FLY FUNGAL INTERPLAY

Dissecting innate immunity to airborne opportunistic fungi through a genome-wide screen in Drosophila

 Coordinatore FOUNDATION FOR RESEARCH AND TECHNOLOGY HELLAS 

 Organization address address: N PLASTIRA STR 100
city: HERAKLION
postcode: 70013

contact info
Titolo: Prof.
Nome: Dimitrios
Cognome: Boumpas
Email: send email
Telefono: 302810000000
Fax: 302810000000

 Nazionalità Coordinatore Greece [EL]
 Totale costo 100˙000 €
 EC contributo 100˙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-2010-RG
 Funding Scheme MC-IRG
 Anno di inizio 2010
 Periodo (anno-mese-giorno) 2010-10-01   -   2014-09-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    FOUNDATION FOR RESEARCH AND TECHNOLOGY HELLAS

 Organization address address: N PLASTIRA STR 100
city: HERAKLION
postcode: 70013

contact info
Titolo: Prof.
Nome: Dimitrios
Cognome: Boumpas
Email: send email
Telefono: 302810000000
Fax: 302810000000

EL (HERAKLION) coordinator 100˙000.00

Mappa


 Word cloud

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

zygomycetes    therapeutic    causes    defense    mechanisms    strategies    opportunistic    virulence    aspergillus    invasive    antifungal    genetics    expand    airborne    flies    drosophila    fungal    infections    model    genes    immune    molecular    host    immunity    humans    fungi   

 Obiettivo del progetto (Objective)

'In recent years, airborne filamentous fungi have become major causes of life-threatening infections in an expanding population of severely immunocompromised individuals. Aspergillus remains the most common fungal pathogen in these patients, whereas Zygomycetes are emerging causes of fatal invasive fungal infections in many cancer institutions. Overall, the increasing frequency and spectrum of invasive fungal infections and the alarming rates of resistance to antifungal agents in fungi underscores the need to expand our knowledge on the immunopathogenesis of opportunistic fungal infections and develop novel therapeutic strategies. Importantly, the versatility of virulence mechanisms of fungi and the complexity of host defense mechanisms against fungi highlights the importance of understanding the molecular aspects of host-fungal interplay in robust experimental systems. Over the past decade, invertebrate mini-host models with well-characterized genetics and less complex immunity have been effectively used to explore several aspects of both fungal pathogenicity and antifungal host defense. These properties coupled with the robust genetics in Drosophila, make flies an ideal model to study the molecular aspects of host-fungal interaction. We have recently implemented Drosophila melanogaster as a model to study virulence mechanisms and the molecular aspects of host immune response to Zygomycetes. Surprisingly, we found that key aspects of the pathophysiology of zygomycosis in humans were appropriately modeled in fruit flies. In this proposal we expand on our previous work to: (a) Identify novel genes involved in Drosophila immunity against the most important airborne opportunistic fungi, Aspergillus and Zygomycetes, by performing a genome-wide screening strategy in Drosophila RNAi lines. (b) Confirm in humans the functional role of novel Drosophila host defense genes by silencing the relevant homologues in human phagocytic cells'

Introduzione (Teaser)

Fungi are emerging pathogens across a broad range of hosts including plants and humans. Delineating the mechanism of immune evasion is central to designing efficacious therapeutic strategies.

Altri progetti dello stesso programma (FP7-PEOPLE)

RNABIC (2009)

"Structure, assembly and metal ion binding properties of the catalytic core of a group II intron ribozyme."

Read More  

LATEST (2014)

Advanced LAnguage TEchnology Platform for TranSlaTors (LATEST)

Read More  

PCDMC (2012)

Control of programmed cell death by metacaspases in plants

Read More