Endocrine influence upon the development of vitellogenic competency in Oncopeltus fasciatus

Immunoelectrophoretic analysis of the blood of precocious adult females of Oncopeltus demonstrated the presence of the A form of vitellogenin but no detectable AB form, the form present in mature adult-female haemolymph. Although the appearance of the AB form could be induced by topical treatment of precocious adult females with juvenile hormone, no yolk deposition was induced in these females. Histological examination revealed that the ovaries of precocious adult females reached only a previtellogenic stage of development with or without treatment with juvenile hormone. Topical treatment of normal larvae and adults with the hormone demonstrated that vitellogenin synthesis could not be induced with juvenile hormone treatment alone until after adult emergence. Since the precocious adult females are chronologically younger than normal last-stage larval instars, we suggest that a transition period during which juvenile hormone is absent (i.e. the precocious moult in treated animals; the final moult in control animals) must occur before some tissue of the precocious or normal adult females, presumably the fat body, becomes competent to respond to further exposure to the hormone by making the AB form of vitellogenin. The ovary requires a similar transition period prior to becoming capable of depositing vitellogenin; however, the times when the fat body and the ovary become competent to respond to the transition period differ.     

Juvenile hormone induced ovarian uptake of a female-specific blood protein in Oncopeltus fasciatus

An adult female-specific blood protein was demonstrated in Oncopeltus by gel electrophoresis. This protein is the major band in soluble yolk fractions. It is also present at substantial concentrations in the haemolymph of starved and diapausing adult females. Thus, the failure of the ovaries to form yolk under these conditions is characterized by an inability to remove vitellogenin from the blood. Application of a juvenile hormone analog (JHA) restored protein yolk deposition in starved and diapausing adult females. Whereas other blood proteins decreased no more than two-fold upon JHA treatment, the vitellogenin concentration decreased 20-fold in starved females. The vitellogenin concentration in the blood of diapausing females was not significantly affected by JHA, apparently because synthesis kept pace with ovarian uptake in this case.     

Expression and regulation of vitellogenin messenger RNA in the mosquito,Aedes aegypti

Vitellogenin (yolk protein) gene expression in the mosquito was investigated at the level of mRNA using a subcloned fragment (403-1c) of the vitellogenin DNA derived from an Aedes aegypti genomic library. Message appeared 1–3 hr after a blood meal, peaked at 36 hr and was rapidly degraded thereafter. Fluctuations in levels of 20-hydroxyecdysone after a blood meal coincided with accumulation of vitellogenin message. Blood-fed, decapitated females injected with 5 μg of 20-hydroxyecdysone accumulated up to 75% of the message found in blood-fed controls. Fat bodies from non-blood-fed females incubated with physiological levels of 20-hydroxyecdysone and the juvenile hormone analog methoprene contained twice as much vitellogenin message as those incubated with 20-hydroxyecdysone alone. Methoprene alone had no effect.     

Cyanoprotein: Developmental stage,sex and diapause-dependent expression,and synthesis regulation by juvenile hormone in the bean bug,Riptortus clavatus

Cyanoprotein (CP) synthesis was studied in nymphal and nondiapause adult, diapause adult, and juvenile hormone (JH) treated adult bean bugs, Riptortus clavatus. Hemolymph collected from bugs injected with [³⁵S]-methionine was analyzed by native polyacrylamide gel electrophoresis (PAGE) and fluorography, and CP synthesis was also determined quantitatively by rocket immunoelectrophoresis of hemolymph and counting. In the nymphal stages synthesis of CP-1, 2, 3, and 4 (with CP-4 synthesis predominant) reached a maximum at mid-instar and was not detected at each ecdysis, so that the synthetic activity of CPs changed cyclically in each instar. During the nymphal stages CP synthesis showed the same pattern and level in both females and males, and both diapause and nondiapause oriented bugs. In the adult stage, however, CP synthesis differed in the two sexes and nondiapause or diapause conditions. In nondiapause males CP synthesis was not detected in the adult, but in nondiapause females CP (only CP-1) was synthesized through the reproductive stages. CP-1 accumulated in the egg yolk together with vitellogenin. In diapause adults (both females and males) CP-1 to 4 were synthesized at a very low rate for over 2 months and accumulated in the hemolymph. JH or JH analog (JHA) methoprene and also long day condition, which terminate diapause, switched the main CP synthesis CP-4 to CP-1 in females. CP synthesis in diapause males stopped after JH(A) treatment. The activities of CP synthesis, thus, changed in developmental stages, sexes, and diapause. This is an excellent system for study of specific gene expression and switching controlled by insect hormones and sex. © 1992 Wiley-Liss, Inc.     

EFFECT OF ECDYSTERONE ON VITELLOGENIN CONCENTRATION IN HAEMOLYMPH OF MALE AND FEMALE SARCOPHAGA BULLATA

Using Polyacrylamide gel electrophoresis, cycloheximide, incorporation of ³H-labelled amino acids and immunological methods, we have demonstrated that injection of ecdy- sterone induces de novo synthesis and release of vitellogenin in both sexes of Sarcophaga bullata. Vitellogenin concentrations were measured by the Mancini-radial immunodiffusion technique. In males a dose as low as 1 ng always makes vitellogenin appear in the haemolymph but very reproducible results are only obtained when doses varying from 10 to 250 ng were injected. In this range, the dose-response curve was linear on a semi- logarithmic scale.

In females, vitellogenin concentration remained low until a few hours after liver feeding and thereafter it rose sharply and reached its maximum about 24 h after the protein meal. 100 μg 6-hydroxydopamine HCl, injected before liver feeding in 4-day-old females, inhibited vitellogenin synthesis and yolk deposition, probably by interfering with the release of a brain hormone. This inhibitory effect on vitellogenin synthesis, but not that on yolk deposition, could be overruled by injection of ecdysterone. Juvenile hormone was ineffective on both. Females, ovariectomized on day 2 or 3, accumulated vitellogenin in their haemolymph, indicating that the continuous presence of the ovaries was not required for vitellogenin synthesis. The possible relation between the gonadotrophs hormone from the brain, vitellogenin synthesis and moulting hormone metabolism is discussed.     

Vitellogenin fluctuations in haemolymph and fat body and dynamics of uptake into oöcytes during the reproductive cycle of Diploptera punctata

Haemolymph and fat body soluble protein titres have been examined during the reproductive cycle of Diploptera punctata, with particular emphasis on the occurrence of vitellogenin and its uptake into the developing oöcytes. Vitellogenin was first detected in the haemolymph of mated females 2 days after adult eclosion at about the same time that vitellin deposition in basal oöcytes began. Peak haemolymph titres of vitellogenin occurred on day 6, correlated with the completion of yolk uptake. Thereafter vitellogenin levels declined and were generally undetectable throughout most of gestation, rising again shortly before parturition in association with the second gonotrophic cycle. Total haemolymph protein levels were not correlated with vitellogenesis.Soluble fat body vitellogenin titres of mated females remained low during the first oöcyte growth period but then rose several-fold at its completion and remained high throughout pregnancy and the second gonotrophic cycle. Total fat body soluble proteins decline after adult eclosion in association with oöcyte growth.Vitellin accumulation in basal oöcytes was related linearly to increase in volume until the onset of chorion formation. Thus no post-vitellogenic growth period was detected.     

Hormonal control of vitellogenin synthesis in Oncopeltus fasciatus

Previous work indicated the existence of two vitellogenins (A and B) in the haemolymph of Oncopeltus fasciatus, and that vitellogenin B was juvenile hormone (JH)-dependent whereas A was not (Kelly and Telfer, 1977). We have extended these results using several electrophoretic techniques in combination with limited proteolysis of key proteins to show that (1) vitellogenin B is present in eggs in a modified form while vitellogenin A cannot be detected in eggs. (2) Vitellogenin A may be a precursor of B since it has a molecular weight of 200,000D, approximately three times that of vitellogenin B (68,000D) and analysis by limited proteolysis shows that two proteins to be nearly identical. (3) Neither ovariectomy nor treatment with the anti-allatotropin, precocene II prohibits the appearance of vitellogenins A and B in the haemolymph. (4) Injection of ecdysone or 20-hydroxyecdysone into adult, male Oncopeltus fasciatus induces the appearance of both vitellogenin A and B in the haemolymph, suggesting the possible involvement of ecdysteroids in the control of vitellogenin synthesis in this species. (5) We have no evidence for JH control of the synthesis of vitellogenin, however, the ratio of vitellogenin A to B in the haemolymph is higher in the precocene-treated females.     

Vitellogenin induced in adult male Diploptera punctata by juvenile hormone and juvenile hormone analogue: Identification and quantitative aspects

The effect of the juvenile hormone analogue hydroprene on the appearance in the haemolymph of the yolk-protein precursor vitellogenin in male Diploptera punctata has been assessed using rocket immuno-electrophoresis. Vitellogenin was induced in a dose-dependent fashion, with a minimum dose of 10 μg hydroprene required for its appearance. Implantation of male corpora allata into male and female hosts also resulted in the appearance of vitellogenin in the haemolymph of the hosts, with females showing apparent greater sensitivity to the implantation.The identity of vitellogenin in male haemolymph was further confirmed using Ouchterlony double immunodiffusion and SDS polyacrylamide gel electrophoresis of immunoprecipitates. The electrophoretic pattern of immunoprecipitated haemolymph from females and hydroprene-treated males was similar, further confirming that the immunoprecipitable product was in fact vitellogenin.     

Cyanoprotein: Quantitative changes and synthesis in diapause and juvenile hormone analog treated bean bug,Riptortus clavatus

Quantitative changes of cyanoproteins (CPs) in diapause and juvenile hormone (JH) analog treated bean bug, Riptortus clavatus, were analyzed by rocket immunoelectrophoresis (RIE). In diapause-oriented nymphal females and males, CP-A (CP-1, 2 and 3) and CP-B (CP-4) increased and reached a maximum level just before nymphal-adult ecdysis, which was the same in non-diapause female and male nymphs. Both CP-A and B disappeared immediately after adult emergence. After this initial decline CP-4 appeared again in the hemolymph, followed after a few days by CP-1, 2 and 3. CP-A and B then increased slowly but constantly in both diapause female and male adults. Both diapause females and males at day 30 after adult emergence had large amounts of CP-A (CP-1, 2 and 3) and CP-B (CP-4). Treatment of diapause females (day 30) with methoprene induced only CP-1 synthesis and increased CP-A content about twice in both the whole body and the hemolymph, but did not effect on CP-B content. Methoprene treated females developed ovaries which accumulated yolk containing CPegg and vitellin (Vn). In diapause males treated with methoprene CP-A and B were not induced and decreased gradully in concentration, eventually disappearing completely, similar to post-diapause males (30 days after transferred to long day condition) in which CPs were not detected. These results show that methoprene treatment of diapause females and males induced the same dynamical situations of CP-A and B seen in non-diapause adults, i.e. only CP-A was induced in females and CPs disappeared in males. This suggests that CP synthesis is regulated by juvenile hormone.     

Activation of vitellogenin synthesis in the mosquito Aedes aegypti by ecdysone

Injected β-ecdysone was found to induce the synthesis of yolk protein (vitellogenin) in adult female Aedes aegypti without a blood meal. After injection of 5 μg ecdysone per mosquito, vitellogenin constituted 80 per cent of the total protein secreted by explanted fat body, a proportion comparable to that produced by fat body from blood-fed females. Moreover, the time course of induction of vitellogenin synthesis in ecdysone-injected mosquitoes was similar to that triggered by a blood meal. Response to ecdysone is dosedependent: 0·5 μg per female was required to stimulate synthesis to 50 per cent of the level found 18 hr after a blood meal. Ecdysone was effective in decapitated or ovariectomized mosquitoes, and also when applied directly to fat body preparations in vitro. Thus it appears that ecdysone acts directly on the fat body to induce specific protein synthesis, as does the vitellogenin stimulating hormone (VSH) from the ovary of blood-fed mosquitoes. These results suggest that ecdysone can replace VSH in inducing vitellogenin synthesis in the unfed mosquito.     

GENERAL ACCOUNTS ON THE OÖCYTE GROWTH AND THE IDENTIFICATION OF VITELLOGENIN BY MEANS OF IMMUNOSPECIFICITY IN THE COCKROACH, BLATTELLA GERMANICA (L.)

The female Blattella germanica pushes out an oötheca 11 days after adult ecdysis and carries it for about 25 days until nymphs hatch out. The terminal oöcyte begins to accumulate yolk abruptly 4 or 5 days after adult ecdysis and grows fully on day 10 when its volume reaches 180 times as compared to that at adult ecdysis.
Vitellogenin, the vitellogenic female-specific protein, was identified by immunoelectrophoresis and Ouchterlony's test. Fluctuation of vitellogenin in the blood, ovary and embryo at various stages was analyzed. Vitellogenin appears in the female blood 3 or 4 days after adult ecdysis and disappears soon after terminal oöcytes have been released to an oötheca. In the ovary, it appears 4 or 5 days after adult ecdysis and disappears when terminal oöcytes leave the ovary. It remains in embryos until shortly before hatching, but is absent in newly hatched nymphs.     

Nonvitellogenic female sterile mutants and the regulation of vitellogenesis in Drosophila melanogaster.

The genetic and endocrine regulation of vitellogenesis was investigated by studying 18 female sterile mutations that disrupt the development of normal vitellogenic follicles. Applications of exogenous juvenile hormone analog and reciprocal ovarian transplants between flies of different genotypes were employed to accomplish our first two objectives: to find (1) whether the mutation blocked development of the ovary directly, and (2) whether the mutation altered the hormonal milieu. In 15 of the mutants the developmental defect was localized to the ovary, but in the other 3 the ovary was competent to respond to a permissive environment. The internal milieu of these three mutants (ap⁴, fs(3)A1, fs(2)A18) was unable to provoke normal development in wild-type ovaries, suggesting that these mutations cause endocrine defects. Our third objective was to find whether an endocrine organ was itself defective in any of these mutants. The corpus allatum from two of the mutants was unable to provoke vitellogenesis in isolated wild-type abdomens, but corpora allata from wild-type females or from other mutants were able to promote maturation of ovarian follicles in isolated abdomens. Our fourth objective was to find whether any of the mutants were able to produce yolk proteins. Immunoelectrophoresis of fly hemolymph demonstrated that in all mutants tested vitellogenins were found in the blood. These experiments permit four main conclusions. First, they identify the first Drosophila mutants in which an endocrine gland is shown to be intrinsically defective during adulthood. Second, they show that the production of morphologically normal late previtellogenic follicles is not required for the induction of vitellogenin synthesis and secretion. Third, they show that juvenile hormone can cause ovarian follicles to sequester yolk in mutant flies. And finally, they show that mutants with defective corpora allata still synthesize and secrete vitellogenin. Taken together, these conclusions suggest that in Drosophila melanogaster the uptake of vitellogenin into follicles depends upon the availability of juvenile hormone, but that the synthesis and secretion of vitellogenin are independent of both normal ovaries and totally normal corpora allata.     

Juvenile hormone-controlled vitellogenin synthesis in Locusta migratoria fat body. Hormonal induction in vivo.

Biosynthetic processes related to the production of vitellogenin (yolk precursor protein) have been examined in the fat body of adult female Locusta migratoria. Vitellogenin-producing capacity was assayed by incubation of fat body with [³H]leucine, followed by precipitation from the medium with specific antiserum. In normal development, vitellogenin synthesis began at about Day 7 after emergence and became maximal at about Day 13, when this protein accounted for 60% of the total fat body protein output. The production of other proteins increased to a lesser extent, becoming maximal at about Day 6. The incorporation of uridine into fat body RNA rose to a maximum at Day 8, which coincided with a marked increase in tissue RNA content. The DNA content in adult female fat body approximately doubled between Days 3 and 8. Vitellogenin synthesis, and the increases in RNA and DNA, were prevented by removal of the corpora allata (the source of juvenile hormone). In allatectomized locusts, vitellogenin synthesis was induced by JH or an analog, ZR-515. Applied topically in acetone, these gave steep dose-response curves, half-maximal at 75 and 150 μg, respectively. After a single treatment with ZR-515, fat body vitellogenin production rose slowly during 48 hr, then steeply to a maximum at 72 hr, but after decay of this effect during 10 days, a second application of ZR-515 induced renewed synthesis with little initial lag. Hormone treatment produced a smaller increase in the output of other proteins, and an increase in incorporation into RNA which preceded the major rise in vitellogenin synthesis. Male fat body produced little or no vitellogenin. These results are consistent with action of JH at the gene level.     

Control of vitellogenin synthesis in the Monarch butterfly by juvenile hormone.

Yolk formation in the Monarch butterfly, as in many other insects, entails juvenile hormone-induced synthesis in the fat body, transport in the hemolymph, and uptake into the oocytes of specific sex-limited protein, the vitellogenin. In the Monarch, vitellogenin first appears in the hemolymph 1 day after emergence of the adult butterfly and then rises rapidly in concentration for at least 3 days. The synthesis of vitellogenin in adult females was shown by the incorporation of [³H]leucine. Active labeling was observed at the same time as the presence of vitellogenin in the hemolymph was first detectable, and the radioactivity in vitellogenin expressed as a percentage of radioactivity in total blood proteins reached 50–60% 3 days after adult emergence. The appearance of vitellogenin was prevented by ligature of freshly emerged butterflies at the neck and restored by injection of juvenile hormone. A low yet significant stimulation of vitellogenin synthesis could be detected as early as 10 hr after administration of the hormone into neck-ligated butterflies, and after 30 to 50 hr about 40% of the total blood protein label was found in the specific protein. With C₁₈-juvenile hormone (JH-I), 0.1 μg per animal was effective in inducing a low level of vitellogenin synthesis, and between 0.01 and 1 μg, a linear relationship between synthesis and log dose was observed. The synthetic analog ZR-512 was also active. In a preliminary experiment, actinomycin D effectively blocked the induction of vitellogenin synthesis.     

Release of egg development neurosecretory hormone in Aedes aegypti and Aedes taeniorhynchus induced by an ovarian factor

Ovariectomized Aedes aegypti do not synthesize vitellogenin after a blood meal, unless an ovary from a blood-fed donor is implanted. Decapitation, however, prior to implantation inhibits vitellogenin synthesis. A female ovariectomized and decapitated 6 hr after a blood meal, synthesizes vitellogenin if an ovary from a blood-fed donor is implanted. On the other hand, females that are fed on blood and immediately decapitated can not be stimulated to synthesize vitellogenin with implanted ovaries removed from blood-fed donors. These experiments led to the hypothesis that the blood meal stimulates the ovary to secrete a corpus cardiacum stimulating factor, that in turn promotes release of egg development neurosecretory hormone stored in the corpus cardiacum.Injection of 20-hydroxy-ecdysone or ovarian extract prepared from ovaries removed from unfed females does not release egg development neurosecretory hormone. Thus corpus cardiacum stimulating factor is not 20-hydroxy-ecdysone, and ovaries removed from unfed females do not store it.The rate of inactivation of egg development neurosecretory hormone released from the corpus cardiacum after a blood meal was investigated by implanting an ovary into females that were blood fed for various intervals than decapitated and ovariectomized. Seventy per cent of implants grow when the operation is done 18 hr after feeding, and 30% when the operation is done between 18 and 24 hr after feeding, indicating that egg development neurosecretory hormone is stable for the first 18 hr after a blood meal.Aedes taeniorhynchus females ovariectomized 24 hr after adult emergence do not synthesize vitellogenin. When such a female is implanted with an ovary removed from a sugar-fed or blood-fed Aedes aegypti donor vitellogenin synthesis is initiated, and the implant grows. Decapitation prior to implantation inhibit vitellogenin synthesis and implants do not grow. These results indicate that corpus cardiacum stimulating factor is not species specific.     

Endocrine biology of the Painted Lady butterfly Vanessa cardui

Experiments dealing with the role of juvenile hormone, adipokinetic hormone and diuretic hormone in the Painted Lady butterfly Vanessa cardui are reported. The results demonstrate an important role of JH in the regulation of ovarian and colleterial gland development in females, and in the regulation of accessory gland, tubular gland and ejaculatory duct development in males. In addition, the presence of an adult reproductive diapause, characterized by decreased effective juvenile hormone haemolymph titres, is suggested. Evidence for the existence of both adipokinetic and diuretic hormones in the Painted Lady is also presented, as is data indicating that both hormones may be similar or identical to those previously described in Monarch butterflies. Owing to the above results, and the existence of an artificial diet suitable for mass rearing in the laboratory, the Painted Lady appears to be an excellent species for studies on adult lepidopteran neuroendocrinology.     

Precocious induction of vitellogenin with JH III in the twospotted stink bug, Perillus bioculatus (Heteroptera: Pentatomidae)

The effect of juvenile hormone (JH) III on the hemolymph composition of vitellogenin was examined in Perillus bioculatus. Adult females were treated topically with JH III, and the premature presence of vitellogenin in the hemolymph was then detected using electrophoresis and Western blot analyses. JH III treatment resulted in a dose-dependent early production of vitellogenin that was detectable 48 h before vitellogenin was present in non-treated insects. Vitellogenin was not observed in the hemolymph of JH III-treated adult males. The techniques reported here may be useful for the detection, isolation and characterization of compounds with JH-like activity in P. bioculatus and other species of Heteroptera (which are thought to have JH-like substances other than the JHs with known chemical identity). These same techniques may also provide a method for researchers to investigate the interactions of JH-like compounds and other substances, such as ecdysteroid, in the regulation of vitellogenesis in Heteroptera.