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

被引:9
|
作者
Zhu, Jia-ying [1 ,2 ,3 ,4 ]
Fang, Qi [1 ,2 ]
Ye, Gong-yin [1 ,2 ]
Hu, Cui [1 ,2 ]
机构
[1] Zhejiang Univ, Inst Insect Sci, Minist Agr, State Key Lab Rice Biol, Hangzhou 310029, Zhejiang, Peoples R China
[2] Zhejiang Univ, Inst Insect Sci, Minist Agr, Key Lab Mol Biol Crop Pathol & Insects, Hangzhou 310029, Zhejiang, Peoples R China
[3] SW Forestry Univ, Minist Educ, Key Lab Forest Disaster Warning & Control Yunnan, Kunming 650224, Peoples R China
[4] SW Forestry Univ, Minist Educ, Key Lab SW Mt Forest Resources Conservat & Utiliz, Kunming 650224, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Proteomics; Plasma; Parasitism; Gene cloning; Pteromalus puparum; Pieris rapae; MOLECULAR-CLONING; HYMENOPTERA PTEROMALIDAE; CHELONUS-INANITUS; VENOM PROTEINS; HOST; LARVAE; LEPIDOPTERA; GROWTH; POLYDNAVIRUS; STRATEGIES;
D O I
10.1631/jzus.B1000158
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
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 parasitoidinduced host alterations associated with innate immune responses, detoxification, and energy metabolism.
引用
收藏
页码:93 / 102
页数:10
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