A molecular survey using a validated real-time PCR assay finds no evidence of bovine alphaherpesvirus 2 in samples from animals with suspected vesicular disease in Brazil between 2014 and 2017
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作者:
Felipe Augusto de Souza
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机构:Centro Universitário Newton Paiva,
Felipe Augusto de Souza
Mateus Laguardia-Nascimento
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机构:Centro Universitário Newton Paiva,
Mateus Laguardia-Nascimento
Marcela Ribeiro Gasparini
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机构:Centro Universitário Newton Paiva,
Marcela Ribeiro Gasparini
Luciana Rabello Ferreira
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机构:Centro Universitário Newton Paiva,
Luciana Rabello Ferreira
Érica Bravo Sales
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机构:Centro Universitário Newton Paiva,
Érica Bravo Sales
Juliana F. Cargnelutti
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机构:Centro Universitário Newton Paiva,
Juliana F. Cargnelutti
Marcelo Fernandes Camargos
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机构:Centro Universitário Newton Paiva,
Marcelo Fernandes Camargos
Antônio Augusto Fonseca Júnior
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机构:Centro Universitário Newton Paiva,
Antônio Augusto Fonseca Júnior
机构:
[1] Centro Universitário Newton Paiva,
[2] Laboratório Nacional Agropecuário de Minas Gerais (Lanagro/MG),undefined
Bovine alphaherpesvirus 2 (BoHV-2) is the etiologic agent of bovine mammillitis (BM) and pseudo-lumpy skin disease. BM is also important because its clinical presentation can be confused with foot-and-mouth disease (FMD), making it necessary to establish differential diagnoses and perform additional laboratory tests. The objective of this work was to use a validated real-time PCR assay to test for the presence of BoHV-2 in samples from cattle and buffalo with suspected vesicular disease in Brazil. The method could detect the virus at a concentration of 0.5 fg/μL and had 99.4% amplification efficiency, a repeatability error of only 4.1%, and good reproducibility with other reagents. No evidence of BoHV-2 causing vesicular disease in cattle and buffalo was found in this work. This study was able to validate a new methodology for detection of BoHV-2 and evaluate its usefulness for investigating outbreaks of vesicular disease Brazil. The importance of BoHV-2 in cases involving other clinical signs should still be studied using the qPCR developed in this work.