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Pyrazinamide susceptibility testing in Mycobacterium tuberculosis using the fast resazurin microtiter assay plate

dc.contributor.authorPina, R. Z.
dc.contributor.authorCaleffi-Ferracioli, K. R.
dc.contributor.authorCampanerut-Sa, R. A. Z.
dc.contributor.authorGhiraldi-Lopez, L. D.
dc.contributor.authorPavan, F. R. [UNESP]
dc.contributor.authorSiqueira, V. L. D.
dc.contributor.authorScodro, R. B. L.
dc.contributor.authorCardoso, R. F.
dc.contributor.institutionUniversidade Estadual de Maringá (UEM)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-11-26T15:31:40Z
dc.date.available2018-11-26T15:31:40Z
dc.date.issued2016-11-01
dc.description.abstractSETTING: Department of Clinical Analysis and Biomedicine, State University of Maringa, Maringa, PR, Brazil. OBJECTIVE: To evaluate the performance of the resazurin microtiter assay (REMA) plate at pH 5.5 in detecting Mycobacterium tuberculosis susceptibility to pyrazinamide (PZA). DESIGN: The minimal inhibitory concentration (MIC) of PZA in M. tuberculosis H(37)Rv and M. bovis AN5 reference strains and in 34 clinical M. tuberculosis isolates (26 PZA-susceptible and eight PZA-resistant) was determined using REMA at pH 5.5 and compared to REMA at pH 6.0. RESULTS: REMA at pH 5.5 was helpful in discriminating PZA-susceptible from resistant M. tuberculosis isolates when <= 50 mu g/ml PZA was considered as the cut-off for PZA susceptibility. Furthermore, it provided results in 8 days. However, two PZA-resistant isolates failed to grow at pH 5.5. CONCLUSION: As the REMA method is rapid, inexpensive, easy to perform and read, it would be of great usefulness in low-income countries for detecting PZA-resistant M. tuberculosis. REMA at pH 5.6-5.9 should be evaluated on an extended panel of clinical M. tuberculosis isolates with a greater range of MIC values in different laboratories for a better understanding of its utility in differentiating PZA-resistant from PZA-susceptible isolates.en
dc.description.affiliationUniv Estadual Maringa, Postgrad Programme Hlth Sci, Maringa, Parana, Brazil
dc.description.affiliationUniv Estadual Maringa, Dept Clin Anal & Biomed, Maringa, Parana, Brazil
dc.description.affiliationSao Paulo State Univ, Sch Pharmaceut Sci, Sao Paulo, Brazil
dc.description.affiliationUnespSao Paulo State Univ, Sch Pharmaceut Sci, Sao Paulo, Brazil
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.format.extent1535-1538
dc.identifierhttp://dx.doi.org/10.5588/ijtld.16.0304
dc.identifier.citationInternational Journal Of Tuberculosis And Lung Disease. Paris: Int Union Against Tuberculosis Lung Disease (i U A T L D), v. 20, n. 11, p. 1535-1538, 2016.
dc.identifier.doi10.5588/ijtld.16.0304
dc.identifier.issn1027-3719
dc.identifier.urihttp://hdl.handle.net/11449/159169
dc.identifier.wosWOS:000386986700020
dc.language.isoeng
dc.publisherInt Union Against Tuberculosis Lung Disease (i U A T L D)
dc.relation.ispartofInternational Journal Of Tuberculosis And Lung Disease
dc.relation.ispartofsjr1,533
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.subjecttuberculosis
dc.subjectPZA resistance
dc.subjectREMA
dc.titlePyrazinamide susceptibility testing in Mycobacterium tuberculosis using the fast resazurin microtiter assay plateen
dc.typeArtigopt
dcterms.rightsHolderInt Union Against Tuberculosis Lung Disease (i U A T L D)
dspace.entity.typePublication
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt

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