{"title":"Sugar transporter protein gene LdST59 of Lymantria dispar mediates lethality of larvae infected by its viral pathogen, LdMNPV","authors":"Xiang Liu , Tong-Xian Liu , Dun Wang","doi":"10.1016/j.pestbp.2025.106871","DOIUrl":null,"url":null,"abstract":"<div><div>Viral infection triggers an immune response in insects, causing a shift in energy resources to immune defense mechanisms. Although sugar transporters are known to be involved in carbohydrate transport in insects, their specific function in metabolic process of viral defense has not been well understood. The genes encoded <em>Lymantria dispar</em> sugar transporter proteins <em>(LdSTs</em>) were characterized and functionally analyzed for their roles in sugar transportation in response to viral infection to this insect host by <em>Lymantria dispar</em> nucleopolyhedrovirus (LdMNPV). Totally, 82 <em>LdSTs</em> were identified from the transcriptomic data. Expression levels for most of these sugar transporter genes significantly changed during LdMNPV infection determined by post-infection temporal analysis. The trehalose and glucose were transported significantly from peripheral tissues (e.g., fat body) to the hemolymph of host insect during the viral infection. Interestingly, silencing <em>LdST59</em> impaired glucose enrichment to hemolymph and suppressed expression of antimicrobial peptides (<em>AMPs</em>) genes, which led to increased lethality and the DNA replication levels of LdMNPV from viral infection. These results suggest that LdST59 is involved in the redistribution of glucose between different larval tissues after viral infection and that this shift in energy supply pattern plays an important role in the lethality of LdMNPV to larvae.</div></div>","PeriodicalId":19828,"journal":{"name":"Pesticide Biochemistry and Physiology","volume":"217 ","pages":"Article 106871"},"PeriodicalIF":4.8000,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pesticide Biochemistry and Physiology","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S004835752500584X","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/12/3 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Viral infection triggers an immune response in insects, causing a shift in energy resources to immune defense mechanisms. Although sugar transporters are known to be involved in carbohydrate transport in insects, their specific function in metabolic process of viral defense has not been well understood. The genes encoded Lymantria dispar sugar transporter proteins (LdSTs) were characterized and functionally analyzed for their roles in sugar transportation in response to viral infection to this insect host by Lymantria dispar nucleopolyhedrovirus (LdMNPV). Totally, 82 LdSTs were identified from the transcriptomic data. Expression levels for most of these sugar transporter genes significantly changed during LdMNPV infection determined by post-infection temporal analysis. The trehalose and glucose were transported significantly from peripheral tissues (e.g., fat body) to the hemolymph of host insect during the viral infection. Interestingly, silencing LdST59 impaired glucose enrichment to hemolymph and suppressed expression of antimicrobial peptides (AMPs) genes, which led to increased lethality and the DNA replication levels of LdMNPV from viral infection. These results suggest that LdST59 is involved in the redistribution of glucose between different larval tissues after viral infection and that this shift in energy supply pattern plays an important role in the lethality of LdMNPV to larvae.
期刊介绍:
Pesticide Biochemistry and Physiology publishes original scientific articles pertaining to the mode of action of plant protection agents such as insecticides, fungicides, herbicides, and similar compounds, including nonlethal pest control agents, biosynthesis of pheromones, hormones, and plant resistance agents. Manuscripts may include a biochemical, physiological, or molecular study for an understanding of comparative toxicology or selective toxicity of both target and nontarget organisms. Particular interest will be given to studies on the molecular biology of pest control, toxicology, and pesticide resistance.
Research Areas Emphasized Include the Biochemistry and Physiology of:
• Comparative toxicity
• Mode of action
• Pathophysiology
• Plant growth regulators
• Resistance
• Other effects of pesticides on both parasites and hosts.