Some observations on the development and cyclic changes of the oöcytes in a brooding starfish, Leptasterias hexactis

There are two ovaries in each arm and each ovary bears a single oviduct which opens orally at the interradial angle. The ovarian wall consists of three layers: mesothelium, muscular-connective tissue layer and germinal epithelium. The haemal space between the germinal epithelium and muscular-connective tissue layer is filled with a PAS positive fluid. It is suggested that this space may provide storage and transportation of nutrient to the germ cells.
The oögonium, situated along the germinal epithelium, is distinguished from the surrounding follicle cells by its clear cytoplasm and large nucleus with a single nucleolus. It measures 10 to 15 μ in diameter.
The development of primary oöcytes is divided into premeiotic, growth and germinal vesicle migration stages. The distribution of mitochondria seems to indicate the existence of a definite polarity in the young oöcytes; but this soon disappears at the beginning of vitellogenesis. Morphological evidence seems to suggest that some of the yolk granules may be synthesized first in follicle cells and then transferred into the oöcyte. Histochemical tests indicate that the yolk platelet is a carbohydrate-protein-lipid complex.
The first meiotic division occurs six hours after sperm penetration and the second meiotic division follows two hours later.
Monthly measurement of the oöcyte throughout a year indicates a well-defined annual spawning cycle; however, the growth of an oöcyte from an oögonium to a mature oöcyte requires about two years.     

Some observations on the histology of the ovary and RNA synthesis in the ovarian tissues of the starfish, Henrida sanguinolenta

The general histology of the ovary and the cellular morphology of oöcytes in Henricia sanguinolenta (Muller) Bell is described.
The single nucleolus in the germinal vesicle begins to multiply when the oöcyte is 90 μm in diameter, either by fragmentation or by budding and it reaches several hundred in number in a full grown oöcyte of 1200 μm in diameter. At no time during the oöcyte growth is RNA synthesis in the nucleolus or any other parts of the oöcyte detected by autoradiographic techniques. However, follicle cells and coelomocytes in the ovary are actively synthesizing RNA during this period.
The inactivity of RNA synthesis in oöcytes is discussed.     

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.     

Reproductive allocation by the blow fly Lucilia sericata in response to protein limitation

Adult females of the anautogenous blow fly Lucilia sericata (Meigen) (Diptera: Calliphoridae) were fed standardized meals of liquidized liver, in quantities shown to range around the minimum required to initiate yolk deposition. Females from each feeding regime were dissected at daily intervals between 4 and 11 days of age; the number and stage of development of all oöcytes were recorded. Once an initial threshold quantity of protein was ingested, yolk deposition was initiated in all available oöcytes. Subsequently, one of two distinct developmental pathways was followed: arrested development in all oöcytes at an early stage of yolk deposition, or more extensive yolk deposition followed by progressive oösorbtion and the maturation of small batches of eggs. The proportion of females showing oösorbtion relative to arrested follicular development increased with increasing protein meal size, suggesting that the difference in response may be triggered by a second protein threshold, either side of which the arrested development or oösorbtion pathways are followed. The behaviour observed may reflect strategies to maximize reproductive output in this short‐lived, resource‐limited insect species. Flies that display arrested development may have sufficient protein to mature few if any complete eggs, but may subsequently be able to mature a full egg‐batch if they obtain further protein meals; this possibility is offset by the risk of death before finding such a meal. Flies that show oöcyte development and oösorbtion produce smaller egg batches more quickly and hence have a higher probability of achieving at least some reproductive output. By initiating yolk deposition in all oöcytes, female L. sericata retain the potential to adopt either developmental pathway, depending on subsequent protein intake.     

Endocrine control of vitellogenesis in the harlequin bug, Dindymus versicolor

An active corpus allatum is essential for the maturation of eggs in the harlequin bug, Dindymus versicolor. The corpus allatum of virgin females remains virtually inactive and the oöcytes are resorbed once they have grown to the stage at which they become competent to incorporate yolk. Mating provides a stimulus which is essential for the initiation and maintenance of corpus allatum activity and, therefore, vitellogenesis. Corpus allatum activity (and vitellogenesis) can be induced in virgin females either by cutting the allatic nerves or by excision of a certain part of the protocerebrum. It is concluded that the corpus allatum of virgin females is inhibited nervously by the brain and that copulation provides a nervous stimulus which lifts this cerebral inhibition thereby permitting allatum activity.The median neurosecretory cells are not essential for vitellogenesis in Dindymus; however, it is suggested that they are necessary for maximum allatum activity. Evidence is provided to show that the growth and maintenance of the previtellogenic oöcytes are also under the control of the corpus allatum. A mechanism is described whereby the number of vitellogenic oöcytes in the ovarioles is maintained constant.     

A neurosecretory hormone-releasing factor from ovaries of mosquitoes fed blood

In mosquitoes, a hormone (egg development neurosecretory hormone or EDNH), produced by the medial neurosecretory cells and stored in the corpus cardiacum soon after eclosion, is released after a blood meal, and vitellogenesis begins a few hours later. When either the ovaries or the neurosecretory cells and corpus cardiacum are removed before the blood meal, vitellogenin is not synthesized. Therefore, we tested the hypothesis that the release of EDNH from the corpus cardiacum is dependent on the secretion of a releasing factor from the ovaries.Using a bioassay for EDNH in the corpus cardiacum, we found that the gland of an ovariectomized female remained active after blood feeding, and therefore, has not released EDNH. When an ovary was implanted before the blood meal, the corpus cardiacum was inactive, and therefore, had released EDNH. We concluded that the ovaries secrete an EDNH-releasing factor, and that this factor and EDNH must both be in circulation before vitellogenesis can begin. Although releasing factor alone did not stimulate vitellogenesis, it was the rate limiting process that controlled the onset of vitellogenesis.Using a bioassay for the EDNH-releasing factor from the ovaries and using rocket-immuno-electrophoresis, we showed that a Culex ovary, but not an Anopheles ovary, could replaces Aedes ovaries as a source of the releasing factor.In Ae. aegypti, EDNH-releasing factor was required again after oviposition in order to reinitiate the vitellogenic process in females that took a second blood meal. Thus, the releasing factor is part of the mechanism regulating cyclic egg maturation in mosquitoes.     

Endocrine control of vitellogenin synthesis and vitellogenesis in Triatoma protracta.

The corpus allatum (CA) is required for vitellogenesis in the blood-sucking reduviid, Triatoma protracta, as seen by the total lack of yolk deposition in allatectomized females. Normally the CA becomes active within a day after emergence. After a period of activity during which unfed virgins may mature a few eggs, the CA is inhibited via its neural connectives from the brain. The CA is activated by mating, while a blood meal provides an additional stimulus for vitellogenesis. If the ventral nerve cord (VNC) is severed within 48 hr after copulation, the mating stimulus does not get through. However, the pathway of the feeding stimulus does not involve the VNC. The brain does not have any allatotropic or gonadotropic function in this species.A female-specific protein (vitellogenin) was identified by immunoelectrophoresis in the haemolymph of egg-maturing females. This protein is taken up by the oöcytes immunologically unaltered and forms the bulk of the yolk. Allatectomy at emergence prevents the appearance of the vitellogenin, and the topical application of JH_III to allatectomized females led to its synthesis de novo, as shown by the incorporation of labelled precursors into vitellogenin. From its mobility in polyacrylamide gels of different concentrations, the molecular weight of the yolk protein is estimated to be 4.37 × 10⁵ daltons.     

The role of factors from the head in the regulation of egg development in the mosquito Aedes aegypti

The relationships between the release of factors from the head after blood-feeding, subsequent levels of ecdysteroids and vitellin, and the ultimate maturation of eggs in Aedes aegypti were investigated. Females were decapitated at various times after a blood meal, at 20 or 48 h after feeding the animals were dissected and divided into two groups, those with arrested oöcytes (yolk length < 100 μm) and those with maturing oöcytes (yolk length > 100 μm). These yolk lengths correspond with the levels of oöcyte growth believed to accompany the proposed initiation and promotion phases of egg development. Animals dissected at 20 h were assayed for ecdysteroid by radioimmunoassay; those dissected at 48 h were assayed for vitellin by rocket immunoelectrophoresis.Non-blood-fed unoperated females contained 8% as much ecdysteroid as blood-fed controls and no measurable vitellin. Females with arrested oöcytes (< 100 μm) were obtained only if decapitations were performed before 8 h; these females had about 20% of the ecdysteroids and 8% of the vitellogenin normally found in blood-fed animals. Females decapitated between 2 and 8 h with maturing oöcytes contained 50–60% as much ecdysteroid and vitellin as blood-fed unoperated controls. Normal ecdysteroid and vitellin levels were reached only when decapitations were delayed for 12 and 24 h, respectively. The number of developing oöcytes was also decreased by early decapitation and was closely correlated with vitellin levels.We conclude that the egg development neurosecretory hormone is released twice, once before 8 h and once after 8 h, to control ecdysteroid levels. We also suggest the presence of other factors from the head that control vitellin levels, the number of developing oöcytes, and the early growth of the oöcyte (initiation).     

Artifactual stimulation of vitellogenesis in Aedes aegypti by 20-hydroxyecdysone

Single or repeated, non-physiological, high doses (0.5–5.0 μg/female) of 20-hydroxyecdysone or ecdysone injected into sugar-fed female Aedes aegypti stimulated follicular growth and deposition of yolk, but suppressed accumulation of protein yolk to approximately one-third, and lipid yolk to one-half that in an equal number of follicles with equivalent yolk length taken from blood-fed controls. Physiological doses (500 pg/female) of ecdysone or 20-hydroxyecdysone or the implantation of ecdysone-secreting ovaries (verified by bioassay), into sugar-fed females failed to induce any yolk deposition. In these experiments, yolk precursors were not the limiting factor, because in decapitated females, digesting a blood meal, the injection of a physiological dose of 20-hydroxyecdysone or the implantation of ecdysone-secreting ovaries still did not stimulate vitellogenesis. Finally, continuous infusion of 500 pg or even 50 ng 20-hydroxyecdysone/hr for 22 hr was as ineffective as single or multiple injections of equivalent doses of hormone. Consequently, rapid excretion or catabolism of 20-hydroxyecdysone by the sugar-fed female does not explain the need for high doses to induce vitellogenesis, or the failure of oöcytes to mature with normal protein and lipid content. Apparently, ovarian ecdysone is not the factor by which normal vitellogenesis is initiated and maintained in this mosquito.     

Pattern of sea bass oocyte development after ovarian stimulation by LHRHa

The cyclic pattern of oocyte development in the sea bass, Dicentrarchus labrax L., was studied after induction of spawning by two injections, 24 h apart, of a luteinizing hormone releasing-hormone analog (LHRHa) administered at the end of vitellogenesis. The first difference in the developmental stage of the ovary and in the size-frequency distribution of oocytes between the LHRHa treated group and the control group, was detected 32 h after the first injection, the LHRHa group showing a higher proportion of the 900 μm diameter oocyte class (maturing oocytes) ( P <0.01). At 48 h LHRHa-treated females showed an increase in the 1000 and 1100 μm classes (maturing oocyte and ovulated eggs) ( P <0.01) and at 72 h these females exhibited a bimodal pattern, reaching the highest proportions in the 1100 (27.4%) and the 600 (14.7%) μm classes (ovulated eggs and advanced vitellogenic oocytes, respectively). Bimodal distributions were present in 80% of the LHRHa-treated females. Once oocyte final maturation was triggered by LHRHa the time needed for ovulation was about 48 h and the interval between consecutive ovulations and spawnings seemed to be 48–72 h.     

Autonomous yolk protein synthesis in ovaries ofDrosophila cultured in vivo

Summary Immature ovaries ofDrosophila mercatorum were injected into young larvae and into adult males ofD. mercatorum, D. melanogaster, D. hydei, D. virilis, andZaprionius vittiger. These homo- and heteroplastic transplantations allow normal vitellogenesis to occur in the donor ovary. By SDS gel electrophoresis, we identified the major species-specific yolk proteins of mature eggs (stage 14) which were exclusively of donor-specific origin. Other experiments withD. hydei andZ. vittiger showed that, when females were used as hosts, the host-specific yolk proteins became incorporated into the donor eggs. When two immature ovaries, one ofD. mercatorum and one ofD. hydei, were co-cultured in males, again only the donor-specific yolk proteins were found in the mature eggs implying that these yolk proteins were not released into the host hemolymph.A parthenogenetic strain ofD. mercatorum was used to demonstrate the ability of transplanted immature ovaries to produce viable eggs which can give rise to fertile adults.The role of the species-specific yolk proteins is discussed with respect to the dual origin of these proteins during normal vitellogenesis, i.e., an autonomous synthesis within the ovary itself in addition to the well-known production by the fat body. Further experiments with pupae as hosts indicate that even in the absence of juvenile hormone and in the presence of high doses of ecdysone, vitellogenesis can proceed within the donor ovary.Based on these experiments, a new hyopthesis on the hormonal control of vitellogenesis inDrosophila is presented. We propose that yolk proteins derived from the fat body are controlled by juvenile hormone, whereas the independent and autonomous vitellogenesis within the ovary itself is controlled by endogenously synthesized ecdysone.     

Leucine aminopeptidase,HlLAP, from the ixodid tick Haemaphysalis longicornis,plays vital roles in the development of oocytes

Female ixodid ticks are amazing invertebrate animals which efficiently convert a large amount of nutrients derived from their ingested blood meals into eggs. Although oocyte development (vitellogenesis) in ticks is triggered by a blood meal and is assumed to be supported by nutrition derived from ovarian cells connecting oocytes, little is known about the ovarian molecules processing nutrient materials for the vitellogenesis. In this study, we have suggested a putative function of leucine aminopeptidase (HlLAP) in the ovary of parthenogenetic adult ixodid tick Haemaphysalis longicornis regarding a negative output of reproduction following disruption of HlLAP gene by RNA interference. Endogenous HlLAP was shown to be localized in the ovarian cells, including ovarian epithelial and pedicel cells which were assumed to provide nutrients for the developing oocytes. Histological studies demonstrated that a majority of immature oocytes in HlLAP gene knockdown ticks were transformed into abnormal morpho-histological oocytes with vacuolated cytoplasm and/or condensed nucleus. Taken together, a reduction of the numbers of laid eggs in the HlLAP gene knockdown ticks may be due to the degeneration of immature oocytes following deprivation of nutrients such as amino acids supplied not only by midgut HlLAP but also by the ovarian HlLAP. Regulation of the tick molecules involved in nutrient metabolism for the reproduction, including blood digestion and vitellogenesis, would help in controlling the tick population and tick-borne pathogens.     

Biological differences in reproductive strategy between the mosquito sibling species Anopheles gambiae sensu stricto and An. quadriannulatus

Females of the afrotropical mosquito species Anopheles gambiae Giles sensu stricto and An. quadriannulatus (Theobald) (Diptera: Culicidae) were studied for the effect of blood meal size and the frequency of blood feeding on reproductive development during the first gonotrophic cycle. To standardize the blood meals, meals were administered by enema in some experiments. The effects of insemination, mosquito size, and metabolic reserves at emergence on egg development were also investigated. Maximum insemination was reached after seven days, varying from 62% in An. quadriannulatus to 95% in An. gambiae and was significantly different (P<0.05) between the two species. Insemination had no effect on feeding success. Females of An. quadriannulatus were significantly larger than An. gambiae females (mean wing size 2.90 ±0.01 mm versus 2.82 ±0.01 mm), but the protein, glycogen, and lipid content of newly emerged females of the two species were not significantly different. Without a blood meal, larger females of both species were significantly more likely to develop oocytes up to Christopher's stage II. With one blood meal, 27% of An. gambiae became pre-gravid and 73% matured eggs. In contrast, all An. quadriannulatus females remained in the pre-gravid stage following ingestion of one blood meal. Vitellogenesis was significantly reduced in smaller-sized pre-gravid An. quadriannulatus compared to larger individuals. When given the opportunity to feed up to three times on three successive days, all females of An. gambiae matured eggs but only 85% of An. quadriannulatus did so. When 1 l of human blood was administered by enema, none of the females of either species developed eggs. With a single enema of 1.5 l of human blood, only An. gambiae developed eggs. A similar result was observed with 1 l and 1.5 l enemas of bovine blood although some An. gambiae also developed eggs with 1 l of blood. Anopheles quadriannulatus developed eggs only when given two 1 l enemas on successive days. However, the percentage of females developing eggs was significantly lower than that of An. gambiae. The implications of these differences in reproductive strategy are discussed in the light of behavioural traits in the field.     

Formation of protein yolk in the eggs of a parasitoid hymenopteran,Nasonia vitripennis (Walker) (Pteromalidae: Hym)

Summary Electron micrograph profiles of developing yolk inclusions in the oöcytes and comparative electrophoresis of the haemolymph of males and females and of mature oöcytes, indicates that a fraction is present in the haemolymph of the females, which does not occur in the haemolymph of the males. Changes occur to the protein fractions from the haemolymph which are passed into the egg. This suggests that the egg synthesises some of its own yolk and does not have a synthetically passive role during vitellogenesis.We would like to thank Professor E. W. Knight-Jones in whose Department the work was done.     

Onset of vitellogenin production and vitellogenesis,and their relationship to changes in the midgut epithelium and oocytes in the tickDermacentor variabilis

InDermacentor variabilis (Say), the onset of vitellogenin production and vitellogenesis (up-take of vitellogenin into oocytes) began during the rapid-engorgement feeding period. Mating was required for both vitellogenin production and vitellogenesis to complete the tick's life cycle. Complete immunological identity, as measured by Ouchterlony's double diffusion test, existed between vitellogenin from the fat body, midgut and hemolymph, and vitellin from the ovaries and eggs. Antivitellin antibody did not react with host hemoglobin nor with fat body, midgut, and ovary extracts from feeding females prior to rapid engorgement, feeding unmated females, or unfed or fed males. Some unmated females fed for 13 days and then hand-detached from the host eventually began oviposition after going through a preoviposition period. In these ticks, organ extracts from the midgut, fat body and ovary reacted with antivitellin antibody. The presence or absence of presumed vitellogenic cells in the midgut and yolk bodies in oocytes corresponded with the presence or absence of vitellogenin and vitellogenesis as measured by Ouchterlony's test. Presumed vitellogenic cells increased in size during the preoviposition period. These cells reached their greatest size during the time when the most eggs were being produced, and then declined in size toward the end of oviposition. Vitellogenin was deposited directly into developing yolk bodies in oocytes and was not processed through lysosomes. Feeding was the process that initiated the formation of eggshell cuticle. Detachment from the host was required for the initiation of oviposition.     

Evidence that the ovaries of Musca domestica do not maintain cyclicity by regulating the corpus allatum.

When the female housefly retains eggs, vitellogenesis in the penultimate oöcytes is suppressed during continued protein feeding. Allatectomy of gravid females or of females with developing oöcytes did not prevent maturation of a second batch of eggs. This result does not support the claim of Adams (1970) that an oöstatic hormone, produced by ovaries with retained eggs, inactivates the corpus allatum (CA) and thereby prevents development of the next batch of eggs.The report of Adams and Hintz (1969) that the CA regulates egg maturation depends on their removal of ring gland, which they incorrectly refer to as ‘allatectomy’. In the present report, removal of the ring gland from 1 day old females suppressed egg development, whereas removal of the CA alone did not. Therefore, sufficient CA hormone for reproduction was secreted within 24 hr of emergence, and it was the removal of the corpus cardiacum, and not the CA, that had prevented egg development in the experiments of Adams and Hintz.     

A Critical Role of the Nuclear Receptor HR3 in Regulation of Gonadotrophic Cycles of the Mosquito Aedes aegypti

The orphan nuclear receptor HR3 is essential for developmental switches during insect development and metamorphosis regulated by 20-hydroxyecdysone (20E). Reproduction of female mosquitoes of the major vector of Dengue fever, Aedes aegypti, is cyclic because of its dependence on blood feeding. 20E is an important hormone regulating vitellogenic events in this mosquito; however, any role for HR3 in 20E-driven reproductive events has not been known. Using RNA interference (RNAi) approach, we demonstrated that Aedes HR3 plays a critical role in a timely termination of expression of the vitellogenin (Vg) gene encoding the major yolk protein precursor. It is also important for downregulation of the Target-of-Rapamycin pathway and activation of programmed autophagy in the Aedes fat body at the end of vitellogenesis. HR3 is critical in activating betaFTZ-F1, EcRB and USPA, the expressions of which are highly elevated at the end of vitellogenesis. RNAi depletion of HR3 (iHR3) prior to the first gonadotrophic cycle affects a normal progression of the second gonadotrophic cycle. Most of ovaries 24 h post second blood meal from iHR3 females in the second cycle were small with follicles that were only slightly different in length from of those of resting stage. In addition, these iHR3 females laid a significantly reduced number of eggs per mosquito as compared to those of iMal and the wild type. Our results indicate an important role of HR3 in regulation of 20E-regulated developmental switches during reproductive cycles of A. aegypti females.     

Annual reproductive cycle based on histological changes in the ovary of the female mosquitofish,Gambusia affinis, in central Japan

To clarify the annual reproductive cycle of wild female mosquitofish,Gambusia affinis, in Mie Prefecture, central Japan, changes in ovarian histology were investigated. Female mosquitofish kept in aquaria under constant temperature (25°C) and photoperiod (16L: 8D) conditions produced successive broods at intervals of 22.1±0.46 days (n=7). Between days 0–3 following parturition, females began active vitellogenesis. Between days 3–5, fully grown oocytes matured and were fertilized, and embryonic development began in the follicles. By day 10, as fertilized eggs continued embryonic development, some oocytes at the oil-droplet stage had begun to accumulate yolk globules for the next gestation. Thus, vitellogenesis of the succeeding batch of oocytes overlaps with gestation during reproduction in the mosquitofish. A rearing experiment showed the annual reproductive cycle of mosquitofish breeding in Nagashima to be as follows. Although oocytes had not at that point developed to the yolk globule stage, copulation occurred in February. Females began vitellogenesis in early May, the first pregnancy of the year commencing in mid-May. From mid-May to August, females repeated the gestation cycle (vitellogenesis, maturation, fertilization, pregnancy and parturition) at around one month intervals. In September, oocyte recruitment from the oil-droplet to the yolk globule stage ceased. After the final parturition, the ovaries contained only non-vitellogenic oocytes. Spermatozoa in the ovarian cavity were scare from November to January.     

Nitrogen partitioning and blood meal utilization by Aedes aegypti (Diptera Culicidae)

The utilization of the blood meal by mosquitoes was investigated by first feeding females quantities of blood ranging from 1 to 5 mg, and then analyzing the faeces for the various by-products of protein catabolism that were subsequently eliminated. The nitrogeneous waste products in order of importance were uric acid, histidine, ammonia and arginine. Only traces of the other amino acids were excreted.The total amount of each faecal substance varied linearly with the quantity of blood ingested, however their relative proportions did not change. Regardless of blood meal size the quantily of uric acid and ammonia produced indicates that about 80% of the non-histidine and arginine amino acids are deaminated and utilized for metabolic purposes other than egg protein synthesis.Most of the histidine and about one half of the arginine content of the blood were excreted as free amino acids, but the other amino acids were lost in trace amounts.Nineteen per cent of the total ingested amino acids was incorporated into soluble yolk proteins and this proportion was constant even for small blood meals that result in a reduction in the numbers of eggs produced.The comparative aspects of nitrogen partitioning and blood meal utilization by haematophagous insects, as well as the factors that affect blood meal utilization and fecundity in A. aegypti are discussed.