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A Qualitative PCR Assay for the Discrimination of Bubaline Herpesvirus 1, Bovine Herpesvirus 1 and Bovine Herpesvirus 5. | LitMetric

A Qualitative PCR Assay for the Discrimination of Bubaline Herpesvirus 1, Bovine Herpesvirus 1 and Bovine Herpesvirus 5.

Microorganisms

Istituto Zooprofilattico Sperimentale del Piemonte, Liguria e Valle d'Aosta (IZSPLV), Via Bologna 148, 10154 Torino, Italy.

Published: February 2023

AI Article Synopsis

  • The study focuses on three herpesviruses: Bubaline herpesvirus 1 (BuHV-1), Bovine herpesvirus 1 (BoHV-1), and Bovine herpesvirus 5 (BoHV-5), which affect cattle and water buffaloes in different ways.
  • The research aimed to create a qualitative PCR assay to differentiate these viruses by targeting specific genes (gD, gE, gG) and their unique nucleotide sequences.
  • The developed PCR assay successfully distinguished among BuHV-1, BoHV-1, and BoHV-5 infections in both cattle and water buffaloes, providing a reliable diagnostic tool for identifying these viral infections.

Article Abstract

Bubaline herpesvirus 1 (BuHV-1), Bovine herpesvirus 1 (BoHV-1) and Bovine herpesvirus 5 (BoHV-5) are classified in the genus , subfamily . BoHV-1 is the causative agent of infectious bovine rhinotracheitis, BoHV-5 induces moderate disease in adult cattle while BuHV-1 has instead been associated with a decline in livestock production of water buffaloes. The aim of this study was to develop a qualitative PCR assay that allows the discrimination of BuHV-1, BoHV-1 and BoHV-5. The alignment of homologous genes identified specific nucleotide sequences of BuHV- 1, BoHV-1 and BoHV-5. The design of the primers and the optimization of the PCR assay were focused on the target sequences located on the portions of gD, gE and gG genes. This assay involved the use of three different PCR end-points: the PCR of a portion of the gD gene identified only the presence of BoHV-1; the PCR of a portion of the gE gene confirmed the presence of both BoHV-5 and BuHV-1; the PCR of a portion of the gG gene discriminated between BoHV-5 and BuHV-1, as the amplification product was observed only for BoHV-5. This qualitative PCR assay allowed the differentiation of BoHV-1 and BoHV-5 infections both in cattle and water buffaloes and heterologous BuHV-1 infections in bovine.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10056083PMC
http://dx.doi.org/10.3390/microorganisms11030577DOI Listing

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