Lipopolysaccharides of Pectobacterium atrosepticum and Pseudomonas corrugata induce different defence response patterns in tobacco, tomato, and potato.
Identifieur interne : 002011 ( Main/Exploration ); précédent : 002010; suivant : 002012Lipopolysaccharides of Pectobacterium atrosepticum and Pseudomonas corrugata induce different defence response patterns in tobacco, tomato, and potato.
Auteurs : S. Desender [France] ; O. Klarzynski ; P. Potin ; M-R Barzic ; D. Andrivon ; F. ValSource :
- Plant biology (Stuttgart, Germany) [ 1435-8603 ] ; 2006.
Descripteurs français
- KwdFr :
- Cellules cultivées (MeSH), Concentration en ions d'hydrogène (MeSH), Facteurs temps (MeSH), Lipopolysaccharides (métabolisme), Lipopolysaccharides (pharmacologie), Lipoxygenase (métabolisme), Lycopersicon esculentum (effets des médicaments et des substances chimiques), Lycopersicon esculentum (génétique), Lycopersicon esculentum (métabolisme), Pectobacterium (métabolisme), Peroxyde d'hydrogène (métabolisme), Pseudomonas (métabolisme), Relation dose-effet des médicaments (MeSH), Solanum tuberosum (effets des médicaments et des substances chimiques), Solanum tuberosum (génétique), Solanum tuberosum (métabolisme), Spécificité d'espèce (MeSH), Tabac (effets des médicaments et des substances chimiques), Tabac (génétique), Tabac (métabolisme).
- MESH :
- effets des médicaments et des substances chimiques : Lycopersicon esculentum, Solanum tuberosum, Tabac.
- génétique : Lycopersicon esculentum, Solanum tuberosum, Tabac.
- métabolisme : Lipopolysaccharides, Lipoxygenase, Lycopersicon esculentum, Pectobacterium, Peroxyde d'hydrogène, Pseudomonas, Solanum tuberosum, Tabac.
- pharmacologie : Lipopolysaccharides.
- Cellules cultivées, Concentration en ions d'hydrogène, Facteurs temps, Relation dose-effet des médicaments, Spécificité d'espèce.
English descriptors
- KwdEn :
- Cells, Cultured (MeSH), Dose-Response Relationship, Drug (MeSH), Hydrogen Peroxide (metabolism), Hydrogen-Ion Concentration (MeSH), Lipopolysaccharides (metabolism), Lipopolysaccharides (pharmacology), Lipoxygenase (metabolism), Lycopersicon esculentum (drug effects), Lycopersicon esculentum (genetics), Lycopersicon esculentum (metabolism), Pectobacterium (metabolism), Pseudomonas (metabolism), Solanum tuberosum (drug effects), Solanum tuberosum (genetics), Solanum tuberosum (metabolism), Species Specificity (MeSH), Time Factors (MeSH), Tobacco (drug effects), Tobacco (genetics), Tobacco (metabolism).
- MESH :
- chemical , metabolism : Hydrogen Peroxide, Lipopolysaccharides, Lipoxygenase.
- chemical , pharmacology : Lipopolysaccharides.
- drug effects : Lycopersicon esculentum, Solanum tuberosum, Tobacco.
- genetics : Lycopersicon esculentum, Solanum tuberosum, Tobacco.
- metabolism : Lycopersicon esculentum, Pectobacterium, Pseudomonas, Solanum tuberosum, Tobacco.
- Cells, Cultured, Dose-Response Relationship, Drug, Hydrogen-Ion Concentration, Species Specificity, Time Factors.
Abstract
Lipopolysaccharides (LPS), ubiquitous cell surface components of Gram-negative bacteria, are directly implicated in plant/pathogen interactions. However, their perception by the plant, the subsequent signal transduction in both compatible and incompatible interactions, as well as the defence reactions induced in compatible interactions are as yet poorly understood. We focused on biochemical and physiological reactions induced in cell suspensions of three Solanaceae species (tobacco, tomato, and potato) by purified lipopolysaccharides from PECTOBACTERIUM ATROSEPTICUM (PA), a pathogen of potato, and PSEUDOMONAS CORRUGATA (PSC), a pathogen of tomato. LPS PA and LPS PSC caused a significant acidification of potato, tomato, and tobacco extracellular media, whereas laminarin (a linear beta-1,3 oligosaccharide elicitor) induced an alkalinisation in tobacco and tomato, but not in potato cell suspensions. None of the two LPS induced the formation of active oxygen species in any of the hosts, while laminarin induced H (2)O (2) production in cells of tobacco but not of tomato and potato. In tomato cells, LPS PA and LPS PSC induced a strong but transitory stimulation of lipoxygenase activity, whereas laminarin induced a stable or slightly increasing LOX activity over the first 24 h of contact. In tobacco, LOX activity was not triggered by either LPS, but significantly increased following treatment with laminarin. In potato, neither LPS nor laminarin induced LOX activity, in contrast with concentrated culture filtrate of PHYTOPHTHORA INFESTANS (CCF). These results demonstrate that LPS, as well as laminarin, are perceived in different ways by SOLANACEAE species, and possibly cultivars. They also suggest that defence responses modulated by LPS depend on plant genotypes rather than on the type of interaction.
DOI: 10.1055/s-2006-924102
PubMed: 16755465
Affiliations:
Links toward previous steps (curation, corpus...)
Le document en format XML
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Potin</name></author><author><name sortKey="Barzic, M R" sort="Barzic, M R" uniqKey="Barzic M" first="M-R" last="Barzic">M-R Barzic</name></author><author><name sortKey="Andrivon, D" sort="Andrivon, D" uniqKey="Andrivon D" first="D" last="Andrivon">D. Andrivon</name></author><author><name sortKey="Val, F" sort="Val, F" uniqKey="Val F" first="F" last="Val">F. 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Potin</name></author><author><name sortKey="Barzic, M R" sort="Barzic, M R" uniqKey="Barzic M" first="M-R" last="Barzic">M-R Barzic</name></author><author><name sortKey="Andrivon, D" sort="Andrivon, D" uniqKey="Andrivon D" first="D" last="Andrivon">D. Andrivon</name></author><author><name sortKey="Val, F" sort="Val, F" uniqKey="Val F" first="F" last="Val">F. Val</name></author></analytic><series><title level="j">Plant biology (Stuttgart, Germany)</title><idno type="ISSN">1435-8603</idno><imprint><date when="2006" type="published">2006</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Cells, Cultured (MeSH)</term><term>Dose-Response Relationship, Drug (MeSH)</term><term>Hydrogen Peroxide (metabolism)</term><term>Hydrogen-Ion Concentration (MeSH)</term><term>Lipopolysaccharides (metabolism)</term><term>Lipopolysaccharides (pharmacology)</term><term>Lipoxygenase (metabolism)</term><term>Lycopersicon esculentum (drug effects)</term><term>Lycopersicon esculentum (genetics)</term><term>Lycopersicon esculentum (metabolism)</term><term>Pectobacterium (metabolism)</term><term>Pseudomonas (metabolism)</term><term>Solanum tuberosum (drug effects)</term><term>Solanum tuberosum (genetics)</term><term>Solanum tuberosum (metabolism)</term><term>Species Specificity (MeSH)</term><term>Time Factors (MeSH)</term><term>Tobacco (drug effects)</term><term>Tobacco (genetics)</term><term>Tobacco (metabolism)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Cellules cultivées (MeSH)</term><term>Concentration en ions d'hydrogène (MeSH)</term><term>Facteurs temps (MeSH)</term><term>Lipopolysaccharides (métabolisme)</term><term>Lipopolysaccharides (pharmacologie)</term><term>Lipoxygenase (métabolisme)</term><term>Lycopersicon esculentum (effets des médicaments et des substances chimiques)</term><term>Lycopersicon esculentum (génétique)</term><term>Lycopersicon esculentum (métabolisme)</term><term>Pectobacterium (métabolisme)</term><term>Peroxyde d'hydrogène (métabolisme)</term><term>Pseudomonas (métabolisme)</term><term>Relation dose-effet des médicaments (MeSH)</term><term>Solanum tuberosum (effets des médicaments et des substances chimiques)</term><term>Solanum tuberosum (génétique)</term><term>Solanum tuberosum (métabolisme)</term><term>Spécificité d'espèce (MeSH)</term><term>Tabac (effets des médicaments et des substances chimiques)</term><term>Tabac (génétique)</term><term>Tabac (métabolisme)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Hydrogen Peroxide</term><term>Lipopolysaccharides</term><term>Lipoxygenase</term></keywords><keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Lipopolysaccharides</term></keywords><keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Lycopersicon esculentum</term><term>Solanum tuberosum</term><term>Tobacco</term></keywords><keywords scheme="MESH" qualifier="effets des médicaments et des substances chimiques" xml:lang="fr"><term>Lycopersicon esculentum</term><term>Solanum tuberosum</term><term>Tabac</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Lycopersicon esculentum</term><term>Solanum tuberosum</term><term>Tobacco</term></keywords><keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Lycopersicon esculentum</term><term>Solanum tuberosum</term><term>Tabac</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Lycopersicon esculentum</term><term>Pectobacterium</term><term>Pseudomonas</term><term>Solanum tuberosum</term><term>Tobacco</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Lipopolysaccharides</term><term>Lipoxygenase</term><term>Lycopersicon esculentum</term><term>Pectobacterium</term><term>Peroxyde d'hydrogène</term><term>Pseudomonas</term><term>Solanum tuberosum</term><term>Tabac</term></keywords><keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr"><term>Lipopolysaccharides</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Cells, Cultured</term><term>Dose-Response Relationship, Drug</term><term>Hydrogen-Ion Concentration</term><term>Species Specificity</term><term>Time Factors</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Cellules cultivées</term><term>Concentration en ions d'hydrogène</term><term>Facteurs temps</term><term>Relation dose-effet des médicaments</term><term>Spécificité d'espèce</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Lipopolysaccharides (LPS), ubiquitous cell surface components of Gram-negative bacteria, are directly implicated in plant/pathogen interactions. However, their perception by the plant, the subsequent signal transduction in both compatible and incompatible interactions, as well as the defence reactions induced in compatible interactions are as yet poorly understood. We focused on biochemical and physiological reactions induced in cell suspensions of three Solanaceae species (tobacco, tomato, and potato) by purified lipopolysaccharides from PECTOBACTERIUM ATROSEPTICUM (PA), a pathogen of potato, and PSEUDOMONAS CORRUGATA (PSC), a pathogen of tomato. LPS PA and LPS PSC caused a significant acidification of potato, tomato, and tobacco extracellular media, whereas laminarin (a linear beta-1,3 oligosaccharide elicitor) induced an alkalinisation in tobacco and tomato, but not in potato cell suspensions. None of the two LPS induced the formation of active oxygen species in any of the hosts, while laminarin induced H (2)O (2) production in cells of tobacco but not of tomato and potato. In tomato cells, LPS PA and LPS PSC induced a strong but transitory stimulation of lipoxygenase activity, whereas laminarin induced a stable or slightly increasing LOX activity over the first 24 h of contact. In tobacco, LOX activity was not triggered by either LPS, but significantly increased following treatment with laminarin. In potato, neither LPS nor laminarin induced LOX activity, in contrast with concentrated culture filtrate of PHYTOPHTHORA INFESTANS (CCF). These results demonstrate that LPS, as well as laminarin, are perceived in different ways by SOLANACEAE species, and possibly cultivars. They also suggest that defence responses modulated by LPS depend on plant genotypes rather than on the type of interaction.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">16755465</PMID><DateCompleted><Year>2006</Year><Month>11</Month><Day>06</Day></DateCompleted><DateRevised><Year>2013</Year><Month>11</Month><Day>21</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Print">1435-8603</ISSN><JournalIssue CitedMedium="Print"><Volume>8</Volume><Issue>5</Issue><PubDate><Year>2006</Year><Month>Sep</Month></PubDate></JournalIssue><Title>Plant biology (Stuttgart, Germany)</Title><ISOAbbreviation>Plant Biol (Stuttg)</ISOAbbreviation></Journal><ArticleTitle>Lipopolysaccharides of Pectobacterium atrosepticum and Pseudomonas corrugata induce different defence response patterns in tobacco, tomato, and potato.</ArticleTitle><Pagination><MedlinePgn>636-45</MedlinePgn></Pagination><Abstract><AbstractText>Lipopolysaccharides (LPS), ubiquitous cell surface components of Gram-negative bacteria, are directly implicated in plant/pathogen interactions. However, their perception by the plant, the subsequent signal transduction in both compatible and incompatible interactions, as well as the defence reactions induced in compatible interactions are as yet poorly understood. We focused on biochemical and physiological reactions induced in cell suspensions of three Solanaceae species (tobacco, tomato, and potato) by purified lipopolysaccharides from PECTOBACTERIUM ATROSEPTICUM (PA), a pathogen of potato, and PSEUDOMONAS CORRUGATA (PSC), a pathogen of tomato. LPS PA and LPS PSC caused a significant acidification of potato, tomato, and tobacco extracellular media, whereas laminarin (a linear beta-1,3 oligosaccharide elicitor) induced an alkalinisation in tobacco and tomato, but not in potato cell suspensions. None of the two LPS induced the formation of active oxygen species in any of the hosts, while laminarin induced H (2)O (2) production in cells of tobacco but not of tomato and potato. In tomato cells, LPS PA and LPS PSC induced a strong but transitory stimulation of lipoxygenase activity, whereas laminarin induced a stable or slightly increasing LOX activity over the first 24 h of contact. In tobacco, LOX activity was not triggered by either LPS, but significantly increased following treatment with laminarin. In potato, neither LPS nor laminarin induced LOX activity, in contrast with concentrated culture filtrate of PHYTOPHTHORA INFESTANS (CCF). These results demonstrate that LPS, as well as laminarin, are perceived in different ways by SOLANACEAE species, and possibly cultivars. They also suggest that defence responses modulated by LPS depend on plant genotypes rather than on the type of interaction.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Desender</LastName><ForeName>S</ForeName><Initials>S</Initials><AffiliationInfo><Affiliation>UMR BiO3P, Biologie des Organismes et des Populations appliquée à la Protection des Plantes, INRA-Agrocampus Rennes, 65 Rue de Saint Brieuc, 35042 Rennes Cedex, France.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Klarzynski</LastName><ForeName>O</ForeName><Initials>O</Initials></Author><Author ValidYN="Y"><LastName>Potin</LastName><ForeName>P</ForeName><Initials>P</Initials></Author><Author ValidYN="Y"><LastName>Barzic</LastName><ForeName>M-R</ForeName><Initials>MR</Initials></Author><Author ValidYN="Y"><LastName>Andrivon</LastName><ForeName>D</ForeName><Initials>D</Initials></Author><Author ValidYN="Y"><LastName>Val</LastName><ForeName>F</ForeName><Initials>F</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2006</Year><Month>06</Month><Day>01</Day></ArticleDate></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>Plant Biol (Stuttg)</MedlineTA><NlmUniqueID>101148926</NlmUniqueID><ISSNLinking>1435-8603</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D008070">Lipopolysaccharides</NameOfSubstance></Chemical><Chemical><RegistryNumber>BBX060AN9V</RegistryNumber><NameOfSubstance UI="D006861">Hydrogen Peroxide</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 1.13.11.12</RegistryNumber><NameOfSubstance UI="D008084">Lipoxygenase</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D002478" MajorTopicYN="N">Cells, Cultured</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D004305" MajorTopicYN="N">Dose-Response Relationship, Drug</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006861" MajorTopicYN="N">Hydrogen Peroxide</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006863" MajorTopicYN="N">Hydrogen-Ion Concentration</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008070" MajorTopicYN="N">Lipopolysaccharides</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName><QualifierName UI="Q000494" MajorTopicYN="Y">pharmacology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008084" MajorTopicYN="N">Lipoxygenase</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018551" MajorTopicYN="N">Lycopersicon esculentum</DescriptorName><QualifierName UI="Q000187" MajorTopicYN="Y">drug effects</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D044043" MajorTopicYN="N">Pectobacterium</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D011549" MajorTopicYN="N">Pseudomonas</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D011198" MajorTopicYN="N">Solanum tuberosum</DescriptorName><QualifierName UI="Q000187" MajorTopicYN="Y">drug effects</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013045" MajorTopicYN="N">Species Specificity</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D013997" MajorTopicYN="N">Time Factors</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D014026" MajorTopicYN="N">Tobacco</DescriptorName><QualifierName UI="Q000187" MajorTopicYN="Y">drug effects</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2006</Year><Month>6</Month><Day>7</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2006</Year><Month>11</Month><Day>7</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2006</Year><Month>6</Month><Day>7</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">16755465</ArticleId><ArticleId IdType="doi">10.1055/s-2006-924102</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>France</li></country><region><li>Région Bretagne</li></region><settlement><li>Rennes</li></settlement></list><tree><noCountry><name sortKey="Andrivon, D" sort="Andrivon, D" uniqKey="Andrivon D" first="D" last="Andrivon">D. Andrivon</name><name sortKey="Barzic, M R" sort="Barzic, M R" uniqKey="Barzic M" first="M-R" last="Barzic">M-R Barzic</name><name sortKey="Klarzynski, O" sort="Klarzynski, O" uniqKey="Klarzynski O" first="O" last="Klarzynski">O. Klarzynski</name><name sortKey="Potin, P" sort="Potin, P" uniqKey="Potin P" first="P" last="Potin">P. Potin</name><name sortKey="Val, F" sort="Val, F" uniqKey="Val F" first="F" last="Val">F. Val</name></noCountry><country name="France"><region name="Région Bretagne"><name sortKey="Desender, S" sort="Desender, S" uniqKey="Desender S" first="S" last="Desender">S. Desender</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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