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Cloning of partial glycoprotein B gene and molecular epidemiological studies of bovine herpes virus-1 isolates.

机译:牛疱疹病毒1分离株糖蛋白B基因的克隆及分子流行病学研究。

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摘要

The study describes genetic grouping and molecular epidemiology of bovine herpes virus-1 (BoHV-1) through cloning of partial glycoprotein B gene of BoHV-1 isolates, with special reference to isolates recovered from cattle breeding stations. Samples were collected from 212 animals (91 bulls and 121 female cattle). Avidin-biotin ELISA employed on serum samples found 74 animals as seropositive for BoHV-1. On inoculation of 212 semen/swab samples to MDBK cell line for virus isolation, samples of 4 seropositive and 5 seronegative animals yielded cytopathic changes characteristic of BoHV-1. Partial gB gene of these isolates were cloned in pGEM T vector, nucleotide sequences were deduced and phylogenetic tree was constructed. Sequence analysis grouped 5 of these isolates under BoHV-1.1 cluster having highest sequence identities with previously described Indian, European and Brazilian isolates of BoHV-1.1. The other 4 isolates were clustered as BoHV-1.2 subtypes having 100% sequence identity with European strain of BoHV1.2. We found that, apparently healthy, seronegative animals can be sources of BoHV-1, attributable to the unique pathogenesis/latency of BoHV-1. This finding necessitates mandatory culling of breeding animals which are positive either in antigen detection or by serology, especially in countries which do not practice vaccination but report high seroprevalance of BoHV-1.
机译:该研究通过克隆BoHV-1分离株的部分糖蛋白B基因,描述了牛疱疹病毒1(BoHV-1)的遗传分组和分子流行病学,特别参考了从牛育种站回收的分离株。从212只动物(91头公牛和121头母牛)收集了样本。对血清样品进行的抗生物素蛋白生物素酶联免疫吸附测定发现74只动物对BoHV-1呈血清反应阳性。在MDBK细胞系中接种212个精液/拭子样品以分离病毒后,对4例血清反应阳性和5例血清阴性的动物进行了BoHV-1特征性细胞病变。将这些分离物的部分gB基因克隆到pGEM T载体中,推导核苷酸序列并构建系统树。序列分析将这些分离株中的5个与先前描述的BoHV-1.1的印度,欧洲和巴西分离株进行了最高序列同一性的BoHV-1.1聚类。其他4个分离物被聚类为与欧洲BoHV1.2菌株具有100%序列同一性的BoHV-1.2亚型。我们发现,显然健康,血清阴性的动物可以是BoHV-1的来源,这归因于BoHV-1的独特发病机理/潜伏期。这一发现使得必须强制淘汰在抗原检测或血清学检查中呈阳性的繁殖动物,特别是在未进行疫苗接种但报告BoHV-1血清阳性率很高的国家。

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