DIFFERENTIAL IDENTIFICATION OF ASCOGREGARINA SPECIES (APICOMPLEXA: LECUDINIDAE) IN AEDES AEGYPTI AND AEDES ALBOPICTUS (DIPTERA: CULICIDAE) BY POLYMERASE CHAIN REACTION

We report 2 polymerase chain reaction (PCR)-based methods for distinguishing morphologically similar gregarine species based on amplification of variable regions of the internal transcribed spacer region of ribosomal DNA. The gregarines we investigated were Ascogregarina barretti (Vavra), A. culicis (Ross), and A. taiwanensis (Lien and Levine), parasites of the mosquitoes Ochlerotatus triseriatus (Say), Aedes aegypti (Linnaeus), and Ae. albopictus (Skuse), respectively. These 3 important vector mosquitoes often utilize the same container habitats, where larval development and infection by the parasite occurs, leaving ample opportunity for cross-species gregarine infection. Because previous studies have shown that the parasites A. culicis and A. taiwanensis variably affect fitness in both normal and abnormal mosquito hosts, distinguishing parasite infection and species is important. The task is complicated by the fact that these 2 parasite species are virtually identical in morphology, whereas A. barretti is morphologically distinct. Of the 2 PCR-based assays reported here, the first provides a rapid, sensitive, and straight- forward means of general ascogregarine detection based on a single PCR amplification. The second method provides a means of differentiation between A. culicis and A. taiwanensis based on a species-specific PCR assay. Together, these assays allow whole mosquitoes to be tested for the presence of Ascogregarina species as well as identification of both A. culicis and A. taiwanensis singly or in dual infections. Ascogregarina (Apicomplexa: Lecudinidae) contains a group of protozoan parasites that naturally infect certain insects. In mosquitoes (Diptera: Culicidae), infections have only been de- scribed from some container-breeding species (Beier and Craig, 1985). Three such species, Aedes aegypti (Linnaeus), Ae. al- bopictus (Skuse), and Ochlerotatus triseriatus(Say), are known or potential vectors of a number of arboviruses (Calisher, 1994). Each of the 3 mosquito species can naturally harbor a specific gregarine parasite that allows the host mosquito to carry out life functions relatively unaffected by its presence. The parasite is transmitted to other mosquitoes in the aquatic environment when feeding larvae ingest oocysts released by defecating or dead adult mosquitoes. Gregarine trophozoites feed intracellu- larly in the midgut epithelium and increase in size during mos- quito larval development; gametogony and sporogony in the Malphigian tubules during the pupal and early adult stages re- sult in new oocysts that are released back into the larval envi