Patterns of plant subcellular responses to successful oomycete infections reveal differences in host cell reprogramming and endocytic trafficking.
Identifieur interne : 001474 ( Main/Exploration ); précédent : 001473; suivant : 001475Patterns of plant subcellular responses to successful oomycete infections reveal differences in host cell reprogramming and endocytic trafficking.
Auteurs : Yi-Ju Lu [Allemagne] ; Sebastian Schornack ; Thomas Spallek ; Niko Geldner ; Joanne Chory ; Swen Schellmann ; Karin Schumacher ; Sophien Kamoun ; Silke RobatzekSource :
- Cellular microbiology [ 1462-5822 ] ; 2012.
Descripteurs français
- KwdFr :
- Arabidopsis (immunologie), Arabidopsis (microbiologie), Interactions hôte-pathogène (MeSH), Maladies des plantes (microbiologie), Microscopie de fluorescence (MeSH), Oomycetes (croissance et développement), Oomycetes (cytologie), Oomycetes (métabolisme), Oomycetes (pathogénicité), Tabac (immunologie), Tabac (microbiologie), Vésicules cytoplasmiques (microbiologie), Vésicules cytoplasmiques (métabolisme).
- MESH :
- croissance et développement : Oomycetes.
- cytologie : Oomycetes.
- immunologie : Arabidopsis, Tabac.
- microbiologie : Arabidopsis, Maladies des plantes, Tabac, Vésicules cytoplasmiques.
- métabolisme : Oomycetes, Vésicules cytoplasmiques.
- pathogénicité : Oomycetes.
- Interactions hôte-pathogène, Microscopie de fluorescence.
English descriptors
- KwdEn :
- Arabidopsis (immunology), Arabidopsis (microbiology), Cytoplasmic Vesicles (metabolism), Cytoplasmic Vesicles (microbiology), Host-Pathogen Interactions (MeSH), Microscopy, Fluorescence (MeSH), Oomycetes (cytology), Oomycetes (growth & development), Oomycetes (metabolism), Oomycetes (pathogenicity), Plant Diseases (microbiology), Tobacco (immunology), Tobacco (microbiology).
- MESH :
- cytology : Oomycetes.
- growth & development : Oomycetes.
- immunology : Arabidopsis, Tobacco.
- metabolism : Cytoplasmic Vesicles, Oomycetes.
- microbiology : Arabidopsis, Cytoplasmic Vesicles, Plant Diseases, Tobacco.
- pathogenicity : Oomycetes.
- Host-Pathogen Interactions, Microscopy, Fluorescence.
Abstract
Adapted filamentous pathogens such as the oomycetes Hyaloperonospora arabidopsidis (Hpa) and Phytophthora infestans (Pi) project specialized hyphae, the haustoria, inside living host cells for the suppression of host defence and acquisition of nutrients. Accommodation of haustoria requires reorganization of the host cell and the biogenesis of a novel host cell membrane, the extrahaustorial membrane (EHM), which envelops the haustorium separating the host cell from the pathogen. Here, we applied live-cell imaging of fluorescent-tagged proteins labelling a variety of membrane compartments and investigated the subcellular changes associated with accommodating oomycete haustoria in Arabidopsis and N. benthamiana. Plasma membrane-resident proteins differentially localized to the EHM. Likewise, secretory vesicles and endosomal compartments surrounded Hpa and Pi haustoria revealing differences between these two oomycetes, and suggesting a role for vesicle trafficking pathways for the pathogen-controlled biogenesis of the EHM. The latter is supported by enhanced susceptibility of mutants in endosome-mediated trafficking regulators. These observations point at host subcellular defences and specialization of the EHM in a pathogen-specific manner. Defence-associated haustorial encasements, a double-layered membrane that grows around mature haustoria, were frequently observed in Hpa interactions. Intriguingly, all tested plant proteins accumulated at Hpa haustorial encasements suggesting the general recruitment of default vesicle trafficking pathways to defend pathogen access. Altogether, our results show common requirements of subcellular changes associated with oomycete biotrophy, and highlight differences between two oomycete pathogens in reprogramming host cell vesicle trafficking for haustoria accommodation. This provides a framework for further dissection of the pathogen-triggered reprogramming of host subcellular changes.
DOI: 10.1111/j.1462-5822.2012.01751.x
PubMed: 22233428
PubMed Central: PMC4854193
Affiliations:
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scheme="KwdEn" xml:lang="en"><term>Arabidopsis (immunology)</term><term>Arabidopsis (microbiology)</term><term>Cytoplasmic Vesicles (metabolism)</term><term>Cytoplasmic Vesicles (microbiology)</term><term>Host-Pathogen Interactions (MeSH)</term><term>Microscopy, Fluorescence (MeSH)</term><term>Oomycetes (cytology)</term><term>Oomycetes (growth & development)</term><term>Oomycetes (metabolism)</term><term>Oomycetes (pathogenicity)</term><term>Plant Diseases (microbiology)</term><term>Tobacco (immunology)</term><term>Tobacco (microbiology)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Arabidopsis (immunologie)</term><term>Arabidopsis (microbiologie)</term><term>Interactions hôte-pathogène (MeSH)</term><term>Maladies des plantes (microbiologie)</term><term>Microscopie de fluorescence (MeSH)</term><term>Oomycetes (croissance et développement)</term><term>Oomycetes (cytologie)</term><term>Oomycetes (métabolisme)</term><term>Oomycetes (pathogénicité)</term><term>Tabac (immunologie)</term><term>Tabac (microbiologie)</term><term>Vésicules cytoplasmiques (microbiologie)</term><term>Vésicules cytoplasmiques (métabolisme)</term></keywords><keywords scheme="MESH" qualifier="croissance et développement" xml:lang="fr"><term>Oomycetes</term></keywords><keywords scheme="MESH" qualifier="cytologie" xml:lang="fr"><term>Oomycetes</term></keywords><keywords scheme="MESH" qualifier="cytology" xml:lang="en"><term>Oomycetes</term></keywords><keywords scheme="MESH" qualifier="growth & development" xml:lang="en"><term>Oomycetes</term></keywords><keywords scheme="MESH" qualifier="immunologie" xml:lang="fr"><term>Arabidopsis</term><term>Tabac</term></keywords><keywords scheme="MESH" qualifier="immunology" xml:lang="en"><term>Arabidopsis</term><term>Tobacco</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Cytoplasmic Vesicles</term><term>Oomycetes</term></keywords><keywords scheme="MESH" qualifier="microbiologie" xml:lang="fr"><term>Arabidopsis</term><term>Maladies des plantes</term><term>Tabac</term><term>Vésicules cytoplasmiques</term></keywords><keywords scheme="MESH" qualifier="microbiology" xml:lang="en"><term>Arabidopsis</term><term>Cytoplasmic Vesicles</term><term>Plant Diseases</term><term>Tobacco</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Oomycetes</term><term>Vésicules cytoplasmiques</term></keywords><keywords scheme="MESH" qualifier="pathogenicity" xml:lang="en"><term>Oomycetes</term></keywords><keywords scheme="MESH" qualifier="pathogénicité" xml:lang="fr"><term>Oomycetes</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Host-Pathogen Interactions</term><term>Microscopy, Fluorescence</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Interactions hôte-pathogène</term><term>Microscopie de fluorescence</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Adapted filamentous pathogens such as the oomycetes Hyaloperonospora arabidopsidis (Hpa) and Phytophthora infestans (Pi) project specialized hyphae, the haustoria, inside living host cells for the suppression of host defence and acquisition of nutrients. Accommodation of haustoria requires reorganization of the host cell and the biogenesis of a novel host cell membrane, the extrahaustorial membrane (EHM), which envelops the haustorium separating the host cell from the pathogen. Here, we applied live-cell imaging of fluorescent-tagged proteins labelling a variety of membrane compartments and investigated the subcellular changes associated with accommodating oomycete haustoria in Arabidopsis and N. benthamiana. Plasma membrane-resident proteins differentially localized to the EHM. Likewise, secretory vesicles and endosomal compartments surrounded Hpa and Pi haustoria revealing differences between these two oomycetes, and suggesting a role for vesicle trafficking pathways for the pathogen-controlled biogenesis of the EHM. The latter is supported by enhanced susceptibility of mutants in endosome-mediated trafficking regulators. These observations point at host subcellular defences and specialization of the EHM in a pathogen-specific manner. Defence-associated haustorial encasements, a double-layered membrane that grows around mature haustoria, were frequently observed in Hpa interactions. Intriguingly, all tested plant proteins accumulated at Hpa haustorial encasements suggesting the general recruitment of default vesicle trafficking pathways to defend pathogen access. Altogether, our results show common requirements of subcellular changes associated with oomycete biotrophy, and highlight differences between two oomycete pathogens in reprogramming host cell vesicle trafficking for haustoria accommodation. This provides a framework for further dissection of the pathogen-triggered reprogramming of host subcellular changes.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">22233428</PMID><DateCompleted><Year>2012</Year><Month>08</Month><Day>08</Day></DateCompleted><DateRevised><Year>2018</Year><Month>11</Month><Day>13</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1462-5822</ISSN><JournalIssue CitedMedium="Internet"><Volume>14</Volume><Issue>5</Issue><PubDate><Year>2012</Year><Month>May</Month></PubDate></JournalIssue><Title>Cellular microbiology</Title><ISOAbbreviation>Cell Microbiol</ISOAbbreviation></Journal><ArticleTitle>Patterns of plant subcellular responses to successful oomycete infections reveal differences in host cell reprogramming and endocytic trafficking.</ArticleTitle><Pagination><MedlinePgn>682-97</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1111/j.1462-5822.2012.01751.x</ELocationID><Abstract><AbstractText>Adapted filamentous pathogens such as the oomycetes Hyaloperonospora arabidopsidis (Hpa) and Phytophthora infestans (Pi) project specialized hyphae, the haustoria, inside living host cells for the suppression of host defence and acquisition of nutrients. Accommodation of haustoria requires reorganization of the host cell and the biogenesis of a novel host cell membrane, the extrahaustorial membrane (EHM), which envelops the haustorium separating the host cell from the pathogen. Here, we applied live-cell imaging of fluorescent-tagged proteins labelling a variety of membrane compartments and investigated the subcellular changes associated with accommodating oomycete haustoria in Arabidopsis and N. benthamiana. Plasma membrane-resident proteins differentially localized to the EHM. Likewise, secretory vesicles and endosomal compartments surrounded Hpa and Pi haustoria revealing differences between these two oomycetes, and suggesting a role for vesicle trafficking pathways for the pathogen-controlled biogenesis of the EHM. The latter is supported by enhanced susceptibility of mutants in endosome-mediated trafficking regulators. These observations point at host subcellular defences and specialization of the EHM in a pathogen-specific manner. Defence-associated haustorial encasements, a double-layered membrane that grows around mature haustoria, were frequently observed in Hpa interactions. Intriguingly, all tested plant proteins accumulated at Hpa haustorial encasements suggesting the general recruitment of default vesicle trafficking pathways to defend pathogen access. Altogether, our results show common requirements of subcellular changes associated with oomycete biotrophy, and highlight differences between two oomycete pathogens in reprogramming host cell vesicle trafficking for haustoria accommodation. This provides a framework for further dissection of the pathogen-triggered reprogramming of host subcellular changes.</AbstractText><CopyrightInformation>© 2012 Blackwell Publishing Ltd.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Lu</LastName><ForeName>Yi-Ju</ForeName><Initials>YJ</Initials><AffiliationInfo><Affiliation>Max-Planck-Institute for Plant Breeding Research, Carl-von-Linné-Weg 10, 50829 Cologne, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Schornack</LastName><ForeName>Sebastian</ForeName><Initials>S</Initials></Author><Author ValidYN="Y"><LastName>Spallek</LastName><ForeName>Thomas</ForeName><Initials>T</Initials></Author><Author ValidYN="Y"><LastName>Geldner</LastName><ForeName>Niko</ForeName><Initials>N</Initials></Author><Author ValidYN="Y"><LastName>Chory</LastName><ForeName>Joanne</ForeName><Initials>J</Initials></Author><Author ValidYN="Y"><LastName>Schellmann</LastName><ForeName>Swen</ForeName><Initials>S</Initials></Author><Author ValidYN="Y"><LastName>Schumacher</LastName><ForeName>Karin</ForeName><Initials>K</Initials></Author><Author ValidYN="Y"><LastName>Kamoun</LastName><ForeName>Sophien</ForeName><Initials>S</Initials></Author><Author ValidYN="Y"><LastName>Robatzek</LastName><ForeName>Silke</ForeName><Initials>S</Initials></Author></AuthorList><Language>eng</Language><GrantList CompleteYN="Y"><Grant><Agency>Howard Hughes Medical Institute</Agency><Country>United States</Country></Grant></GrantList><PublicationTypeList><PublicationType UI="D003160">Comparative Study</PublicationType><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2012</Year><Month>02</Month><Day>15</Day></ArticleDate></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>Cell Microbiol</MedlineTA><NlmUniqueID>100883691</NlmUniqueID><ISSNLinking>1462-5814</ISSNLinking></MedlineJournalInfo><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D017360" MajorTopicYN="N">Arabidopsis</DescriptorName><QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName><QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D022162" MajorTopicYN="N">Cytoplasmic Vesicles</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName><QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D054884" MajorTopicYN="Y">Host-Pathogen Interactions</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008856" MajorTopicYN="N">Microscopy, Fluorescence</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D009868" MajorTopicYN="N">Oomycetes</DescriptorName><QualifierName 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Joanne" uniqKey="Chory J" first="Joanne" last="Chory">Joanne Chory</name><name sortKey="Geldner, Niko" sort="Geldner, Niko" uniqKey="Geldner N" first="Niko" last="Geldner">Niko Geldner</name><name sortKey="Kamoun, Sophien" sort="Kamoun, Sophien" uniqKey="Kamoun S" first="Sophien" last="Kamoun">Sophien Kamoun</name><name sortKey="Robatzek, Silke" sort="Robatzek, Silke" uniqKey="Robatzek S" first="Silke" last="Robatzek">Silke Robatzek</name><name sortKey="Schellmann, Swen" sort="Schellmann, Swen" uniqKey="Schellmann S" first="Swen" last="Schellmann">Swen Schellmann</name><name sortKey="Schornack, Sebastian" sort="Schornack, Sebastian" uniqKey="Schornack S" first="Sebastian" last="Schornack">Sebastian Schornack</name><name sortKey="Schumacher, Karin" sort="Schumacher, Karin" uniqKey="Schumacher K" first="Karin" last="Schumacher">Karin Schumacher</name><name sortKey="Spallek, Thomas" sort="Spallek, Thomas" uniqKey="Spallek T" first="Thomas" last="Spallek">Thomas Spallek</name></noCountry><country name="Allemagne"><region name="Rhénanie-du-Nord-Westphalie"><name sortKey="Lu, Yi Ju" sort="Lu, Yi Ju" uniqKey="Lu Y" first="Yi-Ju" last="Lu">Yi-Ju Lu</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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