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dc.rights.licenseopenen_US
dc.contributor.authorCORRALES, Rosa
dc.contributor.authorVASELEK, Slavica
dc.contributor.authorNEISH, Rachel
dc.contributor.authorBERRY, Laurence
dc.contributor.authorBRUNET, Camille
dc.contributor.authorCROBU, Lucien
dc.contributor.authorKUK, Nada
dc.contributor.authorMATEOS-LANGERAK, Julio
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorROBINSON, Derrick R
dc.contributor.authorVOLF, Petr
dc.contributor.authorMOTTRAM, Jeremy
dc.contributor.authorSTERKERS, Yvon
dc.contributor.authorBASTIEN, Patrick
dc.date.accessioned2023-05-22T13:50:32Z
dc.date.available2023-05-22T13:50:32Z
dc.date.issued2021-06-18
dc.identifier.issn1553-7366en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/182233
dc.description.abstractEnLeishmania parasites possess a unique and complex cytoskeletal structure termed flagellum attachment zone (FAZ) connecting the base of the flagellum to one side of the flagellar pocket (FP), an invagination of the cell body membrane and the sole site for endocytosis and exocytosis. This structure is involved in FP architecture and cell morphogenesis, but its precise role and molecular composition remain enigmatic. Here, we characterized Leishmania FAZ7, the only known FAZ protein containing a kinesin motor domain, and part of a clade of trypanosomatid-specific kinesins with unknown functions. The two paralogs of FAZ7, FAZ7A and FAZ7B, display different localizations and functions. FAZ7A localizes at the basal body, while FAZ7B localizes at the distal part of the FP, where the FAZ structure is present in Leishmania . While null mutants of FAZ7A displayed normal growth rates, the deletion of FAZ7B impaired cell growth in both promastigotes and amastigotes of Leishmania . The kinesin activity is crucial for its function. Deletion of FAZ7B resulted in altered cell division, cell morphogenesis (including flagellum length), and FP structure and function. Furthermore, knocking out FAZ7B induced a mis-localization of two of the FAZ proteins, and disrupted the molecular organization of the FP collar, affecting the localization of its components. Loss of the kinesin FAZ7B has important consequences in the insect vector and mammalian host by reducing proliferation in the sand fly and pathogenicity in mice. Our findings reveal the pivotal role of the only FAZ kinesin as part of the factors important for a successful life cycle of Leishmania .
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.title.enThe kinesin of the flagellum attachment zone in Leishmania is required for cell morphogenesis, cell division and virulence in the mammalian host
dc.typeArticle de revueen_US
dc.identifier.doi10.1371/journal.ppat.1009666en_US
dc.subject.halSciences du Vivant [q-bio]/Microbiologie et Parasitologie/Parasitologieen_US
dc.subject.halSciences du Vivant [q-bio]/Biologie cellulaire/Organisation et fonctions cellulaires [q-bio.SC]en_US
bordeaux.journalPLoS Pathogensen_US
bordeaux.pagee1009666en_US
bordeaux.volume17en_US
bordeaux.hal.laboratoriesMFP (Laboratoire Microbiologie Fondamentale et Pathogénicité) - UMR 5234en_US
bordeaux.issue6en_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcehal
hal.identifierhal-03299396
hal.version1
hal.exportfalse
workflow.import.sourcehal
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=PLoS%20Pathogens&rft.date=2021-06-18&rft.volume=17&rft.issue=6&rft.spage=e1009666&rft.epage=e1009666&rft.eissn=1553-7366&rft.issn=1553-7366&rft.au=CORRALES,%20Rosa&VASELEK,%20Slavica&NEISH,%20Rachel&BERRY,%20Laurence&BRUNET,%20Camille&rft.genre=article


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