EIDPOP

Emerging infectious disease and population genetic structure

 Coordinatore THE UNIVERSITY OF EXETER 

 Organization address address: Northcote House, The Queen's Drive
city: EXETER
postcode: EX4 4QJ

contact info
Titolo: Ms.
Nome: Samantha
Cognome: Irish
Email: send email
Telefono: +44 1392 722375

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 231˙283 €
 EC contributo 231˙283 €
 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-2012-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2013
 Periodo (anno-mese-giorno) 2013-06-01   -   2015-05-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    THE UNIVERSITY OF EXETER

 Organization address address: Northcote House, The Queen's Drive
city: EXETER
postcode: EX4 4QJ

contact info
Titolo: Ms.
Nome: Samantha
Cognome: Irish
Email: send email
Telefono: +44 1392 722375

UK (EXETER) coordinator 231˙283.20

Mappa


 Word cloud

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

diseases    ranavirus    choice    impact    population    disease    amphibian    mate    declines    genes    genotype    offspring    populations    host    yet   

 Obiettivo del progetto (Objective)

'Emerging infectious diseases are increasing worldwide, and have been implicated in population declines and species extinctions. We know that diseases can cause major changes to the genetic composition of host populations through selection and population declines, and in turn that such changes can influence the impact of disease on host populations. We also know that diseases can lead to changes in mate choice behaviour which can alter the population structure, again influencing the impact of disease - yet this has as yet received little attention. This proposal focuses on investigating the interactions between genes, behaviour, and disease, using a model system of Ranavirus (an EU notifiable disease known to be contributing to amphibian declines) in common frogs (Rana temporaria) in the UK. Transcriptomics will be used to gain an understanding of which genes are involved in the host response in the wild to Ranavirus, and controlled laboratory experiments will be used to determine whether these genes are also involved in offspring survivorship. Sequencing of candidate genes in individuals will be used to examine how genotype influences parental mate choice, and the resulting fitness consequences of mate choice on the offspring will be determined. Furthermore, this proposal provides the foundations for a long-term study on how host genotype changes throughout the progression of an epidemic. As such, this proposal addresses fundamental scientific questions relating to the impact of disease on populations, which is critical for our understanding of the wider evolutionary impacts of disease and so for improving our ability to manage such emerging diseases. In addition, this research will directly improve our knowledge of an important driver of global amphibian declines'

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