Polymerase chain reaction characterization of trypanosomes in Glossina morsitans submorsitans and G. tachinoides collected on the game ranch of Nazinga, Burkina Faso.

The polymerase chain reaction was used to characterize the trypanosomes infecting Glossina morsitans submorsitans and G. tachinoides in the game ranch of Nazinga, Burkina Faso, situated near an agropastoral zone. Dissection of 435 tsetse flies, and PCR analysis of 166 infected flies were conducted to assess the epidemiological situation. Trypanosomes of the Nannomonas subgenus were the most abundant in the two tsetse species (80.4% and 73.7% of identified infections in G. m. submorsitans and G. tachinoides respectively). T. vivax and T. brucei infection rates were comparable between the two tsetse species. Mature infection pattern identified by PCR differed from overall infections, mainly because T. simiae infections did not mature, whereas T. vivax represented the predominant taxon. Parasitological and PCR results showed some discrepancies; possibly some typical Duttonella strains could not be recognized by the sets of primers used. The technologies used in this work helped to determine the high trypanosomosis risk in this area.

Microsatellite markers for genetic population studies in Glossina palpalis gambiensis (Diptera: Glossinidae).

Little is known about intraspecific variability in tsetse flies and its consequences for vectorial capacity. Microsatellite markers have been developed for Glossina palpalis gambiensis. Three loci have been identified and showed size polymorphisms for insectarium samples. G. palpalis gambiensis from Burkina Faso were also subjected to PCR to investigate then genetic variability. Amplifications were observed in different species belonging to the palpalis group. These molecular markers will be useful to estimate gene flow within G. palpalis gambiensis populations and analysis could be extended to related species.

[Myiases of economic importance]. / Les myiases d'importance économique.

A simplified list of the principal Diptera capable of causing myiasis is followed by a brief presentation of the biology, lesions inflicted, and methods of treatment and control of the myiases of economic importance. Cochliomyiasis caused by Cochliomyia hominivorax is of greatest interest, in view of the damage and losses caused by this disease. A brief account of the outbreak of infestation in Libya illustrates the danger of this parasite. Other important traumatic myiases are described: that due to Chrysomya bezziana, which causes an African myiasis similar to cochliomyiasis, and those due to Lucilia cuprina and related species. Hypodermyiasis (warble fly infestation) and oestrosis (nasal bot fly infestation in sheep) still cause major economic losses in domestic animals, justifying their inclusion in control campaigns. The same applies to stomach bot flies of the family Gasterophilidae. The account of each myiasis includes notes on parasiticides which have been found to be effective. Given the rapidity with which a parasite can now be transported from one continent to another, it is important for Veterinary Services to be well-informed and vigilant.

[New data on the control of African animal trypanosomiasis]. / Données nouvelles dans la lutte contre la trypanosomose animale africaine.

The glossina control turns towards cheaper, ecological, easier techniques: trapping, which the efficacy might be increased by odour attractants; synthetic pyrethrinoids (impregnated targets; dipping or application of "Pour-on" formulations on skin of cattle). Only one new trypanocide was set up during the last 25 years: Melarsamine, arsenical derivative, effective in camels, cattle, horses infected by Trypanozoon (3.5 mg/kg b. w. by IM or SC routes). The trypanotolerant cattle is characterized by a better control of parasitemia and anaemia, dominant gene A of hemoglobin and gene F of albumin, a better immune response and a smaller drop of hematocrit. Monoclonal antibodies are used to detect, in micro-ELISA plates, circulating somatic trypanosomal antigens of T. brucei (s. l.) and T. evansi (common antigens), T. congolense and T. vivax (species specific antigens).