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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/68414
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dc.contributor.authorFujimura Leite, Clarisse Queico-
dc.contributor.authorDa Silva Rocha, Adalgiza-
dc.contributor.authorDe Andrade Leite, Sergio Roberto-
dc.contributor.authorCarvalho Ferreira, Rosa Maria-
dc.contributor.authorSuffys, Philip N.-
dc.contributor.authorFonseca, Lella de Souza-
dc.contributor.authorFéres Saad, Maria Helena-
dc.date.accessioned2014-05-27T11:21:37Z-
dc.date.accessioned2016-10-25T18:21:08Z-
dc.date.available2014-05-27T11:21:37Z-
dc.date.available2016-10-25T18:21:08Z-
dc.date.issued2005-09-21-
dc.identifierhttp://dx.doi.org/10.1111/j.1348-0421.2005.tb03642.x-
dc.identifier.citationMicrobiology and Immunology, v. 49, n. 7, p. 571-578, 2005.-
dc.identifier.issn0385-5600-
dc.identifier.urihttp://hdl.handle.net/11449/68414-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/68414-
dc.description.abstractThe development of fast, inexpensive, and reliable tests to identify nontuberculous mycobacteria (NTM) is needed. Studies have indicated that the conventional identification procedures, including biochemical assays, are imprecise. This study evaluated a proposed alternative identification method in which 83 NTM isolates, previously identified by conventional biochemical testing and in-house M. avium IS1245-PCR amplification, were submitted to the following tests: thin-layer chromatography (TLC) of mycolic acids and PCR-restriction enzyme analysis of hsp65 (PRA). High-performance liquid chromatography (HPLC) analysis of mycolic acids and Southern blot analysis for M. avium IS1245 were performed on the strains that evidenced discrepancies on either of the above tests. Sixty-eight out of 83 (82%) isolates were concordantly identified by the presence of IS1245 and PRA and by TLC mycolic acid analysis. Discrepant results were found between the phenotypic and molecular tests in 12/83 (14.4%) isolates. Most of these strains were isolated from non-sterile body sites and were most probably colonizing in the host tissue. While TLC patterns suggested the presence of polymycobacterial infection in 3/83 (3.6%) cultures, this was the case in only one HPLC-tested culture and in none of those tested by PRA. The results of this study indicated that, as a phenotypic identification procedure, TLC mycolic acid determination could be considered a relatively simple and cost-effective method for routine screening of NTM isolates in mycobacteriology laboratory practice with a potential for use in developing countries. Further positive evidence was that this method demonstrated general agreement on MAC and M. simiae identification, including in the mixed cultures that predominated in the isolates of the disseminated infections in the AIDS patients under study. In view of the fact that the same treatment regimen is recommended for infections caused by these two species, TLC mycolic acid analysis may be a useful identification tool wherever molecular methods are unaffordable.en
dc.format.extent571-578-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectIS1245-
dc.subjectMycolic acids-
dc.subjectNontuberculous mycobacteria-
dc.subjectPRA-
dc.subjectTLC-
dc.subjectheat shock protein 65-
dc.subjectmycolic acid-
dc.subjectacquired immune deficiency syndrome-
dc.subjectatypical Mycobacterium-
dc.subjectbacterial colonization-
dc.subjectbacterial strain-
dc.subjectbacterium culture-
dc.subjectbacterium detection-
dc.subjectbacterium identification-
dc.subjectbacterium isolate-
dc.subjectbacterium isolation-
dc.subjectcontrolled study-
dc.subjectcost effectiveness analysis-
dc.subjectenzyme assay-
dc.subjecthigh performance liquid chromatography-
dc.subjectintermethod comparison-
dc.subjectmixed cell culture-
dc.subjectMycobacterium avium-
dc.subjectnonhuman-
dc.subjectphenotype-
dc.subjectpolymerase chain reaction-
dc.subjectrestriction mapping-
dc.subjectscreening test-
dc.subjectSouthern blotting-
dc.subjectsuperinfection-
dc.subjectthin layer chromatography-
dc.subjectBacterial Typing Techniques-
dc.subjectChromatography, Thin Layer-
dc.subjectDNA, Bacterial-
dc.subjectMycobacterium-
dc.subjectMycolic Acids-
dc.subjectatypical mycobacterium-
dc.subjectBacteria (microorganisms)-
dc.subjectCorynebacterineae-
dc.titleA comparison of mycolic acid analysis for nontuberculous mycobacteria identification by thin-layer chromatography and molecular methodsen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionOswaldo Cruz Institute-
dc.contributor.institutionUniversidade Federal do Rio de Janeiro (UFRJ)-
dc.contributor.institutionFIOCRUZ-
dc.description.affiliationDepartment of Pharmacy Institute of Chemistry UNESP, Araraquara, São Paulo-
dc.description.affiliationInstitute of Chemistry UNESP, Araraquara, São Paulo-
dc.description.affiliationDepartment of Mycobacterioses Evandro Chagas Hospital Oswaldo Cruz Institute, Fiocruz, Rio de Janeiro, R.J.-
dc.description.affiliationEvandro Chagas Hospital Oswaldo Cruz Institute, Fiocruz, Rio de Janeiro, R.J.-
dc.description.affiliationMycobacteriology Laboratory Microbiology Institute UFRJ, Rio de Janeiro, R.J.-
dc.description.affiliationMicrobiology Institute UFRJ, Rio de Janeiro, R.J.-
dc.description.affiliationDepartment of Mycobacterioses Instituto Oswaldo Cruz FIOCRUZ, Av. Brasil 4365, 21045-900 Rio de Janeiro, RJ-
dc.description.affiliationUnespDepartment of Pharmacy Institute of Chemistry UNESP, Araraquara, São Paulo-
dc.description.affiliationUnespInstitute of Chemistry UNESP, Araraquara, São Paulo-
dc.identifier.doi10.1111/j.1348-0421.2005.tb03642.x-
dc.identifier.wosWOS:000230410300001-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofMicrobiology and Immunology-
dc.identifier.scopus2-s2.0-24744437725-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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