Gross C H, Wolgamot G M, Russell R L, Pearson M N, Rohrmann G F
Department of Agricultural Chemistry, Oregon State University, Corvallis 97331-7301.
J Virol. 1993 Jan;67(1):469-75. doi: 10.1128/JVI.67.1.469-475.1993.
The gene encoding a 37-kDa glycoprotein (gp37) of Orgyia pseudotsugata multinucleocapsid nuclear polyhedrosis virus (OpMNPV) was located and sequenced. gp37 of OpMNPV was found to have 62 and 37% amino acid sequence identity with gp37 of Autographa californica multinucleocapsid nuclear polyhedrosis virus (AcMNPV) and with a protein reported to be a component of occlusion bodies from Choristoneura biennis entomopoxvirus, respectively. The mRNA start site of the OpMNPV gp37 gene was mapped within a late promoter sequence (TTAAG). A TrpE fusion protein containing 55% of the OpMNPV gp37 gene amino acid sequence was used to generate a monospecific antiserum. Western immunoblot analysis of OpMNPV-infected Lymantria dispar cells detected gp37 beginning at 24 h postinfection. Immunoelectron microscopy indicated that the protein is concentrated in cytoplasmic inclusion bodies late in infection. In contrast to gp37 of AcMNPV which was present in the matrix of occlusion bodies, OpMNPV gp37 was not observed in this location. Neither OpMNPV nor AcMNPV gp37 was associated with the polyhedron envelope.
定位并测序了 Pseudotsugata 云杉毒蛾多核衣壳核型多角体病毒(OpMNPV)编码 37 kDa 糖蛋白(gp37)的基因。发现 OpMNPV 的 gp37 与苜蓿银纹夜蛾多核衣壳核型多角体病毒(AcMNPV)的 gp37 以及据报道是双带卷叶蛾昆虫痘病毒包涵体一个组分的一种蛋白质分别具有 62%和 37%的氨基酸序列同一性。OpMNPV gp37 基因的 mRNA 起始位点定位于一个晚期启动子序列(TTAAG)内。使用包含 OpMNPV gp37 基因 55%氨基酸序列的 TrpE 融合蛋白产生了一种单特异性抗血清。对 OpMNPV 感染的舞毒蛾细胞进行的 Western 免疫印迹分析检测到感染后 24 小时开始出现 gp37。免疫电子显微镜表明该蛋白在感染后期集中于细胞质包涵体内。与存在于包涵体基质中的 AcMNPV 的 gp37 不同,未在该位置观察到 OpMNPV 的 gp37。OpMNPV 和 AcMNPV 的 gp37 均与多面体包膜无关。