Quantitative expression analysis of a Glyptapanteles indiensis polydnavirus protein tyrosine phosphatase gene in its natural lepidopteran host, Lymantria dispar

被引:25
作者
Chen, YP
Taylor, PB
Shapiro, M
Gundersen-Rindal, DE
机构
[1] ARS, Insect Biocontrol Lab, USDA, Beltsville, MD 20705 USA
[2] ARS, USDA, Beneficial Insects Intro Res Lab, Newark, DE 19713 USA
关键词
Glyptapanteles indiensis; Lymantria dispar; PDV; gene expression; RT-PCR; RT-qcPCR;
D O I
10.1046/j.1365-2583.2003.00411.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the present study, expression of a newly identified Glyptapanteles indiensis polydnavirus (GiPDV) gene encoding a putative protein tyrosine phosphatase (PDVPTP) was monitored in vivo in the parasitized host, L. dispar , using one step RT-PCR. Expression levels of the PDVPTP transcript were also evaluated in various host tissues at different times post parasitization (pp) using RT quantitative competitive PCR (RT-qcPCR). Expression levels varied, with the most abundant transcript detected in host haemolymph 2 h pp. The high expression level in host haemolymph at an early stage of parasitization suggested a potential role for viral PDVPTP in disruption of the host immune system and protection of the endoparasitoid egg from encapsulation. Additionally, the PDVPTP gene or its homolog(s) mapped to more than one GiPDV genomic DNA segment, which may account for its increased level of expression in the absence of virus replication.
引用
收藏
页码:271 / 280
页数:10
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