Control experiments usingAgrotis segetum granulosis virus againstAgrotis ipsilon [Lep.: Noctuidae] on tobacco seedlings in Northern Pakistan

Agrotis segetum Schiff. granulosis virus propagated in Denmark was applied against released 2nd instar larvae ofAgrotis ipsilon (Hfn.) in tobacco plots in nurseries at Peshawar and Bhurbun (Murree), Northern Pakistan. Nursery bed plots were isolated from the surroundings by net roof and plastic sheets. Granulosis virus concentrations used were 5×10⁷ and 10⁹ capsules per ml water, and 250 ml water per plot (1–4 m²). Reductions of cutworms as well as cutworm damages varied between 72 and 100% as compared to plots only treated with water. Addition of active coal to the GV did not increase reduction percentages. A possible effect of the GV could be traced one year after treatment.

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Résumé Le virus de la granulose d'Agrotis segetum Schiff. multiplié au Danemark a été appliqué contre le 2^e stade des chenilles deAgrotis ipsilon (Hfn.) dans des parcelles expérimentales à Peshawar et Bhurbun (Murree), Pakistan du nord. Les parcelles isolées avec des filets et des feuilles plastiques furent infestées artificiellement en chenilles. Les concentrations de GV utilisées furent de 5×10⁷ et 10⁹ granules par ml d'eau, 250 ml de la suspension préparée étant distribués par parcelle de 1 à 4 m². La réduction du nombre de chenilles et celui des plantes endommagées varie de 72 à 100% par rapport aux notations effectuées dans les parcelles traitées avec de l'eau pure. L'addition du charbon actif au GV n'augmente pas son effet. Une action du traitement a été retrouvée un an après l'application.

     

Isolation and characterization of a granulosis virus from the tomato moth,Lacanobia oleracea,and its potential as a control agent

A disease causing death in Lacanobia oleracea (Lepidoptera: Noctuidae) occurring in glasshouses in Scotland was shown to be caused by a granulosis virus (GV). Structural properties of the virus were examined by electron microscopy, immunodiffusion, polyacrylamide gel electrophoresis, and restriction endonuclease analysis and compared with an isolate of GV from L. oleracea obtained from France. The two isolates were structurally very similar but could be distinguished by analysis of EcoRI digests of their DNAs. Bioassays of the virus gave LD₅₀ values from 10^4.3 capsules for second-instar larvae to 10^6.6 capsules for fifth-instar larvae. The French isolate was bioassayed in third-instar larvae and was not found to differ significantlyfrom the Scottish isolate. Two small glasshouse trials using the virus to control artificial infestations of L. oleracea indicated that high-volume sprays of virus at 10⁸ to 10⁹ capsules/ml achieved good control. An alternative strategy using much smaller amounts of virus to control the insect is discussed.     

Agrotis segetum granulosis virus as a control agent against field populations ofAgrotis ipsilon andA. Segetum [Lep.: Noctuidae] on tobacco,okra, potato and sugar beet in northern pakistan

Agrotis segetum Schiff granulosis virus (AsGV) propagated in Denmark was supplied against naturally occurring cutworm populations (A. ipsilon and to a less extentA. segetum) in experimental field plots of tobacco, okra, potato and sugar beet in northern Pakistan. AsGV doses varied between 4 × 10⁷ and 4 × 10¹¹ capsules per m² plot, and no. of applications between 1 and 3. One treatment with AsGV did not reduce cutworm damage significantly to tobacco seedlings and potato plants. Two treatments with AsGV reduced cutworm damage significantly. In tobacco, reduction was 64–82%, in okra and potato 85% and 77% respectively. Damage in sugar beet was reduced 78%. Three treatments with AsGV dis not reduce damage significantly better than two treatments. AsGV and the chemical insecticides Tamaran and Dieldrin, andBacillus thuringiensis (Thuricide) were about equally effective, reducing damage by 85%, 79%, 87% and 69%, respectively. No difference was found between the efficiency of highly purified AsGV to which activated charcoal was added and partially purified AsGV without charcoal.      

The comparative susceptibilities of Pieris brassicae and P. rapae to a granulosis virus from P. brassicae

A comparison was made of the dosage-mortality responses of larvae of Pieris brassicae and P. rapae to infection by P. brassicae granulosis virus (GV). Bioassays with first, second, third, and fourth-instar larvae of both species revealed a marked difference in susceptibility between instars and between species. Median lethal dosages (LD₅₀s) for P. rapae larvae ranged from five capsules for the first instar to 662 capsules for the fourth instar. With P. brassicae, this range extended from 66 capsules to 2.3 × 10⁷ capsules. The time-mortality responses of the two species were similar when fed virus dosages equivalent to an LD₉₀. Median lethal times (LT₅₀s) ranged from 5 days for first-instar larvae to 7–8 days for fourth-instar larvae. A comparison between a long-established laboratory stock of P. brassicae and a stock recently acquired from the field showed no significant difference in their susceptibility to GV. The implications of the pronounced species differences in susceptibility to GV infection are discussed in relation to the potential field control of P. rapae and P. brassicae.     

Reduction of consumption by grasshoppers (Orthoptera: Acrididae) infected with Nosema locustae canning (Microsporida: Nosematidae)

The effect of ingestion of Nosema locustae Canning spores on feeding by grasshoppers was measured in simultaneous laboratory and field experiments. After 21 days, fourth-instar Melanoplus sanguinipes (F.) nymphs, administered spores at the rates of 0, 2.0 × 10⁴, 2.0 × 10⁵, and 2.0 × 10⁶ per grasshopper, showed dry matter consumption of 102, 87, 64, and 26 mg in 48 hr, respectively. Rate of inoculation was a significant factor in suppression of feeding after correction for the effects of developmental stage, sex, and body weight. The quantity of dry matter consumed decreased linearly with increasing rate of spore ingestion. Experiments on 50 caged 1-m² plots on pasture grass yielded similar trends in per capita consumption independent of the effects of mortality. Field consumption per integrated grasshopper-day was 108, 77, 31, and 27 mg dry wt at the four inoculation rates, over 20 days.     

Quantitative studies on the pathogenicity of Nosema carpocapsae,a microsporidian pathogen of the codling moth,Cydia pomonella,in New Zealand

The pathogenicity of Nosema carpocapsae for codling moth was studied using dose-infectivity experiments. The IC₅₀ (median infective concentration) was similar for the five larval instars (range 4.0 × 10³ to 6.7 × 10⁴ spores/ml). Spore loads in moths ranged from 6.0 × 10⁶ to 7.1 × 10⁷ spores per moth and varied with dose and with larval age at infection. The infection does not cause mortality but does reduce the fecundity and fertility of infected moths. Nosema carpocapsae is transmitted transovarially as well as horizontally. Infected eggs were not produced by healthy females mated with infected males, although such pairs generally produced fewer eggs than healthy pairs.     

Continuous biodegradation of parathion by immobilized Sphingomonas sp. in magnetically fixed-bed bioreactors and evaluation of the enzyme stability of immobilized bacteria

Magnetically-modified Sphingomonas sp. was prepared using covalent binding of magnetic nanoparticles on to the cell surface. The magnetic modified bacteria were immobilized in the fixed-bed bioreactors (FBR) by internal and external magnetic fields for the biodetoxification of a model organophosphate, parathion: 93 % of substrate (50 mg parathion/l) was hydrolyzed at 0.5 ml/min in internal magnetic field fixed-bed bioreactor. The deactivation rate constants (at 1 ml/min) were 0.97 × 10^?3, 1.24 × 10^?3 and 4.17 × 10^?3 h^?1 for immobilized bacteria in external and internal magnetic field fixed-bed bioreactor and FBR, respectively. The deactivation rate constant for immobilized magnetically modified bacteria in external magnetic field fixed-bed bioreactor (EMFFBR) was 77 % lower than that of immobilized cells by entrapping method on porous basalt beads in FBR at 1 ml/min. Immobilized magnetic modified bacteria exhibited maximum enzyme stability in EMFFBR.     

The block to sperm penetration in zonal-free mouse eggs

The rate of sperm penetration and the number of sperm penetrating zona-free mouse eggs were found to be dependent on sperm concentration. At the lowest sperm concentrations examined (10² cells/ml, sperm-egg ratios of approximately 1:1), most eggs were penetrated (75%), and polyspermy was low (19%) following 3 hr of incubation. The number of sperm penetrating the egg was logarithmically related to sperm concentration. All eggs showed a delay of at least 20 min between insemination and penetration, and penetration was complete in approximately 2 hr at 10⁴ sperm/ml; this penetration block was attributed to egg-related changes. The existence and timing of the egg plasma membrane block to polyspermy were evaluated by reinsemination experiments. In this approach, the block was triggered in zona-free eggs with a low concentration of capacitated epididymal sperm at time 0, and the eggs were subsequently challenged with high sperm concentrations. The presence or absence of a block was inferred from the degree of polyspermy observed in these eggs after 3 hr of incubation. Adjusting for sperm concentration-dependent delays between insemination and sperm penetration, a blocking time of approximately 40 min was obtained.     

The effect of tube closures and media on the enrichment of Campylobacter jejuni

Enrichment of C. jejuni in metal, Morton-style capped tubes gave no growth. Cotton wool or sponge rubber plugged tubes yielded enrichment of C. jejuni to 1.6 × 10³ cfu per ml from an inoculation of 0.18 cfu per ml in 10 ml medium.Enrichment of C. jejuni from egg melange in cotton plugged tubes and bottles showed that the ratio of egg melange to broth should not exceed 4:1 in bottles and 2:3 in tubes. When enriching from incubating fertile eggs infected by C. jejuni a decreasing quantitative and qualitative recovery was experienced with increasing time of egg incubation. Five enrichment broths and two selective plating media were compared in this experiment. The medium of Doyle and Roman (Appl. Environ. Microbiol. 43, 1343–1353 (1982)) and a routine enrichment broth plus rifampin (brucella broth containing per litre: 50 ml lysed horse blood, 10 mg rifampin, 5000 IU polymyxin B, 10 mg vancomycin, 5 mg trimethoprim lactate and the reductants of George et al. (J. Clin. Microbiol. 8, 36–41 (1978)) were superior to BNP broth. All media showed decreased enrichment of C. jejuni with increasing time of egg incubation, when growth was only of the order of 2 × 10² cfu per ml at day 15 of egg incubation. Rifampin was required to suppress contamination by Proteus species and Gram-positive cocci.     

Production and field evaluation of codling moth granulosis virus for control of Cydia pomonella in the United Kingdom

Codling moth granulosis virus (Cp GV) was produced in larvae of Cydia pomonella reared on artificial diet. The average yield of virus (9 × 10⁹capsules/larva) was increased by raising the larvae on diet containing methoprene, a juvenile hormone analogue. In field trials in 1978 and 1979, one or two high-volume applications of Cp GV at 7 × 10¹⁰ capsules/litre achieved reductions in numbers of mature larvae and damaged fruit that were little different from those obtained by two applications of azinphos-methyl. A field trial in 1980 showed that at concentrations of Cp GV ≥ 6 × 10⁸ capsules/litre, damaged diminished slowly with increasing virus concentration. Following virus application in 1980, Cp GV infectivity was reduced by half in 3 days, but some activity persisted at least 4–8 wk after spraying. The results indicate that codling moth GV is an effective control agent particularly in reducing numbers of larvae and the more severe forms of fruit damage.     

Virus particle packaging in baculovirus and cytoplasmic polyhedrosis virus inclusion bodies

The structure of the inclusion bodies (IBs) of three multiply enveloped nuclear polyhedrosis viruses (MNPVs), one singly enveloped NPV (SNPV), two granulosis viruses (GVs) and one cytoplasmic polyhedrosis virus (CPV) were compared. A method was devised to calculate the numbers of virus particles and nucleocapsids in IBs using data from light microscopy and thin sections. The three MNPVs, from Agrotis segetum (English and Polish virus isolates) and Mamestra brassicae had similar concentrations of virus particles ranging from 17.3 to 19.6 per μm³ of IB. Plusia gamma SNPV had a higher density of 59.6 virus particles per μm³ of IB, which partly compensated for its having smaller IBs (mean volume 0.65 μm³) than the MNPVs (2.60–9.71 μm³). The English A. segetum MNPV isolate had the most nucleocapsids in each virus particle (mean, 4.04) and the largest IBs (mean volume, 9.71 μm³), giving 674 nucleocapsids per IB on average. The GVs, from A. segetum and Pieris brassicae, mainly contained one nucleocapsid per IB. P. gamma CPV IBs had a much higher density of virus particles than the baculoviruses (260 per μm³ compared with 17–60 per μm³). These data are discussed in relation to the biological properties of these viruses, and possible adaptational advantages of alternative IB designs are considered.     

Effect of Inoculative Releases of Trichogramma ostriniae on Populations of Ostrinia nubilalis and Damage to Sweet Corn and Field Corn

European corn borer (Ostrinia nubilalis) is one of the most injurious pests of sweet and field corn in the United States. We report here on controlled experiments in which an egg parasitoid (Trichogramma ostriniae) was released inoculatively (75,000 females ha⁻¹) early in the growing season (when corn plants were at the early to mid-whorl stage) to test its efficacy as a biological control agent of O. nubilalis. Releases were made in fields of sweet corn and field corn. Numbers of eggs laid in experimental plots, larval tunnels, and larvae and proportion of damaged ears were determined. Mass of ears was determined for field corn plots. In sweet corn, despite greater oviposition by O. nubilalis in T. ostriniae release plots, the number of borer larvae, stalk tunnels, and damaged ears was reduced by ∼50% compared with those in nonrelease plots. This reduction in damage was consistent for early and late-planted sweet corn. In the field corn plots, larger numbers of O. nubilalis eggs were again laid in some release plots than in control plots. However, O. nubilalis damage appeared to be suppressed in T. ostriniae release plots, although no significant differences were found in most. These results were promising, but further work is required in field corn. The results for sweet corn demonstrated that inoculative releases of T. ostriniae provide suppression of O. nubilalis populations adequate to reduce damage significantly.     

Field evaluation of a granulosis virus for control ofPieris rapae [Lep.: Pieridae] in the United Kingdom

A purified granulosis virus isolated fromPieris brassicae (L.) was tested in the field against an introduced population ofPieris rapae (L.) larvae on cabbage (cv January King) in small experimental plots at Littlehampton, Sussex. Experiments were designed to compare the relative efficacy of single and multiple applications of virus (2.1×10¹² and 3.7×10¹² or 2.1×10¹⁴ and 3.7×10¹⁴ virus capsules/ha) in reducing numbers ofP. rapae larvae. An experiment was carried out in June 1978 and repeated in August to coincide approximately with the 2 natural generations ofP. rapae in southern England. Larval populations were monitored by regularin situ assessment of plants and by destructive sampling. Within 10 days of spraying virus there was a significant reduction in the mean larval population on all virus-treated plots compared with untreated controls. Sprays of 2.1×10¹⁴ and 3.7×10¹⁴ capsules/ha reduced larval numbers more quickly than 2.1×10¹² and 3.7×10¹²/ha treatments. In the 1st experiment, three sprays of virus at either 2.1×10¹² or 2.1×10¹⁴ capsules/ha gave no increase over the final level of control achieved by a single spray. However, in the 2nd experiment, a single spray of 3.7×10¹² capsules/ha did not significantly reduce the numbers of larvae. It is likely that this failure could be accounted for by a combination of the larger “natural” population ofP. rapae recorded midway through the 2nd experiment and the rapid inactivation of virus deposits which left little infectious virus to infect these larvae. Virus inactivation was so rapid that only 7–33 % of the initial virus deposits remained 1 day after application. These results suggest that further understanding of virus formulation, persistence and dosage rates are needed before such a virus can be used in a rational manner.     

Plasmid Involvement in Parathion Hydrolysis by Pseudomonas diminuta

An organism identified as Pseudomonas diminuta was found to hydrolyze parathion. Cells grown for 48 h contained 3,400 U of parathion hydrolase activity per liter of broth. Expression of enzymatic activity was lost at a high frequency (9 to 12%) after treatment with mitomycin C. Hydrolase-negative derivatives were missing a plasmid present in the wild-type organism. The molecular mass of this plasmid (pCS1), as determined by electron microscopy, was about 44 × 10⁶ daltons.     

Effect of pH and Chelating Agents on the Heat Resistance and Viability of Salmonella typhimurium Tm-1 and Salmonella senftenberg 775W in Egg White

Supplementation of egg white at pH 8.9 with 5 mg of disodium ethylenediaminetetraacetic acid (EDTA) per ml resulted in a kill of Salmonella typhimurium Tm-1 of greater than 10⁶ per ml after 28 days at 2 C. While at 28 C, supplementation with 7 mg of EDTA per ml resulted in approximately a 10⁶ kill in less than 24 hr. Kena supplementation at 40 mg/ml of egg white resulted in a kill of S. typhimurium Tm-1 of greater than 10⁶ after approximately 60 hr of storage at 28 C. This is in contrast to no reduction in viable count in unsupplemented egg white stored at 2 C and a 100-fold increase in viable count in that stored at 28 C. Supplementation of egg white with EDTA at 7 mg/ml or with Kena at 10 mg/ml also affected the heat resistant characteristics of the two organisms at 52.5 C, reducing the time required to kill 90% of the population (D value) at any pH by a factor of 2 to 6. There was a synergistic effect between EDTA and lactic acid when lactic acid was used to adjust EDTA-supplemented egg white to an acidic pH (5.3) which greatly decreased the heat resistance of Salmonella senftenberg 775W (from 100D to D).     

Bacterial Predator-Prey Interaction at Low Prey Density

A bacterial predator-prey interaction was studied using Bdellovibrio and bioluminescent prey bacteria. The attacking bdellovibrio causes decay of bioluminescence, which is correlated with bdellovibrio penetration into the prey. The behavior of the prey and predator populations over time was found to be well described by a Lotka-Volterra model. By using this model, the probability of bdellovibrio penetration after encountering a prey cell was found to be approximately 3.0%. The prey density required to give the bdellovibrios a 50% chance of survival was calculated to be at least 3.0 × 10⁶ cells per ml, and the density required for population equilibria was calculated to be about 7 × 10⁵ prey bacteria per ml. These values, not generally characteristic of natural habitats, suggest that the existence of Bdellovibrio in nature is limited to special ecological niches.     

The entomogenous nematode Neoaplectana bibionis as a biological control agent of Agrotis segetum in lettuce

Biological control of the soil-inhabitating larvae (cutworms) of Agrotis segetum Schiff. using the entomogenous nematode Neoaplectana bibionis Bovien was investigated under field conditions. Cutworms were introduced to plots planted with lettuce, Lactuca sativa L. After planting and infection with cutworms the plots were treated with either N. bibionis, the insecticide endosulfan or water. The trials were sited on locations with loamy and sandy soil. Adequate control of cutworms was obtained using 2.5×10⁵ nematodes/m² on sandy soil and 1×10⁶ nematodes/m² on loamy soil. Effects of these treatments with nematodes were equal to the effect of endosulfan.

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Neoaplectana bibionis ein entomophager nematode zur biologischen bekämpfung von Agrotis segetum an salat

Zusammenfassung Unter Freilandbedingungen wurde die biologische Bekämpfung von Erdraupen (Agrotis segetum Schiff., Lepidoptera, Noctuidae) mit dem entomophagen Nematoden Neoaplectana bibionis Bovien geprüft. Mit Salat bepflanzte Parzellen wurden mit Erdraupen besetzt. Anschliessend wurde auf die Parzellen N. bibionis, das Insektizid Endosulfan oder Wasser ausgebracht. Die Versuche wurden in Gebieten mit lehmigen und sandigen Böden durchgeführt. Für eine ausreichende Bekämpfung der Erdraupen waren auf dem sandigen Boden 2.5×10⁵ Nematoden/m² und auf dem lehmigen Boden 1×10⁶ Nematoden/m² erforderlich. Die Wirkung dieser Behandlungen entsprach der mit Endosulfan.

     

Development of a direct competitive enzyme-linked immunosorbent assay for parathion residue in food samples

A heterologous direct competitive enzyme-linked immunosorbent assay (ELISA) for parathion residue determination is described based on a monoclonal antibody and a new competitor. The effects of several physicochemical factors, such as methanol concentration, ionic strength, pH value, and sample matrix, on the performance of the ELISA were optimized for the sake of obtaining a satisfactory assay sensitivity. Results showed that when the assay medium was in the optimized condition (phosphate buffer solution [PBS] containing 10% [v/v] methanol and 0.2 mol/L NaCl at a pH value of 5.0), the sensitivity (estimated as the IC₅₀ value) and the limit of detection (LOD, estimated as the IC₁₀ value) were 1.19 and 0.08 ng/ml, respectively. The precision investigation indicated that the intraassay precision values all were below 10% and that the interassay precision values ranged from 4.89 to 19.12%. In addition, the developed ELISA showed a good linear correlation (r² = 0.9962) to gas chromatography within the analyte’s concentration range of 0.1 to 16 ng/ml. When applied to the fortified samples (parathion adding level: 5-15 μg/kg), the developed ELISA presented mean recoveries of 127.46, 122.52, 91.92, 124.01, 129.72, 99.37, and 87.17% for tomato, cucumber, banana, apple, orange, pear, and sugarcane, respectively. Results indicated that the established ELISA is a potential tool for parathion residue determination.     

A functional F analogue of Autographa californica nucleopolyhedrovirus GP64 from the Agrotis segetum granulovirus

The envelope fusion protein F of Plutella xylostella granulovirus is a computational analogue of the GP64 envelope fusion protein of Autographa californica nucleopolyhedrovirus (AcMNPV). Granulovirus (GV) F proteins were thought to be unable to functionally replace GP64 in the AcMNPV pseudotyping system. In the present study the F protein of Agrotis segetum GV (AgseGV) was identified experimentally as the first functional GP64 analogue from GVs. AgseF can rescue virion propagation and infectivity of gp64-null AcMNPV. The AgseF-pseudotyped AcMNPV also induced syncytium formation as a consequence of low-pH-induced membrane fusion.     

Parental size and environmental conditions affect egg capsule production by Nassarius reticulatus (Linnaeus 1758) (Gastropoda: Nassariidae)

In shallow coastal habitats scavenging netted whelks Nassarius reticulatus attached egg capsules to the stipes of red algae Chondrus crispus and occasionally on Furcellaria lumbricalis and Plumaria plumose. In the laboratory egg capsules were laid on aquaria sides and lids by individuals ≥ 21 mm shell length. Larger size classes produced more egg capsules and spawned over a longer period and in doing so partitioned less energy into shell growth. Large netted whelks (25-28.9 mm) produced larger capsules which contained significantly more and larger eggs than those produced by smaller individuals (21-24.9 mm). Egg capsule production continued throughout the year by regularly fed N. reticulatus held at ambient seawater temperatures. Egg production increased in the spring and summer with peak production during June (15 °C), decreased between August and October and resumed again during the winter (November to February at ∼ 7 °C). During the summer (15-16 °C) egg capsules were smaller and contained smaller eggs than those deposited during the winter (7-10 °C), although the number of eggs · capsule⁻¹ was similar. Enforced food limitation reduced the number and size of the egg capsules, the number and size of eggs produced · female⁻¹ and the duration of the breeding period. Hatching success of N. reticulatus egg capsules was high (95%) even at winter seawater temperatures (11-8.5 °C) and the duration of embryonic development was fastest between 15 and 17.5 °C.