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Genomic analysis of globally diverse Mycobacterium tuberculosis strains provides insights into the emergence and spread of multidrug resistance

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dc.contributor.author조상래-
dc.date.accessioned2023-08-09T02:47:27Z-
dc.date.available2023-08-09T02:47:27Z-
dc.date.issued2017-03-
dc.identifier.issn1061-4036-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/195834-
dc.description.abstractMultidrug-resistant tuberculosis (MDR-TB), caused by drug-resistant strains of Mycobacterium tuberculosis, is an increasingly serious problem worldwide. Here we examined a data set of whole-genome sequences from 5,310 M. tuberculosis isolates from five continents. Despite the great diversity of these isolates with respect to geographical point of isolation, genetic background and drug resistance, the patterns for the emergence of drug resistance were conserved globally. We have identified harbinger mutations that often precede multidrug resistance. In particular, the katG mutation encoding p.Ser315Thr, which confers resistance to isoniazid, overwhelmingly arose before mutations that conferred rifampicin resistance across all of the lineages, geographical regions and time periods. Therefore, molecular diagnostics that include markers for rifampicin resistance alone will be insufficient to identify pre-MDR strains. Incorporating knowledge of polymorphisms that occur before the emergence of multidrug resistance, particularly katG p.Ser315Thr, into molecular diagnostics should enable targeted treatment of patients with pre-MDR-TB to prevent further development of MDR-TB.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherNature Pub. Co.-
dc.relation.isPartOfNATURE GENETICS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAntitubercular Agents / therapeutic use-
dc.subject.MESHBacterial Proteins / genetics-
dc.subject.MESHCatalase / genetics-
dc.subject.MESHDrug Resistance, Multiple, Bacterial / genetics*-
dc.subject.MESHGenomics / methods-
dc.subject.MESHHumans-
dc.subject.MESHIsoniazid / therapeutic use-
dc.subject.MESHMutation / genetics-
dc.subject.MESHMycobacterium tuberculosis / drug effects-
dc.subject.MESHMycobacterium tuberculosis / genetics*-
dc.subject.MESHPolymorphism, Genetic / genetics-
dc.subject.MESHRifampin / therapeutic use-
dc.subject.MESHTuberculosis, Multidrug-Resistant / drug therapy-
dc.subject.MESHTuberculosis, Multidrug-Resistant / genetics*-
dc.titleGenomic analysis of globally diverse Mycobacterium tuberculosis strains provides insights into the emergence and spread of multidrug resistance-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Microbiology (미생물학교실)-
dc.contributor.googleauthorAbigail L Manson-
dc.contributor.googleauthorKeira A Cohen-
dc.contributor.googleauthorThomas Abeel-
dc.contributor.googleauthorChristopher A Desjardins-
dc.contributor.googleauthorDerek T Armstrong-
dc.contributor.googleauthorClifton E Barry 3rd-
dc.contributor.googleauthorJeannette Brand TBResist Global Genome Consortium-
dc.contributor.googleauthorSinéad B Chapman-
dc.contributor.googleauthorSang-Nae Cho-
dc.contributor.googleauthorAndrei Gabrielian-
dc.contributor.googleauthorJames Gomez-
dc.contributor.googleauthorAndreea M Jodals-
dc.contributor.googleauthorMoses Joloba-
dc.contributor.googleauthorPontus Jureen-
dc.contributor.googleauthorJong Seok Lee-
dc.contributor.googleauthorLesibana Malinga-
dc.contributor.googleauthorMamoudou Maiga-
dc.contributor.googleauthorDale Nordenberg-
dc.contributor.googleauthorEcaterina Noroc-
dc.contributor.googleauthorElena Romancenco-
dc.contributor.googleauthorAlex Salazar-
dc.contributor.googleauthorWilly Ssengooba-
dc.contributor.googleauthorA A Velayati-
dc.contributor.googleauthorKathryn Winglee-
dc.contributor.googleauthorAksana Zalutskaya-
dc.contributor.googleauthorLaura E Via-
dc.contributor.googleauthorGail H Cassell-
dc.contributor.googleauthorSusan E Dorman-
dc.contributor.googleauthorJerrold Ellner-
dc.contributor.googleauthorParissa Farnia-
dc.contributor.googleauthorJames E Galagan-
dc.contributor.googleauthorAlex Rosenthal-
dc.contributor.googleauthorValeriu Crudu-
dc.contributor.googleauthorDaniela Homorodean-
dc.contributor.googleauthorPo-Ren Hsueh-
dc.contributor.googleauthorSujatha Narayanan-
dc.contributor.googleauthorAlexander S Pym-
dc.contributor.googleauthorAlena Skrahina-
dc.contributor.googleauthorSoumya Swaminathan-
dc.contributor.googleauthorMartie Van der Walt-
dc.contributor.googleauthorDavid Alland-
dc.contributor.googleauthorWilliam R Bishai-
dc.contributor.googleauthorTed Cohen-
dc.contributor.googleauthorSven Hoffner-
dc.contributor.googleauthorBruce W Birren-
dc.contributor.googleauthorAshlee M Earl-
dc.identifier.doi10.1038/ng.3767-
dc.contributor.localIdA03824-
dc.relation.journalcodeJ02294-
dc.identifier.eissn1546-1718-
dc.identifier.pmid28092681-
dc.contributor.alternativeNameCho, Sang Nae-
dc.contributor.affiliatedAuthor조상래-
dc.citation.volume49-
dc.citation.number3-
dc.citation.startPage395-
dc.citation.endPage402-
dc.identifier.bibliographicCitationNATURE GENETICS, Vol.49(3) : 395-402, 2017-03-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Microbiology (미생물학교실) > 1. Journal Papers

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