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伪狂犬病

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Furthermore, this method had a better specificity without cross-reaction with positive sera to PPV、FMD and PRV.

且操作简单,耗时短,与猪细小病毒、口蹄疫和猪伪狂犬病毒阳性血清不发生交叉反应。

The results showed that established PRV PCR technique provided a more sensitive,specific and reliable method for diagnosis and epizootic study of the pseudorabies.

结果病料阳性率为 2 6 2 %( 50 191),猪场阳性率为 71%( 2 2 31)实验结果表明,所建立的PCR技术可用于伪狂犬病的快速诊断和流行病学调查

This indicated that the EPO gene be expressed in BL21(DE3) and the expression products have immunogenicity.

本实验为进一步研究EPO基因的功能以及伪狂犬病病毒的潜伏感染奠定了基础。

At first, the PRV as antigen was purified by overspeed centrifugal method.

试验所用的第一抗体为兔抗伪狂犬病毒鄂A株的IgG。

Result A average positive rate was 21.55% of porcine contagious pleuropneumonia. And the mixed infection between porcine contagious pleuropneumonia and the other pathogens given above was confirmed.

结果]平均阳性率为21.55%,同时在被检猪中又进行了猪瘟、圆环病毒、蓝耳病、伪狂犬病、弓形体等疾病感染的检测,证实猪传染性胸膜肺炎与病毒性、细菌性、寄生虫性疾病有着不同程度的混合感染。

Vaccination is still the most effective and economical means to prevent and control pseudorabies in swine.

伪狂犬病是当今危害养猪业的最重要传染病之一,疫苗免疫接种仍是目前控制和预防该病的主要手段。

Pseudorabies is a intense infectious disease endangering the world porcineculture and make great economic losses in the world.

伪狂犬病是危害世界养猪业的一类烈性传染病,每年在世界范围内造成巨大的经济损失。

In this paper, a recombinant virus expressing ORF2 gene of PCV2 using pseudorabies virus as vector.

伪狂犬病病毒为载体,构建表达猪2型圆环病毒ORF2基因的重组病毒,并研究其生物学特性。

The epidemiological investigation on pathogen of Pseudorabies was conducted in 25 different pig farms in Xinjiang.

应用血清学方法对新疆13 个地区的25 个规模化猪场进行猪伪狂犬病调查,并开展了防治试验研究。

The glycoprotein G gene of pseudorabies virus Hubei strain was amplified by PCR, sequenced and analyzed.

利用PCR技术扩增了伪狂犬病毒湖北株糖蛋白G基因,进行了序列测定和分析。

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