Disruption of pupariation and eclosion behavior in the flesh fly, Sarcophaga bullata Parker (Diptera: Sarcophagidae), by venom from the ectoparasitic wasp Nasonia vitripennis (Walker) (Hymenoptera: Pteromalidae)

The action of venom from the ectoparasitic wasp, Nasonia vitripennis, was monitored by examining alterations in patterned muscular movements characteristic of pupariation and eclosion behavior in the flesh fly, Sarcophaga bullata. Venom injected into larvae prior to pupariation caused a dose-dependent delay in pupariation. Eventually, such larvae did pupariate, but puparia were abnormally formed. Barographic records revealed that all elements of pupariation behavior were present in venom-injected larvae, but pupariation behavior was not well synchronized with tanning, thus implying that the venom caused disruption in the temporal organization of central motor programs. When larvae were ligated and injected with venom posterior to the ligature, no response was evident in the posterior region, suggesting that the venom does not directly stimulate muscles or neuromuscular junctions. Injection of exogenous ecdysteroid into venom-injected larvae restored some elements of pupariation behavior, consistent with ecdysone's role in stimulating the release of anterior retraction factor and puparium tanning factor, two factors that are released from the CNS to regulate pupariation. When the venom was injected into newly emerged imagoes, the duration of extrication behavior was shortened, whereas all phases of post-eclosion behavior were lengthened. These observations imply that the venom affects CNS centers that regulate the muscular systems engaged in extrication and post-eclosion behavior.     

The metabolism of 3H-moulting hormone in Calliphora erythrocephala during larval development

The activity in whole insects for converting ³H-α-ecdysone to ³H-β-ecdysone after injection is low (half-maximal) in young last instar larvae, maximal in mature larvae, and minimal (fourth-maximal) at the white puparial stage. Because moulting hormone titre is low throughout the last larval instar and increases at the formation of the puparium it appears that hydroxylation at C-20 is not a key step in regulating β-ecdysone biosynthesis during larval development.The activity for catabolizing ³H-β-ecdysone is maximal in second instar larvae, about thirdmaximal throughout most of the third instar, and minimal at pupariation (thirtieth-maximal). Thus inactivation may play a rôle in regulating moulting hormone titre during larval development.     

beta-ecdysone levels in pharate pupae of the stable fly, Stomoxys calcitrans and interaction with the chitin inhibitor diflubenzuron.

The β-ecdysone titer in pharate pupae of the stable fly, Stomoxys calcitrans (L.), exposed to diflubenzuron [Thompson-Hayward TH 6040; N-[[(4-chlorophenyl)amino]carbonyl]-2,6-difluorobenzamide] as larvae in artificial diet was analyzed by high-pressure liquid chromatography. No significant differences between treated and control groups were found in the β-ecdysone titers within the first 10 hr after pupariation.     

Under-sized larvae from short-day adults of the blow fly, Calliphora vicina, side-step the diapause programme

Abstract. Larvae of Calliphora vicina R.-D. (Diptera: Calliphoridae) hatching from eggs laid by adult females exposed to short day length, and then raised in darkness at 11^oC, normally enter diapause rather than undergoing prompt pupariation. However, if the feeding stage is curtailed by premature extraction of larvae from their food, or if the larvae are subjected to severe overcrowding, smaller larvae side-step the diapause programme to become miniature puparia, whereas larger larvae proceed to diapause as fully-fed ones. In addition, smaller diapausing larvae show a shorter (or less intense) diapause than full-sized larvae. Apart from the smallest individuals, flies can emerge from these miniature puparia and in some cases are capable of laying eggs; this suggests that avoidance of diapause may allow undersized individuals an opportunity to reproduce before winter sets in. Fat determinations performed on larvae and pupae of various sizes, however, showed that short-day (diapause-destined) individuals lay down the same proportion of fat as long-day (non-diapause) individuals, and the same proportion of fat across all size classes. The possible functional significance of this phenomenon is discussed.     

Developmental inhibition of Drosophila suzukii by ionizing radiation

Spotted wing drosophila (SWD) has emerged as a major invasive insect pest of small berry fruits in the Americas and Europe since the late 2000s. Thus, phytosanitary treatment of commodities for export is imperative to prevent the movement of viable SWD to newer areas. In the present study, all developmental stages of SWD were irradiated with different doses of gamma and electron beam radiation to assess developmental inhibition to identify potential quarantine doses of the radiations. Ionizing radiation induced developmental inhibition of all stages of SWD. The effective doses for 99% inhibition (ED₉₉) of hatching, pupariation, and adult emergence from irradiated eggs for gamma radiation were 882, 395 and 39 Gy, respectively, compared with 2849, 687, and 41 Gy, respectively, for electron beam radiation. The ED₉₉ for inhibition of pupariation and adult emergence in irradiated larvae were 703 and 47 Gy, respectively, for gamma radiation, and 619 and 33 Gy, respectively, for electron beam radiation. Pupal irradiation did not completely inhibit adult emergence, even at 300 Gy. However, irradiation with ≥100 Gy of puparia induced adult sterility, with no egg production at all. The ED₉₉ for inhibition of F₁ egg hatchability from adults irradiated with gamma radiation and electron beam radiation was estimated to be 424 and 125 Gy, respectively. The results of the present study suggest that gamma radiation and electron beam radiation are alternatives for phytosanitary treatment. Irradiation with 100 Gy could be suggested as a potential dose for egg, larval, and pupal quarantine treatment of SWD.     

Biosynthesis of alpha-and beta-ecdysone in isolated abdomens of larvae of Musca domestica.

Abdomens of housefly larvae which are isolated before pupariation and injected with labelled or unlabelled cholesterol are shown by bioassay, thin-layer and gas-liquid chromatography, and tracer experiments to synthesize α- and β-ecdysone. Autoradiography of cross-sections of abdomens injected with labelled cholesterol show that oenocytes are intensively labelled. The results are discussed with respect to the validity of the Calliphora or Musca assay for ecdysones.     

Biosynthesis of ecdysones in isolated prothoracic glands and oenocytes of Tenebrio molitor in vitro

Isolated prothoracic glands from Tenebrio larvae synthesize in vitro α-ecdysone, but not β-ecdysone from 4-¹⁴C-cholesterol. Isolated abdominal oenocytes from the larvae synthesize mainly β-ecdysone, but only little α-ecdysone. When prothoracic glands and oenocytes are cultured together, the α-ecdysone derived from the prothoracic glands is oxidized by the oenocytes to β-ecdysone. The newly synthesized hormones are not stored in the cells, but are secreted into the medium if sufficient amounts of non-labelled hormones are present. If no unlabelled hormones are added to the culture medium, the newly formed hormones are converted to a large extent into polar conjugates.     

Der metabolismus von 3H-α-ecdyson bei larven von Tenebrio molitor

The metabolism of ³H-α-ecdysone has been investigated in larvae of Tenebrio molitor within a moulting cycle. The metabolization occurs by hydroxylation, dehydration, and conjugation. A total of 8 metabolites including α- and β-ecdysone were found. Peak I was cleaved enzymatically up to 56%. The hydrolized part consists of esters of sulfuric- and glucuronic acid with compounds II and III, also with α-ecdysone and 3-dehydroecdysterone to a lesser degree.The hydroxylation of α-ecdysone to β-ecdysone is a very rapid one. Velocity and intensity depends on the physiological stage of the larvae. On days with a large endogenous hormone titer they are maximal and on days with a low endogenous titer they are lower. The rate of conversion of α- to β-ecdysone shows a correlation with the endogenous titer and vice versa.At a low endogenous titer the rate of excretion is very strong, in larvae aged to 2 to 5 days and also 7 to 8 days, 8 h after injection 50 to 80% of injected activity was recovered in the faeces. At the beginning of the moulting cycle 3% and at the 6th day 30% (hormone titer maximum) of activity is excreted. The unexpected high rate of excretion at the first day is compensated by increasing metabolism and storage.The faeces mainly consist of conjugates and α- and β-ecdysone. A correlation between the appearance of these compounds and the physiological stage of the larvae could be found. On those days with low endogenous titer the quota of ecdysone (α and β) is higher.     

Rearing of the fruit fly parasitoid Diachasmimorpha longicaudata (Hymenoptera: Braconidae) on X-ray irradiated larvae of Ceratitis capitata (Diptera: Tephritidae)

We evaluated the effects of X-ray irradiation on larvae of Ceratitis capitata (Wiedemann) (Diptera: Tephritidae), with the aim of finding a treatment that prevented adult fly emergence, yet did not adversely affect larval quality as rearing hosts for the parasitoid Diachasmimorpha longicaudata (Ashmead) (Hymenoptera: Ichneumonidae). Two experiments were carried out. In the first experiment, small numbers of larvae were held in Petri dishes with and without small amounts of rearing media and then irradiated with doses of X-rays ranging from 0 to 8333.6 R (equivalent to 80 Gy). In the second experiment, higher numbers of larvae were held in a manner resembling mass-rearing conditions, and were then irradiated with X-rays ranging from 0 to 10,417 R (equivalent to 100 Gy). In both experiments, the only factor that significantly affected fly emergence was irradiation of larvae. Fly emergence decreased markedly as the irradiation dose increased, and complete suppression of fly emergence was achieved at 6250.2 R (equivalent to 60 Gy) when larvae were irradiated in small batches with or without rearing media. Irradiation also affected the fertility of those flies that did emerge following treatment. In the second experiment, we found the parasitoids reared from irradiated larvae produced a higher parasitism rate and a higher number of female offspring than did parasitoids reared from control (non-irradiated) larvae. Mean fecundity of F1 parasitoids reared from irradiated larvae were affected positively by irradiation only at the 8333.6 R (80 Gy) dose. Our results show that X-ray irradiation can be used to inhibit fruit fly adult emergence and that irradiated larvae are at least as good a rearing substrate as non-irradiated larvae. Future studies should focus on the adjustment of our findings to a mass-rearing scale.     

A comparison of the pupariation acceleration activity of pyrokinin-like peptides native to the flesh fly: Which peptide represents the primary pupariation factor?

Five native pyrokinin-like peptides (Neb-PK-1, Neb-PK-2, Neb-PVK-1, [L9]Neb-PVK-2, [I9]Neb-PVK-2) identified in the neuropeptidome of the flesh fly Neobellieria bullata were compared for their quantitative and/or qualitative effects on puparium formation (pupariation). In a standard pupariation bioassay, both Neb-PVK-1 and [I9]Neb-PVK-2 proved inactive, whereas [L9]Neb-PVK-2 demonstrated only weak activity. In contrast, both Neb-PK-1 and Neb-PK-2 demonstrated potent threshold doses, with Neb-PK-2 about 10-fold more active than Neb-PK-1. Analysis of neuromuscular activity during pupariation using a tensiometric technique demonstrates that the two native Neb-PKs accelerate the onset of immobilization and cuticular shrinkage more than motor programs associated with retraction of the anterior segments and longitudinal body contraction. It was further determined that the sensitivity of various components of the pupariation process to these peptides decreases in the following order: immobilization>cuticular shrinkage>motor program for anterior retraction>motor program for longitudinal contraction congruent to tanning of cuticle of the newly formed puparium. A paradoxical situation was observed whereby the motor programs of pupariation are temporally dissociated from actual morphogenesis of the puparium. The tensiometric data suggest that the most likely candidate for a primary pupariation factor is Neb-PK-2, rather than Neb-PK-1.     

Effects of alpha-ecdysone, beta-ecdysone and inokosterone on the in vitro evagination of Drosophila leg discs and the subsequent differentiation of imaginal integumentary structures

The morphogenetic activity of three hormonal substances—α-ecdysone, β-ecdysone, and inokosterone—has been studied in vitro on isolated imaginal leg discs of third-instar larvae of Drosophila melanogaster.In the presence of α-ecdysone (0.3–3 μg/ml) and also of the phytohormone inokosterone (0.3–3 μg/ml), the discs underwent metamorphosis, as characterized by complete evagination (in less than 24 hr), secretion, and shedding (48 hr after explanation) of the pupal cuticle, secretion, and structural differentiation of the imaginal cuticle, namely pigmentation and formation of claws, bristles, and hairs (during days 3–6).In the presence of β-ecdysone (10, 6, 3, 0.3, 0.03, 0.003 μg/ml), evagination was always abnormal and incomplete. With all concentrations but the lowest, the partially everted legs had a swollen appearance and, at all concentrations, the subsequent development was inhibited. No imaginal differentiation occurred at any of the concentrations tested.Larval fat body or larval epidermis added to the isolated discs had no influence on their response to either α-ecdysone or β-ecdysone.Changing the osmotic pressure of the β-ecdysone containing medium likewise did not alter the noxious effect of β-ecdysone.Discs cultured first in the presence of β-ecdysone (for 24 hr), then transferred to fresh medium containing α-ecdysone were unable to undergo normal development. The inhibitory effect of β-ecdysone thus appears to be irreversible.Discs cultured first in the presence of α-ecdysone (for 24, 48 or 72 hr), then transferred to β-ecdysone containing medium, were unable to continue their normal differentiation. Further development was blocked within a few hours after the transfer.Results are discussed in view of results obtained with other in vitro and in vivo cultivation techniques. In conclusion, isolated leg discs of Drosophila are unable to respond physiologically to exogenous β-ecdysone. Only α-ecdysone and inokosterone will induce complete and normal metamorphosis in leg discs cultured in vitro.     

Immunization of lambs against Oesophagostomum columbianum, using irradiated third stage larvae

The effect of gamma irradiation at doses of 40- and 50 kR on the development of third stage larvae of Oesophagostomum columbianum and the protection conferred by these irradiated larvae against the nematode, was studied in 6-8 week old male Kashmir Merino lambs. At 40- and 50 kR doses, the third stage larvae failed to develop to the adult stage in the intestine. Though single vaccination with 2000, 50 kR irradiated larvae failed to protect the animals against the infection, vaccination with the same number of 40 kR irradiated larvae conferred a partial protection. The presence of adult worms of O. columbianum in sites outside the intestine of 6-8 week old lambs have been demonstrated for the first time.     

Inactivation of ecdysone and the possible feed back control of the titre during pupation of Sarcophaga peregrina

Radioactive β-ecdysone injected into mature larvae or pharate pupae of Sarcophaga peregrina was rapidly metabolized, but the decrease in moulting hormone activity in whole animal extracts was much faster than the decrease of radioactivity. The metabolites were extracted, examined by TLC and HPLC and shown to be conjugates of β-ecdysone in larvae (as shown by enzymatic hydrolysis) but 3-epi-β-ecdysone in pupae. These compounds did not exhibit appreciable activity. The process of inactivation by epimerization may be a mechanism of feed back control of ecdysone, since epimerization is induced by ecdysone itself.     

Hormonal requirements for the larval-pupal transformation of the epidermis of Manduca sexta in vitro

In the tobacco hornworm, Manduca sexta, metamorphosis occurs in response to two releases of ecdysone that occur 2 days apart. Epidermis was explanted from feeding final-instar larvae before the first release of ecdysone and was cultured in Grace's medium. When exposed to 1 μg/ml of β-ecdysone for 24 hr and then to hormone-free medium for 24 hr, followed by 5 μg/ml of β-ecdysone for 4 days, the epidermis produced tanned pupal cuticle in vitro. During the first 24 hr of exposure to β-ecdysone, the epidermis first changed its cellular commitment to that for pupal cuticle formation (ET₅₀ = 14 hr), then later (by 22 hr) it became committed to tan that cuticle. Then, for most of the pupal cuticle to be tanned, at least a 12-hr period of culture in hormone-free medium was required before the cuticle synthesis was initiated. Consequently, some events prerequisite to sclerotization of pupal cuticle not only occur during the ecdysone-induced change in commitment but also during the ecdysone-free period. When the tissue was preincubated in 3 μg/ml of juvenile hormone (JH I or a mimic epoxygeranylsesamole) for 3 hr and then exposed to both ecdysone and juvenile hormone for 24 hr, it subsequently formed larval cuticle. The optimal conditions for this larval cuticle formation were exposure to 5 μg/ml of β-ecdysone in the presence of 3 μg/ml of epoxygeranylsesamole for 48 hr. When the epidermis was cultured in Grace's medium for 3 days and then exposed to 5 μg/ml of β-ecdysone for 4 days, 70% of the pieces formed pupal cuticle. By contrast, if both ecdysone and JH were added, 77% formed larval cuticle. Therefore, the change from larval to pupal commitment of the epidermal cells requires not only the absence of JH, but also exposure to ecdysone.     

The appearance of dopa decarboxylase activity in imaginal discs of Sarcophaga bullata, undergoing development in vitro

During the postembryonic development of Sarcophaga bullata, two large peaks of dopa decarboxylase activity were observed. These were associated with the sclerotization (hardening) of the puparium and the adult cuticle, respectively. A small peak of activity 5.5–6.5 days after pupariation was possibly associated with the sclerotization of the prothoracic spiracles.A premature increase in enzyme activity was observed in young, third-instar larvae injected with 20 μg of β-ecdysone. However, the advantage of studying the effect of the hormone on enzyme activity in vitro led to an attempt to induce² dopa decarboxylase in cultured wing discs.In the presence of β-ecdysone, wing discs underwent evagination and a substantial increase in dopa decarboxylase activity was observed in these discs. The enzyme activity began to appear after the rupture of the peripodial membrane and reached a maximum about the time disc evagination ceased. We suggest that this enzyme activity was responsible for the slight sclerotization of a fine cuticle secreted by the discs. The cultured imaginal discs underwent changes that are very similar to those which occur in intact animals. Therefore, this system appears promising for further studies on the role in differentiation of the hormonal control of enzyme activity.     

Pupal cuticle formation by Manduca sexta epidermis in vitro: Patterns of ecdysone sensitivity

During the larval-pupal transformation, various regions of the epidermis of Manduca sexta larvae have previously been found to require different lengths of exposure to the prothoracic glands in order to form pupal cuticle. To distinguish between requirements for differing threshold concentrations of ecdysone and those for differing durations of exposure to ecdysone, wandering stage larval epidermis was cultured in Grace's medium. When most of the thick larval cuticle was removed, the epidermis responded to concentrations of β-ecdysone of 1.0 μ/ml or greater for 4 days by forming cysts which later formed tanned pupal cuticle. No fat body or protein supplement was required. When the larval integument was explanted intact, similar requirements for cuticle formation and for tanning were found. All regions of the fifth abdominal segment required similar concentrations of β-ecdysone (0.4–0.6 μg/ml) for 4 days for 50% to form pupal cuticle, but gin trap epidermis required the least exposure to a threshold concentration of ecdysone (1.5 days in 0.9 μg/ml). The anterior dorsal intersegmental region required about 0.5 day longer, followed by the posterior intersegmental and the dorsal intrasegmental regions. Thus, the duration of exposure seemed more important. About 1 day longer of exposure to ecdysone was required for subsequent tanning of the new cuticle than for cuticle formation, yet tanning of the cuticle did not occur with prolonged exposure to ecdysone.     

The time during which beta-ecdysone is required for the differentiation in vitro and in situ of wing imaginal discs of Drosophila melanogaster.

The time during which β-ecdysone is required for the apolysis and imaginal differentiation of wing discs of Drosophila both in vitro and in situ has been examined, and it is concluded that β-ecdysone is required as a sustained stimulus rather than as a trigger for differentiation. These results are compared with the requirement for β-ecdysone for the puffing of salivary gland polytene chromosomes during the prepupal stage (Richards, G. P., 1976, Develop. Biol.48, 191–195). It is suggested that imaginal discs and larval salivary glands require different exposures to β-ecdysone to fulfill their developmental commitments and that the drop in β-ecdysone titer during the early prepupal stage, which is necessary for the subsequent puffing of the polytene chromosomes, plays little or no part in imaginal disc differentiation.     

Uptake of beta-ecdysone by the fat body and membrane vesicles of fat body cells of Sarcophaga peregrina larvae.

The fat body of Sarcophaga peregrina larvae was shown to incorporate ³H-β-ecdysone when it was incubated with the hormone in vitro. Most of the incorporated radioactivity was found in the cytoplasmic fraction as free β-ecdysone, not as a protein-β-ecdysone complex.Rapid uptake and accumulation of β-ecdysone was observed in the membrane vesicles of fat body cells in vitro. The apparent K_m value for uptake was estimated to be 1·25 × 10^?7 M. The β-ecdysone in the membrane vesicles was rapidly released when 2,4-dinitrophenol was added. These results suggest that β-ecdysone was incorporated into the membrane vesicles by active transport and not by free diffusion. The hormone is probably incorporated into larval tissues by the same mechanism as it is incorporated into the membrane vesicles of fat body cells.     

The rôle of ecdysone in pupation of Manduca sexta

Slow infusions of β-ecdysone are more effective in eliciting a normal physiological response than are discrete injections of the hormone. Infusion of β-ecdysone into final instar larvae in the presence of juvenile hormone (JH) induces apolysis and the deposition of a normal larval cuticle. In the absence of JH larvae display the prodromal symptoms of pupation (exposure of the heart, purging of the gut, etc.) in response to a β-ecdysone infusion. The occurrence of certain covert physiological events that accompany the exposure of the heart are evidently necessary to prepare a larva for pupation. An infusion of β-ecdysone can induce apolysis and pupal cuticle deposition only after the prodromal signs of pupation have become evident. Of the two pulses of ecdysone that normally precede pupation in Manduca, the first is apparently responsible for the genetic switchover from larval to pupal development whereas the second one triggers apolysis and the subsequent events that lead to pupation. Results obtained from infusion experiments in which the dose and exposure time were varied independently are consistent with the idea that ecdysone has to be present for a certain minimum time above a threshold concentration to induce a physiological response. The requisite exposure time is apparently not dose-dependent.     

The apparent requirement of two hormones, alpha- and beta-ecdysone, for molting induction in insects

Puff formations at loci I-18-C and IV-2-B of the salivary gland chromosomes are early indications of a beginning molting process in Chironomus tentans larvae. The effectiveness of the two ecdysone analogs, α- and β-ecdysone, in inducing these puffs was compared. Incubation of salivary glands in vitro with β-ecdysone causes only puff IV-2-B to appear; incubation with α-ecdysone stimulates initially puffing at only I-18-C. After an injection of α-ecdysone, puffing at I-18-C begins within less than 15 min, whereas puffing at IV-2-B is delayed for more than 30 min. Following an injection of β-ecdysone, puffing at IV-2-B begins within less than 15 min, whereas puffing at I-18-C is delayed. Injected ³H-α-ecdysone is converted to β-ecdysone and a polar compound. Injected ³H-β-ecdysone is converted to a compound less polar than α-ecdysone and a polar metabolite which stimulates puffing at I-18-C, like α-ecdysone. It is suggested that the two ecdysones have different targets in the cell, that they can be rapidly converted to compounds with the activity of the other analog, and that the induction of a complete molt requires the action of both hormones.