Integrated multi-omics analysis and RNAi reveal Toll signaling pathway and melanization as key defenses in Ostrinia furnacalis against Meteorus pulchricornis parasitism
{"title":"Integrated multi-omics analysis and RNAi reveal Toll signaling pathway and melanization as key defenses in Ostrinia furnacalis against Meteorus pulchricornis parasitism","authors":"Ziyuan Tang , Gui Gao , Zhilin Xia , Changli Yang , Changyu Zhang","doi":"10.1016/j.cbd.2025.101537","DOIUrl":null,"url":null,"abstract":"<div><div><em>Ostrinia furnacalis</em>, a worldwide agricultural pest, can be effectively controlled using the endoparasitic wasp <em>Meteorus pulchricornis</em>. However, the molecular mechanisms underlying the host immune response to parasitism remain poorly understood. This study aimed to explore the possible immune molecular mechanisms of <em>O. furnacalis</em> under parasitism by <em>M. pulchricornis</em> for 24 and 48 h (P24 and P48). Overall, 97 differentially expressed genes (DEGs) and 18 differentially expressed proteins (DEPs) associated with immunity were identified, including pattern-recognition receptors (PRRs), antimicrobial peptides (AMPs), antioxidant enzymes, Toll signaling pathway and melanization components. Three Toll signaling pathway downstream genes <em>OfMyD88</em>, <em>OfGlov</em>, and <em>OfLys</em> were chosen for functional analysis by RNA interference (RNAi). The results showed a notable increase in parasitism rate (7–9 %) in immunocompromised hosts and a significant decrease in survival rates (23–27 %), demonstrating that <em>OfMyD88</em>, <em>OfGlov</em>, and <em>OfLys</em> play crucial roles in the parasitic stress response and larvae survival. Our findings reveal novel insights into the immune molecular mechanisms of <em>O. furnacalis</em> and highlight potential targets for enhancing parasitic wasp-based biocontrol strategies.</div></div>","PeriodicalId":55235,"journal":{"name":"Comparative Biochemistry and Physiology D-Genomics & Proteomics","volume":"56 ","pages":"Article 101537"},"PeriodicalIF":2.2000,"publicationDate":"2025-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Comparative Biochemistry and Physiology D-Genomics & Proteomics","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1744117X25001261","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Ostrinia furnacalis, a worldwide agricultural pest, can be effectively controlled using the endoparasitic wasp Meteorus pulchricornis. However, the molecular mechanisms underlying the host immune response to parasitism remain poorly understood. This study aimed to explore the possible immune molecular mechanisms of O. furnacalis under parasitism by M. pulchricornis for 24 and 48 h (P24 and P48). Overall, 97 differentially expressed genes (DEGs) and 18 differentially expressed proteins (DEPs) associated with immunity were identified, including pattern-recognition receptors (PRRs), antimicrobial peptides (AMPs), antioxidant enzymes, Toll signaling pathway and melanization components. Three Toll signaling pathway downstream genes OfMyD88, OfGlov, and OfLys were chosen for functional analysis by RNA interference (RNAi). The results showed a notable increase in parasitism rate (7–9 %) in immunocompromised hosts and a significant decrease in survival rates (23–27 %), demonstrating that OfMyD88, OfGlov, and OfLys play crucial roles in the parasitic stress response and larvae survival. Our findings reveal novel insights into the immune molecular mechanisms of O. furnacalis and highlight potential targets for enhancing parasitic wasp-based biocontrol strategies.
期刊介绍:
Comparative Biochemistry & Physiology (CBP) publishes papers in comparative, environmental and evolutionary physiology.
Part D: Genomics and Proteomics (CBPD), focuses on “omics” approaches to physiology, including comparative and functional genomics, metagenomics, transcriptomics, proteomics, metabolomics, and lipidomics. Most studies employ “omics” and/or system biology to test specific hypotheses about molecular and biochemical mechanisms underlying physiological responses to the environment. We encourage papers that address fundamental questions in comparative physiology and biochemistry rather than studies with a focus that is purely technical, methodological or descriptive in nature.