Field responses of Glossina austeni to sticky panels on Unguja Island, Zanzibar

Abstract .Two designs of cross-shaped sticky panels (XT and XLP) were compared with the royal blue–white legpanel (LPBuWh) in the Jozani forest on Unguja Island as trapping devices for male Glossina austeni . Single coloured royal blue (XTBu) and bi-coloured royal blue–white XT (XTBuWh) caught more than twice as many male G. austeni as the LPBuWh, whereas single coloured black XT trapped significantly fewer flies (10%) than the control LPBuWh. XT's in various horizontal and diagonal blue–white configurations likewise trapped more flies than the LPBuWh, except a horizontally striped blue–white XT which trapped fivefold fewer flies than the LPBuWh. Cross-shaped LP in the blue–white (XLPBuWh) and black–white (XLPBlWh) combination scored significantly better than the control LPBuWh. Similar fly numbers were trapped with XTBuWh and XLPBuWh. Long-term trapping data indicated that the XTBu, XTBuWh and XLPBuWh were three- to fourfold more effective in trapping female flies than the LPBuWh.
The landing bias on bi-coloured panels was low in the blue–white but more pronounced in the blue–black and white–black combinations and was affected by the type of sticky panel used. A high proportion (49%) of the flies alighted on the bottom corners of the XTBu panel, but landing positions were more scattered if white was added.
Increasing the width of the XTBu from 70 to 120 cm improved the catch by a factor of two as compared with standard sized XTBu. The effect of doubling the height of the XT on total fly catch was negligible.
At present, it is the XTBu which can be recommended as the best trapping device for male and female G. austeni.     

Flight behaviour of tsetse flies in host odour plumes: the initial response to leaving or entering odour

ABSTRACT. Free-flying, wild male and female Glossina pallidipes Aust. and G. m. morsitans Westw. were video-recorded in the field in Zimbabwe as they entered or left the side of a host-odour plume in cross-wind flight, or as they overshot a source of host odour in upwind flight (camera 2.5 m up looking down at a 3 times 2.5 m field of view at ground level). 80% of cross-wind odour leavers turned sharply ( turns 95^o), but without regard to wind direction (overshooters behaved essentially the same except that nearly 100% turned). Many fewer flies entering a plume cross wind turned ( c . 60%), and when they did they made much smaller turns ( 58^o); these turns were, however, significantly biassed upwind ( c . 70%). All three classes of fly had similar groundspeeds ( 5.5–6.5 m s^_1) and angular velocities ( 350–400^o s^-1). Clear evidence was obtained of in-flight sensitivity to wind direction: significantly more flies entering odour turned upwind than downwind, and odour losers turning upwind made significantly larger turns than average. The main basis for the different sizes of turn was the different durations of the turning flight, rather than changes in angular velocity or speed. No evidence was found of flies landing after losing contact with odour.     

Behaviour of tsetse flies (Glossina) in host odour plumes in the field

ABSTRACT. In Zimbabwe, studies were made of the responses of Glossina pallidipes Austen and G.morsitans morsitans Westwood to artificial host odour using an incomplete ring of electrocuting nets. In a plume of synthetic host odour tsetse flew generally upwind, with 50–60% flying within 35^o of due upwind. More than 80% of tsetse flew at < 50 cm above ground level. Upon losing contact with odour they executed a reverse turn within about 2 m, and upon regaining contact they turned upwind. There were no clear differences in the responses of G.m.morsitans and G.pallidipes. Using electrocuting nets lying horizontally on the ground it was found that tsetse landed in the vicinity of the odour source, the propensity to land being greater for G.pallidipes than for G.m, morsitans , greater for immature than mature flies, and greater for males than females.     

Use of fluorescent pigments for the automatic marking of tsetse flies in traps

A means of contaminating tsetse flies in the field with fluorescent pigment powders has been developed, using pigment in open-ended plastic chambers at the cage position on traps. Glossina pallidipes Austen and G.morsitans morsitans Westwood passed rapidly through the chambers, and on exit were contaminated with consistent doses of powder: about 90 micrograms/fly when powder was presented on the chamber roof and about 28 micrograms/fly when powder was presented on the chamber floor. The technique automatically marks tsetse flies with pigment, cheaply, simply and with the minimum imposition of stress and is expected to be particularly useful in ecological studies. Its potential for marking other biting flies is discussed.     

Genetic differentiation of some Glossina morsitans morsitans populations

To study the population structure of Glossina morsitans morsitans Westwood (Diptera: Glossinidae), polymerase chain reaction (PCR) and singlestrand conformational polymorphism (SSCP) methods were used to estimate mitochondrial DNA diversity at four loci in six natural populations from Zambia, Zimbabwe and Mozambique, and in two laboratory cultures. The Zambian and Zimbabwean samples were from a single fly belt. Four alleles were recorded at 12S and 16S1, and five alleles at 16S2 and COI. Nucleotide sequencing confirmed their singularities. Chi-square contingency tests showed that allele frequencies differed significantly among populations. Mean allele diversities in populations averaged over loci varied from 0.14 to 0.61. Little loss in haplotype diversity was detected in the laboratory cultures thereby indicating little inbreeding. Wright's fixation index F(ST) in the natural populations was 0.088+/-0.016, the correlation of haplotypes within populations relative to correlations in the total. A function of its inverse allows an estimate of the mean equivalent number of females exchanged per population per generation, 5.2. No correlation was detected between pairwise genetic distance measures and geographical distances. Drift explains the high degree of differentiation.     

Relationships between host blood factors and proteases in Glossina morsitans subspecies infected with Trypanosoma congolense

Abstract. Host blood effects on Trypanosoma congolense establishment in Glossina morsitans morsitans and Glossina morsitans centralis were investigated using goat, rabbit, cow and rhinoceros blood. Meals containing goat erythrocytes facilitated infection in G. m. morsitans , whereas meals containing goat plasma facilitated infection in G. m. centralis. Goat blood effects were not observed in the presence of complementary rabbit blood components. N-acetyl-glucosamine (a midguMectin inhibitor) increased infection rates in some, but not all, blood manipulations. Cholesterol increased infection rates in G. m. centralis only. Both compounds together added to cow blood produced superinfection in G. m. centralis , but not in G. m. morsitans. Midgut protease levels did not differ 6 days post-infection in flies maintaining infections versus flies clearing infections. Protease levels were weakly correlated with patterns of infection, but only in G. m. morsitans. These results suggest that physiological mechanisms responsible for variation in infection rates are only superficially similar in these closely-related tsetse.     

Lectin signalling of maturation of T.congolense infections in tsetse

The process of maturation of Trypanosoma congolense Broden in tsetse has been shown to be initiated by lectin secreted in the fly midgut. In the present study the duration of lectin signal required to induce maturation was determined by the sequential addition or removal of a specific lectin inhibitor (D+glucosamine) to the diet of infected male Glossina morsitans Westwood. An established midgut infection of T.congolense was found to require, at most, 72 h exposure to midgut lectin to begin the process of maturation. Longer exposure to midgut lectin increased the frequency of maturation, suggesting clonal variation in response to lectin stimulation occurs within trypanosome stocks. It is suggested that this variation corresponds to differences in lectin binding sites on the trypanosome surface. Midgut trypanosomes retained their ability to mature throughout their life in the fly; when lectin activity in the midgut was inhibited, the trypanosomes remained as procyclic forms but when this inhibition was removed maturation was able to proceed. This indicates that the process of maturation is dependent upon a signal from the fly and is not predetermined by the trypanosomes undergoing a fixed number of division cycles. The possible role of lectins in the maturation of trypanosomes in vitro is discussed.     

Comment on Barclay and Vreysen: Published dynamic population model for tsetse cannot fit field data

The structure, and assumed parameter values, of a recent dynamic population model for tsetse (Diptera: Glossinidae) render it unable to fit published data on tsetse control programs using odor-baited targets, insecticide-treated cattle and the sterile insect technique (SIT). The underlying problem is a mismatch between the small size of the mapped cells (1 ha) and the long time-step, which allows flies to move only once every 5 days, and then only to an adjacent cell. Assumed rates of tsetse dispersal and killing by odor-baited targets are consequently at least an order of magnitude lower than observed in the field. Suggestions that Glossina pallidipes could be eradicated more rapidly with SIT, than using hundreds of targets per km², is contradicted both by the field data and by three other independent modeling studies.     

Conclusions from a dynamic population model for tsetse: response to comments

The critique by Hargrove et al. (Popul Ecol, 2011) of our recently published paper on a tsetse population model (Barclay and Vreysen in Popul Ecol 53:89–110, 2011) has made some good points but has also misinterpreted the intent of some of our results as we presented them. Hargrove et al. rightly say that there is a mismatch between the size of the unit cells in the model (1 ha) and the iteration rate of the model (every 5 days), yielding too low a dispersal rate to simulate reality. However, they have misconstrued several of our results that we presented as examples to imply that those results were a necessary condition for control of tsetse, especially using traps and targets.