{"title":"拟南芥对多种非适应性炭疽菌介导的黑化附着胞入侵的入侵前非宿主抗性。","authors":"Hiroki Irieda","doi":"10.1080/15592324.2021.2018218","DOIUrl":null,"url":null,"abstract":"<p><p>Nonhost plants effectively block a vast number of nonadapted fungal pathogens at the preinvasive stage. On the host plants, adapted fungal pathogens such as <i>Colletotrichum</i> species invade into plant epidermal cell by penetration peg developed from melanized appressorium, followed by invasive hyphal extension. I reported nonadapted <i>Colletotrichum</i> fungi that showed an increased rate of melanized appressorium-mediated entry (MAE) into the <i>pen2</i> mutant of nonhost <i>Arabidopsis thaliana</i> (hereafter <i>Arabidopsis</i>). It was also found that other MAE-type nonadapted <i>Colletotrichum</i> fungi with no penetration into the <i>pen2</i> mutant invaded <i>Arabidopsis</i> in the presence of additional mutations such as <i>edr1</i>, <i>gsh1</i>, <i>eds5</i>, <i>cas</i>, and <i>chup1</i> in the <i>pen2</i> background. Thus, many immune components contribute to the preinvasive nonhost resistance (NHR) of <i>Arabidopsis</i> against <i>Colletotrichum</i> MAE, and PEN2-related defense takes priority over other defense pathways. Here, I show that among the above nonadapted fungi, <i>Colletotrichum nymphaeae</i> PL1-1-b exhibited relatively lower incompatibility with the nonhost <i>Arabidopsis</i> with increased MAE in each single mutant of <i>edr1</i>, <i>gsh1</i>, <i>eds5</i>, and <i>cas</i>, although other nonadapted fungi almost never invaded these single mutants. Based on the relationships between <i>Colletotrichum</i> MAE and the <i>Arabidopsis</i> immune-related components, <i>Colletotrichum-Arabidopsis</i> incompatibility and multilayered immunity in the preinvasive NHR of <i>Arabidopsis</i> are discussed in this study.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2022-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9176223/pdf/","citationCount":"1","resultStr":"{\"title\":\"Preinvasive nonhost resistance of <i>Arabidopsis</i> against melanized appressorium-mediated entry of multiple nonadapted <i>Colletotrichum</i> fungi.\",\"authors\":\"Hiroki Irieda\",\"doi\":\"10.1080/15592324.2021.2018218\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Nonhost plants effectively block a vast number of nonadapted fungal pathogens at the preinvasive stage. On the host plants, adapted fungal pathogens such as <i>Colletotrichum</i> species invade into plant epidermal cell by penetration peg developed from melanized appressorium, followed by invasive hyphal extension. I reported nonadapted <i>Colletotrichum</i> fungi that showed an increased rate of melanized appressorium-mediated entry (MAE) into the <i>pen2</i> mutant of nonhost <i>Arabidopsis thaliana</i> (hereafter <i>Arabidopsis</i>). It was also found that other MAE-type nonadapted <i>Colletotrichum</i> fungi with no penetration into the <i>pen2</i> mutant invaded <i>Arabidopsis</i> in the presence of additional mutations such as <i>edr1</i>, <i>gsh1</i>, <i>eds5</i>, <i>cas</i>, and <i>chup1</i> in the <i>pen2</i> background. Thus, many immune components contribute to the preinvasive nonhost resistance (NHR) of <i>Arabidopsis</i> against <i>Colletotrichum</i> MAE, and PEN2-related defense takes priority over other defense pathways. Here, I show that among the above nonadapted fungi, <i>Colletotrichum nymphaeae</i> PL1-1-b exhibited relatively lower incompatibility with the nonhost <i>Arabidopsis</i> with increased MAE in each single mutant of <i>edr1</i>, <i>gsh1</i>, <i>eds5</i>, and <i>cas</i>, although other nonadapted fungi almost never invaded these single mutants. Based on the relationships between <i>Colletotrichum</i> MAE and the <i>Arabidopsis</i> immune-related components, <i>Colletotrichum-Arabidopsis</i> incompatibility and multilayered immunity in the preinvasive NHR of <i>Arabidopsis</i> are discussed in this study.</p>\",\"PeriodicalId\":2,\"journal\":{\"name\":\"ACS Applied Bio Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2022-12-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9176223/pdf/\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Bio Materials\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1080/15592324.2021.2018218\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2022/1/3 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, BIOMATERIALS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1080/15592324.2021.2018218","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/1/3 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
Preinvasive nonhost resistance of Arabidopsis against melanized appressorium-mediated entry of multiple nonadapted Colletotrichum fungi.
Nonhost plants effectively block a vast number of nonadapted fungal pathogens at the preinvasive stage. On the host plants, adapted fungal pathogens such as Colletotrichum species invade into plant epidermal cell by penetration peg developed from melanized appressorium, followed by invasive hyphal extension. I reported nonadapted Colletotrichum fungi that showed an increased rate of melanized appressorium-mediated entry (MAE) into the pen2 mutant of nonhost Arabidopsis thaliana (hereafter Arabidopsis). It was also found that other MAE-type nonadapted Colletotrichum fungi with no penetration into the pen2 mutant invaded Arabidopsis in the presence of additional mutations such as edr1, gsh1, eds5, cas, and chup1 in the pen2 background. Thus, many immune components contribute to the preinvasive nonhost resistance (NHR) of Arabidopsis against Colletotrichum MAE, and PEN2-related defense takes priority over other defense pathways. Here, I show that among the above nonadapted fungi, Colletotrichum nymphaeae PL1-1-b exhibited relatively lower incompatibility with the nonhost Arabidopsis with increased MAE in each single mutant of edr1, gsh1, eds5, and cas, although other nonadapted fungi almost never invaded these single mutants. Based on the relationships between Colletotrichum MAE and the Arabidopsis immune-related components, Colletotrichum-Arabidopsis incompatibility and multilayered immunity in the preinvasive NHR of Arabidopsis are discussed in this study.