4.7 Article

Vaccination of Sheep with Bovine Viral Diarrhea Vaccines Does Not Protect against Fetal Infection after Challenge of Pregnant Ewes with Border Disease Virus

Journal

VACCINES
Volume 9, Issue 8, Pages -

Publisher

MDPI
DOI: 10.3390/vaccines9080805

Keywords

Border Disease Virus; sheep; vaccination; fetus; protection; Bovine Viral Diarrhea Virus

Funding

  1. French Regional (Occitanie) Federation of groupements de defense sanitaire
  2. Federation des Organismes de Defense Sanitaire de l'Aveyron

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Border Disease (BD) in sheep is characterized by various symptoms, and control measures include eliminating persistently infected lambs and vaccination. However, vaccines for Bovine Viral Diarrhea Virus (BVDV) may not be effective against BDV infection in sheep, as evidenced by a study showing limited protection against fetal infection.
Border Disease (BD) is a major sheep disease characterized by immunosuppression, congenital disorders, abortion, and birth of lambs persistently infected (PI) by Border Disease Virus (BDV). Control measures are based on the elimination of PI lambs, biosecurity, and frequent vaccination which aims to prevent fetal infection and birth of PI. As there are no vaccines against BDV, farmers use vaccines directed against the related Bovine Viral Diarrhea Virus (BVDV). To date, there is no published evidence of cross-effectiveness of BVDV vaccination against BDV infection in sheep. We tested three commonly used BVDV vaccines, at half the dose used in cattle, for their efficacy of protection against a BDV challenge of ewes at 52 days of gestation. Vaccination limits the duration of virus-induced leukopenia after challenge, suggesting partial protection in transient infection. Despite the presence of BDV neutralizing antibodies in vaccinated ewes on the day of the challenge, fetuses of vaccinated and unvaccinated sheep were, two months after, highly positive for BDV RNA loads and seronegative for antibodies. Therefore, BVDV vaccination at half dose was not sufficient to prevent ovine fetal infection by BDV in a severe challenge model and can only be reconsidered as a complementary mean in BD control.

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