Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros










Intervalo de ano de publicação
1.
Enferm. infecc. microbiol. clín. (Ed. impr.) ; 27(9): 496-502, nov. 2009. tab, ilus
Artigo em Espanhol | IBECS | ID: ibc-78703

RESUMO

Introducción En el complejo Mycobacterium tuberculosis se engloban las especies M. tuberculosis, Mycobacterium africanum, Mycobacterium bovis, Mycobacterium bovis-Calmette y Guérin, Mycobacterium microti, Mycobacterium caprae, Mycobacterium pinnipedii y Mycobacterium canettii. Estas especies son las causantes de la tuberculosis en humanos y animales. Tradicionalmente la identificación de estas especies se ha basado en el estudio de métodos fenotípicos. No obstante, en los últimos años se han desarrollado numerosas técnicas moleculares. El objetivo de este trabajo es la evaluación de cada una de éstas para crear un esquema de identificación rápido y sencillo. Material y métodos Mediante el esquema propuesto se analizaron 251 cepas escogidas al azar entre las estudiadas en el año 2004 y se analizaron 797 cepas recibidas en el Laboratorio de Referencia de Micobacterias entre los años 2005 y 2007. La caracterización fenotípica de 4.183 cepas aisladas en este período se realizó mediante el estudio morfológico de la colonia, el aspecto del cultivo, la reducción de nitratos, la producción de niacina y el crecimiento en presencia de (..) (AU)


Introduction The Mycobacterium tuberculosis complex includes the following species: Mycobacterium tuberculosis, Mycobacterium africanum, Mycobacterium bovis, Mycobacterium bovis-BCG, Mycobacterium microti, Mycobacterium caprae, Mycobacterium pinnipedii, and Mycobacterium canettii. These species cause tuberculosis in humans and animals. Identification of mycobacterial strains has classically been performed by phenotype study. Over the last years, laboratories have developed several molecular techniques to differentiate between these species. The aim of this study is to evaluate these methods and develop a simple, fast, identification scheme. Material and methods We analyzed 251 strains randomly obtained from the strains studied in 2004, and 797 strains received by the Reference Laboratory between 2005 and 2007. Phenotype characterization of 4183 strains isolated during that period was done by studying the colony morphology, characteristics in culture, nitrate (..) (AU)


Assuntos
Humanos , Animais , Bovinos , DNA Bacteriano/genética , Mycobacterium tuberculosis/classificação , Reação em Cadeia da Polimerase/métodos , Polimorfismo de Fragmento de Restrição , Proteínas de Bactérias/genética , Fenótipo , Mycobacterium tuberculosis/classificação
2.
Enferm Infecc Microbiol Clin ; 27(9): 496-502, 2009 Nov.
Artigo em Espanhol | MEDLINE | ID: mdl-19409673

RESUMO

INTRODUCTION: The Mycobacterium tuberculosis complex includes the following species: Mycobacterium tuberculosis, Mycobacterium africanum, Mycobacterium bovis, Mycobacterium bovis-BCG, Mycobacterium microti, Mycobacterium caprae, Mycobacterium pinnipedii, and Mycobacterium canettii. These species cause tuberculosis in humans and animals. Identification of mycobacterial strains has classically been performed by phenotype study. Over the last years, laboratories have developed several molecular techniques to differentiate between these species. The aim of this study is to evaluate these methods and develop a simple, fast, identification scheme. MATERIAL AND METHODS: We analyzed 251 strains randomly obtained from the strains studied in 2004, and 797 strains received by the Reference Laboratory between 2005 and 2007. Phenotype characterization of 4183 strains isolated during that period was done by studying the colony morphology, characteristics in culture, nitrate reduction, niacin accumulation, and growth in the presence of thiophen-2-carboxylic acid hydrazide 10 microg/mL and pyrazinamide 50 microg/mL. The molecular identification scheme designed was as follows: 1) gyrB PCR-RFLP with RsaI, TaqI or SacII and hsp65 RFLP/PCR with HhaI., and 2) multiplex-PCR to determine the presence/absence of the RD9 and RD1 regions. RESULTS: The results showed 100% agreement between phenotype study and the molecular scheme. DISCUSSION: This molecular identification scheme is a simple and fast method, with 100% sensitivity and specificity, that can be implemented in most clinical laboratories at a low cost.


Assuntos
DNA Bacteriano/genética , Mycobacterium tuberculosis/classificação , Reação em Cadeia da Polimerase/métodos , Polimorfismo de Fragmento de Restrição , Tuberculose Bovina/microbiologia , Tuberculose/microbiologia , Animais , Proteínas de Bactérias/genética , Ácidos Carboxílicos , Bovinos , Chaperonina 60/genética , DNA Girase/genética , Humanos , Mycobacterium/classificação , Mycobacterium/efeitos dos fármacos , Mycobacterium/genética , Mycobacterium/metabolismo , Mycobacterium bovis/classificação , Mycobacterium bovis/efeitos dos fármacos , Mycobacterium bovis/genética , Mycobacterium bovis/metabolismo , Mycobacterium tuberculosis/efeitos dos fármacos , Mycobacterium tuberculosis/genética , Mycobacterium tuberculosis/metabolismo , Niacina/metabolismo , Nitratos/metabolismo , Fenótipo , Pirazinamida/farmacologia , Padrões de Referência , Sensibilidade e Especificidade , Especificidade da Espécie , Tiofenos/farmacologia
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...