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A two-step species-specific 16S rRNA PCR assay for the detection of Taylorella equigenitalis in horses

A two-step PCR assay was developed for the molecular detection of Taylorella equigenitalis, a Gram-negative genital bacterial pathogen in horses. Two specific oligonucleotide primers (TE16SrRNABCHf [25mer] and TE16SrRNABCHr [29mer]) were designed from multiple alignments of the 16S rRNA gene loci of...

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Autores principales: Buckley, Thomas C, Millar, B Cherie, Egan, Claire L, Gibson, Paula, Cosgrove, Hazel, Stanbridge, Siobhan, Matsuda, Motoo, Moore, John E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3113911/
https://www.ncbi.nlm.nih.gov/pubmed/21851668
http://dx.doi.org/10.1186/2046-0481-58-3-146
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author Buckley, Thomas C
Millar, B Cherie
Egan, Claire L
Gibson, Paula
Cosgrove, Hazel
Stanbridge, Siobhan
Matsuda, Motoo
Moore, John E
author_facet Buckley, Thomas C
Millar, B Cherie
Egan, Claire L
Gibson, Paula
Cosgrove, Hazel
Stanbridge, Siobhan
Matsuda, Motoo
Moore, John E
author_sort Buckley, Thomas C
collection PubMed
description A two-step PCR assay was developed for the molecular detection of Taylorella equigenitalis, a Gram-negative genital bacterial pathogen in horses. Two specific oligonucleotide primers (TE16SrRNABCHf [25mer] and TE16SrRNABCHr [29mer]) were designed from multiple alignments of the 16S rRNA gene loci of several closely related taxa, including T. asinigenitalis. Subsequent enhanced surveillance of 250 Thoroughbred animals failed to detect the presence of this organism directly from clinical swabs taken from the genital tract of mares and stallions. Such a molecular approach offers a sensitive and specific alternative to conventional culture techniques, and has the potential to lead to improved diagnosis and subsequent management of horses involved in breeding programmes.
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spelling pubmed-31139112011-06-14 A two-step species-specific 16S rRNA PCR assay for the detection of Taylorella equigenitalis in horses Buckley, Thomas C Millar, B Cherie Egan, Claire L Gibson, Paula Cosgrove, Hazel Stanbridge, Siobhan Matsuda, Motoo Moore, John E Ir Vet J Research A two-step PCR assay was developed for the molecular detection of Taylorella equigenitalis, a Gram-negative genital bacterial pathogen in horses. Two specific oligonucleotide primers (TE16SrRNABCHf [25mer] and TE16SrRNABCHr [29mer]) were designed from multiple alignments of the 16S rRNA gene loci of several closely related taxa, including T. asinigenitalis. Subsequent enhanced surveillance of 250 Thoroughbred animals failed to detect the presence of this organism directly from clinical swabs taken from the genital tract of mares and stallions. Such a molecular approach offers a sensitive and specific alternative to conventional culture techniques, and has the potential to lead to improved diagnosis and subsequent management of horses involved in breeding programmes. BioMed Central 2005-03-01 /pmc/articles/PMC3113911/ /pubmed/21851668 http://dx.doi.org/10.1186/2046-0481-58-3-146 Text en
spellingShingle Research
Buckley, Thomas C
Millar, B Cherie
Egan, Claire L
Gibson, Paula
Cosgrove, Hazel
Stanbridge, Siobhan
Matsuda, Motoo
Moore, John E
A two-step species-specific 16S rRNA PCR assay for the detection of Taylorella equigenitalis in horses
title A two-step species-specific 16S rRNA PCR assay for the detection of Taylorella equigenitalis in horses
title_full A two-step species-specific 16S rRNA PCR assay for the detection of Taylorella equigenitalis in horses
title_fullStr A two-step species-specific 16S rRNA PCR assay for the detection of Taylorella equigenitalis in horses
title_full_unstemmed A two-step species-specific 16S rRNA PCR assay for the detection of Taylorella equigenitalis in horses
title_short A two-step species-specific 16S rRNA PCR assay for the detection of Taylorella equigenitalis in horses
title_sort two-step species-specific 16s rrna pcr assay for the detection of taylorella equigenitalis in horses
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3113911/
https://www.ncbi.nlm.nih.gov/pubmed/21851668
http://dx.doi.org/10.1186/2046-0481-58-3-146
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