The Immune Receptor Roq1 Confers Resistance to the Bacterial Pathogens Xanthomonas, Pseudomonas syringae, and Ralstonia in Tomato.
Identifieur interne : 000035 ( Main/Exploration ); précédent : 000034; suivant : 000036The Immune Receptor Roq1 Confers Resistance to the Bacterial Pathogens Xanthomonas, Pseudomonas syringae, and Ralstonia in Tomato.
Auteurs : Nicholas C. Thomas [États-Unis] ; Connor G. Hendrich [États-Unis] ; Upinder S. Gill [États-Unis] ; Caitilyn Allen [États-Unis] ; Samuel F. Hutton [États-Unis] ; Alex Schultink [États-Unis]Source :
- Frontiers in plant science [ 1664-462X ] ; 2020.
Abstract
Xanthomonas species, Pseudomonas syringae and Ralstonia species are bacterial plant pathogens that cause significant yield loss in many crop species. Generating disease-resistant crop varieties can provide a more sustainable solution to control yield loss compared to chemical methods. Plant immune receptors encoded by nucleotide-binding, leucine-rich repeat (NLR) genes typically confer resistance to pathogens that produce a cognate elicitor, often an effector protein secreted by the pathogen to promote virulence. The diverse sequence and presence/absence variation of pathogen effector proteins within and between pathogen species usually limits the utility of a single NLR gene to protecting a plant from a single pathogen species or particular strains. The NLR protein Recognition of XopQ 1 (Roq1) was recently identified from the plant Nicotiana benthamiana and mediates perception of the effector proteins XopQ and HopQ1 from Xanthomonas and P. syringae respectively. Unlike most recognized effectors, alleles of XopQ/HopQ1 are highly conserved and present in most plant pathogenic strains of Xanthomonas and P. syringae. A homolog of XopQ/HopQ1, named RipB, is present in most Ralstonia strains. We found that Roq1 confers immunity to Xanthomonas, P. syringae, and Ralstonia when expressed in tomato. Strong resistance to Xanthomonas perforans was observed in three seasons of field trials with both natural and artificial inoculation. The Roq1 gene can therefore be used to provide safe, economical, and effective control of these pathogens in tomato and other crop species and reduce or eliminate the need for traditional chemical controls.
DOI: 10.3389/fpls.2020.00463
PubMed: 32391034
PubMed Central: PMC7192161
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Thomas</name><affiliation wicri:level="2"><nlm:affiliation>Fortiphyte Inc., Berkeley, CA, United States.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Fortiphyte Inc., Berkeley, CA</wicri:regionArea><placeName><region type="state">Californie</region></placeName></affiliation><affiliation wicri:level="2"><nlm:affiliation>Innovative Genomics Institute, University of California, Berkeley, Berkeley, CA, United States.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Innovative Genomics Institute, University of California, Berkeley, Berkeley, CA</wicri:regionArea><placeName><region type="state">Californie</region></placeName></affiliation></author><author><name sortKey="Hendrich, Connor G" sort="Hendrich, Connor G" uniqKey="Hendrich C" first="Connor G" last="Hendrich">Connor G. Hendrich</name><affiliation wicri:level="2"><nlm:affiliation>Department of Plant Pathology, University of Wisconsin-Madison, Madison, WI, United States.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Plant Pathology, University of Wisconsin-Madison, Madison, WI</wicri:regionArea><placeName><region type="state">Wisconsin</region></placeName></affiliation></author><author><name sortKey="Gill, Upinder S" sort="Gill, Upinder S" uniqKey="Gill U" first="Upinder S" last="Gill">Upinder S. Gill</name><affiliation wicri:level="2"><nlm:affiliation>IFAS, Gulf Coast Research and Education Center, University of Florida, Wimauma, FL, United States.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>IFAS, Gulf Coast Research and Education Center, University of Florida, Wimauma, FL</wicri:regionArea><placeName><region type="state">Floride</region></placeName></affiliation><affiliation wicri:level="2"><nlm:affiliation>Department of Plant Pathology, North Dakota State University, Fargo, ND, United States.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Plant Pathology, North Dakota State University, Fargo, ND</wicri:regionArea><placeName><region type="state">Dakota du Nord</region></placeName></affiliation></author><author><name sortKey="Allen, Caitilyn" sort="Allen, Caitilyn" uniqKey="Allen C" first="Caitilyn" last="Allen">Caitilyn Allen</name><affiliation wicri:level="2"><nlm:affiliation>Department of Plant Pathology, University of Wisconsin-Madison, Madison, WI, United States.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Plant Pathology, University of Wisconsin-Madison, Madison, WI</wicri:regionArea><placeName><region type="state">Wisconsin</region></placeName></affiliation></author><author><name sortKey="Hutton, Samuel F" sort="Hutton, Samuel F" uniqKey="Hutton S" first="Samuel F" last="Hutton">Samuel F. Hutton</name><affiliation wicri:level="2"><nlm:affiliation>IFAS, Gulf Coast Research and Education Center, University of Florida, Wimauma, FL, United States.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>IFAS, Gulf Coast Research and Education Center, University of Florida, Wimauma, FL</wicri:regionArea><placeName><region type="state">Floride</region></placeName></affiliation></author><author><name sortKey="Schultink, Alex" sort="Schultink, Alex" uniqKey="Schultink A" first="Alex" last="Schultink">Alex Schultink</name><affiliation wicri:level="2"><nlm:affiliation>Fortiphyte Inc., Berkeley, CA, United States.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Fortiphyte Inc., Berkeley, CA</wicri:regionArea><placeName><region type="state">Californie</region></placeName></affiliation><affiliation wicri:level="2"><nlm:affiliation>Innovative Genomics Institute, University of California, Berkeley, Berkeley, CA, United States.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Innovative Genomics Institute, University of California, Berkeley, Berkeley, CA</wicri:regionArea><placeName><region type="state">Californie</region></placeName></affiliation></author></analytic><series><title level="j">Frontiers in plant science</title><idno type="ISSN">1664-462X</idno><imprint><date when="2020" type="published">2020</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><i>Xanthomonas</i> species, <i>Pseudomonas syringae</i> and <i>Ralstonia</i> species are bacterial plant pathogens that cause significant yield loss in many crop species. Generating disease-resistant crop varieties can provide a more sustainable solution to control yield loss compared to chemical methods. Plant immune receptors encoded by nucleotide-binding, leucine-rich repeat (NLR) genes typically confer resistance to pathogens that produce a cognate elicitor, often an effector protein secreted by the pathogen to promote virulence. The diverse sequence and presence/absence variation of pathogen effector proteins within and between pathogen species usually limits the utility of a single NLR gene to protecting a plant from a single pathogen species or particular strains. The NLR protein Recognition of XopQ 1 (Roq1) was recently identified from the plant <i>Nicotiana benthamiana</i> and mediates perception of the effector proteins XopQ and HopQ1 from <i>Xanthomonas</i> and <i>P. syringae</i> respectively. Unlike most recognized effectors, alleles of XopQ/HopQ1 are highly conserved and present in most plant pathogenic strains of <i>Xanthomonas</i> and <i>P. syringae</i>. A homolog of XopQ/HopQ1, named RipB, is present in most <i>Ralstonia</i> strains. We found that Roq1 confers immunity to <i>Xanthomonas</i>, <i>P. syringae</i>, and <i>Ralstonia</i> when expressed in tomato. Strong resistance to <i>Xanthomonas perforans</i> was observed in three seasons of field trials with both natural and artificial inoculation. The <i>Roq1</i> gene can therefore be used to provide safe, economical, and effective control of these pathogens in tomato and other crop species and reduce or eliminate the need for traditional chemical controls.</div></front></TEI><pubmed><MedlineCitation Status="PubMed-not-MEDLINE" Owner="NLM"><PMID Version="1">32391034</PMID><DateRevised><Year>2020</Year><Month>09</Month><Day>28</Day></DateRevised><Article PubModel="Electronic-eCollection"><Journal><ISSN IssnType="Print">1664-462X</ISSN><JournalIssue CitedMedium="Print"><Volume>11</Volume><PubDate><Year>2020</Year></PubDate></JournalIssue><Title>Frontiers in plant science</Title><ISOAbbreviation>Front Plant Sci</ISOAbbreviation></Journal><ArticleTitle>The Immune Receptor Roq1 Confers Resistance to the Bacterial Pathogens <i>Xanthomonas</i>, <i>Pseudomonas syringae</i>, and <i>Ralstonia</i> in Tomato.</ArticleTitle><Pagination><MedlinePgn>463</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.3389/fpls.2020.00463</ELocationID><Abstract><AbstractText><i>Xanthomonas</i> species, <i>Pseudomonas syringae</i> and <i>Ralstonia</i> species are bacterial plant pathogens that cause significant yield loss in many crop species. Generating disease-resistant crop varieties can provide a more sustainable solution to control yield loss compared to chemical methods. Plant immune receptors encoded by nucleotide-binding, leucine-rich repeat (NLR) genes typically confer resistance to pathogens that produce a cognate elicitor, often an effector protein secreted by the pathogen to promote virulence. The diverse sequence and presence/absence variation of pathogen effector proteins within and between pathogen species usually limits the utility of a single NLR gene to protecting a plant from a single pathogen species or particular strains. The NLR protein Recognition of XopQ 1 (Roq1) was recently identified from the plant <i>Nicotiana benthamiana</i> and mediates perception of the effector proteins XopQ and HopQ1 from <i>Xanthomonas</i> and <i>P. syringae</i> respectively. Unlike most recognized effectors, alleles of XopQ/HopQ1 are highly conserved and present in most plant pathogenic strains of <i>Xanthomonas</i> and <i>P. syringae</i>. A homolog of XopQ/HopQ1, named RipB, is present in most <i>Ralstonia</i> strains. We found that Roq1 confers immunity to <i>Xanthomonas</i>, <i>P. syringae</i>, and <i>Ralstonia</i> when expressed in tomato. Strong resistance to <i>Xanthomonas perforans</i> was observed in three seasons of field trials with both natural and artificial inoculation. The <i>Roq1</i> gene can therefore be used to provide safe, economical, and effective control of these pathogens in tomato and other crop species and reduce or eliminate the need for traditional chemical controls.</AbstractText><CopyrightInformation>Copyright © 2020 Thomas, Hendrich, Gill, Allen, Hutton and Schultink.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Thomas</LastName><ForeName>Nicholas C</ForeName><Initials>NC</Initials><AffiliationInfo><Affiliation>Fortiphyte Inc., Berkeley, CA, United States.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Innovative Genomics Institute, University of California, Berkeley, Berkeley, CA, United States.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Hendrich</LastName><ForeName>Connor G</ForeName><Initials>CG</Initials><AffiliationInfo><Affiliation>Department of Plant Pathology, University of Wisconsin-Madison, Madison, WI, United States.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Gill</LastName><ForeName>Upinder S</ForeName><Initials>US</Initials><AffiliationInfo><Affiliation>IFAS, Gulf Coast Research and Education Center, University of Florida, Wimauma, FL, United States.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Department of Plant Pathology, North Dakota State University, Fargo, ND, United States.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Allen</LastName><ForeName>Caitilyn</ForeName><Initials>C</Initials><AffiliationInfo><Affiliation>Department of Plant Pathology, University of Wisconsin-Madison, Madison, WI, United States.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Hutton</LastName><ForeName>Samuel F</ForeName><Initials>SF</Initials><AffiliationInfo><Affiliation>IFAS, Gulf Coast Research and Education Center, University of Florida, Wimauma, FL, United States.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Schultink</LastName><ForeName>Alex</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>Fortiphyte Inc., Berkeley, CA, United States.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Innovative Genomics Institute, University of California, Berkeley, Berkeley, CA, United States.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2020</Year><Month>04</Month><Day>23</Day></ArticleDate></Article><MedlineJournalInfo><Country>Switzerland</Country><MedlineTA>Front Plant Sci</MedlineTA><NlmUniqueID>101568200</NlmUniqueID><ISSNLinking>1664-462X</ISSNLinking></MedlineJournalInfo><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Pseudomonas</Keyword><Keyword MajorTopicYN="N">Ralstonia</Keyword><Keyword MajorTopicYN="N">Xanthomonas</Keyword><Keyword MajorTopicYN="N">plant immunity</Keyword><Keyword MajorTopicYN="N">tomato</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2019</Year><Month>12</Month><Day>24</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2020</Year><Month>03</Month><Day>30</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2020</Year><Month>5</Month><Day>12</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2020</Year><Month>5</Month><Day>12</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2020</Year><Month>5</Month><Day>12</Day><Hour>6</Hour><Minute>1</Minute></PubMedPubDate></History><PublicationStatus>epublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">32391034</ArticleId><ArticleId IdType="doi">10.3389/fpls.2020.00463</ArticleId><ArticleId IdType="pmc">PMC7192161</ArticleId></ArticleIdList><ReferenceList><Reference><Citation>Plant Sci. 2019 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Nord</li><li>Floride</li><li>Wisconsin</li></region></list><tree><country name="États-Unis"><region name="Californie"><name sortKey="Thomas, Nicholas C" sort="Thomas, Nicholas C" uniqKey="Thomas N" first="Nicholas C" last="Thomas">Nicholas C. Thomas</name></region><name sortKey="Allen, Caitilyn" sort="Allen, Caitilyn" uniqKey="Allen C" first="Caitilyn" last="Allen">Caitilyn Allen</name><name sortKey="Gill, Upinder S" sort="Gill, Upinder S" uniqKey="Gill U" first="Upinder S" last="Gill">Upinder S. Gill</name><name sortKey="Gill, Upinder S" sort="Gill, Upinder S" uniqKey="Gill U" first="Upinder S" last="Gill">Upinder S. Gill</name><name sortKey="Hendrich, Connor G" sort="Hendrich, Connor G" uniqKey="Hendrich C" first="Connor G" last="Hendrich">Connor G. Hendrich</name><name sortKey="Hutton, Samuel F" sort="Hutton, Samuel F" uniqKey="Hutton S" first="Samuel F" last="Hutton">Samuel F. Hutton</name><name sortKey="Schultink, Alex" sort="Schultink, Alex" uniqKey="Schultink A" first="Alex" last="Schultink">Alex Schultink</name><name sortKey="Schultink, Alex" sort="Schultink, Alex" uniqKey="Schultink A" first="Alex" last="Schultink">Alex Schultink</name><name sortKey="Thomas, Nicholas C" sort="Thomas, Nicholas C" uniqKey="Thomas N" first="Nicholas C" last="Thomas">Nicholas C. Thomas</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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