Development of multiplex PCR to detect and differentiate the categories of diarrheagenic Escherichia coli

INTRODUCTION: Diarrheagenic Escherichia coli (DEC) are considered an important cause of diarrhea in developing countries. The correct identification of these microorganisms depends on their differentiation from non-pathogenic members of the intestinal microbiota. DEC can b...

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Detalles Bibliográficos
Autores: Fusco da Costa, Ana Roberta, Batista Lima, Karla Valéria, Oliveira de Sousa, Cintya, Brito Loureiro, Edvaldo Carlos
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2010
País:Brasil
Institución:Instituto Evandro Chagas (IEC)
Repositorio:Revista Pan-Amazônica de Saúde (RPAS)
Idioma:portugués
OAI Identifier:oai:revista.iec.gov.br:article/1584
Acceso en línea:https://ojs.iec.gov.br/rpas/article/view/1584
Access Level:acceso abierto
Palabra clave:Reacción en Cadena de la Polimerasa
Escherichia coli
Factores de Virulencia
Enfermedades Intestinales
Reação em Cadeia da Polimerase
Fatores de Virulência
Enteropatias
Polymerase Chain Reaction
Virulence Factors
Intestinal Diseases
Descripción
Sumario:INTRODUCTION: Diarrheagenic Escherichia coli (DEC) are considered an important cause of diarrhea in developing countries. The correct identification of these microorganisms depends on their differentiation from non-pathogenic members of the intestinal microbiota. DEC can be classified into one of six categories according to their mechanism of pathogenicity.MATERIALS AND METHODS: Two multiplex PCR systems used to detect enteropathogenic (EPEC), enterotoxigenic (ETEC), enteroinvasive (EIEC) and Shiga Toxin-producing (STEC) E. coli were evaluated and described.RESULTS: Four categories of DEC were detected among isolates of E. coli obtained from individuals infected with HIV. EIEC and EPEC were among the most prevalent pathotypes. Furthermore, two STEC strains that were both stx1-and eae-positive were identified. This is the first report of this kind of isolation in individuals infected with HIV in the State of Pará. Multiplex PCR proved to be an efficient, fast and reproducible technique for detection of DEC isolates. Both multiplex PCR systems described here produced results 100% similar to those obtained from individual PCR reactions.CONCLUSION: Given their simplicity, cost and efficiency, it is possible to use these protocols to expedite the molecular diagnosis of the distinct categories of DEC. In addition to facilitating the development of new research projects, these findings could support the epidemiological surveillance undertaken by public health agencies and institutes.