Mycobacterium tuberculosis complex differentiation using gyrB-restriction fragment length polymorphism analysis
Autor(a) principal: | |
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Data de Publicação: | 2004 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1590/S0074-02762004000700014 http://repositorio.unifesp.br/handle/11600/2267 |
Resumo: | Mycobacterium tuberculosis complex (MTBC) members are causative agents of human and animal tuberculosis. Differentiation of MTBC members is required for appropriate treatment of individual patients and for epidemiological purposes. Strains from six MTBC species - M. tuberculosis, M. bovis subsp. bovis, M. bovis BCG, M. africanum, M. pinnipedii, and M. canetti - were studied using gyrB-restriction fragment length polymorphism (gyrB-RFLP) analysis. A table was elaborated, based on observed restriction patterns and published gyrB sequences. To evaluate applicability of gyrB-RFLP at Instituto Adolfo Lutz, São Paulo, Mycobacterial Reference Laboratory, 311 MTBC clinical isolates, previously identified using traditional methods as M. tuberculosis (306), M. bovis (3), and M. bovis BCG (2), were analyzed by gyrB-RFLP. All isolates were correctly identified by the molecular method, but no distinction between M. bovis and M. bovis BCG was obtained. Differentiation of M. tuberculosis and M. bovis is of utmost importance, because they require different treatment schedules. In conclusion, gyrB-RFLP is accurate and easy-to-perform, with potential to reduce time needed for conventional differentiation methods. However, application for epidemiological studies remains limited, because it cannot differentiate M. tuberculosis from M. africanum subtype II, and M. canetti, M. africanum subtype I from M. pinnipedii, and. M. bovis from M. bovis BCG. |
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Mycobacterium tuberculosis complex differentiation using gyrB-restriction fragment length polymorphism analysisMycobacterium tuberculosis complexgyrBrestriction fragment length polymorphismMycobacterium tuberculosis complex (MTBC) members are causative agents of human and animal tuberculosis. Differentiation of MTBC members is required for appropriate treatment of individual patients and for epidemiological purposes. Strains from six MTBC species - M. tuberculosis, M. bovis subsp. bovis, M. bovis BCG, M. africanum, M. pinnipedii, and M. canetti - were studied using gyrB-restriction fragment length polymorphism (gyrB-RFLP) analysis. A table was elaborated, based on observed restriction patterns and published gyrB sequences. To evaluate applicability of gyrB-RFLP at Instituto Adolfo Lutz, São Paulo, Mycobacterial Reference Laboratory, 311 MTBC clinical isolates, previously identified using traditional methods as M. tuberculosis (306), M. bovis (3), and M. bovis BCG (2), were analyzed by gyrB-RFLP. All isolates were correctly identified by the molecular method, but no distinction between M. bovis and M. bovis BCG was obtained. Differentiation of M. tuberculosis and M. bovis is of utmost importance, because they require different treatment schedules. In conclusion, gyrB-RFLP is accurate and easy-to-perform, with potential to reduce time needed for conventional differentiation methods. However, application for epidemiological studies remains limited, because it cannot differentiate M. tuberculosis from M. africanum subtype II, and M. canetti, M. africanum subtype I from M. pinnipedii, and. M. bovis from M. bovis BCG.Instituto Adolfo Lutz Seção de Bacteriologia Setor de MicobactériasUniversidade Federal de São Paulo (UNIFESP) Escola Paulista de Medicina Departamento de Microbiologia, Imunologia e ParasitologiaUNIFESP, EPM, Depto. de Microbiologia, Imunologia e ParasitologiaSciELOInstituto Oswaldo Cruz, Ministério da SaúdeInstituto Adolfo Lutz Seção de Bacteriologia Setor de MicobactériasUniversidade Federal de São Paulo (UNIFESP)Chimara, EricaFerrazoli, LucilaineLeao, Sylvia Cardoso [UNIFESP]2015-06-14T13:31:19Z2015-06-14T13:31:19Z2004-11-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion745-748application/pdfhttp://dx.doi.org/10.1590/S0074-02762004000700014Memórias do Instituto Oswaldo Cruz. Instituto Oswaldo Cruz, Ministério da Saúde, v. 99, n. 7, p. 745-748, 2004.10.1590/S0074-02762004000700014S0074-02762004000700014.pdf0074-0276S0074-02762004000700014http://repositorio.unifesp.br/handle/11600/2267engMemórias do Instituto Oswaldo Cruzinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-29T15:31:50Zoai:repositorio.unifesp.br/:11600/2267Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-07-29T15:31:50Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Mycobacterium tuberculosis complex differentiation using gyrB-restriction fragment length polymorphism analysis |
title |
Mycobacterium tuberculosis complex differentiation using gyrB-restriction fragment length polymorphism analysis |
spellingShingle |
Mycobacterium tuberculosis complex differentiation using gyrB-restriction fragment length polymorphism analysis Chimara, Erica Mycobacterium tuberculosis complex gyrB restriction fragment length polymorphism |
title_short |
Mycobacterium tuberculosis complex differentiation using gyrB-restriction fragment length polymorphism analysis |
title_full |
Mycobacterium tuberculosis complex differentiation using gyrB-restriction fragment length polymorphism analysis |
title_fullStr |
Mycobacterium tuberculosis complex differentiation using gyrB-restriction fragment length polymorphism analysis |
title_full_unstemmed |
Mycobacterium tuberculosis complex differentiation using gyrB-restriction fragment length polymorphism analysis |
title_sort |
Mycobacterium tuberculosis complex differentiation using gyrB-restriction fragment length polymorphism analysis |
author |
Chimara, Erica |
author_facet |
Chimara, Erica Ferrazoli, Lucilaine Leao, Sylvia Cardoso [UNIFESP] |
author_role |
author |
author2 |
Ferrazoli, Lucilaine Leao, Sylvia Cardoso [UNIFESP] |
author2_role |
author author |
dc.contributor.none.fl_str_mv |
Instituto Adolfo Lutz Seção de Bacteriologia Setor de Micobactérias Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Chimara, Erica Ferrazoli, Lucilaine Leao, Sylvia Cardoso [UNIFESP] |
dc.subject.por.fl_str_mv |
Mycobacterium tuberculosis complex gyrB restriction fragment length polymorphism |
topic |
Mycobacterium tuberculosis complex gyrB restriction fragment length polymorphism |
description |
Mycobacterium tuberculosis complex (MTBC) members are causative agents of human and animal tuberculosis. Differentiation of MTBC members is required for appropriate treatment of individual patients and for epidemiological purposes. Strains from six MTBC species - M. tuberculosis, M. bovis subsp. bovis, M. bovis BCG, M. africanum, M. pinnipedii, and M. canetti - were studied using gyrB-restriction fragment length polymorphism (gyrB-RFLP) analysis. A table was elaborated, based on observed restriction patterns and published gyrB sequences. To evaluate applicability of gyrB-RFLP at Instituto Adolfo Lutz, São Paulo, Mycobacterial Reference Laboratory, 311 MTBC clinical isolates, previously identified using traditional methods as M. tuberculosis (306), M. bovis (3), and M. bovis BCG (2), were analyzed by gyrB-RFLP. All isolates were correctly identified by the molecular method, but no distinction between M. bovis and M. bovis BCG was obtained. Differentiation of M. tuberculosis and M. bovis is of utmost importance, because they require different treatment schedules. In conclusion, gyrB-RFLP is accurate and easy-to-perform, with potential to reduce time needed for conventional differentiation methods. However, application for epidemiological studies remains limited, because it cannot differentiate M. tuberculosis from M. africanum subtype II, and M. canetti, M. africanum subtype I from M. pinnipedii, and. M. bovis from M. bovis BCG. |
publishDate |
2004 |
dc.date.none.fl_str_mv |
2004-11-01 2015-06-14T13:31:19Z 2015-06-14T13:31:19Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1590/S0074-02762004000700014 Memórias do Instituto Oswaldo Cruz. Instituto Oswaldo Cruz, Ministério da Saúde, v. 99, n. 7, p. 745-748, 2004. 10.1590/S0074-02762004000700014 S0074-02762004000700014.pdf 0074-0276 S0074-02762004000700014 http://repositorio.unifesp.br/handle/11600/2267 |
url |
http://dx.doi.org/10.1590/S0074-02762004000700014 http://repositorio.unifesp.br/handle/11600/2267 |
identifier_str_mv |
Memórias do Instituto Oswaldo Cruz. Instituto Oswaldo Cruz, Ministério da Saúde, v. 99, n. 7, p. 745-748, 2004. 10.1590/S0074-02762004000700014 S0074-02762004000700014.pdf 0074-0276 S0074-02762004000700014 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Memórias do Instituto Oswaldo Cruz |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
745-748 application/pdf |
dc.publisher.none.fl_str_mv |
Instituto Oswaldo Cruz, Ministério da Saúde |
publisher.none.fl_str_mv |
Instituto Oswaldo Cruz, Ministério da Saúde |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
_version_ |
1814268310909353984 |