Crabb B S, Allen G P, Studdert M J
School of Veterinary Science, University of Melbourne, Parkville, Victoria, Australia.
J Gen Virol. 1991 Sep;72 ( Pt 9):2075-82. doi: 10.1099/0022-1317-72-9-2075.
A panel of 14 monoclonal antibodies (MAbs) was used to characterize the high abundance glycoproteins of equine herpesviruses 4 (EHV-4) and 1 (EHV-1), and asinine herpesvirus 3 (AHV-3). The specificities of the MAbs, which had been determined previously for strains of EHV-4 and -1 from the U.S.A., in general were confirmed by ELISA for Australian strains of these viruses. Of the 14 MAbs seven were EHV-4 and -1 type-common and cross-reacted with AHV-3. Of the five MAbs that were EHV-1 type-specific, four cross-reacted with AHV-3, whereas neither of the EHV-4 type-specific MAbs reacted with AHV-3, providing further evidence for a closer evolutionary relationship between EHV-1 and AHV-3 than that between either of these viruses and EHV-4. By Western blot and immunoprecipitation analyses, the identity of the six major glycoproteins, gp2, gp10, gp13, gp14, gp18 and gp21/22a, of an Australian EHV-1 isolate was verified, and it was shown that AHV-3 had cross-reactive glycoproteins of very similar Mr to those of EHV-1; five homologous glycoproteins of EHV-4 were also identified. It was determined that the EHV-4 gp13 homologue had a much reduced Mr (67K) when the virus was grown in a continuous cell line than when grown in equine foetal kidney cells (95K). It is suggested that altered glycosylation by the cell line is responsible for this change in Mr. Those glycoproteins acting as major immunogens in the naturally infected host, at least in their ability to elicit antibody, were identified. It was found that gp2, gp13, gp14, gp18 and a glycoprotein at 120K (EHV-1) or 116K (EHV-4) were all important immunogens in mares following EHV-1-induced abortion, and in a specific pathogen-free foal experimentally infected with EHV-1 and later cross-challenged with EHV-4. Gp2, gp14 and gp18 were the major immunogens in the donkey in response to AHV-3 infection. The type specificity associated with these glycoproteins was also examined and it was found that although most if not all contain type-specific epitopes, gp2 and a glycoprotein at 120K, and to a lesser extent gp13 and gp18, were significantly type-specific in the serum from a mare following natural EHV-1 infection and abortion.
使用一组14种单克隆抗体(MAb)对马疱疹病毒4型(EHV - 4)、1型(EHV - 1)和驴疱疹病毒3型(AHV - 3)的高丰度糖蛋白进行表征。这些单克隆抗体先前已针对来自美国的EHV - 4和 - 1毒株确定了特异性,通过酶联免疫吸附测定(ELISA)对这些病毒的澳大利亚毒株进行检测,其特异性总体上得到了证实。在这14种单克隆抗体中,有7种是EHV - 4和 - 1共有的类型,并且与AHV - 3发生交叉反应。在5种EHV - 1型特异性单克隆抗体中,有4种与AHV - 3发生交叉反应,而EHV - 4型特异性单克隆抗体均未与AHV - 3发生反应,这进一步证明了EHV - 1与AHV - 3之间的进化关系比这两种病毒与EHV - 4之间的进化关系更为密切。通过蛋白质印迹法(Western blot)和免疫沉淀分析,验证了澳大利亚EHV - 1分离株的6种主要糖蛋白gp2、gp10、gp13、gp14、gp18和gp21/22a的身份,并表明AHV - 3具有与EHV - 1分子量非常相似的交叉反应性糖蛋白;还鉴定出了EHV - 4的5种同源糖蛋白。已确定,当病毒在连续细胞系中生长时,EHV - 4的gp13同源物的分子量(67K)比在马胎儿肾细胞中生长时(95K)大幅降低。提示细胞系导致的糖基化改变是造成分子量这种变化的原因。确定了那些在自然感染宿主中作为主要免疫原的糖蛋白,至少在其引发抗体的能力方面是如此。研究发现,gp2、gp13、gp14、gp18以及120K(EHV - 1)或116K(EHV - 4)处的一种糖蛋白在EHV - 1诱导流产后的母马以及在实验性感染EHV - 1并随后用EHV - 4进行交叉攻击的无特定病原体幼驹中均为重要免疫原。Gp2、gp14和gp18是驴对AHV - 3感染产生反应的主要免疫原。还研究了与这些糖蛋白相关的类型特异性,发现尽管大多数(如果不是全部)都含有类型特异性表位,但gp2和120K处的一种糖蛋白,以及在较小程度上gp13和gp18,在自然感染EHV - 1并流产后的母马血清中具有显著的类型特异性。