Yao Zhao, Xinyue Zheng, Javier F Tabima, Sheng Zhu, Kelsey L Søndreli, Hope Hundley, Diane Bauer, Kerrie Barry, Yaxin Zhang, Jeremy Schmutz, Yuanchao Wang, Jared M LeBoldus, Qin Xiong
{"title":"杨树叶斑病和茎腐病病原体 Sphaerulina musiva 的分泌效应蛋白以多种方式操纵植物免疫力并增强其毒性。","authors":"Yao Zhao, Xinyue Zheng, Javier F Tabima, Sheng Zhu, Kelsey L Søndreli, Hope Hundley, Diane Bauer, Kerrie Barry, Yaxin Zhang, Jeremy Schmutz, Yuanchao Wang, Jared M LeBoldus, Qin Xiong","doi":"10.1094/MPMI-07-23-0091-R","DOIUrl":null,"url":null,"abstract":"<p><p>Fungal effectors play critical roles in manipulating plant immune responses and promoting colonization. <i>Sphaerulina musiva</i> is a heterothallic ascomycete fungus that causes Septoria leaf spot and stem canker disease in poplar (<i>Populus</i> spp.) plantations. This disease can result in premature defoliation, branch and stem breakage, increased mortality, and plantation failure. However, little is known about the interaction between <i>S. musiva</i> and poplar. Previous work predicted 142 candidate secreted effector proteins in <i>S. musiva</i> (SmCSEPs), 19 of which were selected for further functional characterization in this study. SmCSEP3 induced plant cell death in <i>Nicotiana benthamiana</i>, while 8 out of 19 tested SmCSEPs suppressed cell death. The signal peptides of these eight SmCSEPs exhibited secretory activity in a yeast signal sequence trap assay. Confocal microscopy revealed that four of these eight SmCSEPs target both the cytoplasm and the nucleus, whereas four predominantly localize to discrete punctate structures. Pathogen challenge assays in <i>N. benthamiana</i> demonstrated that the transient expression of six SmCSEPs promoted <i>Fusarium proliferatum</i> infection. The expression of these six <i>SmCSEP</i> genes were induced during infection. SmCSEP2, SmCSEP13, and SmCSEP25 suppressed chitin-triggered reactive oxygen species burst and callose deposition in <i>N. benthamiana</i>. The candidate secreted effector proteins of <i>S. musiva</i> target multiple compartments in the plant cell and modulate different pattern-triggered immunity pathways. [Formula: see text] The author(s) have dedicated the work to the public domain under the Creative Commons CC0 \"No Rights Reserved\" license by waiving all of his or her rights to the work worldwide under copyright law, including all related and neighboring rights, to the extent allowed by law, 2023.</p>","PeriodicalId":3,"journal":{"name":"ACS Applied Electronic Materials","volume":null,"pages":null},"PeriodicalIF":4.3000,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Secreted Effector Proteins of Poplar Leaf Spot and Stem Canker Pathogen <i>Sphaerulina musiva</i> Manipulate Plant Immunity and Contribute to Virulence in Diverse Ways.\",\"authors\":\"Yao Zhao, Xinyue Zheng, Javier F Tabima, Sheng Zhu, Kelsey L Søndreli, Hope Hundley, Diane Bauer, Kerrie Barry, Yaxin Zhang, Jeremy Schmutz, Yuanchao Wang, Jared M LeBoldus, Qin Xiong\",\"doi\":\"10.1094/MPMI-07-23-0091-R\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Fungal effectors play critical roles in manipulating plant immune responses and promoting colonization. <i>Sphaerulina musiva</i> is a heterothallic ascomycete fungus that causes Septoria leaf spot and stem canker disease in poplar (<i>Populus</i> spp.) plantations. This disease can result in premature defoliation, branch and stem breakage, increased mortality, and plantation failure. However, little is known about the interaction between <i>S. musiva</i> and poplar. Previous work predicted 142 candidate secreted effector proteins in <i>S. musiva</i> (SmCSEPs), 19 of which were selected for further functional characterization in this study. SmCSEP3 induced plant cell death in <i>Nicotiana benthamiana</i>, while 8 out of 19 tested SmCSEPs suppressed cell death. The signal peptides of these eight SmCSEPs exhibited secretory activity in a yeast signal sequence trap assay. Confocal microscopy revealed that four of these eight SmCSEPs target both the cytoplasm and the nucleus, whereas four predominantly localize to discrete punctate structures. Pathogen challenge assays in <i>N. benthamiana</i> demonstrated that the transient expression of six SmCSEPs promoted <i>Fusarium proliferatum</i> infection. The expression of these six <i>SmCSEP</i> genes were induced during infection. SmCSEP2, SmCSEP13, and SmCSEP25 suppressed chitin-triggered reactive oxygen species burst and callose deposition in <i>N. benthamiana</i>. The candidate secreted effector proteins of <i>S. musiva</i> target multiple compartments in the plant cell and modulate different pattern-triggered immunity pathways. [Formula: see text] The author(s) have dedicated the work to the public domain under the Creative Commons CC0 \\\"No Rights Reserved\\\" license by waiving all of his or her rights to the work worldwide under copyright law, including all related and neighboring rights, to the extent allowed by law, 2023.</p>\",\"PeriodicalId\":3,\"journal\":{\"name\":\"ACS Applied Electronic Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2023-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Electronic Materials\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1094/MPMI-07-23-0091-R\",\"RegionNum\":3,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2023/12/23 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"ENGINEERING, ELECTRICAL & ELECTRONIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Electronic Materials","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1094/MPMI-07-23-0091-R","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/12/23 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"ENGINEERING, ELECTRICAL & ELECTRONIC","Score":null,"Total":0}
Secreted Effector Proteins of Poplar Leaf Spot and Stem Canker Pathogen Sphaerulina musiva Manipulate Plant Immunity and Contribute to Virulence in Diverse Ways.
Fungal effectors play critical roles in manipulating plant immune responses and promoting colonization. Sphaerulina musiva is a heterothallic ascomycete fungus that causes Septoria leaf spot and stem canker disease in poplar (Populus spp.) plantations. This disease can result in premature defoliation, branch and stem breakage, increased mortality, and plantation failure. However, little is known about the interaction between S. musiva and poplar. Previous work predicted 142 candidate secreted effector proteins in S. musiva (SmCSEPs), 19 of which were selected for further functional characterization in this study. SmCSEP3 induced plant cell death in Nicotiana benthamiana, while 8 out of 19 tested SmCSEPs suppressed cell death. The signal peptides of these eight SmCSEPs exhibited secretory activity in a yeast signal sequence trap assay. Confocal microscopy revealed that four of these eight SmCSEPs target both the cytoplasm and the nucleus, whereas four predominantly localize to discrete punctate structures. Pathogen challenge assays in N. benthamiana demonstrated that the transient expression of six SmCSEPs promoted Fusarium proliferatum infection. The expression of these six SmCSEP genes were induced during infection. SmCSEP2, SmCSEP13, and SmCSEP25 suppressed chitin-triggered reactive oxygen species burst and callose deposition in N. benthamiana. The candidate secreted effector proteins of S. musiva target multiple compartments in the plant cell and modulate different pattern-triggered immunity pathways. [Formula: see text] The author(s) have dedicated the work to the public domain under the Creative Commons CC0 "No Rights Reserved" license by waiving all of his or her rights to the work worldwide under copyright law, including all related and neighboring rights, to the extent allowed by law, 2023.