Phenoloxidase and its zymogen are required for the larval-pupal transition in Bactrocera dorsalis (Diptera: Tephritidae)

被引:14
作者
Bai, Ping-Ping [1 ]
Xie, Yi-Fei [1 ]
Shen, Guang-Mao [1 ]
Wei, Dan-Dan [1 ]
Wang, Jin-Jun [1 ]
机构
[1] Southwest Univ, Coll Plant Protect, Key Lab Entomol & Pest Control Engn, Chongqing 400716, Peoples R China
关键词
Bactrocera dorsalis; Phenoloxidase; Prophenoloxidase; RNA interference; Metal ions; ORIENTAL FRUIT-FLY; GLUTATHIONE S-TRANSFERASES; BIOCHEMICAL-CHARACTERIZATION; MOLECULAR CHARACTERIZATION; POLYPHENOL OXIDASES; MESSENGER-RNA; PROPHENOLOXIDASE; PURIFICATION; EXPRESSION; MELANIZATION;
D O I
10.1016/j.jinsphys.2014.10.013
中图分类号
Q96 [昆虫学];
学科分类号
摘要
Phenoloxidases (POs) play a key role in melanin production, are involved in invertebrate immune mechanisms, and are considered important enzymes in the insect development process. In the present study, we report the developmental stage and tissue-specific expression patterns of BdPPO1 and PO activity from Bactrocera dorsalis. The results showed that the activity of PO and its zymogen expression were closely related to the development of B. dorsalis during the larval-pupal transition, particularly in the integument. Additionally, biochemical characterization showed that PO from different developmental stages and tissues all had maximum activity at pH 7.5 and 37 degrees C. After feeding a metal ion-containing artificial diet, the activity of PO and expression of BdPPO1 were significantly increased, indicating that PO was a metalloprotein and it could be activated by Zn2+, Mg2+, Ca2+, and Cu2+. The functional analysis showed that the expression of BdPPO1 could be regulated by 20-hydroxyecdysone (20E) after injection. Furthermore, injection of the double-stranded RNA of BdPPO1 into the 3rd instar larvae significantly reduced mRNA levels after 24 h and 48 h, and resulted in a lower pupation rate and abnormal phenotype. These results expand the understanding of the important role of PO and its zymogen in the growth of B. dorsalis. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:137 / 146
页数:10
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