DNA hybridization assay for detection of gypsy moth nuclear polyhedrosis virus in infected gypsy moth (Lymantria dispar L.) larvae.

Radiolabeled Lymantria dispar nuclear polyhedrosis virus DNA probes were used in a DNA hybridization assay to detect the presence of viral DNA in extracts from infected larvae. Total DNA was extracted from larvae, bound to nitrocellulose filters, and assayed for the presence of viral DNA by two methods: slot-blot vacuum filtration and whole-larval squashes. To test the assays, neonate larvae were fed droplets containing a known concentration of L. dispar nuclear polyhedrosis virus and observed for up to 10 days to determine the percentage of infected larvae. The average percent mortalities were 88.0, 60.7, 26.0, and 5.3% for larvae fed droplets containing 4.0 x 10(4), 1.0 x 10(4), 2.5 x 10(3), and 6.25 x 10(2) polyhedral inclusion bodies (PIBs) per ml, respectively. Other larvae treated with the same virus concentrations were frozen at 2, 4, and 6 days postinoculation and examined by the hybridization techniques. The average percentage of slot blots containing viral DNA equaled 81.0, 58.0, 18.0, and 6.0% for larvae blotted 4 days after treatment with 4.0 x 10(4), 1.0 x 10(4), 2.5 x 10(3), and 6.25 x 10(2) PIBs per ml, respectively, and 89.9, 52.1, 26.6, and 6.0%, respectively at 6 days postinoculation. Thus, the hybridization results were closely correlated with mortality observed in reared larvae. Hybridization of squashes of larvae frozen 4 days after receiving the above virus treatments also produced accurate measures of the incidence of virus infection.     

Dispersal of first-instar gypsy moth larvae in relation to population quality

Summary Field studies of dispersal by first instar gypsy moth larvae indicate that almost all larvae undergo an initial dispersal episode. However, in laboratory studies large larvae (from large eggs) disperse more frequently than small larvae (from small eggs) in the presence of favored food. Large larvae may be better adapted for dispersal. When larvae encounter unacceptable food or are denied food, larvae disperse more frequently and dispersal by small larvae is nearly as frequent as dispersal by large larvae. Factors affecting egg size may contribute to shifts in dispersal patterns of gypsy moth larvae and distribution of populations.Paper No. 2041, Massachusetts Agricultural Experiment Station, University of Massachusetts at Amherst. This research supported (in part) from Experiment Station Project No. 355     

DNA hybridization assay for detection of gypsy moth nuclear polyhedrosis virus in infected gypsy moth (Lymantria dispar L.) larvae

Radiolabeled Lymantria dispar nuclear polyhedrosis virus DNA probes were used in a DNA hybridization assay to detect the presence of viral DNA in extracts from infected larvae. Total DNA was extracted from larvae, bound to nitrocellulose filters, and assayed for the presence of viral DNA by two methods: slot-blot vacuum filtration and whole-larval squashes. To test the assays, neonate larvae were fed droplets containing a known concentration of L. dispar nuclear polyhedrosis virus and observed for up to 10 days to determine the percentage of infected larvae. The average percent mortalities were 88.0, 60.7, 26.0, and 5.3% for larvae fed droplets containing 4.0 x 10(4), 1.0 x 10(4), 2.5 x 10(3), and 6.25 x 10(2) polyhedral inclusion bodies (PIBs) per ml, respectively. Other larvae treated with the same virus concentrations were frozen at 2, 4, and 6 days postinoculation and examined by the hybridization techniques. The average percentage of slot blots containing viral DNA equaled 81.0, 58.0, 18.0, and 6.0% for larvae blotted 4 days after treatment with 4.0 x 10(4), 1.0 x 10(4), 2.5 x 10(3), and 6.25 x 10(2) PIBs per ml, respectively, and 89.9, 52.1, 26.6, and 6.0%, respectively at 6 days postinoculation. Thus, the hybridization results were closely correlated with mortality observed in reared larvae. Hybridization of squashes of larvae frozen 4 days after receiving the above virus treatments also produced accurate measures of the incidence of virus infection.     

Protein intake by gypsy moth larvae on homogeneous and heterogeneous diets

Abstract. Food selection behaviour, food utilization efficiency and growth performance of a generalist insect, the gypsy moth ( Lymantria dispar (L.), Lepidoptera: Lymantriidae), were examined with respect to variation in food nitrogen concentration. The results suggest that gypsy moth do not suffer physiologically and in fact may benefit from intraplant variation by selective feeding. When provided with diet cubes containing identical nitrogen concentrations, control larvae tended to consume food from a single cube. This behaviour contrasted with that of larvae provided cubes differing in nitrogen concentration. These larvae tended to consume more from the high nitrogen cube, but allocated feeding more evenly among diet cubes than did control larvae. Overall, larvae mixed foods so as to obtain a mean concentration of 2.9-3.2% nitrogen, a concentration assumed to approximate the 'intake target'. Larvae confined to single nitrogen concentrations mitigated the impact of imbalanced diets on body composition via both pre-ingestive and post-ingestive compensation. When confined to a specific nitrogen concentration, larvae adjusted their intake to the point of best compromise. In this case, this was the geometrically closest point to the estimated intake target. Larvae with a choice of foods that deviated more than ±1% from each other in nitrogen concentration grew as well as or better than larvae without a choice but given identical mean nitrogen concentrations. These results demonstrate that selectivity and nitrogen consumption by gypsy moth larvae are altered according to the particular choices available. Insects may benefit from intraplant variation in food quality because such variation provides the opportunity to choose foods and mix them in ways that permit close matching with the intake target. Variation may be particularly important to insects which must offset changing nutritional demands.     

Behaviour of late-instar gypsy moth larvae in high and low density populations

ABSTRACT. 1. Using scaffolding and night-vision equipment, we observed fifth and sixth instars of the gypsy moth, Lymantria dispar (L.), on Quercus velutina Lam. in the field.
2. In low-density populations, larvae fed at night and spent the day resting in sheltered sites away from the canopy. In high-density populations, larvae remained in the canopy throughout the day and night, and the amount of feeding during daylight hours increased with population density.
3. Larvae at all population densities used a similar sequence of behaviours and sampled a number of leaves when selecting feeding sites, but larvae in high-density populations switched feeding sites more frequently and fed continuously for shorter periods.
4. Larvae seldom interfered with each other's feeding in any of the populations.
5. When fifth instars were collected from the field and held for 24 h in an electronic feeding monitor, they maintained feeding rhythms that were characteristic of their source populations. Larvae spent more time crawling and less time feeding when offered foliage from high-density rather than low-density populations.     

Behavioural and physiological plasticity of gypsy moth larvae to host plant switching

Larvae of the gypsy moth, Lymantria dispar L. (Lepidoptera: Lymantriidae), a generalist species, frequently encounter spatial and temporal variations in diet quality. Such variation favoured the evolution of high behavioural and physiological plasticity which, depending on forest stand composition, enables more or less successful exploitation of the environment. Even in mixed oak stands, a suitable habitat, interspecific and intraspecific host quality variation may provoke significant variation in gypsy moth performance and, consequently, defoliation severity. To elucidate the insufficiently explored relationship between gypsy moth and oaks (Fagaceae), we carried out reciprocal switches between Turkey oaks (Quercus cerris L.) and less nutritious Hungarian oaks (Quercus frainetto Ten.) (TH and HT groups), under controlled laboratory conditions, and compared larval performance between the switched larvae and larvae continuously fed on either Turkey oak (TT) or Hungarian oak (HH). We found that larval traits were most strongly affected by among‐tree variation in oak quality and identity of the host consumed during the fourth instar. Switching from Turkey to Hungarian oak (TH) led to a longer period of feeding, decrease of mass gain, growth, and consumption rate, lower efficiency of food use and nutrient conversion, and increase of protease and amylase activities. Larvae exposed to the reverse switch (HT) attained values of these traits characteristic for TT larvae. It appeared that the lower growth in the TH group than in the TT group was caused by both behavioural (consumption, pre‐ingestive) and metabolic (post‐digestive) effects from consuming oaks. Multivariate analyses of growth, consumption, and efficiency of food use revealed that early diet experience influenced the sensitivity of the most examined traits to less suitable Hungarian oaks, suggesting the development of behavioural and physiological adjustments. Our results indicate that lower risks of defoliation by gypsy moth might be expected in mixed stands with a higher proportion of Hungarian oak.     

NADPH-cytochrome-c-reductase: Changes in specific activity in gypsy moth larvae

NADPH-cytochrome-c-reductase from guts of gypsy moth, Porthetria dispar, oxidized NADPH at the following rates: 11·6, 41·9, and 57·6 nmol/30 min per 0·6 mg protein, in the third, fourth and fifth instar, respectively. The increase in specific activity may be due to a natural induction process controlled by materials in the food. This could also explain the observed decreases just prior to ecdysis at which time the larvae have ceased feeding.     

Effects of the ant Formica fusca on the transmission of microsporidia infecting gypsy moth larvae

Transmission plays an integral part in the intimate relationship between a host insect and its pathogen that can be altered by abiotic or biotic factors. The latter include other pathogens, parasitoids, or predators. Ants are important species in food webs that act on various levels in a community structure. Their social behavior allows them to prey on and transport larger prey, or they can dismember the prey where it was found. Thereby they can also influence the horizontal transmission of a pathogen in its host's population. We tested the hypothesis that an ant species like Formica fusca L. (Hymenoptera: Formicidae) can affect the horizontal transmission of two microsporidian pathogens, Nosema lymantriae Weiser (Microsporidia: Nosematidae) and Vairimorpha disparis (Timofejeva) (Microsporidia: Burenellidae), infecting the gypsy moth, Lymantria dispar L. (Lepidoptera: Erebidae: Lymantriinae). Observational studies showed that uninfected and infected L. dispar larvae are potential prey items for F. fusca. Laboratory choice experiments led to the conclusion that F. fusca did not prefer L. dispar larvae infected with N. lymantriae and avoided L. dispar larvae infected with V. disparis over uninfected larvae when given the choice. Experiments carried out on small potted oak, Quercus petraea (Mattuschka) Liebl. (Fagaceae), saplings showed that predation of F. fusca on infected larvae did not significantly change the transmission of either microsporidian species to L. dispar test larvae. Microscopic examination indicated that F. fusca workers never became infected with N. lymantriae or V. disparis after feeding on infected prey.     

Modeling horizontal transmission of microsporidia infecting gypsy moth,Lymantria dispar (L.), larvae

We developed a simulation model that describes the horizontal transmission of three different microsporidia, Endoreticulatus schubergi, Nosema lymantriae and Vairimorpha disparis and their insect host, the gypsy moth, Lymantria dispar. The model describes the stage specific development and mortality of uninfected, latently infected or infectious hosts, the food consumption, the infection by spore-laden feces of E. schubergi and N. lymantriae and by spore-laden cadaver of N. lymantriae and V. disparis. Model results were compared to percent infection of L. dispar test larvae published in earlier studies using caged oak trees and potted oak-plants. When feces were selected as the source of spores for transmission of E. schubergi or N. lymantriae, the model estimated a percent infection in susceptible larvae that was in the range of the experimental studies. When spore-laden cadavers were the source of spores of N. lymantriae or V. disparis, the model did not correctly predict the experimentally measured percent infection in susceptible larvae. The most critical points of the simulation model are exact calculation of spore release, mortality and exact determination of the transmission coefficients when cadavers were included as a source for microsporidian infection.     

Anthropogenic drivers of gypsy moth spread

The gypsy moth, Lymantria dispar (L.), is a polyphagous defoliator introduced to Medford, Massachusetts in 1869. It has spread to over 860,000 km² in North America, but this still only represents ¼ of its susceptible host range in the United States. To delay defoliation in the remaining susceptible host range, the government maintains a barrier zone and a quarantine, reflecting a presumption that anthropogenic factors are important in the spread of gypsy moth. We develop a model framework that relates these factors along with biophysical characteristics to a county’s susceptibility to gypsy moth invasion. We then compile a dataset for counties within 200 km of the infested area and use trap catch data from 1999 to 2007 to estimate the probability of gypsy moth presence. As expected, gypsy moth is more likely to be found close to the population front and to traps that recorded moths in the previous year. However, when controlling for these factors, our most robust finding is that the use of wood for home heating and energy is consistently positively correlated with the presence of gypsy moth. In contrast, the movement of wood products by industry, which is actively regulated by state and federal governments, is rarely correlated with the presence of gypsy moth. This is consistent with effective regulation of the movement of goods by industry, but not by the public. Our findings provide empirical support for the importance and challenge of firewood as a vector for non-native forest insects.     

Effects of microhabitat,time of day,and weather on predation of gypsy moth larvae

Summary Wire cages with different-sized meshes were placed on trunks and around leaves at different heights in oak trees and in forest litter. Gypsy moth, Lymantria dispar, instars II–V tethered with threads were placed in each cage (instars II–III only in leaf cages) as well as outside the cages. Predation of larvae decreased from near ground to mid-crown in trees and was highest in litter and very low on leaves. Predation in litter was not strongly related to cage type, suggesting that small, invertebrate predators were active there, but IV–V instars on trunks were mainly killed by relatively large predators, probably forest mice and shrews. Influences of the time of day and weather on predation were evaluated by observing tethered V–VI instars in litter and on tree trunks hourly. Ants, particularly carpenter ants (Camponotus ferrugineus) and Formica sp., and probably vertebrates, were conspicuous predators in the litter. Ants were most active at lower relative humidities, while other predators were apparently not influenced by humidity. No daily activity rhythms of predation were noted. Invertebrates appear to be important predators of larvae only in the litter whereas vertebrates, such as forest mice and shrews, also readily attack larvae on tree trunks.     

Endogenous and induced monooxygenase activity in gypsy moth larvae feeding on natural and artificial diets

NADPH oxidase activity was measured in third to sixth instar gypsy moth larvae fed oak or pine foliage. Activity levels ranged from 400 to 1,900 pmol NADPH oxidized/min/mg microsomal protein, but enzyme activity was not correlated with host plant ingested. Similarly, activity levels in larvae fed diets containing inducers, such as the terpenoid α-pinene or pentamethylbenzene, ranged from 700 to 1,500 pmol NADPH oxidized/min/mg protein, levels that were comparable to those measured for larvae fed control diets. O-demethylase activity in older instar gypsy moth larvae fed pine averaged 109 pmol p-nitrophenol/min/mg protein, and activity levels in those fed diet containing α-pinene ranged from 22 to 55 pmol/min/mg protein. Although statistically significant, these induced O-demethylase levels are well below those observed for Heliothis zea larvae. Our findings indicate that monooxygenases play a minor, if any, role in the ability of later instar gypsy moth larvae to develop successfully on pine foliage.     

Simulation of litter residence times of young gypsy moth larvae and implications for predation by ants

The length of the time young gypsy moth, Lymantria dispar L. (Lepidoptera: Lymantriidae), larvae remain in litter after failing from trees would help in understanding the impact of predation by ants, as ants appear to be important predators of gypsy moths only in litter. To obtain information on caterpillar litter residence times, visual activity of larvae was investigated in the laboratory by presenting them with vertical dark silhouettes of various widths in a 1 m wide cylindrical arena. Their limit of angular resolution was about 1°. This value helped to determine distances to trees caterpillars could be expected to orient toward from randomly-located points in a forest. These data were used with results on litter crawling speed of instars 1, 2, and 3 in a simulation model that generated litter residence times averaging serveral hours. By combining results with a previously-developed model of ant predation in forest litter, it was estimated that about half of unfed first instars falling into the litter would survive, whereas only about 10% of 2nd and 3rd instars would. The implications these results have for control of the gypsy moth are discussed.

---

Résumé La prédation par les fourmis du genre Formica spp. a une influence importante sur les premiers stades de L. dispar (Lepido., Lymantriidae) en Amérique du Nord. La durée du temps passé dans la litière par les jeunes chenilles après être tombées des arbres doit permettre de comprendre l'impact de la prédation par les fourmis. Pour connaître le temps de séjour des chenilles dans la litière, l'acuité visuelle des chenilles a été examinée au laboratoire en leur présentant des silhouettes noires verticales de différentes largeurs dans une arène circulaire de 1 m de diamètre. La limite de leur angle de résolution était d'environ 1°. Cette valeur a été utilisée pour déterminer les distances (jusqu'à 5 m) quelles que soient les orientations dans la forêt, d'arbres supposés susceptibles d'orienter les chenilles. Les arbres aux silhouettes acceptables étaient distribués uniformément entre 1 et 5 m.Les vitesses de déplacement dans la litière des stades 1, 2, et 3 ont été mesurées par observation directe dans la forêt (elles variaient de 0.9 à 1,54 cm/min). La distance des arbres et la vitesse de déplacement on servi à construire un modèle de simulation qui a donné un temps moyen de séjour de plusieurs heures. En combinant ces résultats avec un modèle précédemment publié de la prédation par les fourmis dans la litière de la forêt, qui utilisait le temps de contact des chenilles avec les fourmis et les taux de captures victorieuses pour estimer la mortalité, nous avons déterminé que la moitié environ des chenilles non alimentées de premier stade tombées dans la litière pourraient survivre, tandis que la survie pour le second et le troisième stade ne serait que de 10%. La discussion porte sur l'importance de ces résultats dans la lutte contre L. dispar.

     

Caterpillar guts and ammonia volatilization: retention of nitrogen by gypsy moth larvae consuming oak foliage

The gypsy moth (Lymantria dispar L.), a major defoliator of hardwood forests in the eastern U.S., has a highly alkaline midgut pH. We hypothesized that the high pH would cause high rates of ammonia (NH₃) volatilization as larvae consumed foliage, leading to potentially large losses of N from the ecosystem to the atmosphere during gypsy moth outbreaks. We measured NH₃ emission during the consumption of oak foliage by larvae in the laboratory. Surprisingly, we found very low amounts of NH₃ release of about 0.1% of the N consumed in foliage. We speculate that digestive mechanisms may limit NH₃ production in the midgut, and that the acidic environment of the hindgut traps most of the small amount of NH₃ that is produced, effectively preventing a potentially very large N loss from both larvae and ecosystem. The estimated rate of NH₃ emission from a defoliated forest is small compared to other inputs and outputs of N from the ecosystem, but could potentially enhance the neutralization of atmospheric acidity during the defoliation period. Received: 12 May 1998 / Accepted: 28 July 1998     

Production of recombinant proteins by baculovirus-infected gypsy moth cells.

An experimental study was undertaken to evaluate alternative insect cell lines to Sf9 [from Spodoptera frugiperda (fall armyworm)] for the production of recombinant proteins. Insect cell lines from two different organisms were considered: IPLB-LdEIta (LdEIta) from Lymantria dispar (gypsy moth) and IPLB-HvT1 (HvT1) from Heliothis virescens (tobacco budworm). Both LdEIta and HvT1 produced higher total activity levels of recombinant beta-galactosidase in monolayer culture than Sf9 after infection with the Autographa californica nuclear polyhedrosis virus (AcMNPV). However, only LdEIta generated a product yield (activity per milligram of total protein) which exceeded that of Sf9 (by 25%), so its growth and production characteristics were investigated in depth. LdEIta generated production levels and yields of a recombinant rotaviral protein, VP4, which exceeded those of Sf9 by 84 and 38%, respectively. In suspension culture, the LdEIta cells grew as aggregates with a doubling time several hours longer than Sf9, but the recombinant product yields of LdEIta were still higher than Sf9 by 38% in this culture environment. beta-Galactosidase expression rates and cell death rates suggested that the difference in productivity between the two hosts was due to the ability of LdEIta to survive the baculovirus infection and produce recombinant proteins longer than Sf9. The presence of LdEIta aggregates in suspension culture may be used as a method to separate live cells from dead cells, labile product, and spent medium in recombinant protein production processes.