Taylor L F, Van Donkersgoed J, Dubovi E J, Harland R J, van den Hurk J V, Ribble C S, Janzen E D
Department of Herd Medicine and Theriogenology, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon.
Can J Vet Res. 1995 Apr;59(2):87-93.
The prevalence of bovine viral diarrhea virus (BVDV) infection was examined in a population of 5129 recently weaned steer calves entering a large feedlot in central Saskatchewan from September to December 1991. Serum samples were collected within 24 h of arrival at the feedlot from every fifth calf processed and again 96 d postarrival. A microtiter virus isolation test was used to determine the prevalence of calves viremic with BVDV on entry to the feedlot. An enzyme-linked immunosorbent assay (ELISA) which detects antibody against glycoprotein 53 of the BVDV was used on paired sera to determine the seroconversion risk during the first 96 d in the feedlot. A virus neutralization (VN) test for BVDV was conducted on a sub-sample of paired sera to measure agreement in determination of seroconversion risk with the ELISA. A polymerase chain reaction (PCR) test which detects BVDV was used to determine if cattle were acutely viremic when treated for disease. The estimated prevalence of persistently infected calves in this population was < 0.1%. The seroconversion risk for BVDV was 27% (236/864) according to the ELISA and it varied from 0 to 63% among the 20 pens sampled. According to the VN test, the seroconversion risk for BVDV was 40% (132/327) and it varied from 0 to 100% among the 11 pens tested. The agreement between the ELISA and VN tests in seroconversion risk to BVDV was very poor (kappa = 0.15 +/- 0.039 SE). The prevalence of acute viremia in calves treated at the feedlot hospital was low at 4% (6/149).(ABSTRACT TRUNCATED AT 250 WORDS)
1991年9月至12月期间,对进入萨斯喀彻温省中部一个大型饲养场的5129头刚断奶的小公牛犊进行了牛病毒性腹泻病毒(BVDV)感染率检测。在牛犊抵达饲养场后的24小时内,从每五头处理的牛犊中采集血清样本,抵达后96天再次采集。采用微量滴定病毒分离试验来确定进入饲养场时感染BVDV的病毒血症牛犊的感染率。对配对血清使用一种检测针对BVDV糖蛋白53抗体的酶联免疫吸附测定(ELISA),以确定在饲养场的前96天内血清转化风险。对配对血清的一个子样本进行BVDV病毒中和(VN)试验,以衡量与ELISA在血清转化风险测定方面的一致性。使用一种检测BVDV的聚合酶链反应(PCR)试验来确定牛在治疗疾病时是否处于急性病毒血症状态。该群体中持续感染牛犊的估计感染率<0.1%。根据ELISA,BVDV的血清转化风险为27%(236/864),在抽样的20个围栏中,其风险从0到63%不等。根据VN试验,BVDV的血清转化风险为40%(132/327),在测试的11个围栏中,其风险从0到100%不等。ELISA和VN试验在BVDV血清转化风险方面的一致性非常差(kappa = 0.15 +/- 0.039标准误)。在饲养场医院接受治疗的牛犊中,急性病毒血症的发生率较低,为4%(6/149)。(摘要截短为250字)