Mosquito Feeding Assays to Determine the Infectiousness of Naturally Infected Plasmodium falciparum Gametocyte Carriers
moustique
Adult
Male
571
Adolescent
[SDV]Life Sciences [q-bio]
Science
Plasmodium falciparum
malaria
gametocyte;malaria;skin infections
test cutané
Young Adult
03 medical and health sciences
0302 clinical medicine
Anopheles
sang
Animals
Humans
Malaria, Falciparum
Child
Q
R
Infant
plasma sanguin
Middle Aged
maladie parasitaire
infection
skin infections
Insect Vectors
3. Good health
[SDV] Life Sciences [q-bio]
paludisme
gametocyte
Child, Preschool
Medicine
Female
N4i 3: Poverty-related infectious diseases NCMLS 1: Infection and autoimmunity
Research Article
DOI:
10.1371/journal.pone.0042821
Publication Date:
2012-08-22T21:29:28Z
AUTHORS (25)
ABSTRACT
In the era of malaria elimination and eradication, drug-based and vaccine-based approaches to reduce malaria transmission are receiving greater attention. Such interventions require assays that reliably measure the transmission of Plasmodium from humans to Anopheles mosquitoes.WE COMPARED TWO COMMONLY USED MOSQUITO FEEDING ASSAY PROCEDURES: direct skin feeding assays and membrane feeding assays. Three conditions under which membrane feeding assays are performed were examined: assays with i) whole blood, ii) blood pellets resuspended with autologous plasma of the gametocyte carrier, and iii) blood pellets resuspended with heterologous control serum.930 transmission experiments from Cameroon, The Gambia, Mali and Senegal were included in the analyses. Direct skin feeding assays resulted in higher mosquito infection rates compared to membrane feeding assays (odds ratio 2.39, 95% confidence interval 1.94-2.95) with evident heterogeneity between studies. Mosquito infection rates in membrane feeding assays and direct skin feeding assays were strongly correlated (p<0.0001). Replacing the plasma of the gametocyte donor with malaria naïve control serum resulted in higher mosquito infection rates compared to own plasma (OR 1.92, 95% CI 1.68-2.19) while the infectiousness of gametocytes may be reduced during the replacement procedure (OR 0.60, 95% CI 0.52-0.70).Despite a higher efficiency of direct skin feeding assays, membrane feeding assays appear suitable tools to compare the infectiousness between individuals and to evaluate transmission-reducing interventions. Several aspects of membrane feeding procedures currently lack standardization; this variability makes comparisons between laboratories challenging and should be addressed to facilitate future testing of transmission-reducing interventions.
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