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比较三种预防牛病毒性腹泻病毒持续感染的商业疫苗。

Comparison of three commercial vaccines for preventing persistent infection with bovine viral diarrhea virus.

机构信息

Department of Animal Sciences, Auburn University, Auburn, Alabama, USA.

出版信息

Theriogenology. 2010 May;73(8):1154-63. doi: 10.1016/j.theriogenology.2010.01.017. Epub 2010 Feb 23.

DOI:10.1016/j.theriogenology.2010.01.017
PMID:20181385
Abstract

Eighty crossbred beef heifers were randomly allocated to four groups to evaluate the efficacy of vaccination in preventing development of calves persistently infected with bovine viral diarrhea virus (BVDV). Group 1 (n=11) was non-vaccinated controls, whereas three groups were vaccinated with commercially available multivalent BVDV vaccines at weaning (approximately 7 mo of age), 28 d post-weaning, approximately 1 y of age, and 28 d later. Groups 2 (n=23) and 3 (n=23) were given a modified-live BVDV vaccine, whereas Group 4 was given an inactivated BVDV vaccine. Heifers were bred by AI and subsequently exposed to two bulls. At 61 d after AI, 70 heifers were pregnant (n=10 for Group 1 and n=20/group for Groups 2, 3, and 4). Three cattle persistently infected with BVDV were commingled with the pregnant heifers (in an isolated pasture) from 68 to 126 d after AI. Thereafter, viremias were detected in pregnant heifers from Groups 1, 3, and 4 (10/10, 1/20, and 10/20, respectively), but not in pregnant heifers from Group 2 (0/20). Resulting calves were assessed for persistent infection using serum PCR, ear notch antigen capture-ELISA, and immunohistochemistry. Persistently infected calves were only produced in Group 1 (10/10) and Group 4 (2/18). In conclusion, commercial vaccines provided effective fetal protection despite prolonged natural exposure to BVDV. Given that viremias were detected in 11 vaccinated heifers after BVDV exposure, and two vaccinated heifers gave birth to persistently infected calves, there is continued need for biosecurity and diagnostic surveillance, in addition to vaccination, to ensure effective BVDV control.

摘要

80 头杂交肉牛犊被随机分配到四组,以评估疫苗接种在预防牛病毒性腹泻病毒(BVDV)持续感染犊牛方面的效果。第 1 组(n=11)为未接种疫苗的对照组,而其余三组在断奶时(约 7 月龄)、断奶后 28 天、约 1 岁和 28 天后使用市售多价 BVDV 疫苗进行接种。第 2 组(n=23)和第 3 组(n=23)接种了改良活 BVDV 疫苗,而第 4 组接种了灭活 BVDV 疫苗。牛犊通过人工授精配种,随后接触两头公牛。在人工授精后 61 天,有 70 头母牛怀孕(第 1 组 10 头,第 2、3 和 4 组各 20 头)。三头 BVDV 持续感染的牛与怀孕的母牛(在一个隔离的牧场上)从人工授精后 68 天到 126 天混群。此后,第 1、3 和 4 组的怀孕母牛均检测到病毒血症(分别为 10/10、1/20 和 10/20),但第 2 组的怀孕母牛未检测到病毒血症(0/20)。通过血清 PCR、耳尖抗原捕获 ELISA 和免疫组织化学检测对犊牛进行持续感染评估。仅在第 1 组(10/10)和第 4 组(2/18)产生了持续感染的犊牛。总之,商业疫苗提供了有效的胎儿保护,尽管犊牛长期自然接触 BVDV。鉴于 BVDV 暴露后,11 头接种疫苗的母牛检测到病毒血症,且 2 头接种疫苗的母牛产下持续感染的犊牛,除了疫苗接种外,还需要持续进行生物安全和诊断监测,以确保有效的 BVDV 控制。

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