Programmed cell death in host-symbiont associations, viewed through the Gene Ontology

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dc.contributor.authorChibucos, Marcus C.en
dc.contributor.authorCollmer, Candace W.en
dc.contributor.authorTorto-Alalibo, Trudyen
dc.contributor.authorGwinn-Giglio, Michelleen
dc.contributor.authorLindeberg, Magdalenen
dc.contributor.authorLi, Donghuien
dc.contributor.authorTyler, Brett M.en
dc.date.accessioned2012-08-24T11:46:54Zen
dc.date.available2012-08-24T11:46:54Zen
dc.date.issued2009-02-19en
dc.date.updated2012-08-24T11:46:54Zen
dc.description.abstractManipulation of programmed cell death (PCD) is central to many host microbe interactions. Both plant and animal cells use PCD as a powerful weapon against biotrophic pathogens, including viruses, which draw their nutrition from living tissue. Thus, diverse biotrophic pathogens have evolved many mechanisms to suppress programmed cell death, and mutualistic and commensal microbes may employ similar mechanisms. Necrotrophic pathogens derive their nutrition from dead tissue, and many produce toxins specifically to trigger programmed cell death in their hosts. Hemibiotrophic pathogens manipulate PCD in a most exquisite way, suppressing PCD during the biotrophic phase and stimulating it during the necrotrophic phase. This mini-review will summarize the mechanisms that have evolved in diverse microbes and hosts for controlling PCD and the Gene Ontology terms developed by the Plant-Associated Microbe Gene Ontology (PAMGO) Consortium for describing those mechanisms.en
dc.description.versionPublished versionen
dc.format.mimetypeapplication/pdfen
dc.identifier.citationBMC Microbiology. 2009 Feb 19;9(Suppl 1):S5en
dc.identifier.doihttps://doi.org/10.1186/1471-2180-9-S1-S5en
dc.identifier.urihttp://hdl.handle.net/10919/18871en
dc.language.isoenen
dc.rightsCreative Commons Attribution 4.0 Internationalen
dc.rights.holderMarcus C Chibucos et al.; licensee BioMed Central Ltd.en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.titleProgrammed cell death in host-symbiont associations, viewed through the Gene Ontologyen
dc.title.serialBMC Microbiologyen
dc.typeArticle - Refereeden
dc.type.dcmitypeTexten

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