Publication:
Drug Susceptibility Testing of Mycobacterium Tuberculosis by the Broth Microdilution Method With 7H9 Broth

dc.authorscopusid7007135107
dc.authorscopusid6701577980
dc.authorscopusid6603655021
dc.authorscopusid7003532093
dc.contributor.authorÇoban, A.Y.
dc.contributor.authorBirinci, A.
dc.contributor.authorEkinci, B.
dc.contributor.authorDurupínar, B.
dc.date.accessioned2020-06-21T15:43:22Z
dc.date.available2020-06-21T15:43:22Z
dc.date.issued2004
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Çoban] Ahmet Yilmaz, Department of Microbiology and Clinical Microbiology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Birinci] Asuman, Department of Microbiology and Clinical Microbiology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Ekinci] Bora, Department of Microbiology and Clinical Microbiology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Durupínar] Belma, Department of Microbiology and Clinical Microbiology, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractIn this study, we have evaluated the broth microdilution method (BMM) for susceptibility testing of Mycobacterium tuberculosis. A total of 43 clinical isolates of M. tuberculosis and H37Rv as a control strain were studied. All isolates were tested by the proportion method and the BMM for isoniazid (INH), rifampicin (RIF), streptomycin (STR), and ethambutol (ETM). The proportion method was carried out according to the National Committee for Clinical Laboratory Standards (NCCLS) on Löwenstein-Jensen (LJ) medium. The BMM was carried out using 7H9 broth with 96 well-plates. All strains were tested at 3.2-0.05 μg/ml, 16-0.25 μg/ml, 32-0.5 μg/ml, and 32-0.5 μg/ml concentrations for INH, RIF, STR, and ETM, respectively. When the BMM was compared with the proportion method, sensitivity was 100, 100, 96.9, and 90.2%, while specificity was 100, 85.7, 90.9, and 100% for INH, RIF, STR, and ETM, respectively. The plates were examined 7, 10, 14, and 21 days after incubation. The majority of the result were obtained at 14th days after incubation, while the proportion method result were ended in 21-28 days. According to our results, it may be suggested that the BMM is suitable for early determining of multidrug-resistance-M. tuberculosis strains in developed or developing countries.en_US
dc.identifier.doi10.1590/S0074-02762004000100020
dc.identifier.endpage113en_US
dc.identifier.issn0074-0276
dc.identifier.issn1678-8060
dc.identifier.issue1en_US
dc.identifier.pmid15057358
dc.identifier.scopus2-s2.0-1642485763
dc.identifier.scopusqualityQ2
dc.identifier.startpage111en_US
dc.identifier.urihttps://doi.org/10.1590/S0074-02762004000100020
dc.identifier.volume99en_US
dc.identifier.wosWOS:000220161500020
dc.identifier.wosqualityQ1
dc.language.isoenen_US
dc.publisherFundacao Oswaldo Cruzen_US
dc.relation.ispartofMemorias Do Instituto Oswaldo Cruzen_US
dc.relation.journalMemorias Do Instituto Oswaldo Cruzen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectBroth Microdilution Methoden_US
dc.subjectMycobacterium Tuberculosisen_US
dc.subjectSusceptibility Testingen_US
dc.titleDrug Susceptibility Testing of Mycobacterium Tuberculosis by the Broth Microdilution Method With 7H9 Brothen_US
dc.typeArticleen_US
dspace.entity.typePublication

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