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Fundamental Roles of the Golgi-Associated Toxoplasma Aspartyl Protease, ASP5, at the Host-Parasite Interface
PM. Hammoudi, D. Jacot, C. Mueller, M. Di Cristina, SK. Dogga, JB. Marq, J. Romano, N. Tosetti, J. Dubrot, Y. Emre, M. Lunghi, I. Coppens, M. Yamamoto, D. Sojka, P. Pino, D. Soldati-Favre,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Directory of Open Access Journals
od 2005
Free Medical Journals
od 2005
Public Library of Science (PLoS)
od 2005
PubMed Central
od 2005
Europe PubMed Central
od 2005
ProQuest Central
od 2005-09-01
Open Access Digital Library
od 2005-01-01
Open Access Digital Library
od 2005-01-01
Open Access Digital Library
od 2005-09-01
Medline Complete (EBSCOhost)
od 2005-09-01
Health & Medicine (ProQuest)
od 2005-09-01
- MeSH
- aspartátové proteasy metabolismus MeSH
- ELISA MeSH
- fluorescenční protilátková technika MeSH
- genový knockout MeSH
- Golgiho aparát enzymologie MeSH
- interakce hostitele a parazita fyziologie MeSH
- kultivované buňky MeSH
- kvantitativní polymerázová řetězová reakce MeSH
- lidé MeSH
- molekulární sekvence - údaje MeSH
- myši inbrední C57BL MeSH
- myši MeSH
- Toxoplasma enzymologie patogenita MeSH
- toxoplazmóza enzymologie MeSH
- transfekce MeSH
- transmisní elektronová mikroskopie MeSH
- transport proteinů MeSH
- western blotting MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Toxoplasma gondii possesses sets of dense granule proteins (GRAs) that either assemble at, or cross the parasitophorous vacuole membrane (PVM) and exhibit motifs resembling the HT/PEXEL previously identified in a repertoire of exported Plasmodium proteins. Within Plasmodium spp., cleavage of the HT/PEXEL motif by the endoplasmic reticulum-resident protease Plasmepsin V precedes trafficking to and export across the PVM of proteins involved in pathogenicity and host cell remodelling. Here, we have functionally characterized the T. gondii aspartyl protease 5 (ASP5), a Golgi-resident protease that is phylogenetically related to Plasmepsin V. We show that deletion of ASP5 causes a significant loss in parasite fitness in vitro and an altered virulence in vivo. Furthermore, we reveal that ASP5 is necessary for the cleavage of GRA16, GRA19 and GRA20 at the PEXEL-like motif. In the absence of ASP5, the intravacuolar nanotubular network disappears and several GRAs fail to localize to the PVM, while GRA16 and GRA24, both known to be targeted to the host cell nucleus, are retained within the vacuolar space. Additionally, hypermigration of dendritic cells and bradyzoite cyst wall formation are impaired, critically impacting on parasite dissemination and persistence. Overall, the absence of ASP5 dramatically compromises the parasite's ability to modulate host signalling pathways and immune responses.
Citace poskytuje Crossref.org
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