Objective To detect malaria in mosquitoes.
Methods A nested polymerase chain reaction (nested PCR) procedure which amp
lifies a 121 bp DNA of a SSUrRNA gene specific to Plasmodium vivax was used
.
Results In laboratory-infected mosquitoes, nested PCR could detect as few a
s 3 sporozoites or 1 infected mosquito mixed in a group of 99 normal ones.
Furthermore, no specific 121 bp band was seen with DNA templates from other
malaria parasites or negative mosquitoes.
Conclusion Sensitivity and specificity obtained indicated an advantage of t
he nested PCR over DNA probes or direct PCR for the detection of Plasmodium
vivax sporozoites in mosquitoes with low-grade parasitic infections.