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Diversity of binary toxin positive Clostridioides difficile in Korea

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dc.contributor.authorKim, Jieun-
dc.contributor.authorKim, Bongyoung-
dc.contributor.authorPai, Hyunjoo-
dc.date.accessioned2023-07-05T02:34:38Z-
dc.date.available2023-07-05T02:34:38Z-
dc.date.created2023-02-08-
dc.date.issued2023-01-
dc.identifier.issn2045-2322-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/186072-
dc.description.abstractThe objective of this study is to determine the trend and diversity of binary toxin-positive Clostridioides difficile over 10 years in Korea. Binary toxin-positive strains were selected from a tertiary hospital in Korea in 2009–2018. The multi-locus sequence typing and antibiotic susceptibility test were performed. Among the 3278 isolates in 2009–2018, 58 possessed binary toxin genes (1.7%). The proportion of CDT- positive isolates was 0.51–4.82% in 2009–2018, which increased over the 10-year period (P = 0.023). Thirteen sequence types (STs) were identified; ST5 (14 [24%]), ST11 (11 [19%]), ST221 (10 [17%]), ST201 (7 [12%]) and ST1 (5 [9%]) were popular. All 58 isolates were susceptible to vancomycin and piperacillin/tazobactam, and clindamycin and moxifloxacin were active in 69.0% and 62% of isolates, respectively. ST1 strains were resistant to several antibiotics, including moxifloxacin (80%), clindamycin (60%) and rifaximin (60%). Moreover, four of five ST1 presented a metronidazole minimum inhibitory concentration of 4 µg/mL. Moxifloxacin resistance was highest (72.3%) for ST11. In conclusion, binary toxin-positive strains are non-prevalent in Korea and involve diverse STs. ST1 strains were resistant to several antibiotics.-
dc.language영어-
dc.language.isoen-
dc.publisherNATURE PORTFOLIO-
dc.titleDiversity of binary toxin positive Clostridioides difficile in Korea-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Jieun-
dc.contributor.affiliatedAuthorKim, Bongyoung-
dc.contributor.affiliatedAuthorPai, Hyunjoo-
dc.identifier.doi10.1038/s41598-023-27768-0-
dc.identifier.scopusid2-s2.0-85146140717-
dc.identifier.wosid000986510100029-
dc.identifier.bibliographicCitationSCIENTIFIC REPORTS, v.13, no.1, pp.1 - 6-
dc.relation.isPartOfSCIENTIFIC REPORTS-
dc.citation.titleSCIENTIFIC REPORTS-
dc.citation.volume13-
dc.citation.number1-
dc.citation.startPage1-
dc.citation.endPage6-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.subject.keywordPlusPCR RIBOTYPE 027-
dc.subject.keywordPlusSTRAIN-
dc.subject.keywordPlusEPIDEMIOLOGY-
dc.subject.keywordPlusINFECTION-
dc.subject.keywordPlusREGION-
dc.subject.keywordPlusHUMANS-
dc.identifier.urlhttps://www.nature.com/articles/s41598-023-27768-0-
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