Objective
Bacterial pathogens encountering host cells employ several attachment factors, which promote direct contact and trigger distinct signalling pathways in the host. The stimulation of particular signalling pathways subverts the eucaryotic cell and enables sur vival and persistence of bacteria within the host. Identification and characterisation of communicative tools between the bacteria and the host cells should lead to a better understanding of the infectious process and the development of new anti-infectious treatment. Pseudomonas aeruginosa is a Gram-negative bacterium causing nosocomial infections, wound infections, and lethal infections in Cystic Fibrosis patients. In the context of this proposal we aim at characterising the function of proteins encoded wi thin the P. aeruginosa cupB cluster, particularly that of the putative adhesins cupB6 and cupB5. The approach will employ cupB promoter studies to identify signals stimulating adhesion to eucaryotic cells. Expression levels of host cellular components upon infection with the wild type or cupB mutant strains will be analysed by high density DNA arrays. Cell lines with the Cystic fibrosis (CF) phenotype and Non CF cell lines will be used. Such an approach could be extended to other adhesins specific for epith elial cell - binding. The results will provide a specific profiling of gene expression and signalling pathways in response to the presence of particular adhesion factors in different P. aeruginosa strains.
Fields of science (EuroSciVoc)
CORDIS classifies projects with EuroSciVoc, a multilingual taxonomy of fields of science, through a semi-automatic process based on NLP techniques. See: The European Science Vocabulary.
CORDIS classifies projects with EuroSciVoc, a multilingual taxonomy of fields of science, through a semi-automatic process based on NLP techniques. See: The European Science Vocabulary.
- natural sciences biological sciences microbiology bacteriology
- natural sciences biological sciences genetics DNA
- natural sciences biological sciences biochemistry biomolecules proteins
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Keywords
Project’s keywords as indicated by the project coordinator. Not to be confused with the EuroSciVoc taxonomy (Fields of science)
Project’s keywords as indicated by the project coordinator. Not to be confused with the EuroSciVoc taxonomy (Fields of science)
Programme(s)
Multi-annual funding programmes that define the EU’s priorities for research and innovation.
Multi-annual funding programmes that define the EU’s priorities for research and innovation.
Topic(s)
Calls for proposals are divided into topics. A topic defines a specific subject or area for which applicants can submit proposals. The description of a topic comprises its specific scope and the expected impact of the funded project.
Calls for proposals are divided into topics. A topic defines a specific subject or area for which applicants can submit proposals. The description of a topic comprises its specific scope and the expected impact of the funded project.
Call for proposal
Procedure for inviting applicants to submit project proposals, with the aim of receiving EU funding.
Procedure for inviting applicants to submit project proposals, with the aim of receiving EU funding.
FP6-2002-MOBILITY-5
See other projects for this call
Funding Scheme
Funding scheme (or “Type of Action”) inside a programme with common features. It specifies: the scope of what is funded; the reimbursement rate; specific evaluation criteria to qualify for funding; and the use of simplified forms of costs like lump sums.
Funding scheme (or “Type of Action”) inside a programme with common features. It specifies: the scope of what is funded; the reimbursement rate; specific evaluation criteria to qualify for funding; and the use of simplified forms of costs like lump sums.
Coordinator
PARIS
France
The total costs incurred by this organisation to participate in the project, including direct and indirect costs. This amount is a subset of the overall project budget.