of toxins from toxin A-positive, toxin B-positive Clostridium difficile variants [J].
Blake, JE ;
Mitsikosta, F ;
Metcalfe, MA .
JOURNAL OF MEDICAL MICROBIOLOGY, 2004, 53 (03) :197-205
[3]  
BORIELLO SP, 1987, J MED MICROBIOL, V24, P53
[4]   Typing of Clostridium difficile [J].
Brazier, JS .
CLINICAL MICROBIOLOGY AND INFECTION, 2001, 7 (08) :428-431
[5]   Clostridium difficile-associated diseases: Comparison of symptomatic infection versus carriage on the basis of risk factors, toxin production, and genotyping results [J].
Cheng, SH ;
Lu, JJ ;
Young, TG ;
Perng, CL ;
Chi, WM .
CLINICAL INFECTIOUS DISEASES, 1997, 25 (01) :157-158
[6]   THE SIGNIFICANCE OF QUANTITATIVE RESULTS OF C-DIFFICILE CULTURES AND TOXIN ASSAYS IN PATIENTS WITH DIARRHEA [J].
CHURCH, JM ;
FAZIO, VW .
DISEASES OF THE COLON & RECTUM, 1985, 28 (11) :765-769
[7]   MODULATION OF CYTO-TOXIN PRODUCTION BY CLOSTRIDIUM-DIFFICILE IN THE INTESTINAL TRACTS OF GNOTOBIOTIC MICE INOCULATED WITH VARIOUS HUMAN INTESTINAL BACTERIA [J].
CORTHIER, G ;
DUBOS, F ;
RAIBAUD, P .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1985, 49 (01) :250-252
[8]   VIRULENCE OF 10 SEROGROUPS OF CLOSTRIDIUM-DIFFICILE IN HAMSTERS [J].
DELMEE, M ;
AVESANI, V .
JOURNAL OF MEDICAL MICROBIOLOGY, 1990, 33 (02) :85-90
[9]   Molecular epidemiology of endemic Clostridium difficile infection and the significance of subtypes of the United Kingdom epidemic strain (PCR ribotype 1) [J].
Fawley, WN ;
Parnell, P ;
Verity, P ;
Freeman, J ;
Wilcox, MH .
JOURNAL OF CLINICAL MICROBIOLOGY, 2005, 43 (06) :2685-2696
[10]   Evidence to support the existence of subgroups within the UK epidemic Clostridium difficile strain (PCR ribotype 1) [J].
Fawley, WN ;
Freeman, J ;
Wilcox, MH .
JOURNAL OF HOSPITAL INFECTION, 2003, 54 (01) :74-77