Liangxuan Qi, Jing Li, Han Wang, Shuai Li, Lei Yang, Jichao Fang, Rui Ji
{"title":"飞虱蛋白Nlsp5是唾液鞘形成所必需的,是诱导植物抗虫的HAMP。","authors":"Liangxuan Qi, Jing Li, Han Wang, Shuai Li, Lei Yang, Jichao Fang, Rui Ji","doi":"10.1111/pbi.70223","DOIUrl":null,"url":null,"abstract":"<p><p>During herbivore feeding, plants can recognize herbivore-associated molecular patterns (HAMPs) present in saliva and trigger pattern-triggered immunity (PTI). Piercing-sucking insects secrete gel saliva, forming salivary sheaths that aid in feeding. However, the role of proteins within these salivary sheaths in modulating plant defences remains poorly understood. In this study, we identified a novel HAMP, Nlsp5, from the salivary sheath of the brown planthopper (Nilaparvata lugens, BPH). Nlsp5 is a planthopper-specific protein and acts as an elicitor of BAK1-dependent PTI responses in both tobacco and rice plants. Moreover, the 19-amino-acid peptide (NP19) within Nlsp5 functions as a minimal immunogenic epitope, which is specifically recognized by plants, stimulating jasmonic acid and hydrogen peroxide pathways. Through exogenous treatment with synthetic NP19 and overexpressing Nlsp5 in rice, we further found that the induced defence responses not only impaired planthopper performance directly but also triggered the emission of volatile compounds that attract a common parasitoid. Additionally, NP19 treatment enhanced the resistance of rice, tobacco, and cotton to several chewing and sap-sucking insects. However, silencing Nlsp5 in BPH disrupted salivary sheath formation, reducing insect feeding efficiency. This study demonstrates that Nlsp5 from the BPH salivary sheath acts as an unavoidable HAMP, triggering resistance in multiple plants to various insect pests. The critical role of this protein in insect feeding precludes evolutionary adaptations to evade detection by plants.</p>","PeriodicalId":221,"journal":{"name":"Plant Biotechnology Journal","volume":" ","pages":""},"PeriodicalIF":10.1000,"publicationDate":"2025-06-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Planthopper protein Nlsp5 is essential for salivary sheath formation and acts as a HAMP inducing plant resistance to insects.\",\"authors\":\"Liangxuan Qi, Jing Li, Han Wang, Shuai Li, Lei Yang, Jichao Fang, Rui Ji\",\"doi\":\"10.1111/pbi.70223\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>During herbivore feeding, plants can recognize herbivore-associated molecular patterns (HAMPs) present in saliva and trigger pattern-triggered immunity (PTI). Piercing-sucking insects secrete gel saliva, forming salivary sheaths that aid in feeding. However, the role of proteins within these salivary sheaths in modulating plant defences remains poorly understood. In this study, we identified a novel HAMP, Nlsp5, from the salivary sheath of the brown planthopper (Nilaparvata lugens, BPH). Nlsp5 is a planthopper-specific protein and acts as an elicitor of BAK1-dependent PTI responses in both tobacco and rice plants. Moreover, the 19-amino-acid peptide (NP19) within Nlsp5 functions as a minimal immunogenic epitope, which is specifically recognized by plants, stimulating jasmonic acid and hydrogen peroxide pathways. Through exogenous treatment with synthetic NP19 and overexpressing Nlsp5 in rice, we further found that the induced defence responses not only impaired planthopper performance directly but also triggered the emission of volatile compounds that attract a common parasitoid. Additionally, NP19 treatment enhanced the resistance of rice, tobacco, and cotton to several chewing and sap-sucking insects. However, silencing Nlsp5 in BPH disrupted salivary sheath formation, reducing insect feeding efficiency. This study demonstrates that Nlsp5 from the BPH salivary sheath acts as an unavoidable HAMP, triggering resistance in multiple plants to various insect pests. The critical role of this protein in insect feeding precludes evolutionary adaptations to evade detection by plants.</p>\",\"PeriodicalId\":221,\"journal\":{\"name\":\"Plant Biotechnology Journal\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":10.1000,\"publicationDate\":\"2025-06-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant Biotechnology Journal\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://doi.org/10.1111/pbi.70223\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Biotechnology Journal","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1111/pbi.70223","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
Planthopper protein Nlsp5 is essential for salivary sheath formation and acts as a HAMP inducing plant resistance to insects.
During herbivore feeding, plants can recognize herbivore-associated molecular patterns (HAMPs) present in saliva and trigger pattern-triggered immunity (PTI). Piercing-sucking insects secrete gel saliva, forming salivary sheaths that aid in feeding. However, the role of proteins within these salivary sheaths in modulating plant defences remains poorly understood. In this study, we identified a novel HAMP, Nlsp5, from the salivary sheath of the brown planthopper (Nilaparvata lugens, BPH). Nlsp5 is a planthopper-specific protein and acts as an elicitor of BAK1-dependent PTI responses in both tobacco and rice plants. Moreover, the 19-amino-acid peptide (NP19) within Nlsp5 functions as a minimal immunogenic epitope, which is specifically recognized by plants, stimulating jasmonic acid and hydrogen peroxide pathways. Through exogenous treatment with synthetic NP19 and overexpressing Nlsp5 in rice, we further found that the induced defence responses not only impaired planthopper performance directly but also triggered the emission of volatile compounds that attract a common parasitoid. Additionally, NP19 treatment enhanced the resistance of rice, tobacco, and cotton to several chewing and sap-sucking insects. However, silencing Nlsp5 in BPH disrupted salivary sheath formation, reducing insect feeding efficiency. This study demonstrates that Nlsp5 from the BPH salivary sheath acts as an unavoidable HAMP, triggering resistance in multiple plants to various insect pests. The critical role of this protein in insect feeding precludes evolutionary adaptations to evade detection by plants.
期刊介绍:
Plant Biotechnology Journal aspires to publish original research and insightful reviews of high impact, authored by prominent researchers in applied plant science. The journal places a special emphasis on molecular plant sciences and their practical applications through plant biotechnology. Our goal is to establish a platform for showcasing significant advances in the field, encompassing curiosity-driven studies with potential applications, strategic research in plant biotechnology, scientific analysis of crucial issues for the beneficial utilization of plant sciences, and assessments of the performance of plant biotechnology products in practical applications.