Efficacy of Vaccination with the DIVENCE® Vaccine Against Bovine Viral Diarrhea Virus Types 1 and 2 in Terms of Fetal Protection.

IF 1.7 Q2 VETERINARY SCIENCES Veterinary medicine (Auckland, N.Z.) Pub Date : 2024-12-10 eCollection Date: 2024-01-01 DOI:10.2147/VMRR.S474655
Ester Taberner, Marta Gibert, Carlos Montbrau, Irene Muñoz Ruiz, Joaquim Mallorquí, Héctor Santo Tomás, Antoni Prenafeta, Ricard March
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Abstract

Purpose: To demonstrate the efficacy of DIVENCE®, a vaccine against BVDV types 1 and 2 (BVDV-1 and BVDV-2) transplacental infection, following a booster regimen in heifers.

Materials and methods: Calves of two-to-three months of age were given two intramuscular doses three weeks apart and a booster vaccine six months later. Efficacy was evaluated by means of a challenge with virulent BVDV-1 or BVDV-2 administered via the intranasal route at 85 days of gestation. Clinical signs, serology, viral shedding, WBC count and viremia were monitored after the challenge. Sixty-six days post-challenge, the fetuses were assessed for BVDV to detect transplacental infection.

Results: Vaccinated animals showed a significant (p < 0.05) reduction in hyperthermia after both challenges. The WBC counts in vaccinated animals were significantly (p < 0.05) higher than in control animals on Days 5 and 6 after both challenges. Vaccinated animals exhibited no shedding after BVDV-1 challenge and the percentage of shedding animals was significantly (p < 0.05) higher among control animals compared to vaccinated animals after BVDV-2 challenge. Viremia were detected in pregnant heifers from all control animals, while only 3/14 and 3/17 pregnant vaccinated heifers showed viremia after BVDV-1 and BVDV-2 challenges, respectively. All the fetuses (n=8) from the control animals were positive for BVDV-1 via virus titration after BVDV-1 challenge. Only one out of fourteen fetuses from the vaccinated animals was positive for BVDV-1. After BVDV-2 challenge, all the control animals had BVDV-2 in all fetal tissues assessed and only one of the seventeen vaccinated animals had BVDV-2 in its fetal samples.

Conclusion: DIVENCE® administered prior to breeding protected 94% of the fetuses against BVDV transplacental infection overall across both challenge trials (BVDV-1 and BVDV-2). A reduction in the hyperthermia, leukopenia, viral shedding, and viremia in vaccinated animals post-challenge with BVDV-1 and BVDV-2 was achieved. The efficacy of DIVENCE® against BVDV-1 and BVDV-2 transplacental infection has been demonstrated in this study.

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目的:证明 DIVENCE® 疫苗预防 BVDV 1 型和 BVDV 2 型(BVDV-1 和 BVDV-2)经胎盘感染的效果:对两到三个月大的犊牛进行两次肌肉注射,每次间隔三周,六个月后再注射一次加强免疫。在犊牛妊娠 85 天时,通过鼻内途径接种毒性 BVDV-1 或 BVDV-2 疫苗,评估疫苗的效力。挑战后对临床症状、血清学、病毒脱落、白细胞计数和病毒血症进行了监测。挑战后66天,对胎儿进行BVDV评估,以检测胎儿是否经胎盘感染:结果:接种疫苗的动物对 BVDV 感染有显著的抑制作用(p p p 结论):在两次挑战试验(BVDV-1 和 BVDV-2)中,配种前接种 DIVENCE® 可保护 94% 的胎儿免受 BVDV 经胎盘感染。接种疫苗的动物在BVDV-1和BVDV-2挑战后的高热、白细胞减少、病毒脱落和病毒血症均有所减少。本研究证明了 DIVENCE® 对 BVDV-1 和 BVDV-2 经胎盘感染的有效性。
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