Isolation and characterisation of toxin A-negative, toxin B-positive Clostridium difficile in Dublin, Ireland

被引:65
作者
Drudy, D. [1 ]
Harnedy, N.
Fanning, S.
O'Mahony, R.
Kyne, L.
机构
[1] Univ Coll Dublin, Ctr Food Safety, Sch Agr Food Sci & Vet Med, Dublin 4, Ireland
[2] Mater Misericordiae Univ Hosp, Dept Med Older Person, Dublin 7, Ireland
关键词
Clostridium difficile; cytotoxicity assay; ELISA; molecular characterisation; PCR; toxins;
D O I
10.1111/j.1469-0691.2006.01634.x
中图分类号
R51 [传染病];
学科分类号
100401 [流行病与卫生统计学];
摘要
Clostridium difficile is a major cause of infectious diarrhoea in hospitalised patients. Most pathogenic C. difficile strains produce two toxins, A and B; however, clinically relevant toxin A-negative, toxin B-positive (A(-)B(+)) strains of C. difficile that cause diarrhoea and colitis in humans have been isolated worldwide. The aims of this study were to isolate and characterise A(-)B(+) strains from two university hospitals in Dublin, Ireland. Samples positive for C. difficile were identified daily by review of ELISA results and were cultured on selective media. Following culture, toxin-specific immunoassays, IMR-90 cytotoxicity assays and PCR were used to analyse consecutive C. difficile isolates from 93 patients. Using a toxin A-specific ELISA, 52 samples produced detectable toxin. All isolates were positive using a toxin A/B ELISA. Similarly, all isolates were positive with the cytoxicity assay, although variant cytopathic effects were observed in 41 cases. PCR amplification of the toxin A and toxin B genes revealed that 41 of the previous A(-)B(+) strains had a c. 1.7-kb deletion in the 3'-end of the tcdA gene. Restriction enzyme analysis of these amplicons revealed the loss of polymorphic restriction sites. These 41 A(-)B(+) isolates were designated toxinotype VIII by comparison with C. difficile strain 1470. PCR ribotyping revealed that all A(-)B(+) isolates belonged to PCR-ribotype 017. A(-)B(+)C. difficile isolates accounted for 44% of the isolates examined in this study, and appeared to be isolated more frequently in Dublin, Ireland, than reported rates for other countries.
引用
收藏
页码:298 / 304
页数:7
相关论文
共 38 条
[1]
al-Barrak A, 1999, Can Commun Dis Rep, V25, P65
[2]
Characterization of a toxin A-negative, toxin B-positive strain of Clostridium difficile responsible for a nosocomial outbreak of Clostridium difficile-associated diarrhea [J].
Alfa, MJ ;
Kabani, A ;
Lyerly, D ;
Moncrief, S ;
Neville, LM ;
Al-Barrak, A ;
Harding, GKH ;
Dyck, B ;
Olekson, K ;
Embil, JM .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (07) :2706-2714
[3]
[Anonymous], CLIN MICROBIOL IN S2
[4]
Secular trends in hospital-acquired Clostridium difficile disease in the United States, 1987-2001 [J].
Archibald, LK ;
Banerjee, SN ;
Jarvis, WR .
JOURNAL OF INFECTIOUS DISEASES, 2004, 189 (09) :1585-1589
[5]
A European survey of diagnostic methods and testing protocols for Clostridium difficile [J].
Barbut, F ;
Delmée, M ;
Brazier, JS ;
Petit, JC ;
Poxton, IR ;
Rupnik, M ;
Lalande, V ;
Schneider, C ;
Mastrantonio, P ;
Alonso, R ;
Kuipjer, E ;
Tvede, M .
CLINICAL MICROBIOLOGY AND INFECTION, 2003, 9 (10) :989-996
[6]
Prevalence and genetic characterization of toxin A variant strains of Clostridium difficile among adults and children with diarrhea in France [J].
Barbut, F ;
Lalande, V ;
Burghoffer, B ;
Thien, HV ;
Grimprel, E ;
Petit, JC .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (06) :2079-2083
[7]
Antibiotic-associated diarrhea [J].
Bartlett, JG .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (05) :334-339
[8]
MOLECULAR, IMMUNOLOGICAL, AND BIOLOGICAL CHARACTERIZATION OF A TOXIN-A-NEGATIVE, TOXIN-B-POSITIVE STRAIN OF CLOSTRIDIUM-DIFFICILE [J].
BORRIELLO, SP ;
WREN, BW ;
HYDE, S ;
SEDDON, SV ;
SIBBONS, P ;
KRISHNA, MM ;
TABAQCHALI, S ;
MANEK, S ;
PRICE, AB .
INFECTION AND IMMUNITY, 1992, 60 (10) :4192-4199
[9]
ANALYSIS OF LATEX AGGLUTINATION-TEST FOR CLOSTRIDIUM-DIFFICILE TOXIN-A (D-1) AND DIFFERENTIATION BETWEEN CLOSTRIDIUM-DIFFICILE TOXIN-A AND TOXIN-B AND LATEX REACTIVE PROTEIN [J].
BORRIELLO, SP ;
BARCLAY, FE ;
REED, PJ ;
WELCH, AR ;
BROWN, JD ;
BURDON, DW .
JOURNAL OF CLINICAL PATHOLOGY, 1987, 40 (05) :573-580
[10]
Brazier JS, 1999, J HOSP INFECT, V42, P248