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Cited 28 time in webofscience Cited 28 time in scopus
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Thiostrepton: A Novel Therapeutic Drug Candidate for Mycobacterium abscessus Infection

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dc.contributor.authorKim, Tae Ho-
dc.contributor.authorHanh, Bui Thi Bich-
dc.contributor.authorKim, Guehye-
dc.contributor.authorLee, Da-Gyum-
dc.contributor.authorPark, June-Woo-
dc.contributor.authorLee, So Eui-
dc.contributor.authorKim, Jae-Sung-
dc.contributor.authorKim, Byoung Soo-
dc.contributor.authorRyoo, Sungweon-
dc.contributor.authorJo, Eun-Kyeong-
dc.contributor.authorJang, Jichan-
dc.date.accessioned2022-12-26T14:17:40Z-
dc.date.available2022-12-26T14:17:40Z-
dc.date.issued2019-12-
dc.identifier.issn1420-3049-
dc.identifier.issn1420-3049-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/8473-
dc.description.abstractMycobacterium abscessus is a rapid-growing, multidrug-resistant, non-tuberculous mycobacterial species responsible for a variety of human infections, such as cutaneous and pulmonary infections. M. abscessus infections are very difficult to eradicate due to the natural and acquired multidrug resistance profiles of M. abscessus. Thus, there is an urgent need for the development of effective drugs or regimens against M. abscessus infections. Here, we report the activity of a US Food and Drug Administration approved drug, thiostrepton, against M. abscessus. We found that thiostrepton significantly inhibited the growth of M. abscessus wild-type strains, subspecies, clinical isolates, and drug-resistant mutants in vitro and in macrophages. In addition, treatment of macrophages with thiostrepton significantly decreased proinflammatory cytokine production in a dose-dependent manner, suggesting an inhibitory effect of thiostrepton on inflammation induced during M. abscessus infection. We further showed that thiostrepton exhibits antimicrobial effects in vivo using a zebrafish model of M. abscessus infection.-
dc.language영어-
dc.language.isoENG-
dc.publisherMDPI-
dc.titleThiostrepton: A Novel Therapeutic Drug Candidate for Mycobacterium abscessus Infection-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.3390/molecules24244511-
dc.identifier.scopusid2-s2.0-85076489950-
dc.identifier.wosid000507299600089-
dc.identifier.bibliographicCitationMOLECULES, v.24, no.24-
dc.citation.titleMOLECULES-
dc.citation.volume24-
dc.citation.number24-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusRESISTANCE-
dc.subject.keywordPlusEFFICACY-
dc.subject.keywordPlusCLARITHROMYCIN-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusMODEL-
dc.subject.keywordPlusHOST-
dc.subject.keywordAuthorthiostrepton-
dc.subject.keywordAuthorMycobacterium abscessus-
dc.subject.keywordAuthorzebrafish bacterial infection-
dc.subject.keywordAuthordrug resistance-
dc.subject.keywordAuthornon-tuberculous mycobacteria-
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