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A Venom Serpin Splicing Isoform of the Endoparasitoid Wasp Pteromalus puparum Suppresses Host Prophenoloxidase Cascade by Forming Complexes with Host Hemolymph Proteinases.

J Biol Chem. 2017; 
Yan Z, Fang Q, Liu Y, Xiao S, Yang L, Wang F, An C, Werren JH, Ye G.
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Catalog Antibody For detection of recombi- nant proteins with His tag, the primary antibody was THETM His tag mouse antibody (GenScript, Nanjin, China; diluted 1:2000).... The secondary antibody was HRP- or alkaline phos- phatase-conjugated goat anti-mouse IgG antibody (GenScript; diluted 1:2000). Get A Quote

摘要

To ensure successful parasitism, parasitoid wasps inject venom along with their eggs into their hosts. The venom serves to suppress host immune responses, including melanization. Venom from Pteromalus puparum, a pupal endoparasitoid, inhibits melanization of host hemolymph in vitro in a dose-dependent manner. Using assay-guided fractionation, a serpin splicing isoform with phenoloxidase inhibitory activity was identified as P puparum serpin-1, venom isoform (PpS1V). This serpin gene has 16 predicted splicing isoforms that differ only in the C-terminal region. RT-PCR results show that the specific serpin isoform is differentially expressed in the venom gland. Recombinant PpS1V (rPpS1V) suppresses host prophenolo... More

关键词

alternative splicing; insect immunity; melanization; parasitoid wasp; parasitology; proteinase; serpin; venom