Vaccination of calves at day of birth with attenuated vaccines against bovine respiratory syncytial virus, bovine parainfluenza type 3 virus and respiratory bovine coronavirus

Mark H. van Rooij , Mélodie Schmitz , Joris M.H. Meessen , Pieter A.W.M. Wouters , Mieke P. Vrijenhoek , Birgit Makoschey
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Abstract

Bovine Respiratory Disease (BRD) is a major cause of calfhood mortality. Bovine Respiratory Syncytial Virus (BRSV), Bovine Parainfluenza 3 Virus (BPIV3), Bovine Herpes Virus-1 (BHV-1), and Bovine Corona Virus (BCV) are major pathogens in BRD outbreaks.

The importance of early protection of newborn calves is undoubted. The BRD vaccines licensed in Europe can be applied from one or two weeks of age onwards. We have investigated the safety and immunity of a commercial intranasal live BRSV-BPIV3 combination vaccine and a live-attenuated BCV vaccine (in development) in calves at day of birth.

In the safety study the calves were revaccinated two weeks after the first vaccination. In the efficacy studies, the calves were experimentally infected with field isolates six days (BRSV, study #2), seven days (BPIV3, study #3) and five days (BCV, study #4), post vaccination.

Animals were monitored for any adverse effects of the vaccination and clinical disease following the challenge infection. Samples were collected and tested for RNA specific for the respective vaccine and challenge viruses. Fourteen days after the BRSV challenge infection, the animals in study #2 were euthanized and a necropsy was performed.

The frequency and degree of symptoms of abnormal health observed in the safety study, were comparable to those observed in older animals after vaccination with the same vaccines.

Mild to moderate signs of upper respiratory tract disease (URTD) were the predominant clinical signs after challenge infection. The average scores in the vaccinated groups were lower than in the control groups, but the differences did not reach statistical significance.

Moreover, the virus load in nasal swabs was significantly lower in the vaccinated group as was the BCV virus load in rectal swab samples taken from the vaccinated animals.

From the four studies it can be concluded that the vaccines used in these studies can be applied from the day of birth onwards.

在犊牛出生当天接种牛呼吸道合胞病毒、牛副流感3型病毒和牛呼吸道冠状病毒减毒疫苗
牛呼吸系统疾病(BRD)是导致小牛死亡的主要原因。牛呼吸道合胞病毒(BRSV)、牛3型副流感病毒(BPIV3)、牛疱疹病毒-1(BHV-1)和牛冠状病毒(BCV)是BRD爆发的主要病原体。早期保护初生牛犊的重要性是毋庸置疑的。在欧洲获得许可的BRD疫苗可以从一到两周大开始使用。我们研究了商业鼻内BRSV-BPIV3联合活疫苗和BCV减毒活疫苗(正在开发中)在小牛出生当天的安全性和免疫力。在安全性研究中,小牛在第一次接种疫苗两周后重新接种疫苗。在疗效研究中,小牛在接种疫苗后6天(BRSV,研究#2)、7天(BPIV3,研究#3)和5天(BCV,研究#4)用现场分离物进行实验感染。监测动物接种疫苗的任何不良反应和激发感染后的临床疾病。收集样本并测试针对各自疫苗和攻击病毒的特异性RNA。BRSV激发感染14天后,对研究2中的动物实施安乐死,并进行尸检。安全性研究中观察到的异常健康症状的频率和程度与接种相同疫苗后在老年动物身上观察到的症状频率和程度相当。上呼吸道疾病(URTD)的轻度至中度症状是激发感染后的主要临床症状。接种疫苗组的平均得分低于对照组,但差异未达到统计学意义。此外,接种疫苗组鼻拭子中的病毒载量显著较低,从接种疫苗的动物身上采集的直肠拭子样本中的BCV病毒载量也显著较低。从这四项研究可以得出结论,这些研究中使用的疫苗可以从出生当天起使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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