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Analysis of nubbin expression patterns in insects.

Previous studies have shown that the gene nubbin (nub) exhibits large differences in expression patterns between major groups of arthropods. This led us to hypothesize that nub may have evolved roles that are unique to particular arthropod lineages. However, in insects, nub has been studied only in Drosophila. To further explore its role in insects in general, we analyzed nub expression patterns in three hemimetabolous insect groups: zygentomans (Thermobia domestica, firebrat), dyctiopterans (Periplaneta americana, cockroach), and hemipterans (Oncopeltus fasciatus, milkweed bug). We discovered three major findings. First, observed nub patterns in the ventral central nervous system ectoderm represent a synapomorphy (shared derived feature) that is not present in other arthropods. Furthermore, each of the analyzed insects exhibits a species-specific nub expression in the central nervous system. Second, recruitment of nub for a role in leg segmentation occurred early during insect evolution. Subsequently, in some insect lineages (cockroaches and flies), this original role was expanded to include joints between all the leg segments. Third, the nub expression in the head region shows a coordinated change in association with particular mouthpart morphology. This suggests that nub has also gained an important role in the morphological diversification of insect mouthparts. Overall, the obtained data reveal an extraordinary dynamic and diverse pattern of nub evolution that has not been observed previously for other developmental genes.

Amino Acid Sequence↗

Acoustic information available to bats using frequency-modulated sounds for the perception of insect prey.

Through the present study, the acoustic information available to an echolocating bat that uses brief frequency-modulated (FM) sonar sounds for the pursuit and capture of insect prey has been characterized. Computer-generated sonar pulses were broadcast at tethered insects, and the returning echoes were recorded on analog tape at high speed for off-line analyses. Echoes from stationary and fluttering insects were displayed using time waveform, spectrogram, power spectrum, and cross-correlation representations. The results show echo signatures for the different insect species studied, which change with the angle of incident sound. Sequences of echoes from fluttering insects show irregular changes in sound amplitude and time-frequency structure, reflecting a random temporal relation between the changing wing position and the arrival of incident sound. A set of recordings that controlled the temporal relation between incident sound and insect wing position suggests that information about the spatial profile of a flying insect could be enhanced if the bat were to produce a sequence of sounds that synchronized briefly with the moving target's wing-beat cycle. From this study, it has been proposed that the FM bat receives stroboscopic-like glimpses of fluttering prey whose spatial representation depends on the operation of the bat's sonar receiver.

Animals↗

The multifunctional deoxynucleoside kinase of insect cells is a target for the development of new insecticides.

The antiherpetic agent (E)-5-(2-bromovinyl)-2'-deoxyuridine (BVDU) was found to be an efficient substrate for recombinant Drosophila melanogaster-deoxyribonucleoside kinase with a K(m) of 4.5 microM and a V(max) of 400 nmol/microg protein/h compared with 1.3 microM and 62.5 nmol/microg protein/h, respectively, for the natural substrate thymidine. Mammalian cytosolic thymidine kinase-1 does not recognize BVDU as a substrate. In sharp contrast to mammalian cells, the insect D. melanogaster and Spodoptera frugiperda (Sf) embryonic cells proved highly sensitive to the cytostatic action of BVDU. BVDU was efficiently metabolized to its 5'-mono-, 5'-di- and 5'-triphosphate derivatives in the insect cell cultures and abundantly incorporated into the insect cell DNA. BVDU prevented the D. melanogaster cells to initiate the S phase of their cell cycle, and exposure of S. frugiperda cells to BVDU led to a dose-dependent retardation of the insect cells in the S phase of their cell cycle. Both inhibition of nucleic acid synthesis (through the 5'-triphosphate of BVDU) and inhibition of thymidylate synthase (through the 5'-monophosphate of BVDU) would account for the cytostatic activity of BVDU against the insect cells. Because of the virtual lack of cytotoxicity of BVDU against mammalian cells, the drug should be considered highly selective in its cytostatic action against the insect cells. When added to the food of S. frugiperda larvae, BVDU caused a remarkable decrease in the weight gain of the larvae and heavily compromised the transformation of the larvae to the pupae and their subsequent adult (moth) phase. Our data indicate that insect multifunctional deoxyribonucleoside kinase should be considered an entirely novel and attractive target in the development of new nucleoside types of highly selective insecticidal drugs.

Animals↗

Thermoregulation in endothermic insects.

On the basis of body weight, most flying insects have higher rates of metabolism, and hence heat production, than other animals. However, rapid rates of cooling because of small body size in most cases precludes appreciable endothermy. The body temperature of small flies in flight is probably close to ambient temperature, and that of flying butterflies and locusts is 5 degrees to 10 degrees C above ambient temperature. Many moths and bumblebees are insulated with scales and hair, and their metabolism during flight can cause the temperature of the flight muscles to increase 20 degrees to 30 degrees C above ambient temperature. Curiously, those insects which (because of size, insulation) retain the most heat in the thorax during flight, also require the highest muscle temperature in order to maintain sufficient power output to continue flight. The minimum muscle temperature for flight varies widely between different species, while the maximum temperature varies over the relatively narrow range of 40 degrees to 45 degrees C. As a consequence, those insects that necessarily generate high muscle temperatures during flight must maintain their thoracic temperature within a relatively narrow range during flight. Active heat loss from the thorax to the abdomen prevents overheating of the flight motor and allows some large moths to be active over a wide range of ambient temperatures. Bumblebees similarly transfer heat from the flight musculature into the abdomen while incubating their brood by abdominal contact. Many of the larger insects would remain grounded if they did not actively increase the temperature of their flight muscles prior to flight. Male tettigoniid grasshoppers elevate their thoracic temperature prior to singing. In addition, some of the social Hymenoptera activate the "flight" muscles specifically to produce heat not only prior to flight but also during nest temperature regulation. During this "shivering" the "flight" muscles are often activated in patterns different from those during flight. The muscles contract primarily against each other rather than on the wings. However, the rate of heat production during shivering and flight is primarily a function of the action potential frequency rather than of the patterns of activation. Thermoregulation is a key factor in the energetics of foraging of some of the flower-visiting insects. The higher their muscle temperature the more flowers they can visit per unit time. When food supplies are ample, bees may invest relatively large amounts of energy for thermoregulation. While shivering to maintain high body temperatures during the short intervals they are perched on flowers (as well as while in the nest), bumblebees often expend energy at rates similar to the rates of energy expenditure in flight. Unlike vertebrates, which usually regulate their body temperature at specific set points, the body temperature of insects is labile. It often appears to be maintained near the lower temperature at which the muscles are able to perform the function at hand. The insects' thermal adaptations may not differ as much from those of vertebrates as previously supposed when size, anatomy, and energy requirements are taken into account.

Animals↗

The Bacillus thuringiensis vegetative insecticidal protein Vip3A lyses midgut epithelium cells of susceptible insects.

The Vip3A protein is a member of a newly discovered class of vegetative insecticidal proteins with activity against a broad spectrum of lepidopteran insects. Histopathological observations indicate that Vip3A ingestion by susceptible insects such as the black cutworm (Agrotis ipsilon) and fall armyworm (Spodoptera frugiperda) causes gut paralysis at concentrations as low as 4 ng/cm2 of diet and complete lysis of gut epithelium cells resulting in larval death at concentrations above 40 ng/cm2. The European corn borer (Ostrinia nubilalis), a nonsusceptible insect, does not develop any pathology upon ingesting Vip3A. While proteolytic processing of the Vip3A protein by midgut fluids obtained from susceptible and nonsusceptible insects is comparable, in vivo immunolocalization studies show that Vip3a binding is restricted to gut cells of susceptible insects. Therefore, the insect host range for Vip3A seems to be determined by its ability to bind gut cells. These results indicate that midgut epithelium cells of susceptible insects are the primary target for the Vip3A insecticidal protein and that their subsequent lysis is the primary mechanism of lethality. Disruption of gut cells appears to be the strategy adopted by the most effective insecticidal proteins.

Animals↗

Enterococci in insects.

Enterococci were obtained from 213 of 403 insects cultured during a 14-month period, in numbers from 10(3) to 3 x 10(7)/g of insect. Insects were taken only from nonurban, wild, and cultivated fields and woods. In species of insects carrying them, enterococci were not always present in every individual cultured, and often more than one species of enterococcus occurred within a species. Enterococci were obtained from certain insects taken in the field during the dormant season, suggesting their role as overwintering agents. They were generally present in species feeding on nectar, succulent plant parts, and on and ir forest litter, but not from insects feeding on less succulent leaves and stems. Streptococcus faecalis was recovered from 32%, Streptococcus faecium from 22.4%, and Streptococcus faecium var. casseliflavus from 43.5% of members of the 37 taxa of insects. S. faecalis and S. faecium var. casseliflavus exhibit a high percent of conformity to the properties published for them. The heterogeneity in properties of S. faecium is similar to that found for the species taken from plants. Many fail to grow in broth at 45 C or in broth containing 6.5% NaCl; 50% of the cultures ferment both melezitose and melibiose, and a few ferment neither sugar. The remainder ferment melibiose only. Failure to reduce methylene blue in milk by S. faecalis and S. faecium is correlated with the inability to ferment lactose. More than 93% of the cultures of S. faecalis digest casein in milk from the top downward, following the production of a soft, flowing curd. Because this property is not characteristic of S. faecalis taken from humans, the reaction in litmus milk is suggested as a means of differentiation between cultures of remote and innocent origin in nature and recent, human pollution.

Animal Feed↗

Measuring virulence factor expression by the pathogenic bacterium Photorhabdus luminescens in culture and during insect infection.

During insect infection Photorhabdus luminescens emits light and expresses virulence factors, including insecticidal toxin complexes (Tcs) and an RTX-like metalloprotease (Prt). Using quantitative PCR and protein assays, we describe the expression patterns of these factors both in culture and during insect infection and compare them to the associated bacterial growth curves. In culture, light and active Prt protease are produced in stationary phase. Tca also appears in stationary phase, whereas Tcd is expressed earlier. These patterns seen in a culture flask are strikingly similar to those observed during insect infection. Thus, in an infected insect, bacteria grow exponentially until the time of insect death at approximately 48 h, when both light and the virulence factors Prt protease and Tca are produced. In contrast, Tcd appears much earlier in insect infection. However, at present, the biological significance of this difference in timing of the production of the two toxins in unclear. This is the first documentation of the expression of Tcs and Prt in an insect and highlights the malleability of Photorhabdus as a model system for bacterial infection.

Animals↗

Comparative physiology of insect renal function.

Transport mechanisms and their control in various segments of insect excretory systems are reviewed and compared to those of vertebrate nephrons, exocrine glands, and hindguts. Formation of the primary urine in most insect Malpighian tubules (MT) is by isosmotic secretion, which is driven by an apical cation (K+) pump rather than by Na+-K+-ATPase. Unlike the glomerular filtrate of vertebrates, insect MT fluid is very different from the blood in composition, often having very high K+-to-Na+ ratios, and urine-to-plasma values much less than unity for most other solutes. The total surface area of insect MT is some 20 times that of vertebrate glomeruli per unit body weight. Secretion of MT fluid is regulated by neuropeptides over a wide range of rats, similar to glomerular filtration rate values for many vertebrate kidneys. Several secretory mechanisms for selected solutes are probably common to insect and vertebrate tubules. Unlike vertebrates, insects usually reabsorb most of the filtered water, ions, and metabolites in the rectum, which has a small surface area relative to the MT. The rectum is also where ionic and osmotic composition of the excreta is finally adjusted, under the control of neuropeptide hormones. In the rectum, insect excreta can become as hyperosmotic as mammalian urine, even though a countercurrent multiplier system is not present. Active transport of Cl- predominates in both locust rectum and the thick ascending limb of Henle's loop, but the characteristics of the anion transfer process are quite different in these two epithelia.

Animals↗

The insect frontal ganglion and stomatogastric pattern generator networks.

Insect neural networks have been widely and successfully employed as model systems in the study of the neural basis of behavior. The insect frontal ganglion is a principal part of the stomatogastric nervous system and is found in most insect orders. The frontal ganglion constitutes a major source of innervation to foregut muscles and plays a key role in the control of foregut movements. Following a brief description of the anatomy and development of the system in different insect groups, this review presents the current knowledge of the way neural networks in the insect frontal ganglion generate and control behavior. The frontal ganglion is instrumental in two distinct and fundamental insect behaviors: feeding and molting. Central pattern-generating circuit(s) within the frontal ganglion generates foregut rhythmic motor patterns. The frontal ganglion networks can be modulated in-vitro by several neuromodulators to generate a variety of motor outputs. Chemical modulation as well as sensory input from the gut and input from other neural centers enable the frontal ganglion to induce foregut rhythmic patterns under different physiological conditions. Frontal ganglion neurons themselves are also an important source of neurosecretion. The neurosecretory material from the frontal ganglion can control and modulate motor patterns of muscles of the alimentary canal. The current and potential future importance of the insect stomatogastric nervous system and frontal ganglion in the study of the neural mechanisms of behavior are discussed.

Animals↗

The effect of air resistance on the jumping performance of insects.

A spring gun was constructed to propel objects at known velocities of between 1 and 4.5 m.s-1. This was used to project insects and various models in a vertical trajectory. By comparing the height attained in air by the insects or models with the height theoretically possible in vacuo, the energy lost against air resistance was observed. Small insects have a higher frontal area to mass ratio than larger ones so have relatively more aerodynamic drag and attain lower heights. The observed effect may be expressed in terms of the drag coefficient, CD. Fleas and locusts have CD of about 1. Winged flies have CD of about 1.5 which falls to about 1 when the wings are amputated and to about 0.8 when the legs are amputated. Aptery is advantageous in jumping insects. From experiments with models, it appears that the optimal condition for small jumping insects is that the body should be as compact as possible to reduce the frontal area to mass ratio. Thus dense spherical bodies are favoured. Some species of jumping insect have densities of about 1 mg.mm-3 while some flying beetles and flies have densities between 0.3 and 0.8 mg.mm-3. The Reynolds number at which the experiments were performed was from 65-205 for fleas up to 740-2340 for locusts. The models operated in similar ranges. At a velocity which would propel a larger animal to a height of 1 m, fleas weighing 0.4 mg only reach about 0.4 m. At lower initial velocities, proportionately less energy is wasted against air resistance so the jump efficiency is higher. Most fleas jump to a height of about 0.1 m with an efficiency of 0.8 while locusts jump to a height of 0.35 m with an efficiency of over 0.9. Air resistance is thus an important scale effect in jumping insects and provides its own design constraints.

Air↗

Spatiotemporal distribution of insects and mites in horizontally stored wheat.

Samples were taken from a flat storage facility located in central Greece, filled with approximately 45 tons of hard wheat, to assess the spatiotemporal distribution of stored-product insects and mites. The wheat was stored in a 1.5-m-deep bulk from June 2001 until March 2002. The samples were taken with a partitioned grain trier during the entire storage period, at 10-d intervals. The trier samples were examined separately for the upper, medial, and lower 0.5 m of the bulk. The spatial distribution of the insect and mite species found was examined by contour analysis based on the numbers of individuals in the trier samples. Nine insect and 20 mite taxa were found during the sampling period. The most abundant insect species were Tribolium castaneum (Herbst), Cryptolestes ferrugineus (Stephens), and Rhyzopertha dominica (F.); the most abundant mite species were Lepidoglyphus destructor (Schrank), Acarus siro L., and the predator Cheyletus malaccensis Oudemans. The highest population densities for the majority of the insect and mite species were recorded during autumn. The majority of the individuals of the most abundant insect and mite species were found in the upper 0.5 m of the bulk, with the exception of C. malaccensis, which was equally distributed in the upper and medial 0.5 m of the bulk. The spatiotemporal distribution during the entire experimental period was notably varied according to the insect and mite species.

Animals↗

Influence of metal exposure history on the bioaccumulation and subcellular distribution of aqueous cadmium in the insect Hydropsyche californica.

The influence of metal exposure history on rates of aqueous Cd accumulation, elimination, and subcellular distribution was examined in the aquatic insect Hydropsyche californica. Specimens were obtained from a reference site and a metal-contaminated site and returned to the laboratory where they were continuously exposed to aqueous Cd (518 ng/L, nominal) for 6 d, followed by 9 d of depuration. Rates of Cd accumulation and elimination were similar in insects from the two sites. Efflux rate constants, k((e), ranged from 0.20 to 0.24/d (t 1/2 approximately 3 d). Immediately following exposure, the cytosol accounted for 40% of the body burden in insects from both sites; however, 89 +/- 2% of the cytosolic Cd was associated with metallothionein-like proteins (MTLP) in insects from the contaminated site, compared to 60 +/- 0% in insects from the reference site. The concentration of Cd bound to non-MTLPs (representing potentially Cd-sensitive proteins) was significantly greater in the insects from the reference site (134 +/- 7 ng/g) than in those from the contaminated site (42 +/- 2 ng/g). At the end of the depuration period, 90% of the accumulated Cd body burden had been eliminated, and Cd concentrations in MTLPs and non-MTLPs were similar between the sites. Results suggested that differences in exposure history had no influence on the bioaccumulation of Cd, but did affect the concentrations of Cd bound to MTLP during Cd exposure in these insects.

Animals↗

Representation of perceptual dimensions of insect prey during terminal pursuit by echolocating bats.

The echolocating big brown bat, Eptesicus fuscus, broadcasts brief frequency-modulated (FM) ultrasonic sounds and perceives objects from echoes of these sounds returning to its ears. Eptesicus is an insectivorous species that uses sonar to locate and track flying prey. Although the bat normally hunts in open areas, it nevertheless is capable of chasing insects into cluttered environments such as vegetation, where it completes interceptions in much the same manner as in the open except that it has to avoid the obstacles as well as catch the insect. During pursuit, the bat shortens its sonar signals and increases their rate of emission as it closes in to seize the target, and it keeps its head pointed at the insect throughout the maneuver. In the terminal stage of interception, the bat makes rapid adjustments in its flight-path and body posture to capture the insect, and these reactions occur whether the bat is pursuing its prey in the open or close to obstacles such as vegetation. Insects can be distinguished from other objects by the spectrum and phase of their echoes, and Eptesicus is very good at discriminating these acoustic features. To identify the insect in the open, but especially to distinguish which object is the insect in clutter, the bat must have some means for representing these features throughout the interception maneuver. Moreover, continuity for perception of these features is necessary to keep track of the prey in complex surroundings, so the nature of the auditory representations for the spectrum and phase of echoes has to be conserved across the approach, tracking, and terminal stages. The first problem is that representation of changes in the phase of echoes requires neural responses in the bat's auditory system to have temporal precision in the microsecond range, which seems implausible from conventional single-unit studies in the bat's inferior colliculus, where the temporal jitter of responses typically is hundreds of microseconds. Another problem is that echoes do not explicitly evoke neural responses in the inferior colliculus distinct from responses evoked by the broadcast during the terminal stage because the delay of echoes is too short for responsiveness to recover from the emissions. In contrast, each emission and each echo evokes its own responses during the approach and tracking stages of pursuit. How does the bat consistently represent the phase of echoes in spite of these evident limitations in neural responses? Local multiunit responses recorded from the inferior colliculus of Eptesicus reveal a novel format for encoding the phase of echoes at all stages of interception. Changes in echo phase (0 degree or 180 degrees) produce shifts in the latency of responses to the emission by hundreds of microseconds, an unexpected finding that demonstrates the existence of expanded time scales in neural responses representing the target at all stages of pursuit.

Animals↗

Metabolism of radiolabeled insecticides in insects and related arthropods: a critical study of various techniques.

The metabolism of radiolabeled insecticides in insects and acarina is studied largely by coupling radiotracer techniques with analytical methods, such as TLC, paper and column chromatography, gel-permeation chromatography, and enzymatic assays. These techniques in various combinations yield both the identification and quantification of the metabolites. Other analytical methods such as gas chromatography or IR spectrometry may also be used to obtain additional support for identification of metabolites. In the absence of authentic chromatographic standards, however, NMR and mass spectrometry are necessary in the identification of the unknown compound. The quantity of the radiolabeled insecticide administered should be within the toxicological range of the insect. Therefore, the dosage-mortality response of the insect using unlabeled material should be determined. A dose should be selected that keeps insect mortality to a minimum in order to avoid complications in the computation of the balance data. The radiolabeled insecticide is usually applied topically to the insect. Alternately, the material may be administered by dipping in a solution containing the radiolabeled compound or by exposure to filter paper impregnated with radiolabeled material. Administration of the radiolabeled material by the oral route presents several problems. Sterile rearing conditions are mandatory to avoid contamination of treated diet with microorganisms. Some knowledge of the insect's feeding rhythm is desirable so that the labeled diet is given at peak feeding time. Synthetic diets should be adjusted to pH 7.0. These precautions minimize degradation of the insecticide in the diet prior to consumption by the insect. Precise doses of radiolabeled materials may be administered by injection. The technique is mainly useful in metabolism studies of intermediate materials resulting from the biotransformation of the parent compound.

Animals↗

Density-dependent insect-mold interactions: effects on fungal growth and spore production.

Larvae of saprophagous insects often have been suspected of being competitors of filamentous fungi on decaying organic matter, which negatively influence mold development. Of interest, the role of insects in determining fungal growth and the onset of sporulation largely has been ignored. I used Aspergillus niger and the vinegar fly Drosophila melanogaster as an ecological model system to analyze the influence of insect larvae on daily fungal growth and the start of conidiospore production. I used an artificial substrate to test whether the effect of larval density (one, five and 10 larvae) and inoculation date of the mold (2 and 3 d ahead of the addition of larvae) significantly altered fungal growth. Fungal growth (area covered by hyphal tissue of the artificial patch) was affected negatively by the number of larvae and by the time that elapsed between inoculation with fungal spores and transfer of larvae to the patches. Whereas one larva had only a minor effect on fungal growth, five or 10 larvae strongly hampered mold development. As time between inoculation with spores and introduction of fly larvae increased, mold increased, indicating a priority effect for the fungus. When 10 larvae were transferred at the same time as the patches were inoculated with spores, almost no mold was visible within the period of observation (after 12 d). In comparison with control treatment (no insect larvae), an increase in larval density caused an increasing delay of several days in the start of spore production. Thus only minor changes in the density of insect larvae and the time that larvae entered the patches after inoculation with spores had an enormous effect on fungal growth and spore production. Therefore insects co-occurring with mold on ephemeral resources might constitute an important biotic factor driving local fungal population dynamics. The mechanisms leading to the suppression of fungal growth and the evolutionary implications of insect-mold interactions are discussed.

Animals↗

Retrospective study of clinical observations on insect hypersensitivity and response to immunotherapy in allergic dogs.

A retrospective study was conducted to evaluate the importance of insect hypersensitivity in atopic dogs in the northeastern United States. Fifty (63%) of 79 dogs tested with 7 insect allergens, other than flea, had positive reactions to one or more insects. No dog had positive reactions to insects only. Forty-four dogs underwent immunotherapy. Thirty-one had insect antigens in their prescription mixture and 13 had only conventional environmental allergens. There was no statistical difference in the response rate between the 2 groups. Thus, testing with insect allergens did not decrease the number of dogs with negative skin tests, and including insect allergens in immunotherapy mixtures did not improve the response rate.

Allergens↗

Effectiveness of introduced biocontrol insects on the weed Parthenium hysterophorus (Asteraceae) in Australia.

Six species of insects and a rust fungus have been successfully established for biocontrol of the weed Parthenium hysterophorus L. in Queensland, Australia. Effectiveness of biocontrol insects was evaluated at two properties in Queensland during 1996-97 based on an exclusion experiment using insecticides. Parthenium-infested plots with and without biocontrol insects were sampled at monthly intervals and the impact of biocontrol insects on parthenium at individual plant and whole population levels monitored. Biocontrol insects were more effective at Mt Panorama (central Queensland) than at Plain Creek (north Queensland). At Mt Panorama, the leaf-feeding beetle Zygogramma bicolorata Pallister caused 96% defoliation and the stem-galling moth Epiblema strenuana Walker affected 100% of the plants, resulting in reductions of 90% in weed density, 40% in plant height, and 82% in flower production. Exclusion of biocontrol insects resulted in a 52% increase in seedling emergence and a seven-fold increase in the soil seed bank in the following season. At Plain Creek, E. strenuana was the only prominent agent. It affected 92% of the plants and prevented 32% of plants from producing any flowers, reduced plant height by 40% and flower production by 49%, but did not reduce the plant biomass, weed density or soil seed bank. However, exclusion of biocontrol insects resulted in an eight-fold increase in the soil seed bank in the following season.

Animals↗

[Expression and purification of varicella-zoster virus glycoprotein I gene in insect cells].

OBJECTIVE: To express the cloned gene glycoprotein I (gpI) of varicella-zoster virus (VZV), Beijing VZV 84-7 strain in insect cells and to purify its expression product. METHODS: The gene coding for gpI of VZV was amplified from viral DNA by PCR and cloned into baculovirus transfer vector (pBacPAK9), and recombinant transfer vector plasmid pBacVZVgpI was obtained. The inserted gpI gene in the pBacVZVgpI was sequenced. Insect cells Sf 9 were co-transfected with the recombinant transfer vector plasmid pBacVZVgpI and wild type linear baculovirus BacPAK6 (digested with Bsu36I) DNA. The recombinant baculoviruses containing the VZV 84-7 gpI gene was isolated through several rounds of limited dilution. Recombinant protein gpI was expressed in insect cells Sf 9, postinfected with recombinant baculoviruses. The expressed recombinant gpI was purified by lectin affinity chromatography and its antigenicity and immunogenicity were investigated. RESULTS: The gene coding for gpI of VZV was obtained by PCR and the gpI gene of pBacPAK9 was confirmed by DNA sequencing. The recombinant gpI was expressed in insect cells Sf 9, post-infected with recombinant baculovirus and identified by SDS-PAGE and western blotting, with its product in cell culture reaching the peak in 72 hours and with a molecular mass of 58 kd and 70 kd, the same as theoretical values. Results of immunoassay with cell lysates infected by recombinant baculoviruses indicated that recombinant protein expressed in insect cells had ability of eliciting specific antibodies against native VZV in mice and complement-dependent neutralizing antibodies. The purified recombinant gpI gave a product with a purity of more than 80%. ELISA and Western-blot analysis demonstrated that purified protein had specific VZV antibody-binding activity. This suggested that the recombinant gpI expressed in insect cells had the same biological characteristics as its native counterpart. CONCLUSION: Baculovirus-insect cells could be used to express the gene of VZV gpI, which could provide a basis for quantitative analysis of VZV antigen, and preparation of its subunit vaccine.

Animals↗