Molecular analysis of Clostridium difficile PCR ribotype 027 isolates from Eastern and Western Canada

被引:136
作者
MacCannell, Duncan R.
Louie, Thomas J.
Gregson, Dan B.
Laverdiere, Michel
Labbe, Annie-Claude
Laing, Felicia
Henwick, Scott
机构
[1] Univ Calgary, Dept Microbiol & Infect Dis, Calgary, AB, Canada
[2] Calgary Hlth Reg, Infect Prevent & Control Program, Calgary, AB, Canada
[3] Calgary Lab Serv, Calgary, AB, Canada
[4] Hop Maison Neuve Rosemont, Montreal, PQ H1T 2M4, Canada
[5] Fraser Hlth Author, Surrey, BC, Canada
关键词
D O I
10.1128/JCM.02563-05
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The prevalence and characteristics of PCR ribotype 027 strains of Clostridium difficile have come into question following recent outbreaks in Eastern Canada and elsewhere. In order to determine the distribution of this strain in other regions in Canada, we screened a bank of 1,419 isolates recovered from three different Canadian health regions between 2000 and 2004. Among isolates from a Montreal area hospital, PCR ribotype 027 strains represented 115/153 strains (75.2%) from 2003 to 2004, but ribotype 027 strains were absent in 2000 and 2001. In Calgary, by contrast, ribotype 027 rates have remained relatively stable over 4 years of surveillance, representing 51/685 (7.4%) hospital isolates and 62/373 (16.6%) strains from the community (P < 0.001). PCR ribotype 027 accounted for 8/135 (5.9%) hospital isolates in the Fraser Health Region in 2004. repetitive extragenic palindromic PCR was used to subtype a random selection of 027 isolates from each region. All 10 of the isolates from Quebec were of a single subtype, which was also dominant among isolates from Alberta (8/10 isolates) and British Columbia (6/8 isolates). Comparative sequencing of the tcdC repressor gene confirmed the documented 18-bp deletion and identified a second, single-base-pair deletion at position 117. Both deletions were conserved across all three provinces and were identified in a United Kingdom reference strain. The presence of a frameshift in the early portion of the tcdC gene implies serious functional disruption and may contribute to the hypervirulence of the 027 phenotype. PCR ribotype 027 strains appear to be widely distributed, to predate the Montreal outbreak, and to have measurable community presence in Western Canada.
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页码:2147 / 2152
页数:6
相关论文
共 24 条
[1]   An improved protocol for pulsed-field gel electrophoresis typing of Clostridium difficile [J].
Alonso, R ;
Martín, A ;
Peláez, T ;
Marín, M ;
Rodríguez-Creixéms, M ;
Bouza, E .
JOURNAL OF MEDICAL MICROBIOLOGY, 2005, 54 (02) :155-157
[2]   Binary bacterial toxins:: Biochemistry, biology, and applications of common Clostridium and Bacillus proteins [J].
Barth, H ;
Aktories, K ;
Popoff, MR ;
Stiles, BG .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2004, 68 (03) :373-+
[3]   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
[4]   Analysis of the pathogenicity locus in Clostridium difficile strains [J].
Cohen, SH ;
Tang, YJ ;
Silva, J .
JOURNAL OF INFECTIOUS DISEASES, 2000, 181 (02) :659-663
[5]   Risk of Clostridium difficile diarrhea among hospital inpatients prescribed proton pump inhibitors:: cohort and case-control studies [J].
Dial, S ;
Alrasadi, K ;
Manoukian, C ;
Huang, A ;
Menzies, D .
CANADIAN MEDICAL ASSOCIATION JOURNAL, 2004, 171 (01) :33-38
[6]   Genomic analysis of the erythromycin resistance element Tn5398 from Clostridium difficile [J].
Farrow, KA ;
Lyras, D ;
Rood, JI .
MICROBIOLOGY-SGM, 2001, 147 :2717-2728
[7]   A modified pulsed-field get electrophoresis (PFGE) protocol for subtyping previously non-PFGE typeable isolates of Clostridium difficile polymerase chain reaction ribotype 001 [J].
Gal, M ;
Northey, G ;
Brazier, JS .
JOURNAL OF HOSPITAL INFECTION, 2005, 61 (03) :231-236
[8]   Prevalence and characterization of a binary toxin (actin-specific ADP-ribosyltransferase) from Clostridium difficile [J].
Gonçalves, C ;
Decré, D ;
Barbut, F ;
Burghoffer, B ;
Petit, JC .
JOURNAL OF CLINICAL MICROBIOLOGY, 2004, 42 (05) :1933-1939
[9]   Transcription analysis of the genes tcdA-E of the pathogenicity locus of Clostridium difficile [J].
Hundsberger, T ;
Braun, V ;
Weidmann, M ;
Leukel, P ;
Sauerborn, M ;
vonEichelStreiber, C .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1997, 244 (03) :735-742
[10]  
Krausz S, 2005, Ned Tijdschr Geneeskd, V149, P2081