Variant forms of the binary toxin CDT locus and tcdC gene in Clostridium difficile strains

被引:41
作者
Stare, Barbara Geric
Delmee, Michel
Rupnik, Maja
机构
[1] Inst Publ Hlth Maribor, Maribor 2000, Slovenia
[2] Univ Maribor, Maribor 2000, Slovenia
[3] Agr Inst Slovenia, Ljubljana 1000, Slovenia
[4] Catholic Univ Louvain, Fac Med, Unite Microbiol, B-1200 Brussels, Belgium
关键词
D O I
10.1099/jmm.0.46931-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Variability in the genes for toxin A, toxin B and other pathogenicity locus regions is well known and is the basis for the distribution of Clostridium difficile strains into variant toxinotypes. Previous data have indicated that some C. difficile strains have a non-functional truncated form of the binary toxin (CDT) locus. This study analysed variability in the CDT locus and the presence of deleted tcdC genes in C. difficile strains. A total of 146 strains were screened, including known variant toxinotypes and non-variant A(+)B(+) (toxinotype 0) and A(-)B(-) C. difficile strains. In all of the strains studied, only two forms of the CDT locus were found: a full-length 4.3 kb fragment encoding the functional binary toxin or a truncated 2.3 kb fragment. Whilst the full-length CDT locus was found almost exclusively in variant toxinotypes, the truncated form was detected in 79 % of toxinotype 0 strains. Non-toxinogenic A(-)B(-) strains with a truncated version were not found and only rarely possessed the full-length CDT locus (A(-)B(-)CDT(+) strains). Four different forms of the tcdC gene were found; three represented deleted versions and typically were found in toxinotypes III-VII, XI, XIV-XVI and XXIV.
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页码:329 / 335
页数:7
相关论文
共 39 条
[11]   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
[12]   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
[13]  
Joseph R., 2005, EUROSURVEILLANCE, P4
[14]  
Kuijper EJ, 2006, EMERG INFECT DIS, V12, P827
[15]   MEGA3: Integrated software for molecular evolutionary genetics analysis and sequence alignment [J].
Kumar, S ;
Tamura, K ;
Nei, M .
BRIEFINGS IN BIOINFORMATICS, 2004, 5 (02) :150-163
[16]   A predominantly clonal multi-institutional outbreak of Clostridium difficile-associated diarrhea with high morbidity and mortality [J].
Loo, VG ;
Poirier, L ;
Miller, MA ;
Oughton, M ;
Libman, MD ;
Michaud, S ;
Bourgault, AM ;
Nguyen, T ;
Frenette, C ;
Kelly, M ;
Vibien, A ;
Brassard, P ;
Fenn, S ;
Dewar, K ;
Hudson, TJ ;
Horn, R ;
René, P ;
Monczak, Y ;
Dascal, A .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (23) :2442-2449
[17]   Molecular analysis of Clostridium difficile PCR ribotype 027 isolates from Eastern and Western Canada [J].
MacCannell, Duncan R. ;
Louie, Thomas J. ;
Gregson, Dan B. ;
Laverdiere, Michel ;
Labbe, Annie-Claude ;
Laing, Felicia ;
Henwick, Scott .
JOURNAL OF CLINICAL MICROBIOLOGY, 2006, 44 (06) :2147-2152
[18]   Clostridium difficile infection in patients discharged from US short-stay hospitals, 1996-2003 [J].
McDonald, LC ;
Owings, M ;
Jernigan, DB .
EMERGING INFECTIOUS DISEASES, 2006, 12 (03) :409-415
[19]   An epidemic, toxin gene-variant strain of Clostridium difficile [J].
McDonald, LC ;
Killgore, GE ;
Thompson, A ;
Owens, RC ;
Kazakova, SV ;
Sambol, SP ;
Johnson, S ;
Gerding, DN .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (23) :2433-2441
[20]   A hospital outbreak of Clostridium difficile disease associated with isolates carrying binary toxin genes [J].
McEllistrem, MC ;
Carman, RJ ;
Gerding, DN ;
Genheimer, CW ;
Zheng, L .
CLINICAL INFECTIOUS DISEASES, 2005, 40 (02) :265-272