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被内寄生蜂 Pteromalus puparum 寄生的菜粉蝶血浆中的蛋白质组变化。

Proteome changes in the plasma of Pieris rapae parasitized by the endoparasitoid wasp Pteromalus puparum.

机构信息

State Key Laboratory of Rice Biology and Key Laboratory of Molecular Biology of Crop Pathology and Insects of Ministry of Agriculture, Institute of Insect Sciences, Zhejiang University, Hangzhou 310029, China.

出版信息

J Zhejiang Univ Sci B. 2011 Feb;12(2):93-102. doi: 10.1631/jzus.B1000158.

Abstract

Parasitism by the endoparasitoid wasp Pteromalus puparum causes alterations in the plasma proteins of Pieris rapae. Analysis of plasma proteins using a proteomic approach showed that seven proteins were differentially expressed in the host pupae after 24-h parasitism. They were masquerade-like serine proteinase homolog (MSPH), enolase (Eno), bilin-binding protein (BBP), imaginal disc growth factor (IDGF), ornithine decarboxylase (ODC), cellular retinoic acid binding protein (CRABP), and one unknown function protein. The full length cDNA sequences of MSPH, Eno, and BBP were successfully cloned using rapid amplification of cDNA ends-polymerase chain reaction (RACE-PCR). Reverse transcriptase-polymerase chain reaction (RT-PCR) analysis indicated that the transcript levels of MSPH and BBP in the fat bodies of host pupae were inducible in response to the parasitism and their variations were consistent with translational changes of these genes after parasitism, while the transcript levels of Eno and IDGF were not affected by parasitism. This study will contribute to the better understanding of the molecular bases of parasitoid-induced host alterations associated with innate immune responses, detoxification, and energy metabolism.

摘要

内寄生蜂蛹期姬小蜂寄生能引起菜粉蝶幼虫血浆蛋白发生改变。采用蛋白质组学方法分析血浆蛋白,结果表明寄生后 24 小时,宿主蛹中有 7 种蛋白的表达水平存在差异。它们分别是伪装酶样丝氨酸蛋白酶同源物(MSPH)、烯醇酶(Eno)、结合胆红素蛋白(BBP)、成虫盘生长因子(IDGF)、鸟氨酸脱羧酶(ODC)、细胞视黄醇结合蛋白(CRABP)和一个未知功能蛋白。采用快速扩增 cDNA 末端聚合酶链反应(RACE-PCR)成功克隆了 MSPH、Eno 和 BBP 的全长 cDNA 序列。反转录聚合酶链反应(RT-PCR)分析表明,MSPH 和 BBP 在宿主蛹脂肪体中的转录水平可被寄生诱导,其变化与寄生后这些基因的翻译变化一致,而 Eno 和 IDGF 的转录水平不受寄生影响。本研究将有助于深入了解与先天免疫反应、解毒和能量代谢相关的寄生诱导宿主改变的分子基础。

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