Juvenile hormone regulates the expression of the gene encoding ceratotoxin a,an antibacterial peptide from the female reproductive accessory glands of the medfly Ceratitis capitata

Ceratotoxin A is an antibacterial peptide produced by the reproductive female accessory glands of the medfly Ceratitis capitata. To investigate whether ceratotoxin A gene expression was affected by juvenile hormone, which has gonadotropic functions in adult insects, newly emerged female medflies were treated with precocene II, an antiallotropin compound capable of inhibiting juvenile hormone biosynthesis. Daily treatment of newly emerged flies with precocene II blocked ceratotoxin A gene expression in a dose-dependent manner. Ceratotoxin A gene expression could be recovered after withdrawl of precocene II treatment. Moreover, the effect of precocene II on ceratotoxin A gene expression could be countered by simultaneous treatment with methoprene, a juvenile hormone analogue. The effects of precocene II and methoprene treatments on the growth of both ovaries and accessory glands was also investigated. Our data suggest that ceratotoxin A gene expression is modulated by juvenile hormone.     

Growth of the male accessory gland in adult locusts: Roles of juvenile hormone,JH esterase,and JH binding proteins

The participation of juvenile hormone (JH) in the regulation of growth and protein synthesis in the accessory reproductive gland of male Locusta migratoria has been investigated. After elimination of endogenous JH with ethoxyprecocene, the accessory gland failed to grow, but growth was restored by a single application of the JH analog, pyriproxyfen. Pyriproxyfen appeared to stimulate total protein synthesis by 3 h, with a significant effect by 12 h, in contrast to 24 h observed in fat body. The dose curve for stimulation of protein synthesis 12 h after applying pyriproxyfen gave an ED₅₀ of 0.1 μg; the dose curve for gland growth at 72 h was biphasic, with steps at about 0.01 μg and 10 μg, suggesting two phases in JH action. SDS-PAGE analysis showed several components that were stimulated by pyriproxyfen, the effect being strongest in an 11 kDa band. A 5 kDa component was enhanced in the soluble and reduced in the particulate fraction after precocene treatment. The accessory gland contained JH esterase activity at levels about 100 times those in fat body or hemolymph, and was higher in precocene treated locusts. Binding activity for [³H]10R -JH III was high in cytosolic and nuclear fractions, and was identified immunologically as due to the previously described hemolymph JH binding protein. The results indicate that the mode of action of JH in the accessory gland may differ from that in the fat body. The presence of intracellular JH binding protein suggests a direct action of JH within the gland, that may be modulated by JH esterase. © 1995 Wiley-Liss, Inc.     

Precocenes as pro-allatocidins in adult female Diploptera punctata: A functional and ultrastructural study

Adult mated females of the viviparous cockroach Diploptera punctata are moderately sensitive to precocenes. Oöcyte growth is inhibited and oviposition is delayed in insects topically treated with precocene II or precocene III. C₁₆ juvenile hormone release by corpora allata of precocene-treated insects is markedly inhibited when compared to corpora allata of acetone-treated controls. Electron microscopy of the corpora allata reveals that precocene treatment results in a disorganisation of the intracellular organelles. Topically applied precocene II reaches a high concentration in the haemolymph (0.5 mM 2 hr after topical application of 250 μg). C₁₆ juvenile hormone release by isolated corpora allata is inhibited by precocenes in vitro; half-maximal inhibition over a 3 hr period is obtained at 0.4 mM precocene II. In vitro inhibition of corpora allata by precocene II concentrations higher than 1 mM rapidly destroys the glands as evidenced by electron microscopy (total disintegration of cellular organelles) and by the virtual cessation of C₁₆ juvenile hormone synthesis by the corpora allata. Inhibition of C₁₆ juvenile hormone release by precocene is time-dependent and is not reversible over the short-term incubation in vitro. This inhibition does not appear to be related to the spontaneous activity of the glands in vitro, and it can be reduced by two epoxidase inhibitors. Precocenes are pro-allatocidins in this species: they are bioactivated within the corpora allata to cytotoxic epoxides.     

The effects of precocene treatment on egg wax production in Gené's organ and egg viability in the cattle tickBoophilus microplus (Acarina ixodidae): An ultrastructural study

Was synthesis by Gené's organ, the egg waxing organ of ticks, is disrupted by precocene treatment of engorged femaleBoophilus microplus, resulting in desiccated nonviable eggs due to the absence of a waterproofing wax layer. Electron microscopy shows that precocene has a destructive effect on the glandular cells of Gené's organ. The precocene also inhibited in vitro was synthesis by the gland cells, indicating a selective cytotoxic effect. Oogenesis and oviposition were otherwise unaffected, also suggesting that precocene affects the gland cells directly, rather than indirectly by antagonism of juvenile hormone.     

Mating and hormonal triggers regulate accessory gland gene expression in male Drosophila

Drosophila melanogaster males transfer accessory gland proteins, as part of their seminal fluid, to females during each mating. Since accessory gland proteins are important for male reproductive success, it is important that the male replenish the proteins he transferred during mating. Previous studies had shown that mating induces the resynthesis of accessory gland proteins, but since mating includes a set of stereotyped behavior patterns as well as the act of copulation, it was not known which aspect of the mating process induces accessory gland protein synthesis. By exposing males to females whose ovipositors had been sealed shut, we have shown that resynthesis of accessory gland proteins occurs only when seminal fluid is transferred to females. By applying juvenile hormone or 20-hydroxyecdysone topically to the cuticle of male flies, we showed that these hormones can act in vivo to stimulate the synthesis of accessory gland proteins to levels similar to those observed after mating.     

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.     

NEUROENDOCRINE REGULATION OF PROTEIN ACCUMULATION BY THE TRANSPARENT ACCESSORY REPRODUCTIVE GLAND OF MALE RHODNIUS PROLIXUS

Surgical removal of the corpus allatum or neurosecretory cells of the brain results in a marked reduction in protein accumulation in the transparent accessory reproductive gland (TARG) of the male. Topical application of C₁₈ juvenile hormone stimulates a dose-dependent accumulation of protein in allatectomized males. These results suggest that a direct or indirect stimulation by the neuroendocrine system is normally required for TARG protein synthesis.     

Extraglandular synthesis of accessory reproductive gland components in male Melanoplus sanguinipes

The accessory reproductive glands (ARG) of the male migratory grasshopper, Melanoplus sanguinipes, are able to accumulate injected labelled ARG protein from the haemolymph. Accumulation is slight in the ARG of 2-day-old virgins, or 7-day-old allatectomized (CA^?) insects. The ARG of 7-day-old virgins, or 7-day-old CA^? insects treated with synthetic juvenile hormone, accumulate about 1.5 times more label than those of 2-day-old insects in a 24-hr period. The ARG of recently mated males accumulate almost four times more label than those of 2-day-old controls. Immunoprecipitation studies indicate that about one fifth of the labelled protein is accumulated unchanged.The fat body and haemolymph contain proteins which are precipitable by antiserum to whole ARG homogenate. The concentration of these proteins in the fat body increases after removal of the ARG, or after copulation. It is concluded that the fat body synthesizes certain proteins which are accumulated by the ARG. Both the synthesis and the accumulation of these proteins are regulated by the corpora allata.     

外用保幼激素与早熟素对丽斗蟋翅二型个体飞行与生殖发育间生理权衡的影响（英文）

为探讨丽斗蟋Velarifictorus ornatus翅二型个体飞行与生殖发育间生理权衡的内分泌控制机理, 本研究调查了外用保幼激素Ⅲ(JH-III)与早熟素Ⅰ(P-I)对丽斗蟋翅二型个体飞行肌与生殖发育的影响。结果表明： 成虫羽化后当日分别注射1, 5, 10和25 μg保幼激素7 d后, 显著促进了丽斗蟋长翅雌虫卵巢发育, 卵巢重量分别从对照组的16.8±11.4 mg/♀增加到43.9±10.7, 33.6±14.0, 56.8±7.6和 39.3±30.7 mg/♀; 但对卵巢内怀卵量无显著影响。相反, 外用保幼激素则诱发飞行肌降解, 1, 5和10 μg JH-III处理组飞行肌重量分别下降为12.9±4.7, 11.7±4.8和8.8±0.8 mg/♀, 显著低于对照组飞行肌重量(17.7±1.6 mg)。对短翅雌虫注射P-I时, 当注射的剂量超过50 μg/♀时, 能够显著抑制卵巢发育, 而低于50 μg/♀时则对卵巢发育无明显影响。外用JH-III对丽斗蟋长翅雄虫飞行肌、 精巢、 附腺的发育无明显影响; 外用P-I对短翅型雄虫精巢与附腺的发育也无明显影响。因此, 丽斗蟋翅二型雌虫与雄虫的飞行肌与生殖器官的内分泌控制机理可能存在差异。     

S-Adenosylmethionine:Juvenile hormone acid methyltransferase in male accessory reproductive glands of Hyalophora cecropia (L.)

The accessory reproductive glands of the adult male Hyalophora cecropia contain S-adenosylmethionine:juvenile hormone acid methyltransferase. The enzyme is soluble and can be found in the gland epithelium as well as in the glandular secretion, but not in any other part of the genital tract of the unmated male. The appearance of this enzyme activity in the pharate adult precedes the formation of a measurable pool of its substrate, juvenile hormone acid, and the onset of the juvenile hormone accumulation in the accessory reproductive glands. The accessory reproductive glands of Antherea pernyi and Manduca sexta, species which do not accumulate juvenile hormone, lack methyltransferase activity. It is concluded that the methyltransferase is an essential component of the juvenile hormone accumulation mechanism in H. cecropia.     

Effects of juvenile hormone and precocene II on the metabolic rate of the digestive system, fat body and ovaries of the insect Oncopeltus fasciatus

The metabolic rate of midgut, fat body and ovaries from Oncopeltus fasciatus adult female has been studied, comparing the results with that from juvenile hormone or precocene II treated insects. Neither juvenile hormone nor precocene II had any effect on midgut and fat body. Precocene II treatment increased the oxygen consumption rate of ovaries, which in turn remained undeveloped. Juvenile hormone had no detectable effects on the metabolic rate of ovaries, other than accelerate their development.     

早熟素II对家蝇卵黄发生的影响

本实验通过卵巢发育分级的解剖观察、可溶性蛋白质和核酸的定量测定、火箭免疫电泳定量测定卵黄原蛋白及激素处理等方法,研究了早熟素对家蝇(Muscadomestica vicina)卵黄发生的影响。试验结果表明用20ug早熟素处理每头刚羽化家蝇时,家蝇卵黄发生处于不完全抑制状态,其卵黄发生过程比对照组“延迟”约12小时。处理后48小时,血淋巴中卵黄原蛋白的滴度为lo.5ug/ul,接近对照组,而其卵巢鲜重和发育等级明显低于对照组,这种不完全抑制状态表明卵母细胞对卵黄原蛋白的吸收作用受到抑制。当用高剂量100ug早熟素11处理每头刚羽化家蝇时,血淋巴中卵黄原蛋白滴度、卵巢鲜重及其发育均受到明显的抑制,这种抑制效应能自然恢复。 当早熟素11和保幼激素(JH-III)、20-羟基蜕皮酮共同处理时,保幼激素具有明显的去抑制作用,可使血淋巴中卵黄蛋白浓度成倍增加,20-羟基蜕皮酮的去抑制效应不明显。本文还对早熟素作用于双翅目昆虫的方式作了讨论。     

Development of the accessory reproductive glands and genital ducts in female Schistocerca gregaria

The accessory reproductive glands of female S. gregaria are tubular extensions of the paired genital ducts, which in the mature female contain large amounts of a proteinaceous secretion used in the formation of the egg pod. In the 4th and 5th-instar female the glands are indistinguishable from the remainder of the mesodermally derived genital ducts. Towards the end of the 5th stadium, however, the accessory gland region only acquires characteristic convolutions which persist throughout the adult stages. At this time the epithelium of the entire ducts becomes reorganized into a unicellular epithelium. Only one cell type occurs throughout the length of the glands, and also in the egg calyces and lateral oviducts. The cells are inactive immediately after final ecdysis and remain in this state until the level of juvenile hormone in the haemolymph rises. The hormone acts directly on the cells triggering a rapid proliferation of organelles associated with protein secretion, and thereby increasing the volume of apical cytoplasm. Microvilli develop at the luminar plasma membrane, while irregular infoldings form at the base of the cells. As the gland matures the major organelle, the rough endoplasmic reticulum, changes from the lamellar to the vesicular form. Secretion is released into the lumen by the ‘microapocrine’ method.     

Effects of Juvenile Hormone and Precocene on the Reproduction of Brachionus calyciflorus

We studied the effects of juvenile hormone and precocene on reproduction of the rotifer Brachionus calyciflorus. Amictic females of B. calyciflorus that were 2‐4 hours old were exposed to different concentrations of juvenile hormone (0.004, 0.02, 0.1, 0.5, 2.5, 12.5 mg/L) and/or precocene (0.05, 0.25, 0.75, 3.75, 7.5 mg/L) for 24 h. They were then transferred to a new medium without hormone and checked every 2 h during the next 48 h, and thereafter monitored daily until the individual died. Precocene had no effects on the length of the rotifer juvenile period, hatching time of the first neonate, lifetime reproduction, or the mixis ratio. In contrast, juvenile hormone at 0.5, 2.5, and 12.5 mg/L significantly prolonged the juvenile period by 6.1, 9.2, and 8.6%, respectively. When 26‐28‐h‐old amictic females were exposed to the same concentration series of juvenile hormone or precocene, precocene at 3.75 mg/L resulted in an increase in lifetime reproduction of 30.39%. However, at 0.75 and 3.75 mg/L precocene, a significantly lower percentage of mictic females was found, whereas juvenile hormone had no effect on the lifetime reproduction or mixis ratio. The population growth test showed that juvenile hormone had significant effects on the population growth rate and mixis ratio, but no effect on resting egg production. In comparison, precocene had no effect on any of these parameters. (© 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Precocene I and II inhibition of vitellogenic oöcyte development in Drosophila melanogaster

Adult female Drosophila melanogaster were exposed to precocene I and II, antiallatropin compounds which result in juvenile hormone deficiency in many insects. The presence of juvenile hormone in Drosophila adults was evaluated by examining vitellogenic oöcyte development, a process regulated by juvenile hormone in these flies. Both precocenes reduced the number of vitellogenic oöcytes present 43 hr after exposure in a dose-dependent manner. Precocene I was effective when applied to either newly eclosed females prior to vitellogenic oöcyte development or to gravid females. Precocene I was also effective in decapitated females, indicating that the action of the compound is not mediated by the brain. Corpus allatum volume, presumably a reflection of secretory activity, increased between 0 and 24 hr after eclosion in control females but not in precocene-treated females even after 48 hr. However, when females were removed from precocene medium, gland volumes increased within 48 hr to approximately those of control flies. This result is consistent with the reversibility of the precocene effect on Drosophila adults. These results suggest that precocene acts on the corpus allatum of Drosophila adult females to produce juvenile hormone deficiency.     

Effects of methoprene,a juvenile hormone analogue,on the larval and pupal stages of the yellow fever mosquito, Aedes aegypti

Exposure of early fourth-instar larvae of Aedes aegypti to the juvenile hormone analogue Altosid ZR15^® (methoprene) significantly increased the concentration of carbohydrates in the haemolymph of late fourth-instar larvae and reduced the haemolymph carbohydrate concentration of 24-h-old pupae relative to controls. Such treatment also effected a decline in haemolymph amino nitrogen levels of the pupal stage and a depletion of haemolymph proteins in late fourth-instar larvae as well as pupae. Two of nine protein fractions in the haemolymph of larvae were significantly depleted following methoprene treatment. Fourteen soluble protein fractions were present in the haemolymph of control pupae; two of these were missing from the pupae which were treated as larvae with methoprene. A further protein fraction, common to the haemolymph of both treated and control pupae, was significantly reduced in concentration as a consequence of exposure to methoprene. The juvenile hormone analogue impaired the capacity of the fat bodies of late fourth-instar larvae and pupae to synthesise proteins, resulting in a lowered concentration of fat body proteins. Glycogen levels in the fat bodies of treated larvae were significantly lower than in controls and glycogenolysis was suppressed due to an overall depletion of glycogen phosphorylase and, in pupae, a lowered ratio of active: inactive enzyme. The data are consistent with the proposition that the juvenile hormone analogue elicits neuroendocrinological changes in the target insect.     

The hormonal control of migratory flight behaviour in the convergent ladybird beetle, Hippodamia convergens

ABSTRACT. Topical application of the juvenile hormone mimic, Altosid, to Hippodamia convergens (Guérin-Méneville) (Coccinellidae) stimulated a significant increase in long-term flight behaviour in both males and females. Altosid treatment also stimulated ovarian development in females. Topical application of precocene II to H.convergens inhibited flight activity in treated animals of both sexes for about 10 days. Altosid treatment to precocene-treated beetles significantly increased their migratory behaviour over that of precocene-treated or acetone-treated controls. These results indicate that juvenile hormone stimulates migratory flight behaviour in this species along with reproductive development. It is likely that the hormone serves to coordinate migration with reproduction in the young adult.     

Inhibition of vitellogenin synthesis in Apis mellifera workers by a juvenile hormone analogue,pyriproxyfen

Insect juvenile hormone (JH) has been related to modulation of vitellogenin (Vg) synthesis, a protein produced by fat body cells, secreted in haemolymph and sequestered by developing oocytes. A stimulatory JH action has been described for the majority of species studied thus far. In some insects, however, Vg synthesis has been inhibited or unaffected by JH. The aim of this study was to re-examine the action of JH on Vg synthesis in Apis mellifera workers, since contrasting effects of this hormone were described. Newly emerged worker bees were treated with different doses of pyriproxyfen (PPN), a potent JH analogue. Vg and total protein were quantified in haemolymph samples of newly emerged up to 6-day-old worker bees. Protein synthesis activity of fat body cultured in vitro and ultrastructure of fat body cells were also examined. High doses (1.25, 2.5, 5 and 10 &mgr;g) of PPN inhibited the onset and accumulation of Vg in the haemolymph of young worker bees in a dose-dependent fashion. This inhibition was not a result of fat body cell degeneration or death, as illustrated by fat body cells ultrastructure analysis, but by impairing Vg synthesis, as demonstrated by in vitro culture of fat body cells. Low doses (0.001, 0.01 and 0.1 &mgr;g) neither affected the normal synthesis and secretion of Vg into the haemolymph nor caused an early onset of Vg in treated bees (which could be interpreted as a JH-activating effect), as shown by Vg quantification at 24-h intervals. The results suggest that a low JH titre in honey bee workers permits the onset and accumulation of Vg in haemolymph, whereas high JH levels turn off Vg synthesis.     

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.     

The roles of juvenile hormone and 20-hydroxy-ecdysone during vitellogenesis in isolated abdomens of Drosophila melanogaster

Both juvenile hormone and 20-hydroxy-ecdysone seem to be involved in the regulation of vitellogenesis in Drosophila melanogaster. It is the purpose of this paper to begin to define the functions of these two hormones. Although vitellogenin synthesis does not occur at a high rate in 1-day-old female abdomens isolated from the head and thorax before 0.75 hr after eclosion, both ZR515 (a juvenile hormone analogue) and 20-hydroxy-ecdysone can cause in these preparations vitellogenin synthesis and secretion into the haemolymph. The synthesis and secretion into the haemolymph of all three vitellogenins which are detectable by electrophoresis in sodium dodecyl sulphate-containing gels of polyacrylamide is promoted by both hormones. That result excludes the hypothesis that these two hormones regulate the synthesis of different vitellogenins. A dose-response curve showed that an injection of 0.2 μl of a 10^?6 M 20-hydroxy-ecdysone solution was sufficient to promote vitellogenin synthesis and secretion in isolated abdomens. Ovaries from isolated female abdomens treated with juvenile hormone analogue showed nearly normal amounts of all three vitellogenins and morphologically normal advanced vitellogenic follicles, whereas ovaries from isolated abdomens treated with 20-hydroxy-ecdysone contained little vitellogenin and no vitellogenic follicles. We conclude that under the conditions used, juvenile hormone permits vitellogenin uptake into the oöcyte much more readily than does 20-hydroxy-ecdysone.