Mettenleiter T C
Institut für Molekulare und Zelluläre Virologie, Friedrich-Loeffler-Institute der Bundesforschungsanstalt für Viruskrankheiten der Tiere, Insel Riems.
Tierarztl Prax. 1995 Dec;23(6):570-4.
New insights into the molecular biology of pseudorabies virus (PrV), the causative agent of Aujeszky's disease (AD) of pigs, led to novel concepts for eradication of the disease. Virus mutants, which lack certain nonessential glycoproteins, formed the basis for the development of the first available marked vaccines. They allow a differentiation between infected and vaccinated animals. Further molecular studies resulted in the identification of several PrV genes whose products modulate virulence and pathogenicity of the virus, and which are therefore targeted by genetic engineering methods to develop new attenuated virus strains. The isolation of virus mutants, which cannot be shed in infectious form by vaccinated animals, led to an increase in the biological safety of respective PrV vaccines. The availability of these mutants now provides the basis for the development of safe PrV vector vaccines, in which recombinant PrV express immunogenic proteins of other, unrelated viruses leading to a broad antiviral immunity. Based on PrV vectors marked vaccines against other viral diseases are being developed which represent powerful tools for combatting infectious diseases in animals.
对猪奥耶斯基氏病(AD)病原体伪狂犬病病毒(PrV)分子生物学的新见解,为根除该疾病带来了新的理念。缺乏某些非必需糖蛋白的病毒突变体,构成了首个可用标记疫苗研发的基础。它们能够区分感染动物和接种疫苗的动物。进一步的分子研究确定了几个PrV基因,其产物可调节病毒的毒力和致病性,因此通过基因工程方法针对这些基因来开发新的减毒病毒株。无法通过接种疫苗的动物以感染性形式排出的病毒突变体的分离,提高了相应PrV疫苗的生物安全性。这些突变体的可用性现在为开发安全的PrV载体疫苗提供了基础,其中重组PrV表达其他无关病毒的免疫原性蛋白,从而产生广泛的抗病毒免疫力。基于PrV载体,正在开发针对其他病毒性疾病的标记疫苗,这些疫苗是对抗动物传染病的有力工具。