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The changes of PCR ribotype and antimicrobial resistance of Clostridium difficile in a tertiary care hospital over 10 years

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dc.contributor.authorLee, Jong-Han-
dc.contributor.authorLee, Yang soon-
dc.contributor.authorLee, Kyungwon-
dc.contributor.authorRiley, Thomas V.-
dc.contributor.authorKim, Heejung-
dc.date.accessioned2022-07-16T04:19:29Z-
dc.date.available2022-07-16T04:19:29Z-
dc.date.created2021-05-13-
dc.date.issued2014-06-
dc.identifier.issn0022-2615-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/159691-
dc.description.abstractThe aims of this study were to investigate any change in PCR ribotypes and to determine the antimicrobial resistance of common PCR ribotypes over a 10-year period in a tertiary care hospital. We conducted PCR ribotyping, antimicrobial susceptibility testing and DNA gyrase sequencing to identify changes in 1407 Clostridium difficile non-duplicated isolates obtained between 2000 and 2009. A total of 74 different ribotypes were found. The most prevalent ribotype was ribotype 001 (26.1 %). The prevalence of ribotype 017 was 17% and that of ribotype 014/020 was 9.6 %. Ribotyping showed that the prevalence of ribotype 001 decreased and the prevalence of ribotypes 017, 014/020 and 018 increased over the 10 years. Antimicrobial resistance rates in prevalent ribotypes were: clindamycin, 81 %; cefotetan, 19%; moxifloxacin, 42 %; imipenem, 8%; ciprofloxacin, 100% and erythromycin, 80 %. Ribotype 018 showed greater antimicrobial resistance than other ribotypes. All ribotype 018 strains showing moxifloxacin resistance had a substitution of a gyrA coding amino acid (Thr82 to Ile). This study will help the understanding of PCR ribotype trends and antimicrobial resistance of C. difficile in Korea.-
dc.language영어-
dc.language.isoen-
dc.publisherSOC GENERAL MICROBIOLOGY-
dc.titleThe changes of PCR ribotype and antimicrobial resistance of Clostridium difficile in a tertiary care hospital over 10 years-
dc.typeArticle-
dc.contributor.affiliatedAuthorLee, Yang soon-
dc.identifier.doi10.1099/jmm.0.072082-0-
dc.identifier.scopusid2-s2.0-84901365137-
dc.identifier.wosid000338815500007-
dc.identifier.bibliographicCitationJOURNAL OF MEDICAL MICROBIOLOGY, v.63, no.6, pp.819 - 823-
dc.relation.isPartOfJOURNAL OF MEDICAL MICROBIOLOGY-
dc.citation.titleJOURNAL OF MEDICAL MICROBIOLOGY-
dc.citation.volume63-
dc.citation.number6-
dc.citation.startPage819-
dc.citation.endPage823-
dc.type.rimsART-
dc.type.docType정기학술지(Article(Perspective Article포함))-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaMicrobiology-
dc.relation.journalWebOfScienceCategoryMicrobiology-
dc.subject.keywordPlusBINARY TOXIN-
dc.subject.keywordPlusMOXIFLOXACIN-
dc.subject.keywordPlusINFECTIONS-
dc.subject.keywordPlusMUTATIONS-
dc.subject.keywordPlusGYRB-
dc.identifier.urlhttps://www.microbiologyresearch.org/content/journal/jmm/10.1099/jmm.0.072082-0-
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