Prevalence and characterization of a binary toxin (actin-specific ADP-ribosyltransferase) from Clostridium difficile

被引:126
作者
Gonçalves, C
Decré, D
Barbut, F
Burghoffer, B
Petit, JC
机构
[1] Univ Paris 06, UFR St Antoine, Fac Med, UPRES EA 2392, Paris, France
[2] Hop St Antoine, Assist Publ Hop Paris, Bacteriol Lab, F-75571 Paris, France
[3] Hop St Antoine, Assist Publ Hop Paris, Unite Hyg & Lutte Contre Infect Nosocomiales, F-75571 Paris, France
关键词
D O I
10.1128/JCM.42.5.1933-1939.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In addition to the two large clostridial cytotoxins (TcdA and TcAB), some strains of Clostridium difficile also produce an actin-specific ADP-ribosyltransferase, called binary toxin CDT. We used a PCR method and Southern blotting for the detection of genes encoding the enzymatic (CDTa) and binding (CDTb) components of the binary toxin in 369 strains isolated from patients with suspected C. difficile-associated diarrhea or colitis. Twenty-two strains (a prevalence of 6%) harbored both genes. When binary toxin production was assessed by Western blotting, 19 of the 22 strains reacted with antisera against the iota toxin of C. perfringens (anti-la and anti-Ib). Additionally, binary toxin activity, detected by the ADP-ribosyltransferase assay, was present in only 17 of the 22 strains. Subsequently, all 22 binary toxin-positive strains were tested for the production of toxins TcdA and TcAB, toxinotyped, and characterized by serogrouping, PCR ribotyping, arbitrarily primed PCR, and pulsed-field gel electrophoresis. All binary toxin-positive strains also produced TcdB and/or TcdA. However, they had significant changes in the tcdA and tcdB genes and belonged to variant toxinotypes III, IV, V, VII, IX, and XIII. We could differentiate 16 profiles by using typing methods, indicating that most of the binary toxin-positive strains were unrelated.
引用
收藏
页码:1933 / 1939
页数:7
相关论文
共 46 条
  • [1] MECHANISMS OF THE CYTOPATHIC ACTION OF ACTIN-ADP-RIBOSYLATING TOXINS
    AKTORIES, K
    WEGNER, A
    [J]. MOLECULAR MICROBIOLOGY, 1992, 6 (20) : 2905 - 2908
  • [2] DIARRHEA ASSOCIATED WITH TOXIGENIC CLOSTRIDIUM-SPIROFORME
    BABUDIERI, S
    BORRIELLO, SP
    PANTOSTI, A
    LUZZI, I
    TESTORE, GP
    PANICHI, G
    [J]. JOURNAL OF INFECTION, 1986, 12 (03) : 278 - 279
  • [3] BANNO Y, 1984, REV INFECT DIS, V6, pS11
  • [4] Barbut F, 2000, J CLIN MICROBIOL, V38, P2386
  • [5] Prevalence and genetic characterization of toxin A variant strains of Clostridium difficile among adults and children with diarrhea in France
    Barbut, F
    Lalande, V
    Burghoffer, B
    Thien, HV
    Grimprel, E
    Petit, JC
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (06) : 2079 - 2083
  • [6] COMPARISON OF 3 ENZYME IMMUNOASSAYS, A CYTOTOXICITY ASSAY, AND TOXIGENIC CULTURE FOR DIAGNOSIS OF CLOSTRIDIUM-DIFFICILE ASSOCIATED DIARRHEA
    BARBUT, F
    KAJZER, C
    PLANAS, N
    PETIT, JC
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (04) : 963 - 967
  • [7] NUCLEOTIDE-SEQUENCE OF CLOSTRIDIUM-DIFFICILE TOXIN-B GENE
    BARROSO, LA
    WANG, SZ
    PHELPS, CJ
    JOHNSON, JL
    WILKINS, TD
    [J]. NUCLEIC ACIDS RESEARCH, 1990, 18 (13) : 4004 - 4004
  • [8] CLOSTRIDIUM-DIFFICILE - HISTORY OF ITS ROLE AS AN ENTERIC PATHOGEN AND THE CURRENT STATE OF KNOWLEDGE ABOUT THE ORGANISM
    BARTLETT, JG
    [J]. CLINICAL INFECTIOUS DISEASES, 1994, 18 : S265 - S272
  • [9] Antibiotic-associated diarrhea
    Bartlett, JG
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (05) : 334 - 339
  • [10] Development of a new PCR-ribotyping method for Clostridium difficile based on ribosomal RNA gene sequencing
    Bidet, P
    Barbut, F
    Lalande, V
    Burghoffer, B
    Petit, JC
    [J]. FEMS MICROBIOLOGY LETTERS, 1999, 175 (02) : 261 - 266