Dynamics of Aspen Roots Colonization by Pseudomonads Reveals Strain-Specific and Mycorrhizal-Specific Patterns of Biofilm Formation.
Identifieur interne : 000F47 ( Main/Exploration ); précédent : 000F46; suivant : 000F48Dynamics of Aspen Roots Colonization by Pseudomonads Reveals Strain-Specific and Mycorrhizal-Specific Patterns of Biofilm Formation.
Auteurs : Marie-Francoise Noirot-Gros [États-Unis] ; Shalaka Shinde [États-Unis] ; Peter E. Larsen [États-Unis] ; Sarah Zerbs [États-Unis] ; Peter J. Korajczyk [États-Unis] ; Kenneth M. Kemner [États-Unis] ; Philippe H. Noirot [États-Unis]Source :
- Frontiers in microbiology [ 1664-302X ] ; 2018.
Abstract
Rhizosphere-associated Pseudomonas fluorescens are known plant growth promoting (PGP) and mycorrhizal helper bacteria (MHB) of many plants and ectomycorrhizal fungi. We investigated the spatial and temporal dynamics of colonization of mycorrhizal and non-mycorrhizal Aspen seedlings roots by the P. fluorescens strains SBW25, WH6, Pf0-1, and the P. protegens strain Pf-5. Seedlings were grown in laboratory vertical plates systems, inoculated with a fluorescently labeled Pseudomonas strain, and root colonization was monitored over a period of 5 weeks. We observed unexpected diversity of bacterial assemblies on seedling roots that changed over time and were strongly affected by root mycorrhization. P. fluorescens SBW25 and WH6 stains developed highly structured biofilms with internal void spaces forming channels. On mycorrhizal roots bacteria appeared encased in a mucilaginous substance in which they aligned side by side in parallel arrangements. The different phenotypic classes of bacterial assemblies observed for the four Pseudomonas strains were summarized in a single model describing transitions between phenotypic classes. Our findings also reveal that bacterial assembly phenotypes are driven by interactions with mucilaginous materials present at roots.
DOI: 10.3389/fmicb.2018.00853
PubMed: 29774013
PubMed Central: PMC5943511
Affiliations:
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Kemner</name><affiliation wicri:level="2"><nlm:affiliation>Biosciences Division, Argonne National Laboratory, Lemont, IL, United States.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Biosciences Division, Argonne National Laboratory, Lemont, IL</wicri:regionArea><placeName><region type="state">Illinois</region></placeName></affiliation></author><author><name sortKey="Noirot, Philippe H" sort="Noirot, Philippe H" uniqKey="Noirot P" first="Philippe H" last="Noirot">Philippe H. Noirot</name><affiliation wicri:level="2"><nlm:affiliation>Biosciences Division, Argonne National Laboratory, Lemont, IL, United States.</nlm:affiliation><country xml:lang="fr">États-Unis</country><wicri:regionArea>Biosciences Division, Argonne National Laboratory, Lemont, IL</wicri:regionArea><placeName><region type="state">Illinois</region></placeName></affiliation></author></analytic><series><title level="j">Frontiers in microbiology</title><idno type="ISSN">1664-302X</idno><imprint><date when="2018" type="published">2018</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Rhizosphere-associated <i>Pseudomonas fluorescens</i> are known plant growth promoting (PGP) and mycorrhizal helper bacteria (MHB) of many plants and ectomycorrhizal fungi. We investigated the spatial and temporal dynamics of colonization of mycorrhizal and non-mycorrhizal Aspen seedlings roots by the <i>P. fluorescens</i> strains SBW25, WH6, Pf0-1, and the <i>P. protegens</i> strain Pf-5. Seedlings were grown in laboratory vertical plates systems, inoculated with a fluorescently labeled <i>Pseudomonas</i> strain, and root colonization was monitored over a period of 5 weeks. We observed unexpected diversity of bacterial assemblies on seedling roots that changed over time and were strongly affected by root mycorrhization. <i>P. fluorescens</i> SBW25 and WH6 stains developed highly structured biofilms with internal void spaces forming channels. On mycorrhizal roots bacteria appeared encased in a mucilaginous substance in which they aligned side by side in parallel arrangements. The different phenotypic classes of bacterial assemblies observed for the four <i>Pseudomonas</i> strains were summarized in a single model describing transitions between phenotypic classes. Our findings also reveal that bacterial assembly phenotypes are driven by interactions with mucilaginous materials present at roots.</div></front></TEI><pubmed><MedlineCitation Status="PubMed-not-MEDLINE" Owner="NLM"><PMID Version="1">29774013</PMID><DateRevised><Year>2020</Year><Month>10</Month><Day>01</Day></DateRevised><Article PubModel="Electronic-eCollection"><Journal><ISSN IssnType="Print">1664-302X</ISSN><JournalIssue CitedMedium="Print"><Volume>9</Volume><PubDate><Year>2018</Year></PubDate></JournalIssue><Title>Frontiers in microbiology</Title><ISOAbbreviation>Front Microbiol</ISOAbbreviation></Journal><ArticleTitle>Dynamics of Aspen Roots Colonization by Pseudomonads Reveals Strain-Specific and Mycorrhizal-Specific Patterns of Biofilm Formation.</ArticleTitle><Pagination><MedlinePgn>853</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.3389/fmicb.2018.00853</ELocationID><Abstract><AbstractText>Rhizosphere-associated <i>Pseudomonas fluorescens</i> are known plant growth promoting (PGP) and mycorrhizal helper bacteria (MHB) of many plants and ectomycorrhizal fungi. We investigated the spatial and temporal dynamics of colonization of mycorrhizal and non-mycorrhizal Aspen seedlings roots by the <i>P. fluorescens</i> strains SBW25, WH6, Pf0-1, and the <i>P. protegens</i> strain Pf-5. Seedlings were grown in laboratory vertical plates systems, inoculated with a fluorescently labeled <i>Pseudomonas</i> strain, and root colonization was monitored over a period of 5 weeks. We observed unexpected diversity of bacterial assemblies on seedling roots that changed over time and were strongly affected by root mycorrhization. <i>P. fluorescens</i> SBW25 and WH6 stains developed highly structured biofilms with internal void spaces forming channels. On mycorrhizal roots bacteria appeared encased in a mucilaginous substance in which they aligned side by side in parallel arrangements. The different phenotypic classes of bacterial assemblies observed for the four <i>Pseudomonas</i> strains were summarized in a single model describing transitions between phenotypic classes. Our findings also reveal that bacterial assembly phenotypes are driven by interactions with mucilaginous materials present at roots.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Noirot-Gros</LastName><ForeName>Marie-Francoise</ForeName><Initials>MF</Initials><AffiliationInfo><Affiliation>Biosciences Division, Argonne National Laboratory, Lemont, IL, United States.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Shinde</LastName><ForeName>Shalaka</ForeName><Initials>S</Initials><AffiliationInfo><Affiliation>Biosciences Division, Argonne National Laboratory, Lemont, IL, United States.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Larsen</LastName><ForeName>Peter E</ForeName><Initials>PE</Initials><AffiliationInfo><Affiliation>Biosciences Division, Argonne National Laboratory, Lemont, IL, United States.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Zerbs</LastName><ForeName>Sarah</ForeName><Initials>S</Initials><AffiliationInfo><Affiliation>Biosciences Division, Argonne National Laboratory, Lemont, IL, United States.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Korajczyk</LastName><ForeName>Peter J</ForeName><Initials>PJ</Initials><AffiliationInfo><Affiliation>Biosciences Division, Argonne National Laboratory, Lemont, IL, United States.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Kemner</LastName><ForeName>Kenneth M</ForeName><Initials>KM</Initials><AffiliationInfo><Affiliation>Biosciences Division, Argonne National Laboratory, Lemont, IL, United States.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Noirot</LastName><ForeName>Philippe H</ForeName><Initials>PH</Initials><AffiliationInfo><Affiliation>Biosciences Division, Argonne National Laboratory, Lemont, IL, United States.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2018</Year><Month>05</Month><Day>03</Day></ArticleDate></Article><MedlineJournalInfo><Country>Switzerland</Country><MedlineTA>Front Microbiol</MedlineTA><NlmUniqueID>101548977</NlmUniqueID><ISSNLinking>1664-302X</ISSNLinking></MedlineJournalInfo><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Laccaria bicolor</Keyword><Keyword MajorTopicYN="N">Populus tremuloides</Keyword><Keyword MajorTopicYN="N">Pseudomonas fluorescens</Keyword><Keyword MajorTopicYN="N">biofilms</Keyword><Keyword MajorTopicYN="N">mucilage</Keyword><Keyword MajorTopicYN="N">mycorrhization</Keyword><Keyword MajorTopicYN="N">plant-root colonization</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate 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Kemner</name><name sortKey="Korajczyk, Peter J" sort="Korajczyk, Peter J" uniqKey="Korajczyk P" first="Peter J" last="Korajczyk">Peter J. Korajczyk</name><name sortKey="Larsen, Peter E" sort="Larsen, Peter E" uniqKey="Larsen P" first="Peter E" last="Larsen">Peter E. Larsen</name><name sortKey="Noirot, Philippe H" sort="Noirot, Philippe H" uniqKey="Noirot P" first="Philippe H" last="Noirot">Philippe H. Noirot</name><name sortKey="Shinde, Shalaka" sort="Shinde, Shalaka" uniqKey="Shinde S" first="Shalaka" last="Shinde">Shalaka Shinde</name><name sortKey="Zerbs, Sarah" sort="Zerbs, Sarah" uniqKey="Zerbs S" first="Sarah" last="Zerbs">Sarah Zerbs</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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