Yang Jie, Wang Xiaonan, Tang Shunming, Shen Zhongyuan, Wu Jinmei
College of Biotechnology, Jiangsu University of Science and Technology, Zhenjiang 212018, China.
The Sericultural Research Institute, Chinese Academy of Agricultural Sciences, Zhenjiang 212018, China.
J Insect Sci. 2015 Mar 22;15(1). doi: 10.1093/jisesa/iev007. Print 2015.
Peptidoglycan recognition protein (PGRP) binds specifically to peptidoglycan and plays an important role as a pattern recognition receptor in the innate immunity of insects. The cDNA of a short-type PGRP, an open reading frame of 588 bp encoding a polypeptide of 196 amino acids, was cloned from Bombyx mori. A phylogenetic tree was constructed, and the results showed that BmPGRP-S2 was most similar to Drosophila melanogaster PGRP (DmPGRP-SA). The induced expression profile of BmPGRP-S2 in healthy Escherichia coli- and Bacillus subtilis-challenged B. mori was measured using semiquantitative reverse transcriptase polymerase chain reaction analysis. The expression of BmPGRP-S2 was upregulated at 24 h by E. coli and Ba. subtilis challenge. In addition, in the integument of B. mori, RNAi knockdown of BmPGRP-S2 caused an obvious reduction in the transcription expression of the transcription factor Relish and in antibacterial effector genes Attacin, Gloverin, and Moricin. The results indicated that BmPGRP-S2 participates in the signal transduction pathway of B. mori.
肽聚糖识别蛋白(PGRP)特异性结合肽聚糖,并作为模式识别受体在昆虫先天免疫中发挥重要作用。从家蚕中克隆出一种短型PGRP的cDNA,其开放阅读框为588 bp,编码一个由196个氨基酸组成的多肽。构建了系统发育树,结果表明家蚕PGRP-S2(BmPGRP-S2)与黑腹果蝇PGRP(DmPGRP-SA)最为相似。使用半定量逆转录聚合酶链反应分析测定了健康家蚕在受到大肠杆菌和枯草芽孢杆菌攻击后BmPGRP-S2的诱导表达谱。大肠杆菌和枯草芽孢杆菌攻击后24小时,BmPGRP-S2的表达上调。此外,在家蚕的体表,RNA干扰敲低BmPGRP-S2导致转录因子Relish以及抗菌效应基因Attacin、Gloverin和Moricin的转录表达明显降低。结果表明,BmPGRP-S2参与家蚕的信号转导途径。