Isolation, Characterization, and Pathogenicity of Two Pseudomonas syringae Pathovars from Populus trichocarpa Seeds.
Identifieur interne : 000303 ( Main/Exploration ); précédent : 000302; suivant : 000304Isolation, Characterization, and Pathogenicity of Two Pseudomonas syringae Pathovars from Populus trichocarpa Seeds.
Auteurs : Patricia Mb Saint-Vincent [États-Unis] ; Mary Ridout [États-Unis] ; Nancy L. Engle [États-Unis] ; Travis J. Lawrence [États-Unis] ; Meredith L. Yeary [États-Unis] ; Timothy J. Tschaplinski [États-Unis] ; George Newcombe [États-Unis] ; Dale A. Pelletier [États-Unis]Source :
- Microorganisms [ 2076-2607 ] ; 2020.
Abstract
Pseudomonas syringae is a ubiquitous plant pathogen, infecting both woody and herbaceous plants and resulting in devastating agricultural crop losses. Characterized by a remarkable specificity for plant hosts, P. syringae pathovars utilize a number of virulence factors including the type III secretion system and effector proteins to elicit disease in a particular host species. Here, two Pseudomonas syringae strains were isolated from diseased Populustrichocarpa seeds. The pathovars were capable of inhibiting poplar seed germination and were selective for the Populus genus. Sequencing of the newly described organisms revealed similarity to phylogroup II pathogens and genomic regions associated with woody host-associated plant pathogens, as well as genes for specific virulence factors. The host response to infection, as revealed through metabolomics, is the induction of the stress response through the accumulation of higher-order salicylates. Combined with necrosis on leaf surfaces, the plant appears to quickly respond by isolating infected tissues and mounting an anti-inflammatory defense. This study improves our understanding of the initial host response to epiphytic pathogens in Populus and provides a new model system for studying the effects of a bacterial pathogen on a woody host plant in which both organisms are fully genetically sequenced.
DOI: 10.3390/microorganisms8081137
PubMed: 32731357
PubMed Central: PMC7465253
Affiliations:
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Engle</name><affiliation wicri:level="2"><nlm:affiliation>Bioscience Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Bioscience Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831</wicri:regionArea><placeName><region type="state">Tennessee</region></placeName></affiliation></author><author><name sortKey="Lawrence, Travis J" sort="Lawrence, Travis J" uniqKey="Lawrence T" first="Travis J" last="Lawrence">Travis J. Lawrence</name><affiliation wicri:level="2"><nlm:affiliation>Bioscience Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Bioscience Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831</wicri:regionArea><placeName><region type="state">Tennessee</region></placeName></affiliation></author><author><name sortKey="Yeary, Meredith L" sort="Yeary, Meredith L" uniqKey="Yeary M" first="Meredith L" last="Yeary">Meredith L. Yeary</name><affiliation wicri:level="2"><nlm:affiliation>Bioscience Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Bioscience Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831</wicri:regionArea><placeName><region type="state">Tennessee</region></placeName></affiliation></author><author><name sortKey="Tschaplinski, Timothy J" sort="Tschaplinski, Timothy J" uniqKey="Tschaplinski T" first="Timothy J" last="Tschaplinski">Timothy J. Tschaplinski</name><affiliation wicri:level="2"><nlm:affiliation>Bioscience Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Bioscience Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831</wicri:regionArea><placeName><region type="state">Tennessee</region></placeName></affiliation></author><author><name sortKey="Newcombe, George" sort="Newcombe, George" uniqKey="Newcombe G" first="George" last="Newcombe">George Newcombe</name><affiliation wicri:level="2"><nlm:affiliation>Department of Forest, Rangeland and Fire Sciences, University of Idaho, Moscow, ID 83844, USA.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Forest, Rangeland and Fire Sciences, University of Idaho, Moscow, ID 83844</wicri:regionArea><placeName><region type="state">Idaho</region></placeName></affiliation></author><author><name sortKey="Pelletier, Dale A" sort="Pelletier, Dale A" uniqKey="Pelletier D" first="Dale A" last="Pelletier">Dale A. Pelletier</name><affiliation wicri:level="2"><nlm:affiliation>Bioscience Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Bioscience Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831</wicri:regionArea><placeName><region type="state">Tennessee</region></placeName></affiliation></author></analytic><series><title level="j">Microorganisms</title><idno type="ISSN">2076-2607</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>Pseudomonas syringae</i> is a ubiquitous plant pathogen, infecting both woody and herbaceous plants and resulting in devastating agricultural crop losses. Characterized by a remarkable specificity for plant hosts, <i>P. syringae</i> pathovars utilize a number of virulence factors including the type III secretion system and effector proteins to elicit disease in a particular host species. Here, two <i>Pseudomonas syringae</i> strains were isolated from diseased <i>Populus</i><i>trichocarpa</i> seeds. The pathovars were capable of inhibiting poplar seed germination and were selective for the <i>Populus</i> genus. Sequencing of the newly described organisms revealed similarity to phylogroup II pathogens and genomic regions associated with woody host-associated plant pathogens, as well as genes for specific virulence factors. The host response to infection, as revealed through metabolomics, is the induction of the stress response through the accumulation of higher-order salicylates. Combined with necrosis on leaf surfaces, the plant appears to quickly respond by isolating infected tissues and mounting an anti-inflammatory defense. This study improves our understanding of the initial host response to epiphytic pathogens in <i>Populus</i> and provides a new model system for studying the effects of a bacterial pathogen on a woody host plant in which both organisms are fully genetically sequenced.</div></front></TEI><pubmed><MedlineCitation Status="PubMed-not-MEDLINE" Owner="NLM"><PMID Version="1">32731357</PMID><DateRevised><Year>2020</Year><Month>09</Month><Day>28</Day></DateRevised><Article PubModel="Electronic"><Journal><ISSN IssnType="Print">2076-2607</ISSN><JournalIssue CitedMedium="Print"><Volume>8</Volume><Issue>8</Issue><PubDate><Year>2020</Year><Month>Jul</Month><Day>28</Day></PubDate></JournalIssue><Title>Microorganisms</Title><ISOAbbreviation>Microorganisms</ISOAbbreviation></Journal><ArticleTitle>Isolation, Characterization, and Pathogenicity of Two <i>Pseudomonas syringae</i> Pathovars from <i>Populus trichocarpa</i> Seeds.</ArticleTitle><ELocationID EIdType="pii" ValidYN="Y">E1137</ELocationID><ELocationID EIdType="doi" ValidYN="Y">10.3390/microorganisms8081137</ELocationID><Abstract><AbstractText><i>Pseudomonas syringae</i> is a ubiquitous plant pathogen, infecting both woody and herbaceous plants and resulting in devastating agricultural crop losses. Characterized by a remarkable specificity for plant hosts, <i>P. syringae</i> pathovars utilize a number of virulence factors including the type III secretion system and effector proteins to elicit disease in a particular host species. Here, two <i>Pseudomonas syringae</i> strains were isolated from diseased <i>Populus</i><i>trichocarpa</i> seeds. The pathovars were capable of inhibiting poplar seed germination and were selective for the <i>Populus</i> genus. Sequencing of the newly described organisms revealed similarity to phylogroup II pathogens and genomic regions associated with woody host-associated plant pathogens, as well as genes for specific virulence factors. The host response to infection, as revealed through metabolomics, is the induction of the stress response through the accumulation of higher-order salicylates. Combined with necrosis on leaf surfaces, the plant appears to quickly respond by isolating infected tissues and mounting an anti-inflammatory defense. This study improves our understanding of the initial host response to epiphytic pathogens in <i>Populus</i> and provides a new model system for studying the effects of a bacterial pathogen on a woody host plant in which both organisms are fully genetically sequenced.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Saint-Vincent</LastName><ForeName>Patricia Mb</ForeName><Initials>PM</Initials><AffiliationInfo><Affiliation>Bioscience Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>Geologic and Environmental Systems Directorate, National Energy Technology Laboratory, Pittsburgh, PA 15236, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Ridout</LastName><ForeName>Mary</ForeName><Initials>M</Initials><AffiliationInfo><Affiliation>Department of Forest, Rangeland and Fire Sciences, University of Idaho, Moscow, ID 83844, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Engle</LastName><ForeName>Nancy L</ForeName><Initials>NL</Initials><AffiliationInfo><Affiliation>Bioscience Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Lawrence</LastName><ForeName>Travis J</ForeName><Initials>TJ</Initials><Identifier Source="ORCID">0000-0002-7380-489X</Identifier><AffiliationInfo><Affiliation>Bioscience Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Yeary</LastName><ForeName>Meredith L</ForeName><Initials>ML</Initials><AffiliationInfo><Affiliation>Bioscience Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Tschaplinski</LastName><ForeName>Timothy J</ForeName><Initials>TJ</Initials><Identifier Source="ORCID">0000-0002-9540-6622</Identifier><AffiliationInfo><Affiliation>Bioscience Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Newcombe</LastName><ForeName>George</ForeName><Initials>G</Initials><Identifier Source="ORCID">0000-0002-9330-7356</Identifier><AffiliationInfo><Affiliation>Department of Forest, Rangeland and Fire Sciences, University of Idaho, Moscow, ID 83844, USA.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Pelletier</LastName><ForeName>Dale A</ForeName><Initials>DA</Initials><AffiliationInfo><Affiliation>Bioscience Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><GrantList CompleteYN="Y"><Grant><GrantID>DE-SC0014547</GrantID><Agency>U.S. Department of Energy</Agency><Country></Country></Grant></GrantList><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2020</Year><Month>07</Month><Day>28</Day></ArticleDate></Article><MedlineJournalInfo><Country>Switzerland</Country><MedlineTA>Microorganisms</MedlineTA><NlmUniqueID>101625893</NlmUniqueID><ISSNLinking>2076-2607</ISSNLinking></MedlineJournalInfo><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Pseudomonas</Keyword><Keyword MajorTopicYN="N">germination</Keyword><Keyword MajorTopicYN="N">metabolomics</Keyword><Keyword MajorTopicYN="N">pathogen</Keyword><Keyword MajorTopicYN="N">virulence</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2020</Year><Month>06</Month><Day>02</Day></PubMedPubDate><PubMedPubDate PubStatus="revised"><Year>2020</Year><Month>07</Month><Day>21</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2020</Year><Month>07</Month><Day>23</Day></PubMedPubDate><PubMedPubDate 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Engle</name><name sortKey="Lawrence, Travis J" sort="Lawrence, Travis J" uniqKey="Lawrence T" first="Travis J" last="Lawrence">Travis J. Lawrence</name><name sortKey="Newcombe, George" sort="Newcombe, George" uniqKey="Newcombe G" first="George" last="Newcombe">George Newcombe</name><name sortKey="Pelletier, Dale A" sort="Pelletier, Dale A" uniqKey="Pelletier D" first="Dale A" last="Pelletier">Dale A. Pelletier</name><name sortKey="Ridout, Mary" sort="Ridout, Mary" uniqKey="Ridout M" first="Mary" last="Ridout">Mary Ridout</name><name sortKey="Saint Vincent, Patricia Mb" sort="Saint Vincent, Patricia Mb" uniqKey="Saint Vincent P" first="Patricia Mb" last="Saint-Vincent">Patricia Mb Saint-Vincent</name><name sortKey="Tschaplinski, Timothy J" sort="Tschaplinski, Timothy J" uniqKey="Tschaplinski T" first="Timothy J" last="Tschaplinski">Timothy J. Tschaplinski</name><name sortKey="Yeary, Meredith L" sort="Yeary, Meredith L" uniqKey="Yeary M" first="Meredith L" last="Yeary">Meredith L. 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