Accessory gland protein regulates pairing process and oviposition in the subterranean termite Reticulitermes chinensis after swarming

Author:

Liu Yutong1,Zhang Fei2,Hassan Ali1,Zhou Xuguo3ORCID,Huang Qiuying1ORCID

Affiliation:

1. Hubei Insect Resources Utilization and Sustainable Pest Management Key Laboratory Huazhong Agricultural University Wuhan China

2. National Key Laboratory of Crop Genetic Improvement Huazhong Agricultural University Wuhan China

3. Department of Entomology University of Kentucky Lexington KY USA

Abstract

AbstractSwarming and pairing behaviors are significant to population dispersal of termites. Tandem running is a key process in pairing behavior of dealates to find a mate. Succinylation can lead to significant changes in protein structure and function, which is widely involved in metabolism and behavior regulation in many organisms. However, whether succinylation modification regulates termites’ tandem running is currently unknown. In this research, we performed quantitative modified proteomics of the subterranean termite Reticulitermes chinensis Snyder before and after alate swarming. The succinylation levels of accessory gland protein (ACP) were significantly altered after alate swarming. We found that ACP is enriched in male accessory gland and female oocytes of termites. The acetylation and succinylation sites of ACP affected tandem running of dealates. The transcriptome and metabolome analyses of alates injected with ACP and its mutant proteins showed that β‐alanine metabolism pathway was the major downstream pathway of ACP. Silencing the significantly differentially expressed genes in the β‐alanine metabolic pathway (acyl‐CoA dehydrogenase, enoyl‐CoA hydratase, 3‐hydroxyisobutyrate dehydrogenase, methylmalonate‐semialdehyde dehydrogenase) suppressed tandem running and altered oviposition of paired dealates. These findings demonstrate that protein translation modification is an important regulator of tandem running behavior of termites, which implies that the succinylation and acetylation modification sites of ACP could be potential targets for insecticide action. Our research offers a potential approach for developing novel dispersal inhibitors against social insect pests.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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