PACI

Adaptation of Pseudomonas aeruginosa to the human host during chronic infections

 Coordinatore UNIVERSITE DE FRANCHE-COMTE 

 Organization address address: CLAUDE GOUDIMEL 1
city: BESANCON
postcode: 25030

contact info
Titolo: Ms.
Nome: Fournier
Cognome: Pauline
Email: send email
Telefono: 33381665814
Fax: 33381501103

 Nazionalità Coordinatore France [FR]
 Totale costo 334˙410 €
 EC contributo 334˙410 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-IOF-2008
 Funding Scheme MC-IOF
 Anno di inizio 2009
 Periodo (anno-mese-giorno) 2009-07-01   -   2012-06-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITE DE FRANCHE-COMTE

 Organization address address: CLAUDE GOUDIMEL 1
city: BESANCON
postcode: 25030

contact info
Titolo: Ms.
Nome: Fournier
Cognome: Pauline
Email: send email
Telefono: 33381665814
Fax: 33381501103

FR (BESANCON) coordinator 334˙410.20

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

pa    pseudomonas    resistance    yellow    clinical    aeruginosa    deleted    infections    metabolism    pigment    bppa    fibrosis    antibiotics    chronic    cystic    data    green    genes    university    mutants    virulence    emergence    cf    ci    respiratory    dpt    patients    bacterial    position    france   

 Obiettivo del progetto (Objective)

'Pseudomonas aeruginosa (PA) is an important bacterial pathogen causing a wide range of acute and chronic infections (CI). It usually expresses a yellow-green pigment. It is a major cause of respiratory CI in patients with underlying diseases such as cystic fibrosis (CF) leading to a progressive lung damage. Pathogenesis in CI implies a genetic diversification of PA, with emergence of atypical mutants such as brown pigment producing PA (bpPA). PACI study aims to explore the adaptation process of PA in CI, through the example of bpPA and to evaluate the clinical outcome of the emergence of such mutants. Ten clinical (CF and non-CF) or laboratory bpPA, and their isogenic yellow-green counterparts, have been identified. Preliminary data showed a large deletion in the same chromosomal region in bpPA when compared to their parental strains. Deleted genes are involved in chimiotactism, metabolism, resistance to antibiotics, synthesis of lipopolysaccharides, biofilm formation, anaerobic respiration and regulation. This strongly suggests that bpPA deeply modify their behaviour and virulence strategy in patients. The applicant will identify the deleted genes in bpPA using comparative genomic DNA hybridization microarrays and to assess variations in resistance to antibiotics and pyocins, growth under diverse conditions, metabolism, motility and virulence factor production. He will correlate the emergence of bpPA in CF-patients with disease progression using existing clinical data and bacterial collection. This proposal will permit the fellow, now in position of Associate Professor/Hospital Practitioner in the Dpt of Bacteriology, University of Franche-Comté (Besançon, France), to conduct the project during 2 years in the Dpt of Microbiology, University of Washington (Seattle, USA) before resuming his position in France. Characterization of these chronically-adapted clinical isolates will contribute to define new therapeutical options for the treatments of CI due to PA.'

Introduzione (Teaser)

The reason behind chronic respiratory infections was the study of a European effort. Scientists studied mutated bacterial forms of Pseudomonas aeruginosa (PA) and their link to cystic fibrosis patient infections.

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