A common pathway for metabolism of 4-hydroxybenzylglucosinolate in Pieris and Anthocaris (Lepidoptera: Pieridae)

Caterpillars of Pieris rapae L. (Lepidoptera: Pieridae) convert 4-hydroxybenzylglucosinolate (sinalbin) in brassicaceous plants into 4-hydroxybenzylcyanide sulfate (HBC sulfate), with 4-hydroxybenzylcyanide (HBC) as intermediate. This apparently serves as a detoxification, because alternative formation of a mustard oil is avoided. We confirmed the capacity of P. rapae to convert the intermediate HBC into HBC sulfate. Four additional Pieridae – Anthocaris cardamines L., Pieris virginiensis Harris, Pieris napi oleracea Edwards and Pieris brassicae L., likewise excreted HBC sulfate after ingesting leaves with topically added HBC or leaves naturally containing sinalbin and myrosinase, but not after ingesting control leaves devoid of HBC and sinalbin. We confirmed the capacity of the most distantly related pierid species (A. cardamines) for converting ingested (topically added) sinalbin into HBC sulfate. Larvae of two non-pierid Brassicaceae-feeding insects, the oligophagous sawfly Athalia rosae L. (Hymenoptera: Tenthrenidae) and the polyphagous moth Spodoptera frugiperda (Smith) (Lepidoptera: Noctuidae), did not excrete HBC sulfate after ingesting sinalbin-containing leaves or topically added HBC.     

Daily changes of neurosecretory type-II cell structure of Pieris larvae entrained by short and long days

The neurosecretory type-II cell (NS-II cell) group of each brain hemisphere consists of three kinds of cells: two small cells, six large ones, and two others having characteristic vacuolated endoplasmic reticulum (ER).Ultrastructural changes of large NS-II cells were observed through the fifth instar and diurnally when short-day and long-day larvae were compared. There were little differences between short-day and long-day larvae in cell structures on corresponding developmental days except for daily changes, but remarkable changes were observed every day through the instar. A secretory cycle through the instar was supposed being based on the ultrastructural changes in NS-II cells: reduced secretory activity on the first day, formation of organelles necessary for the synthesis of secretory materials throughout the instar on the second day, active synthesis and secretion of secretory material during the middle stage (third-fourth day), and reversion to a reduced level of cell activity after the cessation of feeding.In short-day larvae on the third to fourth day, NS-II cells contained large aggregates of secretory granules during the day except for the time of 13 hr after the onset of photophase when a decrease of secretory granules occurred. In long-day larvae, only a small amount of secretory granules was observed at 8 and 13 hr after the onset. Rough ER changed daily paralleling with the quantitative change of the secretory granules.Based on these differences of daily changes in NS-II cell activity between short-day and long-day larvae, it was concluded that photoperiodic time measurement of diapause induction depends on the daily secretory cycle entrained by the photoperiods during the larval stage.     

Lipid metabolism of the male crab Pachygrapsus marmoratus during the moulting cycle

The moult induces important variations in the concentrations and fatty acid composition of lipid classes during the moulting cycle of the male crab Pachygrapsus marmoratus. Phospholipids are the predominant lipid class. The high levels in total saturated fatty acids but also in oleic and palmitic acids result of the semi-terrestrial ethology of this grapsidae. The hepatopancreas presents the most notable variations in the lipid concentration during the moulting cycle. Transport of hepatopancreatic lipids through the hemolymph to the periphery occurs during the end of premolt, just before the new tissues constitution.     

Ecdysone metabolism and endogenous moulting hormone titre during larval-pupal development in Choristoneura fumiferana

The titre and metabolism of ecdysone were studied in the last larval instar of the spruce budworm, Choristoneura fumiferana. Both in males and females a distinct ecdysone peak is present just before ecdysis. Injection of radioactive α-ecdysone into the insect when the endogenous level is low results in the transformation of most of the injected hormone into 3-dehydro-α-ecdysone and conjugates, with very little conversion to β-ecdysone. Whereas when the labelled material is administered when the endogenous level is high, the α-ecdysone is for the most part converted to β-ecdysone. The significance of the correlation between the endogenous titre of ecdysone and the metabolism of injected α-ecdysone is discussed.     

Stretch-induced moulting in Oncopeltus fasciatus

Fifth instar nymphs of Oncopeltus fasciatus initiate a moulting cycle when they reach a critical weight of 27.9±1.1 (±S.D.) mg for females or 23.7±1.2 mg for males. This critical weight is not absolute. Its precise value depends on the somatic size of the individual. Large-bodied individuals have a higher critical weight than small-bodied ones. Sexual size-dimorphism accounts largely for sex differences in critical weights. Animals of a subcritical weight can be induced to moult by means of a saline injection, in the absence of further food intake or growth. Since a saline injection only stretches the abdominal wall it is suggested that moulting in Oncopeltus is triggered by stimulation of abdominal stretch receptors, as in bloodsucking Reduviidae. The critical weight is thus an index of the size at which a critical degree of stretch is achieved.     

Changes in lipid and protein during starvation and the moulting cycle in the tiger prawn, Penaeus esculentus Haswell

Tiger prawns, Penaeus esculentus Haswell (mean wt 20.8 ± 0.3 g, range 13.9–27.7 g) contained 1–2% extractable lipid, 13% protein (biuret method) and 71–74% water (wet wt). In 21 days, the weight of fed prawns increased by 3% and that of starved prawns decreased by 4.4%. Protein was the major energy source during 14 days of starvation, with a loss of 550 mg of total protein compared with a loss of 84 mg of total lipid. The absolute amount of water present remained constant. Of three different tissue compartments, abdomen, cephalothorax, and digestive gland, the abdomen contributed the most protein (330 mg) and lipid (35 mg) during 14 days of starvation. Digestive gland, although containing the largest percentage wet wt of lipid, accounted for only 8.3% of the total lipid in the prawn, and contributed only 18 mg of lipid in 14 days of starvation. Lipid concentration in the digestive gland increased during early premoult (stage D₄) and dropped in late premoult (stage D₄). Resting oxygen consumption rate remained constant at ≈0.1 ml · g^?1 · h^?1 at 25°C during 21 days of starvation.     

Resistance of Apanteles eggs to the haemocytic encapsulation by their habitual host, Pieris

The calyx fluid in the lateral oviduct of a gregarious parasitoid, Apanteles glomeratus contained ellipsoid particles of ca. 130 × 200 nm. These calyx fluid particles did not appear to be embedded in a fibrous outer layer on the surface of eggs in the lateral oviduct. They were not observed on the surfaces of the eggs 3 to 4 hr after being deposited into the host haemocoele. Oviposition experiments indicated that the occurrence of haemocytic defence reactions of the late 2nd instar larvae of the Pieris rapae crucivora against 1 st instar larvae of the parasitoid increased with a decreasing number of the parasitoid eggs introduced into a host, and that more than 5 to 9 parasitoid eggs were needed for suppressing the ability of the host to encapsulate its parasitoid larvae immediately after hatching. When eggs with calyx fluid obtained from egg reservoir were injected into the host, they were found to be encapsulated 1 to 2 days after the injection. They could not start their embryonic development. When calyx fluid-free 3-hr-old eggs were injected in a number of more than 5 eggs into a 5th instar larva of Pieris, 58% of 31 eggs injected had normally hatched without evoking encapsulation reactions by the host. Both electron microscopic observations of parasitoid eggs in the host haemocoele and the experimental results suggested that calyx fluid or calyx fluid particles of the parasitoid might not be involved in the encapsulation-inhibiting activity of the parasitoid eggs. Rather it was anticipated that a substance (or substances) might be secreted by the parasitoid eggs into the haemocoele of the host, which suppressed defence reactions of the host.     

Oesophagostomum radiatum: Glucose metabolism of larvae grown in vitro and adults grown in vivo

Larval stages of Oesophagostomum radiatum grown in vitro and adults grown in vivo were incubated in complex media or in a simple salt solution containing radioactive glucose. Glucose disappearance and end product accumulation of third-stage larvae in a simple salt solution indicated that they excreted CO₂ and acetic, propionic, and lactic acids. Larvae in third molt, fourth stage, and adults all excreted CO₂, acetic, propionic, and lactic acids at twice the rate of third-stage larvae plus an additional product, methylbutyric acid. Carbon dioxide arose primarily from the 3 or 4 carbons of glucose. An anaerobic atmosphere (95% N₂:5% CO₂) had no apparent effect on metabolism. When incubation was done in complex media, isobutyric and 3-methylbutyric acids were seen as major excretion products (10 and 24%, respectively). However, these acids were quantitatively minor when incubations took place in simple salts-glucose medium (1 and 0–3%, respectively).     

Control of moulting in the house cricket, Acheta domesticus

Last-instar Acheta domesticus moulted 7–8 days after the beginning of feeding, following ecdysis, or following starvation. Two full days of feeding were required for commitment to moult, and the minimal food consumption was estimated at 80–110 mg. All day-0 larvae weighing 200 mg, that achieved a critical weight of 280–300 mg after 48 hr of feeding, moulted. Two kinds of experiments indicated that an approximate 50% increase in wet-weight gain was required for a commitment to moult, which occurred at the end of the second day of feeding. Neck ligatures indicated that a head factor, presumably prothoracicotropic hormone, (PTTH), was released during the third day after the beginning of feeding provided the critical weight was achieved. Neither PTTH release nor ecdysis appeared to be under photoperiodic control in Acheta.     

Neuroendocrine control of moulting cycle in mealworms: Bioassay of moulting hormone

The moulting hormone content of mealworm homogenates was determined by injection of partially purified fractions into abdomens of mature larvae of Musca domestica. In mealworms with a 12-day interval between ecdyses, moulting hormone was at a maximum at 8 days.     

Seasonal production of moulting hormone in the barnacle Semibalanus balanoides

An analytical procedure for the quantification of ecdysteroids (crustacean moulting hormone) in barnacles was devised so that minimum sample size could be used. A combination of solvent partitions, Sephadex chromatography, silylation and gas chromatography with electron capture detection was devised, enabling ecdysteroids to be determined down to 20 pg. This was used to determine the amount of moulting hormone in a population of barnacles over a 30 month period. Levels varied from barely detectable in winter months to a maximum value of 1.5 μg kg^− 1 of wet weight of barnacles in September. Polar conjugates of 20-hydroxyecdysone were detected only during the winter months. The number of barnacles moulting at any time corresponded roughly to the titre of hormone present at that time.     

Changes in blood serum protein levels during the moulting cycle of the lobster, Homarus gammarus (L.)

The blood serum protein level of lobsters kept in a stable environment rose from a mean value of 36.5 μg protein/ml of blood shortly after moulting to about 70 μg/ml in the first 40 % of the moult cycle; in the next 30 % of the cycle there was little change but in the last 30 % the mean blood protein level rose to ≈ 85 μg/ml. It is concluded that the variation in blood protein level between lobsters is too great at any stage of the moulting cycle for the technique to give an indication of the onset of moulting.     

Growth and moulting in nematodes: Changes in the dimensions and morphology of Rotylenchulus reniformis from start to finish of moulting

At a temperature of 24°C, freshly hatched second stage larvae (L₂) of Rotylenchulus reniformis take 2 weeks to complete moulting and become either adult males or immature females. Measurements of different nematode stages were made using a computer-interfaced digitizer (CID). This proved to be more rapid and reproducible than conventional techniques.Moulting and development were followed in individual living specimens viewed under Nomarski optics and oil immersion. The mean loss in body volume of these specimens from L₂ to immature female is about 17% compared with about 19% for the mean loss in body volume from L₂ to male. The mean volumes for a total of 70 randomly selected living specimens measured are 95·6 pi for L₂s, 72·9 pl for immature females and 74·2 pl for males. Mean losses in body volume during moulting calculated from these randomly selected stages were slightly higher than those observed for individuals, being about 24% for the immature female and about 22% for the male.     

Importance of the methyl-citrate cycle on glycerol metabolism in the yeast Yarrowia lipolytica

A novel approach to trigger lipid accumulation and/or citrate production in vivo through the inactivation of the 2-methyl-citrate dehydratase in Yarrowia lipolytica was developed. In nitrogen-limited cultures with biodiesel-derived glycerol utilized as substrate, the Δphd1 mutant (JMY1203) produced 57.7 g/L of total citrate, 1.6-fold more than the wild-type strain, with a concomitant glycerol to citrate yield of 0.91 g/g. Storage lipid in cells increased at the early growth stages, suggesting that inactivation of the 2-methyl-citrate dehydratase would mimic nitrogen limitation. Thus, a trial of JMY1203 strain was performed with glycerol under nitrogen-excess conditions. Compared with the equivalent nitrogen-limited culture, significant quantities of lipid (up to ∼31% w/w in dry weight, 1.6-fold higher than the nitrogen-limited experiment) were produced. Also, non-negligible quantities of citric acid (up to ∼26 g/L, though 0.57-fold lower than the nitrogen-limited experiment) were produced, despite remarkable nitrogen presence into the medium, indicating the construction of phenotype that constitutively accumulated lipid and secreted citrate in Y. lipolytica during growth on waste glycerol utilized as substrate.     

Effect of the venom of the gregarious parasitoid Apanteles glomeratus on its hemocytic encapsulation by the host, Pieris

When eggs from the lateral oviduct of the gregarious parasitoid Apanteles glomeratus were injected with calyx fluid and venom apparatus material into host larvae, Pieris rapae crucivora, most of the eggs were not encapsulated. Apanteles eggs deposited by the parasitoid from which the venom apparatus was removed were usually encapsulated by the host. These results indicate that the parasitoid venom apparatus material is an important factor in suppressing the encapsulation of 1- or 2-day-old eggs in the host. In order to clearly demonstrate that the venom suppresses egg encapsulation but not the encapsulation of other foreign objects, DEAE-Sephadex A-50 ion-exchange particles stained with 0.001% (w/v) Congo Red solution were injected into hosts together with venom apparatus material. The Sephadex particles were encapsulated by host hemocytes. The results suggest that the venom does not inhibit the encapsulation ability of the host.     

In vitro stimulation of cell death in the moulting glands of Oncopeltus fasciatus by 20-hydroxyecdysone

The moulting glands of the milkweed bug, Oncopeltus fasciatus, normally degenerate just before the time of ecdysis to an adult (day 7 of the fifth instar). Morphologically normal cell death can be prematurely stimulated in vitro by 20-hydroxyecdysone. Breakdown is triggered by a 24-hr period of exposure to 20-hydroxyecdysone, but an additional incubation period is required before clear signs of degeneration are manifested. Glands removed after the onset of endogenous ecdysteroid secretion degenerate in vitro in the absence of added hormones. Thus, in the moulting glands of Oncopeltus, ecdysteroids appear to act as an important trigger for metamorphic cell death.     

Structure of the toad epidermis during the moulting cycle

Summary Skin samples were taken from 17 toads (Bufo bufo) in various phases of the moulting cycle. The phase was determined by recording a number of moulting intervals prior to sacrifice and by study of the macroscopic appearance of the skin and the moulting behaviour at sacrifice. Eight of the toads were in the moult when the samples were taken.Characteristic morphological changes were found to be restricted to a period immediately prior to and after shedding of the slough. Chemical changes of the membranes of stratum corneum (or material adhered to them) were observed already prior to adoption of the moulting posture. The separation from the underlying epidermis prior to shedding was accompanied by a swelling of the stratum corneum cells. After final detachment of the slough the replacement layer was differentiated into a new stratum corneum within 24 hours. Significant changes in the morphology of the flask cells were not observed.The findings are discussed with emphasis on the processes of separation and differentiation of the stratum corneum. Based on the morphology of the epidermis the following terminology is proposed for the phases of the moulting cycle: Intermoult phase, preparation phase, early shedding phase, late shedding phase, and differentiation phase.The authors wish to thank professor C.B. Jørgensen, Dr. D. P. Knight and Dr. E.H. Larsen for valuable discussions. The technical assistance of Miss Susanne Binzer and Mrs. Grete Budtz is gratefully acknowledged. G.B. kept records of the moults. Without her patient and careful observations during several weeks it had not been possible to obtain the present material.     

Studies on the moulting hormones of the desert locust, Schistocerca gregaria

A chemical investigation of the desert locust (Schistocerca gregaria) using an isolated locust abdomen assay has led to the identification of 20-hydroxyecdysone as one of the hormones controlling moulting, but the evidence presented does not favour the prothoracic gland (PTG) as the site of its production. Preliminary information indicates two other active substances are present in higher concentration in the PTG which affect apolysis. Determination of 20-hydroxyecdysone titre at daily intervals in the fifth instar and adult show highest concentrations on the day of ecdysis. Ecdysone was not detected. Histological examination of cuticle suggests that PTG extracts cause growth in epidermal cells, rather than increased cell division.     

Chilled Galleria mellonella larvae: mechanism of supernumerary moulting

ABSTRACT. Supernumerary larval instars were produced when Galleria mellonella L. (Lepidoptera) larvae were chilled at 0°C. Although sensitivity to cooling stress of the last instar and younger larvae were generally the same, only penultimate and the last instar larvae showed a significant correlation between their age and the number of additional larval moults. Chilling stress induced a rapid and persistent increase in the JH titre of the last instar larvae. Severing the ventral nerve cord resulted in a predictable loss of the ability to produce supernumerary moults in chilled last instar larvae. The data suggest that sensory input stimulates allatotropic hormone secretion by the brain of chilled larvae. The possible mechanism controlling supernumerary moulting is discussed.