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.     

Juvenile hormone mimics as effective sterilants for the tsetse fly Glossina morsitans morsitans

The development of puparia of Glossina morsitans morsitans Westwood was disrupted by topical applications of the juvenile hormone mimics S-methoprene (the resolved enantiomer of 11-methoxy-3,7,11-trimethyl-2,4-dodecadienoic acid 1-methyl ester) (Zoecon), S21149 (propionaldoxime-0-4-phenoxyphenoxyethylether) (Sumitomo), or S31183 (2-[1-methyl-2-(4-phenoxyphenoxy)ethoxy]pyridine) (Sumitomo) dissolved in acetone. Puparia so treated during the first 4 days of life suffered developmental abnormalities, the severity of which were dose-dependent. Similarly, puparia produced by adult females treated with these compounds were abnormal. Dose-response data showed that effects were greatest with S31183 and least with S-methoprene. Abnormalities in the form of abdominal lesions and wing crumpling were typical of flies emerging from puparia produced by S-methoprene-treated females. However, arrested development at the red eye and pigmented seta stage within the puparium were typical of offspring of females treated with S21149 and S31183. A dose of 2 micrograms per female of S31183 was sufficient to prevent emergence of offspring produced for the rest of the life of the fly. The same dose resulted in partial recovery of females treated with S21149 some 18 days following treatment. Treatment with 2 micrograms S-methoprene did not suppress completely the production of normal offspring and recovery was complete some 27-35 days after treatment. Exposure of males to 20 micrograms S31183 did not impair their ability to inseminate females; transfer of material during copulation was sufficient to prevent the production of viable offspring by their mates.(ABSTRACT TRUNCATED AT 250 WORDS)     

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.     

Rhythmic pulses of haemolymph pressure associated with parturition and ovulation in the tsetse fly,Glossina morsitans

Abstract Expulsion of the tsetse larva from the uterus of the female is preceded by 1–2 h of rhythmic pulses of haemolymph pressure that can be detected using a barographic technique. At first baseline pressure is maintained and all pulses are positive in relation to baseline. Then, about 1 h before parturition, baseline pressure increases, pulse intensity increases, and the pulses become both positive and negative in relation to baseline. Each pulse correlates with ‘bobbing’ action of the female's proboscis, the only external indication of this internal activity. A single large pressure pulse is observed at parturition, and thereafter the pressure level returns to the original baseline and pulsing action ceases. Around the presumptive time of ovulation, 1–2 h after parturition, another series of pressure pulses is observed. The pulses are the likely consequence of coordinated waves of muscular contraction that are essential preparation for successful parturition and ovulation.     

A study on isoenzyme polymorphism in the tsetse fly Glossina morsitans

Polymorphism was studied for a number of enzyme systems in the tsetse fly Glossina morsitans. Enzyme polymorphism was observed for -glycerophospate dehydrogenase, aldehyde oxidase and esterases. For esterases, the operation of null alleles was assumed, as otherwise no explanation could be given for the observed frequencies of the variants.Two laboratory colonies and two field populations were compared with respect to their variation at the leucine aminopeptidase (Lap) loci, for which polymorphism was shown to occur in previous work. Conspicuous differences were found between material originating from Tanzania and from Rhodesia. In addition, allelic relationships were established for the Lap ₃-locus.

---

Résumé Faisant suite à des études antérieures, le polymorphisme d'un certain nombre de systèmes enzymatiques a été étudié chez Glossina morsitans. Un polymorphisme a été observé pour l' -glycerophosphate déhydrogénase, pour l'aldéhyde-oxydase et pour les estérases. Pour les estérases, on a supposé l'intervention d'allèles nuls, les fréquences observées chez les variants ne pouvant être expliquées d'autre façon.Deux colonies élevées au laboratoire et deux populations naturelles ont été comparées quant à leur variation au niveau des loci (Lap) pour la leucine aminopeptidase, pour lesquels un travail antérieur avait mis en évidence un polymorphisme. Des différences nettes ont été trouvées entre le matériel provenant de Tanzanie et celui de Rhodésie. En outre des parentés alléliques ont été établies en ce qui concerne le locus Lap ₃.

     

Cloning and expression of the yolk protein of the tsetse fly Glossina morsitans morsitans

Two major families of nutritional proteins exist in insects, namely the vitellogenins and the yolk proteins. While in other insects only vitellogenins are found, cyclorraphan flies only contain yolk proteins. Possible sites of yolk protein synthesis are the fat body and the follicle cells surrounding the oocyte. We report the cloning of the yolk protein of the tsetse fly Glossina morsitans morsitans, a species with adenotrophic viviparity. The tsetse fly yolk protein could be aligned with other dipteran yolk proteins and with some vertebrate lipases. In contrast to the situation in most fly species, only a single yolk protein gene was found in the tsetse fly. Northern blot analysis showed that only the ovarian follicle cells, and not the fat body represents the site of yolk protein synthesis.     

Oxidation of proline by sarcosomes of the tsetse fly,Glossina morsitans

Mitochondria isolated from the flight muscles of tsetse flies are capable of oxidizing proline at rates commensurate with the requirements of the flight system. The rate of oxidation of other substrates is negligible by comparison. In the presence of phosphate, the oxidation of proline is completely controlled by ADP, acting at the level of the respiratory chain and not at the level of the dehydrogenases. The amount of alanine formed during the in vitro oxidation of ¹⁴C-proline is substantially less than the amount of proline used. The result is interpreted on the basis of a branching of the metabolic pathway at the level of glutamate, with the aminotransferase accounting for approximately 80% of the flux, and glutamic dehydrogenase for the remainder.     

The control of receptivity and ovulation in the tsetse fly, Glossina morsitans

ABSTRACT. A rapid decline in receptivity of mated female Glossina morsitans morsitans Westwood is shown to depend on both physical and chemical stimuli associated with copulation. Radiolabelling revealed the transfer of substances from the male to the haemolymph of the female during copulation. Implantation of male tissues or their injection as homogenates into virgin females showed the chemical stimulus to come from the male accessory glands. Receptivity decreased in females mated to males with ejaculatory ducts severed or testes removed and also in females which had a glass bead inserted into their uterus and/or the tip of their abdomen covered with wax, suggesting that a physical stimulus inducing refractoriness is provided by distension of the uterus and/or stimulation of their terminalial setae. Exposing virgin females to daily short matings in which no male materials were transferred, confirmed this. Receptivity also declined slowly with age in unexposed virgin females. Transfusion of haemolymph from mated females (up to 11 days old) into virgins did not indicate the existence of a haemolymph-borne ovulation-inducing factor; apparently only physical stimuli from mating are involved in the induction of ovulation, and somehow prime the ovarian tissue so that it responds appropriately later when the egg has matured. Whether the stimulus is transmitted to the ovary neurally or hormonally is unknown.