A white eye color mutant in the tsetse fly Glossina morsitans submotsitans Newstead (Diptera: Glossinidae).

A spontaneous mutation in Glossina morsitans submorsitans Newstead is described. The mutant, designated wht, has white compound eyes but the ocelli and testes have normal coloration. Mutants have lower than normal amounts of xanthommatin and pteridines in their heads. The lesion occurs late in the tryptophan to xanthommatin pathway, in the storage of xanthommatin in the compound eyes, or, most likely, in the transport of precursors into the compound eyes. The locus wht is on the X chromosome.     

Experiments on the elimination of symbionts from the tsetse fly,Glossina morsitans morsitans (Diptera: Glossinidae), by antibiotics and lysozyme

One sulfonamide and ten antibiotics were tested for symbiont elimination in Glossina morsitans morsitans. Only tetracycline, penicillin, and kanamycin could be used in concentrations which destroyed the symbionts and impeded host reproduction, but did not affect host longevity. The later the treatment with penicillin and kanamycin began, the smaller was the damage to symbionts from these two antibiotics. Small doses damaged the symbionts to an extent that flies could produce offspring, but these were free of symbionts. Lysozyme was used as an alternative to antibiotics. After both injection and oral administration of lysozyme the symbionts were damaged, and host reproduction ceased, although host longevity remained unaffected. It can be concluded from the results of these experiments that tsetse flies do not require their symbionts for survival but probably do need them for reproduction.     

Lipophorin from the tsetse fly, Glossina morsitans morsitans.

1. Lipophorin was isolated from the haemolymph of adult tsetse fly, Glossina morsitans morsitans, by ultracentrifugation in a potassium bromide density gradient. 2. The tsetse fly lipophorin (Mr congruent to 600,000) has a density of congruent to 1.11 g/ml and consists of two apoproteins, apolipophorin-I (apoLp-I, Mr congruent to 250,000) and apolipophorin-II (apoLp-II, Mr congruent to 80,000), both of which are glycosylated as shown by staining with periodate-Schiff reagent. The protein complex is composed of 49% protein and 51% lipids. 3. The finding of lipophorin in tsetse fly haemolymph suggests that, although these flies primarily utilize proline for their energy needs, there is an active transport mechanism for the supply of lipid requirements.     

Macrogeographic population structure of the tsetse fly, Glossina pallidipes (Diptera: Glossinidae)

Tsetse flies are confined to sub-Saharan Africa where they occupy discontinuous habitats. In anticipation of area-wide control programmes, estimates of gene flow among tsetse populations are necessary. Genetic diversities were partitioned at eight microsatellite loci and five mitochondrial loci in 21 Glossina pallidipes Austin populations. At microsatellite loci, Nei's unbiased gene diversity averaged over loci was 0.659 and the total number of alleles was 214, only four of which were shared among all populations. The mean number of alleles per locus was 26.8. Random mating was observed within but not among populations (fixation index FST=0.18) and 81% of the genetic variance was within populations. Thirty-nine mitochondrial variants were detected. Mitochondrial diversities in populations varied from 0 to 0.85 and averaged 0.42, and FST=0.51. High levels of genetic differentiation were characteristic, extending even to subpopulations separated by tens and hundreds of kilometres, and indicating low rates of gene flow.     

Characterization of microsatellite markers in the tsetse fly, Glossina pallidipes (Diptera: Glossinidae)

Glossina pallidipes is a vector of African trypanosomiasis. Here we characterize eight new polymorphic microsatellite loci in 288 G. pallidipes sampled from 12 Kenya populations. The number of alleles per locus ranged from four to 36 with a mean of 20.5 +/- 10.1. Expected single locus heterozygosities varied from 0.044 to 0.829. Heterozygosity averaged 0.616 +/- 0.246. No linkage disequilibrium was found. We also report results in eight other tsetse species estimated by using the primers developed in G. pallidipes. The primers worked best in G. swynnertoni and G. austeni and worst in G. m. morsitans and G. m. submorsitans.     

Persistent courtship reduces male and female longevity in captive tsetse flies Glossina morsitans morsitans Westwood (Diptera: Glossinidae)

Where males can increase their mating success by harassing femalesuntil they accept copulation, harassing tactics can be expectedto evolve to a point where they have costs to the longevityof both sexes. By experimentally manipulating the sex ratioin captive groups of tsetse flies Glossina morsitans morsitans,we demonstrated that the longevity of females declines wheresex ratios are biased toward males, while the longevity of malesdeclines where the sex ratio is biased toward females. Neitherirradiation of males nor prevention of copulation by blockingor damaging the external male genitalia increased the longevityof females caged with them, suggesting that female longevitywas reduced by the physical aspects of male harassment ratherthan by components of the ejaculate     

Mark-recapture and Moran curve estimates of the survival probabilities of an island population of tsetse flies Glossina morsitans morsitans (Diptera: Glossinidae)

A study on populations of Glossina morsitans morsitans Westwood on Antelope Island, Lake Kariba, Zimbabwe provided Jolly-Seber (J-S) mark-recapture estimates of adult survival and Moran curve estimates of the overall survival of all developmental stages. For females, Moran survival estimates derived using ox fly-round catches showed similar trends to, but were more variable than, those calculated from J-S population estimates. Regression of one set on the other removed only 26% of the variance. Undue emphasis should not be placed on small changes in Moran survival estimates based on sequences of catches. Catch data cannot provide Moran estimates of male survival probabilities and no comparison is thus possible with estimates from the J-S data. The J-S and the Moran approaches were combined to estimate survival probabilities of the immature stages of male and female tsetse. The overall survival per three-week period averaged 45% for males and 59% for females, comprising mature adult survivals of 27 and 46%, and pooled survivals of immature stages of 59 and 77%, respectively. The high survival of immature flies is due to the sheltered, inactive nature of pupal life. Adult and overall survival probabilities were highly correlated in males (r(2) = 0.61) but less so in females (r(2) = 0.24) where capture rates were lower and variance in the results greater. Immature and overall survival was more highly correlated for both sexes, with r(2) = 0.77 and 0.53 for males and females respectively. When a fixed pupal mortality of 1% per day was assumed, estimates of the survival of young adult males suggested that these were even lower than the survival of mature flies at the harshest times of the year, but were not markedly different when overall survival was high. Assuming equal mortality in all adults enabled the estimation of pupal survival. These had high variances but there was no evidence of any difference between the survival probabilities of male and female pupae.     

Octopamine distribution in the tsetse fly Glossina morsitans

Tissues of Glossina morsitans were assayed for octopamine using an enzymatic technique. Octopamine was detected at the highest concentration in the brain (7.06-7.99 ng mg-1 tissue protein) and thoracic ganglion (10.9-13.89 ng mg-1 tissue protein). Octopamine was present in haemolymph at a concentration of 1.0-1.27 X 10(-7) M. This was not found to vary when insects were flown or mechanically stressed. Nervous tissue, flight muscle and haemolymph showed a significant ability to metabolize octopamine. The greatest enzyme activity was present in the haemolymph.     

Identification and properties of microsatellite markers in tsetse flies Glossina morsitans sensu lato (Diptera: Glossinidae)

Genomic libraries enriched for simple sequence repeats were constructed for Glossina morsitans morsitans, G. m. submorsitans, and G. m. centralis. Sixteen microsatellite markers were isolated from the libraries and evaluated on flies from natural G. m. morsitans populations and other Glossina species in the Morsitans and Palpalis species groups. The primers amplified appropriate sized DNA fragments in the Morsitans and Palpalis groups. In G. morsitans s.l., eight of 12 dinucleotide repeats and four of 12 trinucleotide repeats were polymorphic. The polymorphic loci showed a mean 7.5 +/- 4.8 alleles per locus and their mean heterozygosity was 55.8 +/- 7.7%.     

Genetics of Glossina morsitans morsitans (Diptera: Glossinidae). X. A mutant (sabr) having long scutellar apical bristles in females

A line of Glossina morsitans morsitans Westwood was established in which females have scutellar apical bristles approximately three times as long as normal. In other respects the flies appear normal. The mutant allele, sabr, is recessive to the wild-type allele. The locus for sabr is located in linkage group III, 50 or more map units from the locus for malic dehydrogenase. Scutellar apical bristles in mutant flies are longer in flies emerging from puparia maintained at 30 degrees C than in flies emerging from puparia maintained at 25 degrees C.