A polymorphic tandem repeat potentially useful for typing in the chromosome of Yersinia enterocolitica

1 Servicio de Microbiología, Hospital Universitario Marqués de Valdecilla, Avenida de Valdecilla s/n, 39008-Santander, Spain 2 Departamento de Biología Molecular, Facultad de Medicina, Universidad de Cantabria, Centro Asociado al CIB, CSIC, Cardenal Herrera Oria s/n, 39011, Santander, Spain Correspo...

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Veröffentlicht in:Microbiology (Society for General Microbiology) 2004-01, Vol.150 (1), p.199-204
Hauptverfasser: de Benito, Ines, Cano, Maria Eliecer, Aguero, Jesus, Lobo, Juan M. Garcia
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creator de Benito, Ines
Cano, Maria Eliecer
Aguero, Jesus
Lobo, Juan M. Garcia
description 1 Servicio de Microbiología, Hospital Universitario Marqués de Valdecilla, Avenida de Valdecilla s/n, 39008-Santander, Spain 2 Departamento de Biología Molecular, Facultad de Medicina, Universidad de Cantabria, Centro Asociado al CIB, CSIC, Cardenal Herrera Oria s/n, 39011, Santander, Spain Correspondence Juan M. García Lobo jmglobo{at}unican.es The hexanucleotide CCAGCA was found repeated 15 times in tandem on the 5' side of the virginiamycin acetyl transferase gene of Yersinia enterocolitica strain Y56. The corresponding region was analysed by PCR from 54 clinical strains belonging to the same biotype and serotype, and others from this laboratory collection belonging to different biotypes and serotypes. Each strain produced a single amplification product whose size was variable among strains, revealing that the locus was polymorphic. Nucleotide sequence determination of selected PCR products showed that the polymorphism was due to the precise expansion or reduction in the number of hexanucleotide repeats. Analysis of this locus in a few strains showing the same PFGE pattern showed that it was also polymorphic. These results suggest that this method could be valuable to increase the discriminatory power of current Y. enterocolitica typing schemes. Abbreviations: PA, proline-alanine; VNTR, variable number tandem repeats
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García Lobo jmglobo{at}unican.es The hexanucleotide CCAGCA was found repeated 15 times in tandem on the 5' side of the virginiamycin acetyl transferase gene of Yersinia enterocolitica strain Y56. The corresponding region was analysed by PCR from 54 clinical strains belonging to the same biotype and serotype, and others from this laboratory collection belonging to different biotypes and serotypes. Each strain produced a single amplification product whose size was variable among strains, revealing that the locus was polymorphic. Nucleotide sequence determination of selected PCR products showed that the polymorphism was due to the precise expansion or reduction in the number of hexanucleotide repeats. Analysis of this locus in a few strains showing the same PFGE pattern showed that it was also polymorphic. These results suggest that this method could be valuable to increase the discriminatory power of current Y. enterocolitica typing schemes. 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subjects Amino Acid Sequence
Bacterial Typing Techniques - methods
Bacteriology
Base Sequence
Biological and medical sciences
DNA, Bacterial - genetics
Electrophoresis, Gel, Pulsed-Field
Fundamental and applied biological sciences. Psychology
Humans
Microbiology
Minisatellite Repeats
Miscellaneous
Molecular Sequence Data
Open Reading Frames
Polymorphism, Genetic
Sequence Homology, Amino Acid
Yersinia - classification
Yersinia - genetics
Yersinia enterocolitica
Yersinia enterocolitica - classification
Yersinia enterocolitica - genetics
Yersinia enterocolitica - isolation & purification
title A polymorphic tandem repeat potentially useful for typing in the chromosome of Yersinia enterocolitica
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