Abstract

BackgroundAnopheles gambiae females are the world's most successful vectors of human malaria. However, a fraction of these mosquitoes is refractory to Plasmodium development. L3-5, a laboratory selected refractory strain, encapsulates transforming ookinetes/early oocysts of a wide variety of Plasmodium species. Previous studies on these mosquitoes showed that one major (Pen1) and two minor (Pen2, Pen3) autosomal dominant quantitative trait loci (QTLs) control the melanotic encapsulation response against P. cynomolgi B, a simian malaria originating in Malaysia.ResultsWe have investigated the response of L3-5 to infection with P. cynomolgi Ceylon, a different but related parasite species, in crosses with the susceptible strain 4Arr. Refractoriness to this parasite is incompletely recessive. Infection and genotyping of F2 intercross females at genome-spanning microsatellite loci revealed that 3 autosomal QTLs control encapsulation of this species. Two loci map to the regions containing Pen2 and Pen3. The novel QTL maps to chromosome 3R, probably to polytene division 32 or 33. Thus the relative contribution of any QTL to oocyst encapsulation varies with the species of parasite. Further, different QTLs were most readily identified in different F2 families. This, like the F1 data, suggests that L3-5 is not genetically homogeneous and that somewhat different pathways may be used to achieve an encapsulation response.ConclusionWe have shown here that different QTLs are involved in responses against different Plasmodium parasites.

Highlights

  • Anopheles gambiae females are the world's most successful vectors of human malaria

  • In this study we have investigated the genetics of the encapsulation response against P. cynomolgi Ceylon in crosses between the extant refractory L3-5 and susceptible 4Arr strains using microsatellite markers spanning the genome and QTL analysis

  • Refractoriness to P. cynomolgi Ceylon is incompletely recessive Infection of parental line mosquitoes showed that L3-5 refractory strain mosquitoes encapsulated P. cynomolgi Ceylon, whereas 4Arr did not (Fig. 1A)

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Summary

Introduction

Anopheles gambiae females are the world's most successful vectors of human malaria. a fraction of these mosquitoes is refractory to Plasmodium development. L3-5, a laboratory selected refractory strain, encapsulates transforming ookinetes/early oocysts of a wide variety of Plasmodium species. Previous studies on these mosquitoes showed that one major (Pen1) and two minor (Pen, Pen3) autosomal dominant quantitative trait loci (QTLs) control the melanotic encapsulation response against P. cynomolgi B, a simian malaria originating in Malaysia. BMC Genetics 2003, 4 http://www.biomedcentral.com/1471-2156/4/16 encapsulation of malaria parasites was first observed within a year of the discovery that mosquitoes are the vectors of malaria [5]. Melanotic encapsulation of plasmodia has been observed in a wide variety of mosquito species. Depending on the mosquito and the parasite species, encapsulation is directed against different stages of development [6]

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