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결핵균과 비결핵성항산균 검출에 Real-time PCR의 유용성

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dc.contributor.author윤은영-
dc.contributor.author조수희-
dc.contributor.author고세일-
dc.contributor.author백종하-
dc.contributor.author김유은-
dc.contributor.author마정은-
dc.contributor.author이기동-
dc.contributor.author조유지-
dc.contributor.author정이영-
dc.contributor.author김호철-
dc.contributor.author이종덕-
dc.contributor.author김선주-
dc.contributor.author황영실-
dc.date.accessioned2025-04-08T05:30:15Z-
dc.date.available2025-04-08T05:30:15Z-
dc.date.issued2010-10-
dc.identifier.issn1738-3536-
dc.identifier.issn2005-6184-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/77724-
dc.description.abstractBackground: The purpose of this study was to evaluate recently developed real-time polymerase chain reaction (PCR) assay kit to detect Mycobacterium tuberculosis (MTB) and nontuberculous mycobacteria (NTM) in respiratory specimens. Methods: We assessed the positive rate of the real-time PCR assay to detect MTB and NTM in 87 culture-positive specimens (37 sputum, 50 bronchial washing), which were performed real-time PCR by using Real-Q™ MTB&NTM Kit from January 2009 to June 2009, at Gyeongsang University Hospital. To compare the efficacy with the TB-PCR assay, we evaluated 63 culture-positive specimens (19 sputum, 44 bronchial washing) for MTB or NTM, which were performed TB-PCR by using ABSOLUTE™ MTB II PCR Kit from March 2008 to August 2008. Results: Among 87 specimens tested using real-time PCR, MTB and NTM were cultured in 58 and 29, respectively. The positive rate of real-time PCR assay to detect MTB was 71% (22/31) and 92.6% (25/27) in AFB stain-negative and stain-positive specimens. For NTM, the positive rate of real-time PCR was 11.1% (2/18) and 72.7% (8/11) in AFB stain-negative and stain-positive specimens. Among 63 specimens performed using TB-PCR, MTB and NTM were cultured in 46 and 17, respectively. The positive rate of TB-PCR was 61.7% (21/34) and 100% (12/12) in AFB stain-negative and stain-positive specimens. TB-PCR was negative in all NTM-cultured 17 specimens. Conclusion: TB/NTM real-time PCR assay is useful to differentiate MTB and NTM in AFB stain-positive respiratory specimens and it is as effective in detecting MTB with TB-PCR. Copyright©2010. The Korean Academy of Tuberculosis and Respiratory Diseases. All rights reserved.-
dc.format.extent6-
dc.language한국어-
dc.language.isoKOR-
dc.title결핵균과 비결핵성항산균 검출에 Real-time PCR의 유용성-
dc.title.alternativeUsefulness of real-time PCR to detect Mycobacterium tuberculosis and nontuberculous mycobacteria-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.4046/trd.2010.69.4.250-
dc.identifier.scopusid2-s2.0-78649381785-
dc.identifier.bibliographicCitationTuberculosis and Respiratory Diseases, v.69, no.4, pp 250 - 255-
dc.citation.titleTuberculosis and Respiratory Diseases-
dc.citation.volume69-
dc.citation.number4-
dc.citation.startPage250-
dc.citation.endPage255-
dc.type.docTypeArticle-
dc.identifier.kciidART001491444-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.subject.keywordAuthorMycobacteria, atypical-
dc.subject.keywordAuthorMycobacterium tuberculosis-
dc.subject.keywordAuthorPolymerase chain reaction, real-time-
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