{"title":"根结线虫效应因子Mi1D08B靶向njia家族共同抑制因子,抑制大豆茉莉酸盐的产生,促进侵染","authors":"Peitong Li, Sobhan Bahrami Zadegan, Nicole Coffey, Nandiny Ghosh, J. Hollis Rice, Ahmad El-Messidi, Mohamed Boshnag, Tabibul Islam, Tessa Burch-Smith, Vince Pantalone, Tarek Hewezi","doi":"10.1111/tpj.71095","DOIUrl":null,"url":null,"abstract":"<p>Plant-parasitic nematodes deploy secreted effector proteins that reprogram host cellular processes to establish parasitism. Here, we characterized Mi1D08B, a putative dorsal-gland effector from the root-knot nematode <i>Meloidogyne incognita</i> and defined its role in subverting soybean jasmonate-mediated immunity. Mi1D08B is conserved across several <i>Meloidogyne</i> species and localizes to the plant nucleus and cytoplasm. Overexpression of <i>Mi1D08B</i> significantly increased galling and egg production, demonstrating a strong virulence role. A gall-specific yeast two-hybrid screen identified the NINJA-family co-repressor mc410 as a host target of Mi1D08B. Consistent with the functional relevance of this interaction, <i>mc410</i> promoter activity was detected in galls and giant cells throughout nematode infection. Genetic manipulation of <i>mc410</i> phenocopied Mi1D08B activity as <i>mc410</i> overexpression enhanced susceptibility, whereas <i>mc410</i> silencing reduced nematode infection. Hormone profiling revealed that <i>Mi1D08B</i> overexpression elevated 12-oxo-phytodienoic acid (OPDA) but reduced jasmonic acid (JA) and JA-Ile, consistent with a bottleneck at the peroxisomal OPDA-to-JA conversion. Furthermore, several metabolites associated with this conversion were reduced, indicating that Mi1D08B perturbs metabolic flux through the peroxisomal phase of jasmonate biosynthesis. Gene expression analyses supported this biochemical signature, with upregulation of plastidial OPDA-biosynthetic genes and downregulation of peroxisomal OPDA-reductases, JA-conjugating enzymes, and JA-responsive markers. Together, our data support a model in which Mi1D08B effector interacts with a NINJA co-repressor to suppress JA biosynthesis and signaling, thereby coupling nuclear transcriptional repression to altered metabolism. This mechanism deepens our understanding of nematode manipulation of host hormone networks and highlights the Mi1D08B–mc410 interface and OPDA conversion as promising targets for engineering nematode resistance.</p>","PeriodicalId":233,"journal":{"name":"The Plant Journal","volume":"127 4","pages":""},"PeriodicalIF":6.2000,"publicationDate":"2026-08-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/tpj.71095","citationCount":"0","resultStr":"{\"title\":\"The root-knot nematode effector Mi1D08B targets a NINJA-family co-repressor to suppress jasmonate production and promote infection in soybean\",\"authors\":\"Peitong Li, Sobhan Bahrami Zadegan, Nicole Coffey, Nandiny Ghosh, J. Hollis Rice, Ahmad El-Messidi, Mohamed Boshnag, Tabibul Islam, Tessa Burch-Smith, Vince Pantalone, Tarek Hewezi\",\"doi\":\"10.1111/tpj.71095\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Plant-parasitic nematodes deploy secreted effector proteins that reprogram host cellular processes to establish parasitism. Here, we characterized Mi1D08B, a putative dorsal-gland effector from the root-knot nematode <i>Meloidogyne incognita</i> and defined its role in subverting soybean jasmonate-mediated immunity. Mi1D08B is conserved across several <i>Meloidogyne</i> species and localizes to the plant nucleus and cytoplasm. Overexpression of <i>Mi1D08B</i> significantly increased galling and egg production, demonstrating a strong virulence role. A gall-specific yeast two-hybrid screen identified the NINJA-family co-repressor mc410 as a host target of Mi1D08B. Consistent with the functional relevance of this interaction, <i>mc410</i> promoter activity was detected in galls and giant cells throughout nematode infection. Genetic manipulation of <i>mc410</i> phenocopied Mi1D08B activity as <i>mc410</i> overexpression enhanced susceptibility, whereas <i>mc410</i> silencing reduced nematode infection. Hormone profiling revealed that <i>Mi1D08B</i> overexpression elevated 12-oxo-phytodienoic acid (OPDA) but reduced jasmonic acid (JA) and JA-Ile, consistent with a bottleneck at the peroxisomal OPDA-to-JA conversion. Furthermore, several metabolites associated with this conversion were reduced, indicating that Mi1D08B perturbs metabolic flux through the peroxisomal phase of jasmonate biosynthesis. Gene expression analyses supported this biochemical signature, with upregulation of plastidial OPDA-biosynthetic genes and downregulation of peroxisomal OPDA-reductases, JA-conjugating enzymes, and JA-responsive markers. Together, our data support a model in which Mi1D08B effector interacts with a NINJA co-repressor to suppress JA biosynthesis and signaling, thereby coupling nuclear transcriptional repression to altered metabolism. This mechanism deepens our understanding of nematode manipulation of host hormone networks and highlights the Mi1D08B–mc410 interface and OPDA conversion as promising targets for engineering nematode resistance.</p>\",\"PeriodicalId\":233,\"journal\":{\"name\":\"The Plant Journal\",\"volume\":\"127 4\",\"pages\":\"\"},\"PeriodicalIF\":6.2000,\"publicationDate\":\"2026-08-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1111/tpj.71095\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Plant Journal\",\"FirstCategoryId\":\"2\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/tpj.71095\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Plant Journal","FirstCategoryId":"2","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/tpj.71095","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
The root-knot nematode effector Mi1D08B targets a NINJA-family co-repressor to suppress jasmonate production and promote infection in soybean
Plant-parasitic nematodes deploy secreted effector proteins that reprogram host cellular processes to establish parasitism. Here, we characterized Mi1D08B, a putative dorsal-gland effector from the root-knot nematode Meloidogyne incognita and defined its role in subverting soybean jasmonate-mediated immunity. Mi1D08B is conserved across several Meloidogyne species and localizes to the plant nucleus and cytoplasm. Overexpression of Mi1D08B significantly increased galling and egg production, demonstrating a strong virulence role. A gall-specific yeast two-hybrid screen identified the NINJA-family co-repressor mc410 as a host target of Mi1D08B. Consistent with the functional relevance of this interaction, mc410 promoter activity was detected in galls and giant cells throughout nematode infection. Genetic manipulation of mc410 phenocopied Mi1D08B activity as mc410 overexpression enhanced susceptibility, whereas mc410 silencing reduced nematode infection. Hormone profiling revealed that Mi1D08B overexpression elevated 12-oxo-phytodienoic acid (OPDA) but reduced jasmonic acid (JA) and JA-Ile, consistent with a bottleneck at the peroxisomal OPDA-to-JA conversion. Furthermore, several metabolites associated with this conversion were reduced, indicating that Mi1D08B perturbs metabolic flux through the peroxisomal phase of jasmonate biosynthesis. Gene expression analyses supported this biochemical signature, with upregulation of plastidial OPDA-biosynthetic genes and downregulation of peroxisomal OPDA-reductases, JA-conjugating enzymes, and JA-responsive markers. Together, our data support a model in which Mi1D08B effector interacts with a NINJA co-repressor to suppress JA biosynthesis and signaling, thereby coupling nuclear transcriptional repression to altered metabolism. This mechanism deepens our understanding of nematode manipulation of host hormone networks and highlights the Mi1D08B–mc410 interface and OPDA conversion as promising targets for engineering nematode resistance.
期刊介绍:
Publishing the best original research papers in all key areas of modern plant biology from the world"s leading laboratories, The Plant Journal provides a dynamic forum for this ever growing international research community.
Plant science research is now at the forefront of research in the biological sciences, with breakthroughs in our understanding of fundamental processes in plants matching those in other organisms. The impact of molecular genetics and the availability of model and crop species can be seen in all aspects of plant biology. For publication in The Plant Journal the research must provide a highly significant new contribution to our understanding of plants and be of general interest to the plant science community.