RICKOCHET

Origin and evolution of host-association and pathogenicity in the Rickettsiales

 Coordinatore UPPSALA UNIVERSITET 

 Organization address address: SANKT OLOFSGATAN 10 B
city: UPPSALA
postcode: 751 05

contact info
Titolo: Ms.
Nome: Karin
Cognome: Olsson
Email: send email
Telefono: +46 18 4714961
Fax: +46 18 4716404

 Nazionalità Coordinatore Sweden [SE]
 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-2010-RG
 Funding Scheme MC-ERG
 Anno di inizio 2011
 Periodo (anno-mese-giorno) 2011-01-01   -   2013-12-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UPPSALA UNIVERSITET

 Organization address address: SANKT OLOFSGATAN 10 B
city: UPPSALA
postcode: 751 05

contact info
Titolo: Ms.
Nome: Karin
Cognome: Olsson
Email: send email
Telefono: +46 18 4714961
Fax: +46 18 4716404

SE (UPPSALA) coordinator 45˙000.00

Mappa


 Word cloud

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

pathogen    amoeba    caused    human    bacterial    living    pathogens    evolutionary    free    isolated    pathogenic    species    transition    rickettsiales    bacterium   

 Obiettivo del progetto (Objective)

'Despite that many human diseases are caused by bacterial pathogens, not much is known about how these pathogenic bacteria emerge. The alpha-proteobacterial order Rickettsiales comprises intracellular bacterial pathogens, including the causative agent of epidemic typhus, Rickettsia prowazekii. The overall aim of the current project is to gain insight in the evolutionary transition from free-living bacterium to (human) pathogen, using the Rickettsiales as a model system. To do so, deeply branching Rickettsiales lineages will be isolated from environmental samples and from amoeba that contain Ricketsiales-like endosymbionts. Free-living Rickettsiales species will be isolated from the Sargasso Sea using a single-cell genomics approach. In parallel, protist-associated Rickettsiales species will be isolated from amoeba. Subsequently, an attempt will be made to determine the complete genome sequence of the obtained free-living and ciliate-associated Rickettsiales species. By comparing the obtained genomic data with that of their pathogenic relatives, principle differences will be revealed that should give insight in the evolutionary transition from free-living bacterium to human pathogen. The proposed study aims at enumerating a number of pathogenicity genes that could represent excellent targets for vaccine development for treatment of infections caused by pathogenic Rickettsiales species.'

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