%0 Journal Article
%9 ACL : Articles dans des revues avec comité de lecture répertoriées par l'AERES
%A Morlais, Isabelle
%A Grébaut, Pascal
%A Bodo, J.M.
%A Djoba, S.
%A Cuny, Gérard
%A Herder, Stéphane
%T Detection and identification of trypanosomes by polymerase chain reaction in wild tsetse flies in Cameroon
%D 1998
%L fdi:010078593
%G ENG
%J Acat Tropica
%@ 0001-706X
%K TRYPANOSOMIASE HUMAINE ; MALADIE DU SOMMEIL ; VECTEUR ; ISOLEMENT D'AGENT PATHOGENE ; PREVALENCE
%K PCR.REACTION DE POLYMERISATION EN CHAINE
%K CAMEROUN
%M ISI:000075145200011
%N 1
%P 109-117
%R 10.1016/S0001-706X(98)00014-X
%U https://www.documentation.ird.fr/hor/fdi:010078593
%> https://horizon.documentation.ird.fr/exl-doc/pleins_textes/divers20-07/010078593.pdf
%V 70
%W Horizon (IRD)
%X The prevalence of various species and subgroups of trypanosomes in infected flies from three sleeping sickness foci in Cameroon was determined by the use of polymerase chain reaction (PCR). The predominant tsetse species found were Glossina palpalis palpalis. Microscopical examination of 943 non-teneral tsetse flies revealed an average infection rate of 10.4%. A total of 90 flies were analyzed for trypanosome identification with primer sets specific for Trypanosoma (Trypanozoon) brucei s.l., T. (Duttonella) vivax, T. (Nannomonas) simiae, and forest type T. (Nannamonas) congolense. PCR succeeded in identifying 52 of the 90 infected flies. Other primers were also tested on microscope positive/PCR-negative infections, and trypanosome subgroups were detected (Kilifi type and savannah type T. congolense). PCR amplification allowed identification of immature infections and revealed mixed-infections. The PCR technique failed to identify 42.2% (38/90) of the parasitologically positive flies and the reasons for this failure are discussed.
%$ 052GLOTRY ; 020BIOL