Diferenciación de especies de Rhodococcusmediante una prueba de PCR-RFLP basada en los genes codificantes para la subunidad 16S ribosomal
Differentiation of Species of By Means of a Test of Pcr-Rflp Based On the Coding Genes for the Sub Unit 16s Ribosomal.
Differentiation of Species of By Means of a Test of Pcr-Rflp Based On the Coding Genes for the Sub Unit 16s Ribosomal.
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Pavia, Paula
Calderón, Camila
Puerta PhD, Concepción
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Universidad Colegio Mayor de CundinamarcaCitación
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Dada la dificultad en diferenciar las especies de Rhodococcus por pruebas bioquímicas, se desarrolló una prueba de Reacción en Cadena de la Polimerasa (PCR), seguida de un ensayo de Polimorfismo de Longitud de Fragmentos de Restricción (PCR-RFLP) para la diferenciación de las mismas. R. equi, R. rhodnii y otras bacterias fueron cultivadas en agar sangre y BHI a 37 y 26 °C. El ADN bacteriano fue extraído y amplificado con los iniciadores descritos por Hypsa y Dale. Los productos de amplificación fueron sometidos a digestión con diversas enzimas de restricción y los patrones de restricción obtenidos fueron confirmados mediante análisis in silico. Se obtuvo el fragmento de amplificación esperado de 1300 pb en todas las bacterias analizadas. Se pudo diferenciar R. equi de R. rhodnii con las endonucleasas PstI y HindIII y con respecto a otras bacterias con PstI, HindIII, SstI, BamHI y EcoRI. Los patrones de restricción obtenidos fueron confirmados mediante análisis in silico. La prueba PCR-RFLP constituye una alternativa para la diferenciación entre especies de Rhodococcus tales como R. equi y R. rhodnii. Considering the difficulty to differentiate the species of Rhodococcus by biochemical tests, a Polymerase Chain Reaction-Restriction Fragment Length Polymorphism (PCR-RFLP) has been developed to distinguish the species of the genus Rhodococcus. R. equi, R. rhodnii and other bacterial samples were cultured on Blood agar and BHI at 26 and 37°C. The obtained DNA was amplified with the primers described by Hypsa and Dale. Products of amplification were submitted to digestion with multiple restriction enzymes and the restriction patterns were confirmed by using in silico analysis. The expected amplification fragment of 1300 pb was obtained in all tested samples. R. equi was distinguished from R. rhodnii by using endonucleases such as PstI and HindIII, and from other bacteria with endonucleases PstI, HindIII, SstI, BamHI and EcoRI. The obtained restriction patterns were confirmed by using in silico analysis. This PCR-RFLP establishes an alternative for the differentiation among species of the genus Rhodococcus such as R. equi and R. rhodnii.
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