Histopathological effects of Bacillus thuringiensis on the midgut of tobacco hornworm larvae (Manduca sexta): Low doses compared with fasting

The cytology and ultrastructure of the midgut cells of Manduca sexta larvae are described for untreated controls, larvae which fed on a spore preparation of Bacillus thuringiensis, and larvae which were fasted for either 24 or 48 hr. New observations on the ultrastructure of midgut cells in Manduca larvae included the finding of specialized Golgi vesicles in anteriormost columnar cells and of regular arrays of expanded rough endoplasmic reticulum in goblet cells of the posterior midgut region. The present observations reveal that the columnar cells of the midgut responded cytologically in the same way to fasting as they did to exposure to the toxic spores of B. thuringiensis. The goblet cells, however, appeared unaffected by fasting but became swollen in response to feeding of B. thuringiensis spore preparation.     

Bacillus thuringiensis crystal toxin: Ultrastructural studies of its effect on silkworm midgut cells

Bacillus thuringiensis crystal toxin induced a cytoplasmic response in columnar cells within 1 min after ingestion although external symptoms were not exhibited by larvae until 15 min after ingestion. Microvilli became less consistently uniform in diameter; their organized internal microfilaments were disrupted and disappeared. The cisternae of rough endoplasmic reticulum were enlarged and denuded of ribosomes. By 5 min after ingestion, microvilli of some columnar cells disappeared entirely and gross ultrastructural changes were observed in other regions of the cells. Up to 5 min after ingestion there were few, if any, ultrastructural changes observed within goblet cells. Mitochondria in columnar cells were swollen but did not exhibit the condensed configuration reported by other workers. Both the buffer system used in the fixation medium and its osmolarity influenced the changes in the ultrastructure of midgut cells exposed to B. thuringiensis crystal toxin.     

Inhibition of active K+ transport in the tobacco hornworm (Manduca sexta) midgut after ingestion of Bacillus thuringiensis endotoxin

The effect of Bacillus thuringiensis endotoxin after ingestion on the K⁺ transport of Manduca sexta midgut is described. Direct measurements of short circuit current and transepithelial potential demonstrate that the transport is inhibited at the end of 1 hr with many of the insects exhibiting both negative short circuit current and transepithelial potential by the end of a 4-hr ingestion period.     

The goblet cavity matrix in the larval midgut of Hyalophora cecropia

The larval midgut of the silkmoth Hyalophora cecropia was examined using scanning electron microscopy. Goblet cells were observed to contain within their cavities a matrix plug. This matrix material was extruded onto the lumen side of the epithelium when the tissue was stretched. The rôle of this matrix material in maintenance of the capacity of the midgut to transport ions in vivo and in vitro is discussed.     

Induction of hostplant specificity in the tobacco hornworm, Manduca sexta

The hostplant specificity of the tobacco hornworm, Manduca sexta, is not inherited but is induced. Newly hatched larvae are polyphagous and will feed on many kinds of non-hostplants although they are not able to grow on them. They become oligophagous when they are reared on solanaceous plants but remain polyphagous when reared on diet. The critical period for induction is in the first instar. The induced oligophagous behaviour can be reversed by forcing larvae to feed on diet.     

Neurosecretory cells in the frontal ganglion of the tobacco hornworm, Manduca sexta

The frontal ganglion of the tobacco hornworm, Manduca sexta (L.), was found to contain two neurosecretory (NS) cells (max dia = 40–45 μm). The cytoplasmic inclusions of the NS cells were stained purple with paraldehyde fuchsin, and marked fluctuations in amounts of NS material in the perikarya were observed, depending upon the developmental status of the insect. The perikarya of NS cells in the frontal ganglia of starved larvae and diapause pupae contained large accumulations of NS material, whereas feeding larvae and developing pharate adults showed relatively low amounts of neurosecretion. Electron microscopy revealed large accumulations of NS granules (dia = 80–240 nm) in the frontal ganglia of diapause pupae, but only slight accumulations of granules were seen in the NS cells of developing larvae and pharate adults.It was concluded that axonal transport and release but not synthesis is shut down during starvation and diapause, leading to accumulation of NS material in the perikarya. It is also suggested that the failure of many investigators to differentiate NS cells in the frontal ganglion of various insects may have been due to the selection of very active stages when the amount of available NS material was too low to be visualized by conventional staining techniques.     

Juvenile hormone-specific esterases in the haemolymph of the tobacco hornworm, Manduca sexta

A new sensitive method for determining juvenile hormone (JH) hydrolysis has been developed which measures the release of tritiated methanol from JH labelled in the methyl ester group. Using this assay we investigated the interaction of JH with haemolymph esterases and haemolymph JH-binding protein. Haemolymph from fifth instar larvae of Manduca sexta contains two families of esterases which can be distinguished by their reactivity with diisopropylphosphorofluoridate (DFP). One group consists of general esterases which are capable of hydrolysing free JH but not JH complexed to the binding protein and are completely inhibited by low concentrations of DFP (10⁻⁴ M). The other group (JH-specific esterases), relatively DFP resistant, has little detectable general esterase activity but can hydrolyse JH bound to the binding protein as well as free JH. The major JH-esterase has a sedimentation coefficient of 4·98 S and a diffusion coefficient of 6·4 × 10⁻⁷ cm² sec⁻¹. The molecular weight calculated from these values is 6·7 × 10⁴. The general esterases are present throughout the larval stage, but the JH-specific esterases are barely detectable until the fourth day of the fifth instar when they suddenly appear at a high concentration. Since the general esterases cannot hydrolyse bound JH, one function of the binding protein is to protect JH during transport in the early instars, thus confirming that the binding protein is a true carrier of JH. In the late fifth instar prior to metamorphosis, however, JH-specific esterases appear in the haemolymph resulting in the hydrolysis of JH complexed to the carrier protein. Thus, by lowering JH titre, the JH-esterases play an important rôle in development in M. sexta.     

Photoperiodic induction of the pupal diapause in the tobacco hornworm, Manduca sexta

A study was made of photoperiodic induction of the facultative pupal diapause in the tobacco hornworm, Manduca sexta, reared on artificial diet in the laboratory. The species entered a prolonged diapause when the egg and larval feeding stages were reared in daily photoperiods of 13·5 hr or less. Diapause was induced in all insects at photoperiods ranging from 1 to 13 hr, and part of the population entered diapause at only 15 to 30 min of light per day. Photoperiods of 14 hr or more and continous darkness prevented diapause. Duration of diapause varied with the inductive photoperiod in which the hornworms were reared during the sensitive period. Insects reared in longer diapause-inducing photoperiods within a range of 12 to 13·25 hr remained in diapause longer than those reared in shorter photoperiods. There was no difference in the rate of larval development of hornworms reared in diapause-inducing vs diapause-preventing photoperiods. Temperatures of 26 to 30°C were most favourable for the photoperiodic induction of diapause; at 21°C, the critical photoperiod and incidence of diapause were decreased. Diapause induction was suppressed by low (18°C) and higher (33°C) temperatures. The number of inductive 12L:12D (light = 12 hr; dark = 12 hr) cycles required to induce diapause ranged from as few as 5 for some insects to as many as 12 for others when the post-inductive régimen was continuous light, but with insects previously held in continuous dark, as few as 2 12L:12D cycles during the last 2 days of larval feeding induced diapause in 38 per cent of the population. Only 3 to 4 cycles of 15L:9D during the final larval instar reversed inductive effects of 14 to 15 12L:12D cycles. Photoperiodic sensitivity extended from the late embryo to the end of larval feeding but showed considerable fluctuation during development with maximum sensitivity occurring just before egg hatch and during larval growth.Light breaks applied at different times during the dark period of 12L:12D cycles generated different response curves, depending on the number of cycles in which light breaks were repeated. When repeated for 6 cycles, a unimodal response curve was obtained; 10 cycles produced a bimodal curve and light breaks given for 18 cycles throughout the sensitive period averted diapause regardless of time of night applied. It is suggested that diapause is regulated by a photo- and thermolabile substance that accumulates during long nights (11 hr or more) and acts during the early pupal stage to inhibit the translocation and release of development-promoting neurosecretion from the brain.     

The composition of larval-pupal moulting fluid in the tobacco hornworm, Manduca sexta

The concentrations of sodium, potassium, chloride, bicarbonate, total phosphate, labile phosphate, inorganic phosphate, protein, polypeptides, amino acids, trehalose, and glucose, as well as pH and osmotic pressure of larval-pupal moulting fluid and haemolymph were measured in the tobacco hornworm, Manduca sexta, during the secretion and resorption of moulting fluid. Moulting fluid is a mildly alkaline (pH 7.2), iso-osmotic (330 mOsm) potassium bicarbonate salt solution containing within it the sol form of moulting gel. Bicarbonate is the principal anion in moulting fluid. It is only a minor component of haemolymph. Significant differences in the concentrations of potassium, chloride, bicarbonate, non-labile phosphate, labile phosphate, inorganic phosphate, protein, polypeptide, amino acids, trehalose, and glucose indicate that the integumentary epithelium does not act as a semi-permeable membrane, and that free diffusion between moulting fluid and haemolymph can account for only a small fraction of the molecular species movement between these two fluids.     

The biology of the black larval mutant of the tobacco hornworm, Manduca sexta

A mutant of the tobacco hornworm, Manduca sexta, was found to form black melanized cuticle in the last larval instar. This black phenotype is due to a single sex-linked gene whose expression can be changed by one or more modifier genes. The expression of the mutant phenotype is prevented by juvenile hormone (JH) application at the time of head cap apolysis during the moulting cycle to the last larval instar. The bl mutant is equally as sensitive to JH at this time as is a neck-ligated wild type larva, ruling out an absence of hormone receptors or a difference in JH metabolism. The bl corpora allata were found to be less active at this time than were those of the wild type larva, suggesting that the defect resides in the control of the corpora allata. Since selection for complete expression of the bl phenotype is easy, this mutant provides the basis for an ultrasensitive JH bioassay to be described in a forthcoming paper.     

Wax secretion in non-diapausing and diapausing pupae of the tobacco hornworm, Manduca sexta

Scanning electron microscopy of the epicuticle of the tobacco hornworm, Manduca sexta, showed that pupae in diapause possess thicker wax layers than non-diapausing pupae. Extractions of the epicuticle with CHCl₃ established that diapausing pupae secreted over three times as much wax as non-diapausing pupae, and that the total period of wax secretion in diapausing pupae was two to three times longer than that of non-diapausing pupae. Apparently, the extra thickness of the wax layer of diapausing pupae protects the insect from desiccation during diapause. The deposition of additional wax may result from hormonal changes accompanying entry into diapause.     

Endocrine events during pre-diapause and non-diapause larval-pupal development of the tobacco hornworm, Manduca sexta

The haemolymph ecdysteroid titre and in vitro capacities of prothoracic glands and corpora allata to synthesize ecdysone and juvenile hormone, respectively, during the last-larval instar of diapause-destined (short-day) and non-diapause-destined (long-day) Manduca sexta were investigated. In general, the ecdysteroid titres for both populations of larvae were the same and exhibited the two peaks characteristic of the haemolymph titre during this developmental stage in Manduca. The only difference in the titre occurred between day 7 plus 12 h and day 7 plus 20 h, when the short-day larval titre did not decrease as quickly as the long-day titre. The in vitro synthesis of ecdysone by prothoracic glands of short- and long-day larvae during the pharate pupal phase of the instar were also essentially the same. Activity fluctuated at times which would support the idea that ecdysone synthesis by the glands is a major contributing factor to the changes in the haemolymph ecdysteroid titre. There was one subtle difference in prothoracic gland activity between the two populations, occurring on day 7 plus 2 h. By day 7 plus 10 h, however, rates of ecdysone synthesis by the short- and long-day glands were comparable. This elevated activity of the short-day glands occurred just prior to the period the haemolymph ecdysteroid titre remained elevated in these larvae. The capacities of corpora allata to synthesize juvenile hormone I and III in vitro were not markedly different in long- and short-day last-instar larvae. At the time of prothoracicotropic hormone release in the early pupa, activity of corpora allata from short- and long-day reared animals was low and also essentially the same. There were a few differences in the levels of synthesis at isolated times, but they were not consistent for both homologues. Overall, there are no compelling differences in the fluctuations of ecdysteroids and juvenile hormones between diapause-destined and non-diapause-destined Manduca larvae. Since these hormones do not appear to play any obviously significant role in the induction of pupal diapause in this insect, the photoperiodic induction of diapause in Manduca appears to be a predominantly brain-centred phenomenon not involving endocrine effectors.     

Azadirachtin affects growth and endocrine events in larvae of the tobacco hornworm, Manduca sexta

Injection of azadirachtin in freshly emerged last-instar larvae of Manduca sexta elicited different reactions according to the dose administered. At low doses, pupation occurred in most of the cases, but the resulting pupae were defective for the most part. Individuals treated with higher doses usually did not fully complete development, moulting to supernumerary larvae or dying as larvae (sometimes at the wandering stage) after varying periods of survival. The haemolymph ecdysteroid titre of individuals treated with 2 μg azadirachtin/g bodyweight showed characteristic changes which are presumed to cause the disorders in the last stages that normally lead to pupation. Injection of moulting hormone in azadirachtin-treated individuals at certain times during the penultimate stage elicited no reduction of the azadirachtin-induced effects. It is shown that azadirachtin is able to inhibit development even when individuals performed a complete moult after the treatment.     

Pore-forming properties of the Bacillus thuringiensis toxin Cry9Ca in Manduca sexta brush border membrane vesicles

The toxicity and pore-forming ability of the Bacillus thuringiensis Cry9Ca insecticidal toxin, its single-site mutants, R164A and R164K, and the 55-kDa fragment resulting from its proteolytic cleavage at residue 164 were investigated using Manduca sexta neonate larvae and fifth-instar larval midgut brush border membrane vesicles, respectively. Neither the mutations nor the proteolytic cleavage altered Cry9Ca toxicity. Compared with Cry1Ac, Cry9Ca and its mutants formed large poorly selective pores in the vesicles. Pore formation was highly dependent on pH, however, especially for wild-type Cry9Ca and both mutants. Increasing pH from 6.5 to 10.5 resulted in an irregular step-wise decrease in membrane permeabilization that was not related to a change in the ionic selectivity of the pores. Pore formation was much slower with Cry9Ca and its derivatives, including the 55-kDa fragment, than with Cry1Ac and its rate was not influenced by the presence of protease inhibitors or a reducing agent.     

Midgut and fatbody mitochondrial transhydrogenase activities during larval-pupal development of the tobacco hornworm, Manduca sexta

Midgut and fatbody mitochondria from fifth larval instar Manduca sexta display a membrane-associated transhydrogenase that catalyzes a reversible hydride ion transfer between NADP(H) and NAD(H). The NADPH-forming activity occurs as a nonenergy- or energy-linked activity with energy for the latter derived from either electron transport-dependent NADH or succinate utilization, or ATP hydrolysis by Mg⁺⁺-dependent ATPase. During the ten-day developmental period preceding the larval-pupal molt (fifth larval instar), significant peaks in the mitochondrial transhydrogenase activities of midgut and fatbody tissues were noted and these peaks were coincident with the onset of wandering behavior and with the fifty-fold increase in ecdysone 20-monooxygenase (E20-M) activity previously reported for M. sexta midgut. Since E20-M preferentially uses NADPH in catalyzing ecdysone conversion to the physiologically active molting hormone, 20-hydroxyecdysone, the physiological and developmental significance of the mitochondrial, NADPH-forming energy-linked transhydrogenations were made apparent. Moreover, that the increases in all transhydrogenase activities resulted from de novo enzyme synthesis were indicated by the cycloheximide-dependent reductions in these activities.     

Efflux patterns for organic molecules from the CNS of the tobacco hornworm. Manduca sexta

The efflux of nicotine and its CNS metabolites from the nerve cord of the nicotine-insensitive tobacco hornworm is simpler (two efflux components) than from the nerve cord of the nicotine-sensitive cockroach (three components). This paper looks at the question of whether this disparity is merely a fortuitous species difference, or whether it may have regulatory significance. It is found that Manduca and Periplaneta cords display strikingly similar tripartite efflux patterns of leucine efflux, and that this pattern also characterises efflux of three extracellular markers from Manduca CNS. Efflux of the alkaloid, atropine, and the basic amino acid, arginine, from Manduca CNS follow different patterns from both nicotine/metabolite efflux and the other substances tested. These data support the notion that the simple efflux pattern for nicotine/metabolites in Manduca reflects the activity of special physiological processes, and is not simply imposed by factors such as tissue geometry.     

Effects of cholinesterase inhibitors and metyrapone on wandering and pupation in the tobacco hornworm, Manduca sexta

Eserine, BW 284c51 and neostigmine inhibit larval cholinesterase activity in vitro. Injection of eserine, neostigmine or metyrapone into feeding fifth instar larve had no effect on the normal onset of wandering. Eserine injection during the prepupal stage interfered with the development of the pupa.     

Uptake and metabolism of nicotine by the CNS of a nicotine-resistant insect,the tobacco hornworm (Manduca sexta)

Penetration of the CNS by nicotine occurred equally rapidly in the nicotine-insensitive Manduca cord and the nicotine-sensitive Periplaneta cord, ruling out the possibility that lowered permeability renders Manduca insensitive. Although a saturable concentrative component of nicotine uptake was found in the Manduca cord, it was difficult to examine this component rigorously, because, except at high concentrations, the CNS metabolises the bulk of the nicotine that is taken up. The CNS metabolites of nicotine are water-soluble compounds. They are special first by virtue of the fact that they are formed in the CNS itself and secondly because their chromatographic characteristics are different from mammalian nicotine metabolites (which are not formed by nervous tissue). When subjected to hydrolysis, the metabolites acted like conjugates. Periplaneta CNS also metabolised nicotine, but much less extensively than Manduca. It is speculated that enzymic detoxification of dietary neurotoxins may be a necessary function of the insect CNS, since insects have no anatomical equivalent of a hepatic-portal system for detoxifying ingested compounds before they reach the blood-brain interface.     

Changes in fat body urate synthesizing capacity during the larval-pupal transformation of the tobacco hornworm, Manduca sexta

Large quantities of uric acid or urates are deposited in the fat body of tobacco hornworms, Manduca sexta, between the larval and pupal stages in development. The cause of this increased deposition was investigated by measuring fat body urate synthesizing capacity (USC) during the larval-pupal transformation (LPT). An 85% loss in USC occurs between the late-feeding larval and newly-ecdysed pupal stages. Urate synthesizing capacity, per se, is not responsible for the increase in fat body urate deposition, as evidenced by comparable rates of urate deposition in insects whose USCs differ by a factor of three. Rather, the increased deposition is caused by an increase in substrate availability. The loss in USC is programmed in two steps. The first programmed loss occurs by the end of the feeding fifth larval instar, since hornworms ligated at the pink stripe (PS) stage and measured at the time of the larval-pupal ecdysis (LPE) exhibit an increased retention of USC relative to controls. The second programmed loss in USC occurs between PS + one and PS + two day stages in development. A single administration of 20-hydroxyecdysone to hornworms ligated at the PS stage causes a restoration of this loss in USC by PS + two days, which is further sustained until the LPE. Unexpectedly, when measured immediately after the LPE, the second programmed loss in USC can be delayed until PS + 3 days if non-ligated hornworms are daily administered 20-hydroxyecdysone. The possibility is raised that 20-hydroxyecdysone does not act alone in causing the loss in fat body USC.     

Rôle of gustation and olfaction in food plant discrimination in the tobacco hornworm, Manduca sexta

The rôle of the various chemoreceptors in behavioural discrimination among closely related food plants was studied in Manduca sexta larvae. Amputation of the three types of receptors in various combinations showed that: (1) removal of the maxillary styloconica (gustatory) causes a drastic loss of discrimination; (2) ablation of either the maxillary palpi or antennae (olfactory) also reduces discrimination, but to a lesser degree; and (3) amputation of both palpi and antennae simultaneously causes a severe discriminatory loss comparable to that of gustatory loss. We conclude that both gustation and olfaction are important for host plant discrimination. These chemosensory organs were also shown to play a strong role in the induction of preference. Unilateral extirpations of all three sense organs caused no detectable loss, demonstrating their redundancy in normal animals.