{"title":"灰葡萄孢菌通过多种代谢途径解毒倍半萜类植物雌激素利西汀","authors":"Abriel Salaria Bulasag , Akira Ashida , Atsushi Miura , Sreynich Pring , Teruhiko Kuroyanagi , Maurizio Camagna , Aiko Tanaka , Ikuo Sato , Sotaro Chiba , Makoto Ojika , Daigo Takemoto","doi":"10.1016/j.fgb.2024.103895","DOIUrl":null,"url":null,"abstract":"<div><p><em>Botrytis cinerea</em> is a necrotrophic pathogen that infects across a broad range of plant hosts, including high-impact crop species. Its generalist necrotrophic behavior stems from its ability to detoxify structurally diverse phytoalexins. The current study aims to provide evidence of the ability of <em>B. cinerea</em> to tolerate the sesquiterpenoid phytoalexin rishitin, which is produced by potato and tomato. While the growth of potato pathogens <em>Phytophthora infestans</em> (late blight) and <em>Alternaria solani</em> (early blight) was severely inhibited by rishitin, <em>B. cinerea</em> was tolerant to rishitin. After incubation of rishitin with the mycelia of <em>B. cinerea</em>, it was metabolized to at least six oxidized forms. Structural analysis of these purified rishitin metabolites revealed a variety of oxidative metabolism including hydroxylation at C7 or C12, ketone formation at C5, and dihydroxylation at the 10,11-olefin. Six rishitin metabolites showed reduced toxicity to <em>P. infestans</em> and <em>A. solani</em>, indicating that <em>B. cinerea</em> has at least 5 distinct enzymatic reactions to detoxify rishitin. Four host-specialized phytopathogenic <em>Botrytis</em> species, namely <em>B. elliptica, B. allii, B. squamosa,</em> and <em>B. tulipae</em> also had at least a partial ability to metabolize rishitin as <em>B. cinerea</em>, but their metabolic capacity was significantly weaker than that of <em>B. cinerea</em>. These results suggest that the ability of <em>B. cinerea</em> to rapidly metabolize rishitin through multiple detoxification mechanisms could be critical for its pathogenicity in potato and tomato.</p></div>","PeriodicalId":55135,"journal":{"name":"Fungal Genetics and Biology","volume":"172 ","pages":"Article 103895"},"PeriodicalIF":2.4000,"publicationDate":"2024-04-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Botrytis cinerea detoxifies the sesquiterpenoid phytoalexin rishitin through multiple metabolizing pathways\",\"authors\":\"Abriel Salaria Bulasag , Akira Ashida , Atsushi Miura , Sreynich Pring , Teruhiko Kuroyanagi , Maurizio Camagna , Aiko Tanaka , Ikuo Sato , Sotaro Chiba , Makoto Ojika , Daigo Takemoto\",\"doi\":\"10.1016/j.fgb.2024.103895\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><em>Botrytis cinerea</em> is a necrotrophic pathogen that infects across a broad range of plant hosts, including high-impact crop species. Its generalist necrotrophic behavior stems from its ability to detoxify structurally diverse phytoalexins. The current study aims to provide evidence of the ability of <em>B. cinerea</em> to tolerate the sesquiterpenoid phytoalexin rishitin, which is produced by potato and tomato. While the growth of potato pathogens <em>Phytophthora infestans</em> (late blight) and <em>Alternaria solani</em> (early blight) was severely inhibited by rishitin, <em>B. cinerea</em> was tolerant to rishitin. After incubation of rishitin with the mycelia of <em>B. cinerea</em>, it was metabolized to at least six oxidized forms. Structural analysis of these purified rishitin metabolites revealed a variety of oxidative metabolism including hydroxylation at C7 or C12, ketone formation at C5, and dihydroxylation at the 10,11-olefin. Six rishitin metabolites showed reduced toxicity to <em>P. infestans</em> and <em>A. solani</em>, indicating that <em>B. cinerea</em> has at least 5 distinct enzymatic reactions to detoxify rishitin. Four host-specialized phytopathogenic <em>Botrytis</em> species, namely <em>B. elliptica, B. allii, B. squamosa,</em> and <em>B. tulipae</em> also had at least a partial ability to metabolize rishitin as <em>B. cinerea</em>, but their metabolic capacity was significantly weaker than that of <em>B. cinerea</em>. These results suggest that the ability of <em>B. cinerea</em> to rapidly metabolize rishitin through multiple detoxification mechanisms could be critical for its pathogenicity in potato and tomato.</p></div>\",\"PeriodicalId\":55135,\"journal\":{\"name\":\"Fungal Genetics and Biology\",\"volume\":\"172 \",\"pages\":\"Article 103895\"},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2024-04-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Fungal Genetics and Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S108718452400032X\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fungal Genetics and Biology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S108718452400032X","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0
摘要
灰葡萄孢菌是一种坏死性病原体,可感染多种植物寄主,包括影响较大的作物物种。它的通性坏死行为源于其对结构多样的植物毒素的解毒能力。目前的研究旨在提供证据,证明 B. cinerea 能够耐受马铃薯和番茄产生的倍半萜类植物毒素 rishitin。马铃薯病原体 Phytophthora infestans(晚疫病)和 Alternaria solani(早疫病)的生长会受到 rishitin 的严重抑制,而 B. cinerea 却能耐受 rishitin。利希丁与 B. cinerea 菌丝体培养后,至少代谢成六种氧化形式。对这些纯化的利什亭代谢物进行的结构分析表明,它们进行了多种氧化代谢,包括 C7 或 C12 处的羟基化、C5 处的酮形成以及 10,11- 烯烃处的二羟基化。六种利希丁代谢物对 P. infestans 和 A. solani 的毒性降低,表明 B. cinerea 至少有 5 种不同的酶促反应来解毒利希丁。四种寄主专化植物病原菌,即 B. elliptica、B. allii、B. squamosa 和 B. tulipae 也与 B. cinerea 一样至少具有部分代谢利希菌素的能力,但它们的代谢能力明显弱于 B. cinerea。这些结果表明,B. cinerea 通过多种解毒机制快速代谢利希菌素的能力可能是其在马铃薯和番茄中致病的关键。
Botrytis cinerea detoxifies the sesquiterpenoid phytoalexin rishitin through multiple metabolizing pathways
Botrytis cinerea is a necrotrophic pathogen that infects across a broad range of plant hosts, including high-impact crop species. Its generalist necrotrophic behavior stems from its ability to detoxify structurally diverse phytoalexins. The current study aims to provide evidence of the ability of B. cinerea to tolerate the sesquiterpenoid phytoalexin rishitin, which is produced by potato and tomato. While the growth of potato pathogens Phytophthora infestans (late blight) and Alternaria solani (early blight) was severely inhibited by rishitin, B. cinerea was tolerant to rishitin. After incubation of rishitin with the mycelia of B. cinerea, it was metabolized to at least six oxidized forms. Structural analysis of these purified rishitin metabolites revealed a variety of oxidative metabolism including hydroxylation at C7 or C12, ketone formation at C5, and dihydroxylation at the 10,11-olefin. Six rishitin metabolites showed reduced toxicity to P. infestans and A. solani, indicating that B. cinerea has at least 5 distinct enzymatic reactions to detoxify rishitin. Four host-specialized phytopathogenic Botrytis species, namely B. elliptica, B. allii, B. squamosa, and B. tulipae also had at least a partial ability to metabolize rishitin as B. cinerea, but their metabolic capacity was significantly weaker than that of B. cinerea. These results suggest that the ability of B. cinerea to rapidly metabolize rishitin through multiple detoxification mechanisms could be critical for its pathogenicity in potato and tomato.
期刊介绍:
Fungal Genetics and Biology, formerly known as Experimental Mycology, publishes experimental investigations of fungi and their traditional allies that relate structure and function to growth, reproduction, morphogenesis, and differentiation. This journal especially welcomes studies of gene organization and expression and of developmental processes at the cellular, subcellular, and molecular levels. The journal also includes suitable experimental inquiries into fungal cytology, biochemistry, physiology, genetics, and phylogeny.
Fungal Genetics and Biology publishes basic research conducted by mycologists, cell biologists, biochemists, geneticists, and molecular biologists.
Research Areas include:
• Biochemistry
• Cytology
• Developmental biology
• Evolutionary biology
• Genetics
• Molecular biology
• Phylogeny
• Physiology.