Isolement,action biologique et evolution des substances paragoniales contenues dans le spermatophore d'Acanthoscelides obtectus (Coleoptère)

In Acanthoscelides obtectus, some male secretions deposited in the spermatophore during mating reach the blood of the females and stimulate oögenesis. Water extracts from spermatophores injected into a female abdomen stimulate oögenesis but do not influence egg-laying or sexual receptivity. After column chromatograph of spermatophores, aqueous extracts on Sephadex G 25 Coarse, G 25 Superfine, and G 15, an active fraction has been isolated. This injected into the abdomen of virgin females stimulates oögenesis at low concentrations, but it is toxic at higher concentrations. This fraction was examined by paper electrophoresis at low voltage and then chromatographed on G 10 Sephadex. Two peaks were obtained: the first corresponds to the paragonial substance A which stimulates oögenesis at 0,2 10^?3 μg/μl concentration. The second contains the paragonial substance B. At a 0,3 10^?3 ug/μl concentration this substance is toxic. First this toxicity inhibits oögenesis and then causes the death of most females at higher concentrations. The toxic effect appears 2 or 3 days after injection. These two substances are purified on paper chromatography and the biological activities are contained in a zone of R_f 0.25 to 0.45 (paragonial substance A) and in a zone of 0.16–0.30 R_f (paragonial substance B).The paragonial substances disappear from the spermatophore after mating. Aqueous extracts of spermatophores obtained 6 hr after mating do not stimulate oögenesis and do not have any toxic effect. The chemical nature of these both fractions is not yet determined because the quantity of extracts obtained at the end of the purification is very low.The action of both paragonial substances is similar to the action of hormones. The paragonial substances influence unknown receptors at low concentration after a latent period. The origin of the paragonial B substance was not determined, but this substance which inhibits oögenesis at low concentrations could be an antagonist of paragonial A substance.     

Abdominal distention terminates subsequent host-seeking behaviour of Aedes aegypti following a blood meal

The failure of Aedes aegypti females to engage in host-seeking behaviour following a replete blood meal was investigated. Abdominal distention appears to be responsible for this immediate inhibition after feeding. Large enemas of saline had the same effect as blood in terminating host-seeking; this was not due merely to the presence of large amounts of fluid, but rather to the distention produced by these liquids. Since transection of the ventral nerve cord anterior to the 2nd abdominal ganglion did not release the inhibition in blood-fed females, we restricted the degree of distention of abdominal segments with wax. Distention of the abdomen anteriorly by a blood meal more effectively inhibited host-seeking than did distention posteriorly, suggesting that stretch receptors in the anterior portion of the abdomen regulate the response towards a host.     

Diuresis after a bloodmeal in female Anopheles freeborni

Female Anopheles freeborni discharge urine rapidly and copiously for a brief time after taking a meal of blood. This diuresis begins immediately upon cessation of feeding and continues for about 30 min at a constant rate. A decline in this rate follows and diuresis is completed by 50 min after feeding. This time-course of diuresis is independent of the size of the meal; diuresis after large meals occures at a higher rate, not over a longer time, than diuresis after small meals. Heat-stable and saline-soluble substances that induce rapid excretion by isolated Malpighian tubules can be extracted from the head and thoracic nervous system, suggesting the presence of a neurosecretory diuretic hormone similar to that found in other blood-sucking insects. Decapitation or section of the ventral nerve cord abolishes the rapid phase of diuresis after a bloodmeal. Therefore, in analogy to the situation in the tsetse fly, the head is required either as the source of a diuretic hormone or as link in the pathway that stimulates its release.     

Vitellin and vitellogenin concentrations during oögenesis in the first gonotrophic cycle of the house fly,Musca domestica

The house fly, Musca domestica, contains at least two native vitellin and two vitellogenin proteins. Both vitellins appear to have an identical vitellogenin partner. The major native vitellin has a mol. wt of 281 K Daltons, and the major native vitellogenin has a mol. wt of 283 K Daltons. These proteins are composed of three subunits with mol. wt of 48, 45 and 40 K Daltons. The relationship of the subunits to the native proteins is not known.Haemolymph vitellogenin levels are cyclical during oögenesis with no detectable amounts in previtellogenic flies and low levels in postvitellogenic flies. The highest level of vitellogenin, 10.5 μg/μl, occurred in flies with stage-7 ovaries. The vitellogenin levels during oögenesis fit a parabolic curve and the fat body vitellogenin content during oögenesis showed this same pattern.Uptake of vitellogenin into the ovary during each stage of oögenesis also fit a parabolic curve and produced a high linear correlation with haemolymph vitellogenin levels. The greatest uptake was 37 μg/stage and occurred during stage 6.     

Ecdysone,juvenile hormone and oögenesis in Rhodnius prolixus

Oviposition and oögenesis can be inhibited in female Rhodnius prolixus by ecdysone given by the digestive tract. The inhibition is dose-dependent, and doses higher than 4.0 ng ecdysone/mg body weight drastically reduce the size and shape of the whole ovaries. In ecdysone-treated insects, normal oviposition and oögenesis can be re-established by a subsequent blood meal without ecdysone, or by the application of a juvenile hormone analogue.These results suggest that ecdysone inhibits juvenile hormone production.     

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).     

Vitellogenin synthesis in blood-fed Aedes aegypti in the absence of the head,thorax and ovaries

A blood meal initiates oöcyte maturation in Aedes aegypti, and we have used rocket immunoelectrophoresis to investigate the function of midgut, ovaries, and head in the onset of vitellogenin synthesis. Non-blood-fed females and those fed blood (by enema) containing soybean trypsin inhibitor never contained vitellogenin. This demonstrates that the pressure of an undigested blood meal on stretch receptors of the midgut plays no role in the induction of vitellogenin synthesis, rather the stimulus is a digestion product of blood.When females were ovariectomized or decapitated and then fed blood, the haemolymph contained newly synthesized vitellogenin 24 h later. This was also demonstrated in isolated ovariectomized abdomens. Apparently, induction of vitellogenin synthesis does not require factors from either the head, thorax, or ovaries. When ovariectomy or decapitation was postponed after a blood meal, the level of vitellogenin in the haemolymph rose. Therefore, interaction of factors from the head and ovaries maintain the synthesis needed for oöcyte maturation.     

Dynamics of vitellogenin uptake in Aedes aegypti as demonstrated by trypan blue

Trypan blue has been shown to be a reliable indicator of the micropinocytotic uptake of vitellogenin by developing oöcytes. Trypan blue was injected into the mosquito Aedes aegypti to determine at what times after the blood meal vitellogenin was taken up. Histological sections examined by light microscopy showed that trypan blue began to be sequestered from 2 to 5 hr after the blood meal. Any association between dye and ovariole ended from 39 to 42 hr after the blood meal, in which period no dye was incorporated into spheres of yolk protein. Of the times investigated in this experiment, the greatest amount of dye was seen in the oöcyte at 24 hr after the blood meal. The onset and conclusion of trypan blue uptake correspond with the related events in the synthesis of vitellogenin by the fat body. The presence of trypan blue in occasional interfollicular spaces suggests that the route of entry of vitellogenin in Aedes aegypti is indeed an interfollicular one.     

Juvenile hormone control of oögenesis in bumblebee workers, Bombus terrestris

In queenright workers of Bombus terrestris oögenesis is inhibited by the queen, the activity of the corpora allata is suppressed, and the resulting JH titer in the haemolymph remains low. In contrast, in queenless workers the JH production is stimulated on the first day of adult emergence, the JH titer increases, and eggs are rapidly formed. After injection of JH I in newly emerged workers oögenesis can also be induced in the presence of a queen in the same way as in queenless workers. The induced oögenesis is JH dosage dependent, dosages of less than 8 μg stimulate the production of vitellogenins, whereas a complete oögenesis can be induced by high dosages of about 50 μg. From studies on the rate of JH excretion it can be concluded that such high dosages must be injected to obtain the required JH titer during the whole egg maturation of 5 days. It is evident, therefore, that the initiation and the maintenance of oögenesis depends on JH.The injected JH ester is completely degraded to JH acid and JH diol mainly in the hindgut. The excretion starts quickly after the injection, but only traces of unchanged JH are excreted.From these results it can be suggested that a queen inhibits egg maturation in workers by suppressing the JH production in the corpora allata and thus lowering the JH titer. This influence also enables a queen to block oögenesis once stimulated, for instance in queenless workers. Breakdown of JH and excretion are not under the control of the queen and therefore neither of them play any rôle in regulating egg maturation in the worker caste.     

Mosquito reproduction: Incomplete utilization of the blood meal protein for oögenesis

Fecundity, measured by utilization of dietary protein for the production ofyolk protein was examined in several mosquito species (A. aegypti, A. simpsoni, A. atropalpus, A. triseriatus) using blood from eight vertebrate hosts over a whole range of biological blood mean volumes. All experimental blood meals were injected by enema in measured amounts. The total ovarian and excretory nitrogen produced during each gonotrophic cycle was quantified.Blood proteins are utilized for oögenesis only to a limited extent: two thirds, at the most, are detectable in the mature ovaries. This efficiency decreases with increasing blood meal size to about one fifth. The nitrogen content of each mature egg is constant and species-specific, irrespective of blood meal size or source.There are no significant differences in the efficiency of conversion of protein from different types of vertebrate blood into oöcyte protein except for human blood which led to a drastically reduced efficiency. This is shown to be due to a lack of isoleucine which is essential for reproduction. Hominid primates lack this amino acid in their haemoglobin molecule and it exists at a low titre in human plasma. Apparently, in other vertebrates the amino acids are better balanced in the haemoglobin or, can be mobilized in sufficient amounts from various non-haemoglobin protein fractions.All blood protein is catabolized and the excess nitrogen excreted quantitatively; excretory nitrogen therefore reflects the quantitative demands of a gonotrophic cycle. These processes are not dependent upon receiving a mating stimulus.     

Rate of follicle growth,change in follicle volume and stages of macromolecular synthesis during ovarian development in Musca domestica

At 21°C the first egg generation takes 6 days to develop. During this period the oöcyte volume increases by a factor of ×5000, and compared with an oögonium the growth factor amounts to ×100,000. The growth rate of the oöcyte increases with each stage of oögenesis, until at stage 5 it reaches 2.5 × 10⁶ μm³/hr. About 35% of the substance stored in the oöcyte originates from the nurse chamber. 30% of the volume is formed in the stage where the oöcyte synthesizes almost exclusively glycogen. Accordingly, about 30% of the volume is provided by the euplasmatic protein synthesis and by the yolk uptake.     

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.     

Hormonal aspects of oögenesis in the flies Phormia regina and Sarcophaga bullata

The corpora allata (CA) and median neurosecretory cells (MNC) of Phormia regina and Sarcophaga bullata become active with increasing age of the fly, on a diet of sugar alone. To prevent or retard oögenesis the CA or MNCs must be removed shortly after emergence, with subsequent protein meals. Topical JH application partially compensates for CA or MNC removal. This shows that the MNC activate the CA, and not vice versa. The trauma of either operation slightly depresses egg development.Injection of ecdysone into both species in the stage of initial yolk deposition causes the primary oöcytes to degenerate. This leads to development of the penultimate oöcytes. Older and younger egg stages are not sensitive to ecdysone. In P. regina the application of JH to females with developing primary oöcytes stimulates yolk deposition in the penultimate oöcytes.     

Endocrine control of oögenesis in the housefly,Musca domestica vicina

The endocrine system involved in the control of oögenesis in the housefly, Musca domestica vicina, was investigated. Allatectomy, decapitation, and starvation of newly emerged females resulted in inhibition of oögenesis, showing a close relationship between enlargement of the corpus allatum and growth of follicles during the first oögenesis. Histological observation of sexually matured females showed active secretion of the corpus allatum and the medial neurosecretory cells of pars intercerebralis. Topical application of juvenile hormone analogues (JHA) to the allatectomized fly induced the growth of ovary, and critical doses of methoprene and methyl-7, 11-diethyl-juvenate for the maturation of the ovary were determined. JHA stimulated initiationof oögenesis in the starved or decapitated flies as well as vitellogenesis in the sugar-fed one; subsequently it was found that juvenile hormone acted not only as a gonadotropin but also as a regulator of vitellogenesis. Furthermore, JHA stimulated cell lysis in pupal fat body of female flies, indicating a possible influence of juvenile hormone upon the process of releasing vitellogenin.     

Inhibition of oöcyte development during pregnancy in the cockroach Eublaberus posticus

The corpora allata are inhibited during pregnancy in ovoviviparous Eublaberus posticus, and yolk is not deposited in the basal oöcytes for the entire or almost the entire gestation period.Precocious oöcyte development occurs if the oötheca is removed but this can be prevented by substituting a plastic oötheca for the true egg case in the uterus. Implantation of a uterus containing an oötheca into the abdomen of a female whose oötheca is removed does not prevent precocious oöcyte development even though many of the eggs in the implant grow and stretch the donor uterus. These experiments argue against the hypothesis that an ‘agent’ from the uterine eggs or stretched uterus inhibits the activity of the corpora allata (CA), and supports the hypothesis that inhibition from the uterus is mechanical.Cyclical activity of neurosecretory cells in certain abdominal ganglia in one species of ovoviviparous cockroach has been correlated with the cyclical inhibition of the oöcytes during pregnancy. Mechanoreceptors are found in the uteri of several ovoviviparous species including Eublaberus.In Eublaberus transecting the nerve cord between various ganglia in pregnant females only results in a marked decrease in the percentage of famales showing precocious oöcyte development when the nerves posterior to the sixth abdominal ganglion are severed. However, the results are the same if these nerves are severed after removing the oötheca. It is suggested that pressure of the oötheca on mechanoreceptors in the uterus, or cessation of pressure (after removal of the oötheca), result in sensory information being transmitted to the last abdominal ganglion which affect the CA, perhaps indirectly by controlling the activity of the neurosecretory cells in various abdominal ganglia.     

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 endocrine basis of reproductive inactivity in Monarch butterflies overwintering in central California

Monarch butterflies (Danaus plexippus) collected during winter in central California are reproductively inactive. Oögenesis is stimulated in such animals by environments simulating summer conditions. Allatectomized or neck-ligatured winter animals do not normally undergo oögenesis when placed in summer conditions, but apparently normal oögenesis occurs if they are injected with juvenile hormone isomers. Injections of such isomers into winter animals held in environments simulating winter also promote oögenesis, even though winter conditions typically inhibit ovarian development. Reproductive dormany in winter Monarchs of central California therefore appears to be due (at least partially) to environmentally induced inactivity of the corpora allata.     

Haemolymph ecdysteroid in the housefly,Musca domestica,during oögenesis and its relationship with vitellogenin levels

Ecdysteroid titre in the haemolymph of the housefly, Musca domestica, cycled during oögenesis and peaked at ～50 pg/μl during stages 5, 6 and 7. Levels of 10–20 pg/μl were found in houseflies with pre- and post-vitellogenic ovaries. Removal of the corpus allatum and corpus cardiacum complex resulted in low ecdysteroid levels (10 pg/μl). Ovariectomized flies also had lower ecdysteroid levels than the controls at 2 days (5 pg/μl) after emergence but not at 6 days (22 pg/μl). It is possible that the ecdysteroid peak that occurred during stages 5, 6 and 7 was produced by the ovaries because ovaries secreted and synthesized ecdysteroid in vitro. Endogenous haemolymph ecdysteroid levels had a linear correlation with the amount of vitellogenin that held for hormone concentrations of 5–43 pg/μl. Furthermore, the injection of 20-hydroxyecdysone at doses of 10 ng?1.0 μg/fly increased the amount of vitellogenin from 6 h to 12 h after injection; by 24 h, the vitellogenin returned to control levels. When 20-hydroxyecdysone was injected into ovariectomized flies, it was rapidly degraded and 96% was cleared from the haemolymph within 1 h.     

Some aspects of oögenesis in the stable fly Stomoxys calcitrans (Diptera: Muscidae)

Two distinct patterns of blood ingestion in the female stable fly, Stomoxys calcitrans L. were observed, based on whether or not the female was mated. Mating is not required for oögenesis, but is necessary for oviposition. Virgin females develop eggs but, in the absence of mating, they retain eggs until death. In stable flies, oögenesis appears to be atypical among other dipterans as the penultimate follicles develop and deposit up to 50% yolk before the terminal follicles are matured. Oösorption was seen in the penultimate follicles of virgin females retaining eggs. Accessory-gland implants initiated oviposition in virgin females. However, the total number of eggs laid by such females was 50% less than the number of eggs laid by mated flies.     

Uptake of vitellogenin into developing oöcytes of Locusta migratoria

The selective incorporation of vitellogenin into developing locust oöcytes was studied using ¹²⁵I-vitellin. Vitellogenin incorporation does not start before the oöcytes are 1.5 mm in length. It increases rapidly up to a maximum at 4.7 mm oöcyte length and decreases steadily until the eggs are fully developed (6.5 mm). Concentrations of serum proteins and vitellogenin in the haemolymph show parallel changes, vitellogenin titre reaching a maximum of 7.5 mg/ml. Incorporation rates for vitellogenin increase from 1.5 μg/hr/oöcyte (2.2 mm) up to 13.8 μg/hr/oöcyte (4.7 mm). In this range incorporation per unit surface area increases 4-fold. While the vitelline and chorionic membranes are being formed, the incorporation rates as well as the protein concentrations in the haemolymph decrease steadily until the second gonotrophic cycle starts. The hormonal basis for oögenesis and the mechanism for selective uptake of locust vitellogenin are discussed.