Literature DB >> 20890081

Investigation of toxin gene diversity, molecular epidemiology, and antimicrobial resistance of Clostridium difficile isolated from 12 hospitals in South Korea.

Heejung Kim1, Seok Hoon Jeong, Kyoung Ho Roh, Seong Geun Hong, Jong Wan Kim, Myung-Geun Shin, Mi-Na Kim, Hee Bong Shin, Young Uh, Hyukmin Lee, Kyungwon Lee.   

Abstract

BACKGROUND: Clostridium difficile is a major cause of antibiotic-associated diarrhea. The objective of this study was to characterize clinical isolates of C. difficile obtained from various regions in Korea with regard to their toxin status, molecular type, and antimicrobial susceptibility.
METHODS: We analyzed a total of 408 C. difficile isolates obtained between 2006 and 2008 from 408 patients with diarrhea in 12 South Korean teaching hospitals. C. difficile toxin genes tcdA, tcdB, cdtA, and cdtB were detected by PCR. Molecular genotyping was performed by PCR ribotyping. Antimicrobial susceptibilities of the 120 C. difficile isolates were assessed by agar dilution methods.
RESULTS: Among 337 toxigenic isolates, 105 were toxin A-negative and toxin B-positive (A(-)B(+)) and 29 were binary toxin-producing strains. PCR ribotyping showed 50 different ribotype patterns. The 5 most frequently occurring ribotypes comprised 62.0% of all identified ribotypes. No isolate was susceptible to cefoxitin, and all except 1 were susceptible to piperacillin and piperacillin-tazobactam. The resistance rates of isolates to imipenem, cefotetan, moxifloxacin, ampicillin, and clindamycin were 25%, 34%, 42%, 51%, and 60%, respectively. The isolates showed no resistance to metronidazole or vancomycin.
CONCLUSIONS: This is the first nationwide study on the toxin status, including PCR ribotyping and antimicrobial resistance, of C. difficile isolates in Korea. The prevalence of A-B+ strains was 25.7%, much higher than that reported from other countries. Binary toxin-producing strains accounted for 7.1% of all strains, which was not rare in Korea. The most prevalent ribotype was ribotype 017, and all A-B+ strains showed this pattern. We did not isolate strains with decreased susceptibility to metronidazole or vancomycin.

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Year:  2010        PMID: 20890081     DOI: 10.3343/kjlm.2010.30.5.491

Source DB:  PubMed          Journal:  Korean J Lab Med        ISSN: 1598-6535


  33 in total

1.  Clostridium difficile ribotype diversity at six health care institutions in the United States.

Authors:  Sheila Waslawski; Eugene S Lo; Sarah A Ewing; Vincent B Young; David M Aronoff; Susan E Sharp; Susan M Novak-Weekley; Arthur E Crist; W Michael Dunne; Joan Hoppe-Bauer; Michelle Johnson; Stephen M Brecher; Duane W Newton; Seth T Walk
Journal:  J Clin Microbiol       Date:  2013-04-03       Impact factor: 5.948

2.  Molecular and microbiological characterization of Clostridium difficile isolates from single, relapse, and reinfection cases.

Authors:  Kentaro Oka; Takako Osaki; Tomoko Hanawa; Satoshi Kurata; Mitsuhiro Okazaki; Taki Manzoku; Motomichi Takahashi; Mamoru Tanaka; Haruhiko Taguchi; Takashi Watanabe; Takashi Inamatsu; Shigeru Kamiya
Journal:  J Clin Microbiol       Date:  2012-01-11       Impact factor: 5.948

3.  Characterizations of clinical isolates of clostridium difficile by toxin genotypes and by susceptibility to 12 antimicrobial agents, including fidaxomicin (OPT-80) and rifaximin: a multicenter study in Taiwan.

Authors:  Chun-Hsing Liao; Wen-Chien Ko; Jang-Jih Lu; Po-Ren Hsueh
Journal:  Antimicrob Agents Chemother       Date:  2012-04-16       Impact factor: 5.191

4.  Molecular epidemiology of Clostridium difficile infection in a major chinese hospital: an underrecognized problem in Asia?

Authors:  Peter M Hawkey; Clare Marriott; Wen En Liu; Zi Juan Jian; Qian Gao; Thomas Kin Wah Ling; Viola Chow; Erica So; Raphael Chan; Katie Hardy; Li Xu; Susan Manzoor
Journal:  J Clin Microbiol       Date:  2013-07-31       Impact factor: 5.948

5.  Extended multilocus variable-number tandem-repeat analysis of Clostridium difficile correlates exactly with ribotyping and enables identification of hospital transmission.

Authors:  S E Manzoor; H E Tanner; C L Marriott; J S Brazier; K J Hardy; S Platt; P M Hawkey
Journal:  J Clin Microbiol       Date:  2011-08-17       Impact factor: 5.948

6.  Toxin A-negative toxin B-positive ribotype 017 Clostridium difficile is the dominant strain type in patients with diarrhoea attending tuberculosis hospitals in Cape Town, South Africa.

Authors:  B Kullin; J Wojno; V Abratt; S J Reid
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2016-09-30       Impact factor: 3.267

7.  Characterisation of Clostridium difficile strains isolated from Groote Schuur Hospital, Cape Town, South Africa.

Authors:  B Kullin; T Brock; N Rajabally; F Anwar; G Vedantam; S Reid; V Abratt
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2016-07-27       Impact factor: 3.267

Review 8.  Clostridium difficile Infection.

Authors:  Jae Hyun Shin; Esteban Chaves-Olarte; Cirle A Warren
Journal:  Microbiol Spectr       Date:  2016-06

9.  Evaluation of the Xpert Clostridium difficile assay for the diagnosis of Clostridium difficile infection.

Authors:  Saeam Shin; Minkyung Kim; Myungsook Kim; Heejung Lim; Heejung Kim; Kyungwon Lee; Yunsop Chong
Journal:  Ann Lab Med       Date:  2012-08-13       Impact factor: 3.464

10.  Susceptibility of hamsters to Clostridium difficile isolates of differing toxinotype.

Authors:  Anthony M Buckley; Janice Spencer; Lindsay M Maclellan; Denise Candlish; June J Irvine; Gillian R Douce
Journal:  PLoS One       Date:  2013-05-21       Impact factor: 3.240

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