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A RT-PCR assay for the detection of encephalomycarditis virus infections in pigs

Encephalomyocarditis virus (EMCV) infections can cause losses in pig farms all over the world. Rapid, sensitive and unequivocal detection of this virus is therefore essential for the diagnosis and control of the disease. An RT-PCR assay was developed, optimized and evaluated for encephalomyocarditis...

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Detalles Bibliográficos
Autores principales: Pérez, Lester J., Díaz de Arce, Heidy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Microbiologia 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3768574/
https://www.ncbi.nlm.nih.gov/pubmed/24031451
http://dx.doi.org/10.1590/S1517-838220090004000034
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author Pérez, Lester J.
Díaz de Arce, Heidy
author_facet Pérez, Lester J.
Díaz de Arce, Heidy
author_sort Pérez, Lester J.
collection PubMed
description Encephalomyocarditis virus (EMCV) infections can cause losses in pig farms all over the world. Rapid, sensitive and unequivocal detection of this virus is therefore essential for the diagnosis and control of the disease. An RT-PCR assay was developed, optimized and evaluated for encephalomyocarditis virus detection in organ based on a pair of primers that amplifies a 165 bp DNA fragment from a highly conserved nucleotide region of the viral 3D glycoprotein. PCR products of the expected size were obtained from Cuban EMCV 744/03 strain. Non-specific reactions were not observed when other porcine RNA genome viruses and uninfected cells were used. The analytical sensitivity of the test was estimated to be 2 TCID(50)/50 μL. The analysis of tissue homogenate samples from naturally infected animals proved the potential usefulness of the method for a rapid disease diagnosis from field cases.
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spelling pubmed-37685742013-09-12 A RT-PCR assay for the detection of encephalomycarditis virus infections in pigs Pérez, Lester J. Díaz de Arce, Heidy Braz J Microbiol Veterinarian Microbiology Encephalomyocarditis virus (EMCV) infections can cause losses in pig farms all over the world. Rapid, sensitive and unequivocal detection of this virus is therefore essential for the diagnosis and control of the disease. An RT-PCR assay was developed, optimized and evaluated for encephalomyocarditis virus detection in organ based on a pair of primers that amplifies a 165 bp DNA fragment from a highly conserved nucleotide region of the viral 3D glycoprotein. PCR products of the expected size were obtained from Cuban EMCV 744/03 strain. Non-specific reactions were not observed when other porcine RNA genome viruses and uninfected cells were used. The analytical sensitivity of the test was estimated to be 2 TCID(50)/50 μL. The analysis of tissue homogenate samples from naturally infected animals proved the potential usefulness of the method for a rapid disease diagnosis from field cases. Sociedade Brasileira de Microbiologia 2009 2009-12-01 /pmc/articles/PMC3768574/ /pubmed/24031451 http://dx.doi.org/10.1590/S1517-838220090004000034 Text en © Sociedade Brasileira de Microbiologia http://creativecommons.org/licenses/by-nc/3.0/ All the content of the journal, except where otherwise noted, is licensed under a Creative Commons License
spellingShingle Veterinarian Microbiology
Pérez, Lester J.
Díaz de Arce, Heidy
A RT-PCR assay for the detection of encephalomycarditis virus infections in pigs
title A RT-PCR assay for the detection of encephalomycarditis virus infections in pigs
title_full A RT-PCR assay for the detection of encephalomycarditis virus infections in pigs
title_fullStr A RT-PCR assay for the detection of encephalomycarditis virus infections in pigs
title_full_unstemmed A RT-PCR assay for the detection of encephalomycarditis virus infections in pigs
title_short A RT-PCR assay for the detection of encephalomycarditis virus infections in pigs
title_sort rt-pcr assay for the detection of encephalomycarditis virus infections in pigs
topic Veterinarian Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3768574/
https://www.ncbi.nlm.nih.gov/pubmed/24031451
http://dx.doi.org/10.1590/S1517-838220090004000034
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