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Geographic Differences in the Contribution of ubiA Mutations to High-Level Ethambutol Resistance in Mycobacterium tuberculosis

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dc.contributor.author조상래-
dc.date.accessioned2017-10-26T07:27:58Z-
dc.date.available2017-10-26T07:27:58Z-
dc.date.issued2016-
dc.identifier.issn0066-4804-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/152068-
dc.description.abstractEthambutol (EMB) resistance can evolve through a multistep process, and mutations in the ubiA (Rv3806c) gene appear to be responsible for high-level EMB resistance in Mycobacterium tuberculosis We evaluated the prevalence of ubiA and embB (Rv3795) mutations in EMB-resistant strains originating from Africa and South Korea. No differences in embB mutation frequencies were observed between strains from both origins. However, ubiA mutations were present in 45.5% ± 6.5% of the African EMB-resistant isolates but in only 9.5% ± 1.5% of the South Korean EMB-resistant isolates. The ubiA mutations associated with EMB resistance were localized to regions encoding the transmembrane domains of the protein, whereas the embB mutations were localized to regions encoding the extramembrane domains. Larger studies are needed to investigate the causes of increased ubiA mutations as a pathway to high-level EMB resistance in African countries, such as extended EMB usage during tuberculosis treatment.-
dc.description.statementOfResponsibilityopen-
dc.publisherAmerican Society for Microbiology-
dc.relation.isPartOfANTIMICROBIAL AGENTS AND CHEMOTHERAPY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAntitubercular Agents/pharmacology* Bacterial Proteins/genetics Drug Resistance, Bacterial/genetics Ethambutol/pharmacology* Microbial Sensitivity Tests Mutation/genetics* Mycobacterium tuberculosis/drug effects* Mycobacterium tuberculosis/genetics*-
dc.titleGeographic Differences in the Contribution of ubiA Mutations to High-Level Ethambutol Resistance in Mycobacterium tuberculosis-
dc.typeArticle-
dc.publisher.locationUnited States-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Microbiology-
dc.contributor.googleauthorSubramanya Lingaraju-
dc.contributor.googleauthorLeen Rigouts-
dc.contributor.googleauthorAditi Gupta-
dc.contributor.googleauthorJongseok Lee-
dc.contributor.googleauthorAlaine Nyaruhirira Umubyeyi-
dc.contributor.googleauthorAmy L. Davidow-
dc.contributor.googleauthorSusan German-
dc.contributor.googleauthorEunJin Cho-
dc.contributor.googleauthorJi-im Lee-
dc.contributor.googleauthorSang-Nae Cho-
dc.contributor.googleauthorCheon Tae Kim-
dc.contributor.googleauthorDavid Alland-
dc.contributor.googleauthorHassan Safi-
dc.identifier.doi10.1128/AAC.03002-15-
dc.contributor.localIdA03824-
dc.relation.journalcodeJ00189-
dc.identifier.eissn1098-6596-
dc.identifier.pmid27139478-
dc.contributor.alternativeNameCho, Sang Nae-
dc.contributor.affiliatedAuthorCho, Sang Nae-
dc.citation.volume60-
dc.citation.number7-
dc.citation.startPage4101-
dc.citation.endPage4105-
dc.identifier.bibliographicCitationANTIMICROBIAL AGENTS AND CHEMOTHERAPY, Vol.60(7) : 4101-4105, 2016-
dc.date.modified2017-10-24-
dc.identifier.rimsid46848-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Microbiology (미생물학교실) > 1. Journal Papers

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