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首页> 外文期刊>Journal of Clinical Microbiology >Detection of Bovine Herpesvirus Type 1 in Blood from Naturally Infected Cattle by Using a Sensitive PCR That Discriminates between Wild-Type Virus and Virus Lacking Glycoprotein E
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Detection of Bovine Herpesvirus Type 1 in Blood from Naturally Infected Cattle by Using a Sensitive PCR That Discriminates between Wild-Type Virus and Virus Lacking Glycoprotein E

机译:通过使用区分野生型病毒和缺乏糖蛋白E的敏感PCR,从自然感染牛的血液中检测牛1型疱疹病毒

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In the present study, we report for the first time on the detection of bovine herpesvirus type 1 (BHV-1) in whole-blood samples derived from naturally infected cattle. Sensitive PCR assays specific for glycoprotein B (gB), gC, and gE of BHV-1 allow the detection of one BHV-1 DNA copy in 105 to 107 peripheral blood leukocytes (PBLs). The incidence of BHV-1-positive PBLs in naturally infected cattle appears to be quite high (92.2% positive PBLs among all samples tested), although in most cases only between 10?5 and 10?7 positive leukocytes were present. The results demonstrate that the viral DNA is detectable not only in the peripheral blood of acutely infected animals but, more importantly, also in the peripheral blood of subclinically infected cattle. The gE-specific PCR described in the report allows discrimination between wild-type (WT) virus-infected and vaccinated animals, which is of importance for control programs that use the recently introduced vaccination strategy with a gE-negative virus. The results further show that doubtful serological results can be verified or falsified and that individual animals can be monitored for the presence or absence of WT BHV-1 or gE-negative virus in cattle herds. The PCR protocols allow the detection of BHV-1 prior to seroconversion or in BHV-1-seronegative cattle. Finally, the results indicate the simultaneous presence of WT and gE-negative vaccine virus in the PBLs of several cattle. Therefore, investigations of viremia in naturally and experimentally infected cattle and on the identification of infected cell types of bovine PBLs can be now performed.
机译:在本研究中,我们首次报告了在源自自然感染牛的全血样品中检测1型牛疱疹病毒(BHV-1)的方法。 BHV-1的糖蛋白B(gB),gC和gE特异的灵敏PCR分析可以检测10 5 至10 7 外围的一个BHV-1 DNA拷贝血白细胞(PBL)。在自然感染的牛中,BHV-1阳性PBL的发生率似乎很高(在所有测试样品中阳性PBL的比率为92.2%),尽管在大多数情况下,仅在10 5 和10 之间存在?7 阳性白细胞。结果表明,病毒DNA不仅可以在急性感染动物的外周血中检测到,更重要的是,还可以在亚临床感染牛的外周血中检测到。报告中描述的gE特异性PCR可以区分野生型(WT)病毒感染的动物和疫苗接种的动物,这对于使用最近引入的带有gE阴性病毒的疫苗接种策略的控制程序非常重要。结果进一步表明,可以验证或伪造可疑的血清学结果,并且可以监控单个动物的牛群中是否存在WT BHV-1或gE阴性病毒。 PCR方案可在血清转化之前或在BHV-1-血清阴性牛中检测BHV-1。最后,结果表明在几头牛的PBL中同时存在WT和gE阴性疫苗病毒。因此,现在可以对自然感染和实验感染的牛进行病毒血症调查,并确定牛PBL的感染细胞类型。

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