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The inhibition of the apoptosis pathway by the Coxiella burnetii effector protein CaeA requires the EK repetition motif, but is independent of survivin

dc.contributor.authorBisle, Stephanie
dc.contributor.authorKlingenbeck, Leonie
dc.contributor.authorBorges, Vítor
dc.contributor.authorSobotta, Katharina
dc.contributor.authorSchulze-Luehrmann, Jan
dc.contributor.authorMenge, Christian
dc.contributor.authorHeydel, Carsten
dc.contributor.authorGomes, João Paulo
dc.contributor.authorLührmann, Anja
dc.date.accessioned2016-02-19T13:24:49Z
dc.date.available2017-01-01T01:30:09Z
dc.date.issued2016-01-13
dc.description.abstractCoxiella burnetii is an obligate intracellular bacterium that causes Query (Q) fever, a zoonotic disease. It requires a functional type IV secretion system (T4SS) which translocate bacterial effector proteins into the host cell cytoplasm and thereby facilitates bacterial replication. To date, more than 130 effector proteins have been identified, but their functions remain largely unknown. Recently, we demonstrated that one of these proteins, CaeA (CBU1524) localized to the host cell nucleus and inhibited intrinsic apoptosis of HEK293 or CHO cells. In the present study we addressed the question whether CaeA also affects the extrinsic apoptosis pathway. Ectopic expression of CaeA reduced extrinsic apoptosis and prevented the cleavage of the executioner caspase 7, but did not impair the activation of initiator caspase 9. CaeA expression resulted in an up-regulation of survivin (an inhibitor of activated caspases), which, however, was not causal for the anti-apoptotic effect of CaeA. Comparing the sequence of CaeA from 25 different C. burnetii isolates we identified an EK (glutamic acid/ lysine) repetition motif as a site of high genetic variability. The EK motif of CaeA was essential for the anti-apoptotic activity of CaeA. From these data, we conclude that the C. burnetii effector protein CaeA interferes with the intrinsic and extrinsic apoptosis pathway. The process requires the EK repetition motif of CaeA, but is independent of the upregulated expression of survivin.pt_PT
dc.description.sponsorshipThis work was supported by the Deutsche Forschungsgemeinschaft (SFB796 project B8) to AL and by the ERA-NET PathoGenoMics 3rd call to AL and JPG.pt_PT
dc.identifier.citationVirulence. 2016 May 18;7(4):400-12. doi:10.1080/21505594.2016.1139280. Epub 2016 Jan 13pt_PT
dc.identifier.doi10.1080/21505594.2016.1139280pt_PT
dc.identifier.issn2150-5594
dc.identifier.urihttp://hdl.handle.net/10400.18/3440
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherTaylor & Francispt_PT
dc.relation.publisherversionhttp://www.tandfonline.com/doi/abs/10.1080/21505594.2016.1139280?journalCode=kvir20pt_PT
dc.subjectCoxiella burnetiipt_PT
dc.subjectApoptosispt_PT
dc.subjectEffectorpt_PT
dc.subjectCaeApt_PT
dc.subjectBacterial Pathogenesispt_PT
dc.subjectSurvivingpt_PT
dc.subjectType IV Secretion Systempt_PT
dc.subjectInfecções Sistémicas e Zoonosespt_PT
dc.titleThe inhibition of the apoptosis pathway by the Coxiella burnetii effector protein CaeA requires the EK repetition motif, but is independent of survivinpt_PT
dc.typejournal article
dcterms.descriptionFree PMC Article: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4871633/
dspace.entity.typePublication
oaire.citation.endPage13pt_PT
oaire.citation.startPage1pt_PT
oaire.citation.titleVirulencept_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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