Trudeau D, Witherell R A, Strand M R
Department of Entomology, University of Wisconsin-Madison, Madison, WI 53706, USA1.
J Gen Virol. 2000 Dec;81(Pt 12):3049-3058. doi: 10.1099/0022-1317-81-12-3049.
The braconid wasp Microplitis demolitor carries M. demolitor polydnavirus (MdPDV) and parasitizes the larval stage of the moth Pseudoplusia includens. M. demolitor injects MdPDV into P. includens larvae when it lays an egg and the virus infects various cells including haemocytes. Two new MdPDV transcripts expressed in host haemocytes were characterized in this study. Screening of an MdPDV-infected haemocyte cDNA library identified a 0.4 kb cDNA encoding a predicted protein of 103 amino acids which was named Egf0. 4. This protein contained a cysteine-rich epidermal growth factor (EGF)-like motif at its N terminus that was similar to the EGF-like domains in the previously identified MdPDV genes egf1.5 and egf1.0. Sequencing of the genomic clone pMd-10 indicated that it contained the egf0.4 gene, which consisted of two introns and three exons. This gene was located on MdPDV segment O and appeared to exist in multiple copies. A nucleic acid and expression screen identified a 1. 8 kb cDNA encoding a predicted protein of 515 amino acids designated Glc1.8. This protein consisted of a heavily glycosylated central core of six tandemly arranged repeats flanked by hydrophobic N- and C-terminal domains. Northern blotting and in situ hybridization studies indicated that both egf0.4 and glc1.8 were expressed in MdPDV-infected host haemocytes. Immunocytochemical studies also indicated that Glc1.8 localized to the cell surface.
茧蜂科黄蜂毁侧沟茧蜂携带毁侧沟茧蜂多DNA病毒(MdPDV),并寄生于海灰翅夜蛾幼虫阶段。毁侧沟茧蜂在产卵时将MdPDV注入海灰翅夜蛾幼虫体内,该病毒会感染包括血细胞在内的各种细胞。本研究对在宿主血细胞中表达的两种新的MdPDV转录本进行了表征。对一个受MdPDV感染的血细胞cDNA文库进行筛选,鉴定出一个0.4 kb的cDNA,其编码一个预测的103个氨基酸的蛋白质,命名为Egf0.4。该蛋白质在其N端含有一个富含半胱氨酸的表皮生长因子(EGF)样基序,与先前鉴定的MdPDV基因egf1.5和egf1.0中的EGF样结构域相似。基因组克隆pMd-10的测序表明它包含egf0.4基因,该基因由两个内含子和三个外显子组成。该基因位于MdPDV片段O上,似乎以多个拷贝存在。核酸和表达筛选鉴定出一个1.8 kb的cDNA,其编码一个预测的515个氨基酸的蛋白质,命名为Glc1.8。该蛋白质由六个串联排列的重复序列组成的高度糖基化中央核心以及两侧的疏水N端和C端结构域组成。Northern印迹和原位杂交研究表明,egf0.4和glc1.8均在受MdPDV感染的宿主血细胞中表达。免疫细胞化学研究还表明,Glc1.8定位于细胞表面。