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© Valérie Choumet
Mosquitoes were orally infected with the chikungunya virus. Midguts were dissected at day 5 post-infection, fixed and permeabilised. Virus is shown in red (anti-E2 protein, cyanine 3), the actin network in green (phalloidin 548) and nuclei in blue (DAPI).
Publication : PloS one

Wild Anopheles funestus mosquito genotypes are permissive for infection with the rodent malaria parasite, Plasmodium berghei

Scientific Fields
Diseases
Organisms
Applications
Technique

Published in PloS one - 08 Apr 2013

Xu J, Hillyer JF, Coulibaly B, Sacko M, Dao A, Niaré O, Riehle MM, Traoré SF, Vernick KD

Link to Pubmed [PMID] – 23593423

PLoS ONE 2013;8(4):e61181

Malaria parasites undergo complex developmental transitions within the mosquito vector. A commonly used laboratory model for studies of mosquito-malaria interaction is the rodent parasite, P. berghei. Anopheles funestus is a major malaria vector in sub-Saharan Africa but has received less attention than the sympatric species, Anopheles gambiae. The imminent completion of the A. funestus genome sequence will provide currently lacking molecular tools to describe malaria parasite interactions in this mosquito, but previous reports suggested that A. funestus is not permissive for P. berghei development.

http://www.ncbi.nlm.nih.gov/pubmed/23593423