{"title":"毒液中侧向获得的几丁质酶基因促进了卵类寄生蜂的寄生。","authors":"Xu Chen , Guy Smagghe , Yong-Ming Chen , Lian-Sheng Zang","doi":"10.1016/j.ibmb.2025.104362","DOIUrl":null,"url":null,"abstract":"<div><div>Parasitoid wasps (Hymenoptera) play a crucial role in ecosystems and agroforestry pest management as biological control agents. These wasps utilize venom proteins to suppress host immunity and regulate physiology, facilitating offspring development. Although venom functions have been studied in some parasitoids, their roles in egg parasitoids remain poorly understood. In this study, we employed genomic and transcriptomic sequencing to identify venom proteins in <em>Anastatus japonicus</em> and <em>Anastatus fulloi</em>, two egg parasitoids used in biological control. We discovered a significant expansion of GH19 chitinase in their genomes, with phylogenetic analysis indicating acquisition via lateral gene transfer (LGT) from microsporidian. Functional characterization revealed that four highly expressed GH19 chitinases, <em>Aj13071</em>/<em>Aj13072</em> in <em>A. japonicus</em> and <em>Af23628</em>/<em>Af23629</em> in <em>A. fulloi</em> are essential for host egg penetration; silencing these genes increased penetration time and resulted in smaller or incomplete holes. Additionally, silencing <em>Aj13071</em> and <em>Aj13072</em> in <em>A. japonicus</em> impaired female fecundity, while <em>Af23628</em> and <em>Af23629</em> in <em>A. fulloi</em> affected venom reservoir development and egg load, respectively. These findings underscore the critical roles of GH19 chitinases in host penetration and reproduction, offering new insights into the molecular mechanisms driving parasitism in egg parasitoids. This study advances our understanding of venom evolution and supports the development of targeted biological control strategies.</div></div>","PeriodicalId":330,"journal":{"name":"Insect Biochemistry and Molecular Biology","volume":"183 ","pages":"Article 104362"},"PeriodicalIF":3.7000,"publicationDate":"2025-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Laterally acquired chitinase genes in venom facilitate parasitism in egg parasitoid wasps\",\"authors\":\"Xu Chen , Guy Smagghe , Yong-Ming Chen , Lian-Sheng Zang\",\"doi\":\"10.1016/j.ibmb.2025.104362\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Parasitoid wasps (Hymenoptera) play a crucial role in ecosystems and agroforestry pest management as biological control agents. These wasps utilize venom proteins to suppress host immunity and regulate physiology, facilitating offspring development. Although venom functions have been studied in some parasitoids, their roles in egg parasitoids remain poorly understood. In this study, we employed genomic and transcriptomic sequencing to identify venom proteins in <em>Anastatus japonicus</em> and <em>Anastatus fulloi</em>, two egg parasitoids used in biological control. We discovered a significant expansion of GH19 chitinase in their genomes, with phylogenetic analysis indicating acquisition via lateral gene transfer (LGT) from microsporidian. Functional characterization revealed that four highly expressed GH19 chitinases, <em>Aj13071</em>/<em>Aj13072</em> in <em>A. japonicus</em> and <em>Af23628</em>/<em>Af23629</em> in <em>A. fulloi</em> are essential for host egg penetration; silencing these genes increased penetration time and resulted in smaller or incomplete holes. Additionally, silencing <em>Aj13071</em> and <em>Aj13072</em> in <em>A. japonicus</em> impaired female fecundity, while <em>Af23628</em> and <em>Af23629</em> in <em>A. fulloi</em> affected venom reservoir development and egg load, respectively. These findings underscore the critical roles of GH19 chitinases in host penetration and reproduction, offering new insights into the molecular mechanisms driving parasitism in egg parasitoids. This study advances our understanding of venom evolution and supports the development of targeted biological control strategies.</div></div>\",\"PeriodicalId\":330,\"journal\":{\"name\":\"Insect Biochemistry and Molecular Biology\",\"volume\":\"183 \",\"pages\":\"Article 104362\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2025-07-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Insect Biochemistry and Molecular Biology\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0965174825001067\",\"RegionNum\":2,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Insect Biochemistry and Molecular Biology","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0965174825001067","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Laterally acquired chitinase genes in venom facilitate parasitism in egg parasitoid wasps
Parasitoid wasps (Hymenoptera) play a crucial role in ecosystems and agroforestry pest management as biological control agents. These wasps utilize venom proteins to suppress host immunity and regulate physiology, facilitating offspring development. Although venom functions have been studied in some parasitoids, their roles in egg parasitoids remain poorly understood. In this study, we employed genomic and transcriptomic sequencing to identify venom proteins in Anastatus japonicus and Anastatus fulloi, two egg parasitoids used in biological control. We discovered a significant expansion of GH19 chitinase in their genomes, with phylogenetic analysis indicating acquisition via lateral gene transfer (LGT) from microsporidian. Functional characterization revealed that four highly expressed GH19 chitinases, Aj13071/Aj13072 in A. japonicus and Af23628/Af23629 in A. fulloi are essential for host egg penetration; silencing these genes increased penetration time and resulted in smaller or incomplete holes. Additionally, silencing Aj13071 and Aj13072 in A. japonicus impaired female fecundity, while Af23628 and Af23629 in A. fulloi affected venom reservoir development and egg load, respectively. These findings underscore the critical roles of GH19 chitinases in host penetration and reproduction, offering new insights into the molecular mechanisms driving parasitism in egg parasitoids. This study advances our understanding of venom evolution and supports the development of targeted biological control strategies.
期刊介绍:
This international journal publishes original contributions and mini-reviews in the fields of insect biochemistry and insect molecular biology. Main areas of interest are neurochemistry, hormone and pheromone biochemistry, enzymes and metabolism, hormone action and gene regulation, gene characterization and structure, pharmacology, immunology and cell and tissue culture. Papers on the biochemistry and molecular biology of other groups of arthropods are published if of general interest to the readership. Technique papers will be considered for publication if they significantly advance the field of insect biochemistry and molecular biology in the opinion of the Editors and Editorial Board.