Patel J R, Shilleto R W, Williams J, Alexander D C S
Intervet UK Ltd., Huntingdon, UK.
Arch Virol. 2002 Dec;147(12):2453-63. doi: 10.1007/s00705-002-0878-3.
Results are presented for an experimental validation of the efficacy of an EU licensed, inactivated bovine viral diarrhoea virus vaccine (Bovilis BVDV). This study was designed to assess the quality of efficacy 6 months after a single course of vaccination (two intramuscular doses a month apart). A natural challenge at about 87 days of gestation by 3 persistently infected carrier heifers rapidly infected all experimental heifers. This resulted in transplacental BVDV infection of all 7 unvaccinated dams whereas 11 immunised dams produced 9 live-born calves and 2 aborted foetuses from which no BVDV could be recovered.
本文展示了对一种欧盟许可的灭活牛病毒性腹泻病毒疫苗(Bovilis BVDV)有效性的实验验证结果。本研究旨在评估单次疫苗接种疗程(每月两次肌肉注射,间隔一个月)6个月后的效力质量。在妊娠约87天时,3头持续感染的携带病毒的小母牛进行自然感染,迅速感染了所有实验小母牛。这导致所有7头未接种疫苗的母牛经胎盘感染牛病毒性腹泻病毒,而11头免疫的母牛产下9头活产犊牛和2头流产胎儿,从中未检测到牛病毒性腹泻病毒。