PROTEIN-BIOFILM

Characterization of protein-dependent biofilms by Staphylococcus aureus

 Coordinatore AGENCIA ESTATAL CONSEJO SUPERIOR DE INVESTIGACIONES CIENTIFICAS 

 Organization address address: CALLE SERRANO 117
city: MADRID
postcode: 28006

contact info
Titolo: Prof.
Nome: Iñigo
Cognome: Lasa
Email: send email
Telefono: 0034 948168007
Fax: 0034 948232191

 Nazionalità Coordinatore Spain [ES]
 Totale costo 45˙000 €
 EC contributo 45˙000 €
 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-2007-2-2-ERG
 Funding Scheme MC-ERG
 Anno di inizio 2007
 Periodo (anno-mese-giorno) 2007-09-03   -   2010-09-02

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    AGENCIA ESTATAL CONSEJO SUPERIOR DE INVESTIGACIONES CIENTIFICAS

 Organization address address: CALLE SERRANO 117
city: MADRID
postcode: 28006

contact info
Titolo: Prof.
Nome: Iñigo
Cognome: Lasa
Email: send email
Telefono: 0034 948168007
Fax: 0034 948232191

ES (MADRID) coordinator 0.00

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staphylococcal    biofilm    infections    proteins    aureus   

 Obiettivo del progetto (Objective)

'Nosocomial staphylococcal foreign-body infections related to biofilm formation are important problem in modern medicine and S. aureus has become one of the most important bacteria responsible for these chronic infections. The formation of adherent, multilayered bacterial biofilms is the most important factor in the pathogenesis of these infections, which regularly fail to respond to appropriate antimicrobial therapy. Given the impressive array of surface proteins expressed by S. aureus, it seems reasonable that some of them might be involved in biofilm development either in cooperation or independently of PIA/PNAG. Increasing number of evidences suggest the existence of protein dependent biofilm development on clinical isolates of S. aureus. The general objectives of my research proposal are to identify and characterize proteins involved in biofilm formation. The identification of novel biofilm therapeutic and preventive targets would aid in the development of new and more effective treatments for combating staphylococcal proteinaceous-building biofilm associated infections.'

Introduzione (Teaser)

European research is tackling the source of most outbreaks of hospital infections, Staphylococcus aureus (S. aureus). Attacking the bacterium's anti-microbial defence, the biofilm, the microbe should be easier to control.

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