PARAFROGS

Emerging Protist Parasites of Frogs: Global prevalence and host/parasite interaction

 Coordinatore THE UNIVERSITY OF EXETER 

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

contact info
Titolo: Dr.
Nome: Enda
Cognome: Clarke
Email: send email
Telefono: 441393000000
Fax: 441392000000

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 200˙371 €
 EC contributo 200˙371 €
 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-2011-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2012
 Periodo (anno-mese-giorno) 2012-09-01   -   2015-02-28

 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: Dr.
Nome: Enda
Cognome: Clarke
Email: send email
Telefono: 441393000000
Fax: 441392000000

UK (EXETER) coordinator 200˙371.80
2    NATURAL HISTORY MUSEUM

 Organization address address: CROMWELL ROAD
city: LONDON
postcode: SW7 5BD

contact info
Titolo: Mr.
Nome: Oliver
Cognome: Bacon
Email: send email
Telefono: +44 207 942 6690

UK (LONDON) participant 0.00

Mappa


 Word cloud

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

tadpole    global    group    infection    collection    infects    eukaryotic    animal    microscopy    protist    infectious    molecular    cells    frogs    mass    microbial   

 Obiettivo del progetto (Objective)

'The causes of global decline of amphibian population is still unclear, however it is apparent that this animal group is susceptible to opportunistic infections. Two important infectious agents have been identified: a fungus and a virus, both of which are responsible for mass mortalities. However, since 2003, new mass mortality events have been recorded through out the USA and have been attributed to infection by a protist of the Superphylum Alveolata. This parasite preferentially infects liver tissue leading to the presence of hundred of thousand small spherical cells. In parallel, environmental sequencing of freshwater environments targeting the smallest size of eukaryotic plankton has revealed that this group of protists is globally distributed and has a free-living stage. We have performed a pilot test on 28 tadpoles specimens from the collection of the Natural History Museum of London (UK) in order to confirm the association between the protist and frogs and found three positive cases in distantly related frog taxa. We therefore hypothesise that this protist group represents a global threat to frogs and has a complex lifecycle involving both infectious and freeliving phases and has acquired cellular phenotypes and molecular innovations associated with host infection. Using a combination of molecular pathology of global tadpole samples, microscopy with cell biological staining, and comparative transcriptomics this project will identify the geographic and taxonomic prevalence of this pathogen and how and by what molecular mechanism it infects tadpole cells. As such the project will underpin advanced training in: collection management, histology, immuno-microscopy, comparative genomics and microbial parasitology of animal hosts. This project will provide information important for understanding the diversity of microbial eukaryotic forms, evolution of parasitic mechanisms and understanding disease threats to frogs in order to assists conservation planning.'

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