Molecular detection and genotyping of bovine viral diarrhea virus in Selangor, Malaysia.
5’-UTR region
Bovine viral diarrhea
E2 region
bovine viral diarrhea virus
reverse transcription polymerase chain reaction
Journal
Journal of advanced veterinary and animal research
ISSN: 2311-7710
Titre abrégé: J Adv Vet Anim Res
Pays: Bangladesh
ID NLM: 101647585
Informations de publication
Date de publication:
Jun 2024
Jun 2024
Historique:
received:
18
08
2023
revised:
25
11
2023
accepted:
27
11
2023
medline:
5
8
2024
pubmed:
5
8
2024
entrez:
5
8
2024
Statut:
epublish
Résumé
Bovine viral diarrhea (BVD) disease is a viral infection in cows caused by a single-stranded plus-sense RNA virus of the A reverse transcription polymerase chain reaction (RT-PCR) was performed for antigen detection in 253 plasma samples collected from cows using a cross-sectional study design. We selected the 5 untranslated regions (5'-UTR) region and the E2 region to compare the genetic differences between the isolates. One sample was found to be positive (1/253) following RT-PCR targeting the conserved 5'-UTR region of BVDV. Thus, BVDV antigen prevalence was 0.40% (95% confidence interval: 0.0%-2.2%). By targeting the hypervariable E2 region of the isolated virus, UPM/MAL/BVDV/D17, the virus was classified under the subgenotype BVDV-1a. BVDV is present and circulating on selected cattle farms in Selangor, Malaysia. Given the presence of BVDV in several subgenotypes, the screening of all incoming cattle at Malaysia's border is pertinent to prevent the entry of other BVDV subgenotypes into the country.
Identifiants
pubmed: 39101100
doi: 10.5455/javar.2024.k797
pmc: PMC11296188
doi:
Types de publication
Journal Article
Langues
eng
Pagination
474-482Informations de copyright
© The authors.
Déclaration de conflit d'intérêts
The authors declare that they have no conflict of interest.