{"title":"Bursaphelenchus xylophilus 毒液过敏原样蛋白 BxVAP1 触发植物防御相关的程序性细胞死亡,在调控 Pinus massoniana 萜烯防御反应中发挥重要作用。","authors":"Yuqian Feng, Yongxia Li, Zhenkai Liu, Xuan Wang, Wei Zhang, Dongzhen Li, Xiaojian Wen, Xingyao Zhang","doi":"10.1094/PHYTO-01-24-0026-R","DOIUrl":null,"url":null,"abstract":"<p><p><i>Bursaphelenchus xylophilus</i> (pine wood nematode, PWN), a migratory plant-parasitic nematode, acts as an etiological agent, inflicting considerable damage to pine forests worldwide. Plant immunity constitutes a crucial factor in resisting various pathogenic invasions. The primary defensive responses of host pines against PWN infection encompass terpene accumulation, defense response-related gene expression, and programmed cell death. Venom allergen-like proteins (VAPs), as potential effectors, are instrumental in facilitating the successful colonization of PWNs. In this study, we investigated the inhibition of <i>B. xylophilus</i> VAP (<i>BxVAP1</i>) expression by RNA interference in vitro. Following <i>BxVAP1</i> silencing, the reproduction rate and migration rate of the PWN population in <i>Pinus massoniana</i> decreased, the expression of the α-pinene synthase gene was induced, other terpene synthase and pathogenesis-related genes were inhibited and delayed, the peak times and levels of terpene-related substances were changed, and the degree of cavitation in <i>P. massoniana</i> was diminished. Transient expression of BxVAP1 in <i>Nicotiana benthamiana</i> revealed that BxVAP1 was expressed in both the cell membrane and nucleus, inducing programmed cell death and the expression of pathogen-associated molecular pattern-triggered immunity marker genes (<i>NbAcre31</i> and <i>NbPTI5</i>). This study is the first to demonstrate that silencing the <i>BxVAP1</i> gene affects host defense responses, including terpenoid metabolism in <i>P. massoniana</i>, and that BxVAP1 can be recognized by <i>N. benthamiana</i> as an effector to trigger its innate immunity, expanding our understanding of the parasitic mechanism of <i>B. xylophilus</i>.</p>","PeriodicalId":20410,"journal":{"name":"Phytopathology","volume":" ","pages":"2331-2340"},"PeriodicalIF":2.6000,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"<i>Bursaphelenchus xylophilus</i> Venom Allergen-Like Protein BxVAP1, Triggering Plant Defense-Related Programmed Cell Death, Plays an Important Role in Regulating <i>Pinus massoniana</i> Terpene Defense Responses.\",\"authors\":\"Yuqian Feng, Yongxia Li, Zhenkai Liu, Xuan Wang, Wei Zhang, Dongzhen Li, Xiaojian Wen, Xingyao Zhang\",\"doi\":\"10.1094/PHYTO-01-24-0026-R\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><i>Bursaphelenchus xylophilus</i> (pine wood nematode, PWN), a migratory plant-parasitic nematode, acts as an etiological agent, inflicting considerable damage to pine forests worldwide. Plant immunity constitutes a crucial factor in resisting various pathogenic invasions. The primary defensive responses of host pines against PWN infection encompass terpene accumulation, defense response-related gene expression, and programmed cell death. Venom allergen-like proteins (VAPs), as potential effectors, are instrumental in facilitating the successful colonization of PWNs. In this study, we investigated the inhibition of <i>B. xylophilus</i> VAP (<i>BxVAP1</i>) expression by RNA interference in vitro. Following <i>BxVAP1</i> silencing, the reproduction rate and migration rate of the PWN population in <i>Pinus massoniana</i> decreased, the expression of the α-pinene synthase gene was induced, other terpene synthase and pathogenesis-related genes were inhibited and delayed, the peak times and levels of terpene-related substances were changed, and the degree of cavitation in <i>P. massoniana</i> was diminished. Transient expression of BxVAP1 in <i>Nicotiana benthamiana</i> revealed that BxVAP1 was expressed in both the cell membrane and nucleus, inducing programmed cell death and the expression of pathogen-associated molecular pattern-triggered immunity marker genes (<i>NbAcre31</i> and <i>NbPTI5</i>). This study is the first to demonstrate that silencing the <i>BxVAP1</i> gene affects host defense responses, including terpenoid metabolism in <i>P. massoniana</i>, and that BxVAP1 can be recognized by <i>N. benthamiana</i> as an effector to trigger its innate immunity, expanding our understanding of the parasitic mechanism of <i>B. xylophilus</i>.</p>\",\"PeriodicalId\":20410,\"journal\":{\"name\":\"Phytopathology\",\"volume\":\" \",\"pages\":\"2331-2340\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2024-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Phytopathology\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://doi.org/10.1094/PHYTO-01-24-0026-R\",\"RegionNum\":2,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/9/30 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phytopathology","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1094/PHYTO-01-24-0026-R","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/9/30 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
Bursaphelenchus xylophilus Venom Allergen-Like Protein BxVAP1, Triggering Plant Defense-Related Programmed Cell Death, Plays an Important Role in Regulating Pinus massoniana Terpene Defense Responses.
Bursaphelenchus xylophilus (pine wood nematode, PWN), a migratory plant-parasitic nematode, acts as an etiological agent, inflicting considerable damage to pine forests worldwide. Plant immunity constitutes a crucial factor in resisting various pathogenic invasions. The primary defensive responses of host pines against PWN infection encompass terpene accumulation, defense response-related gene expression, and programmed cell death. Venom allergen-like proteins (VAPs), as potential effectors, are instrumental in facilitating the successful colonization of PWNs. In this study, we investigated the inhibition of B. xylophilus VAP (BxVAP1) expression by RNA interference in vitro. Following BxVAP1 silencing, the reproduction rate and migration rate of the PWN population in Pinus massoniana decreased, the expression of the α-pinene synthase gene was induced, other terpene synthase and pathogenesis-related genes were inhibited and delayed, the peak times and levels of terpene-related substances were changed, and the degree of cavitation in P. massoniana was diminished. Transient expression of BxVAP1 in Nicotiana benthamiana revealed that BxVAP1 was expressed in both the cell membrane and nucleus, inducing programmed cell death and the expression of pathogen-associated molecular pattern-triggered immunity marker genes (NbAcre31 and NbPTI5). This study is the first to demonstrate that silencing the BxVAP1 gene affects host defense responses, including terpenoid metabolism in P. massoniana, and that BxVAP1 can be recognized by N. benthamiana as an effector to trigger its innate immunity, expanding our understanding of the parasitic mechanism of B. xylophilus.
期刊介绍:
Phytopathology publishes articles on fundamental research that advances understanding of the nature of plant diseases, the agents that cause them, their spread, the losses they cause, and measures that can be used to control them. Phytopathology considers manuscripts covering all aspects of plant diseases including bacteriology, host-parasite biochemistry and cell biology, biological control, disease control and pest management, description of new pathogen species description of new pathogen species, ecology and population biology, epidemiology, disease etiology, host genetics and resistance, mycology, nematology, plant stress and abiotic disorders, postharvest pathology and mycotoxins, and virology. Papers dealing mainly with taxonomy, such as descriptions of new plant pathogen taxa are acceptable if they include plant disease research results such as pathogenicity, host range, etc. Taxonomic papers that focus on classification, identification, and nomenclature below the subspecies level may also be submitted to Phytopathology.