Abstract
Glycosylation is a common modification of proteins and critical for a wide range of biological processes. Differences in protein glycosylation between sexes have already been observed in humans, nematodes and trematodes, and have recently also been reported in the rice pest insect Nilaparvata lugens Although protein N-glycosylation in insects is nowadays of high interest because of its potential for exploitation in pest control strategies, the functionality of differential N-glycosylation between sexes is yet unknown. In this study, therefore, the occurrence and role of sex-related protein N-glycosylation in insects were examined. A comprehensive investigation of the N-glycosylation sites from the adult stages of N. lugens was conducted, allowing a qualitative and quantitative comparison between sexes at the glycopeptide level. N-glycopeptide enrichment via lectin capturing using the high mannose/paucimannose-binding lectin Concanavalin A, or the Rhizoctonia solani agglutinin which interacts with complex N-glycans, resulted in the identification of over 1300 N-glycosylation sites derived from over 600 glycoproteins. Comparison of these N-glycopeptides revealed striking differences in protein N-glycosylation between sexes. Male- and female-specific N-glycosylation sites were identified, and some of these sex-specific N-glycosylation sites were shown to be derived from proteins with a putative role in insect reproduction. In addition, differential glycan composition between males and females was observed for proteins shared across sexes. Both lectin blotting experiments as well as transcript expression analyses with complete insects and insect tissues confirmed the observed differences in N-glycosylation of proteins between sexes. In conclusion, this study provides further evidence for protein N-glycosylation to be sex-related in insects. Furthermore, original data on N-glycosylation sites of N. lugens adults are presented, providing novel insights into planthopper's biology and information for future biological pest control strategies.
Highlights
Nilaparvata lugens Stål (Hemiptera: Delphacidae) or the brown planthopper (BPH) is one of the most notorious pest insects in the rice producing countries of Asia [1]
Concanavalin A (ConA) interacts with high mannose and paucimannose N-glycans, while Rhizoctonia solani agglutinin (RSA) binds to complex N-glycans carrying terminal Gal and N-acetylgalactosamine (GalNAc) residues
To evaluate whether differences in protein glycosylation are present between wing forms and/or adult sexes, as was previously observed at the N-glycome level [4], far-western blot analysis was conducted using anti-ConA as the primary antibody to visualize glycoproteins carrying high mannose and/or paucimannose N-glycans
Summary
Nilaparvata lugens Stål (Hemiptera: Delphacidae) or the brown planthopper (BPH) is one of the most notorious pest insects in the rice producing countries of Asia [1]. To evaluate whether differences in protein glycosylation are present between wing forms and/or adult sexes, as was previously observed at the N-glycome level [4], far-western blot analysis was conducted using anti-ConA as the primary antibody to visualize glycoproteins carrying high mannose and/or paucimannose N-glycans. Complete protein extracts were enriched for glycopeptides using the lectins ConA and RSA to select peptides carrying high mannose/paucimannose N-glycans and complex N-glycans, respectively.
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