The evolution of novel host use is unlikely to be constrained by trade‐offs or a lack of genetic variation

The genetic and ecological factors that shape the evolution of animal diets remain poorly understood. For herbivorous insects, the expectation has been that trade‐offs exist, such that adaptation to one host plant reduces performance on other potential hosts. We investigated the genetic architecture of alternative host use by rearing individual Lycaeides melissa butterflies from two wild populations in a crossed design on two hosts (one native and one introduced) and analysing the genetic basis of differences in performance using genomic approaches. Survival during the experiment was highest when butterfly larvae were reared on their natal host plant, consistent with local adaptation. However, cross‐host correlations in performance among families (within populations) were not different from zero. We found that L. melissa populations possess genetic variation for larval performance and variation in performance had a polygenic basis. We documented very few genetic variants with trade‐offs that would inherently constrain diet breadth by preventing the optimization of performance across hosts. Instead, most genetic variants that affected performance on one host had little to no effect on the other host. In total, these results suggest that genetic trade‐offs are not the primary cause of dietary specialization in L. melissa butterflies.     

A quantitative genetic analysis of leaf beetle larval performance on two natural hosts: including a mixed diet

Published quantitative genetic studies of larval performance on different host plants have always compared performance on one host species or genotype vs. performance on another species or genotype. The fact that some insects may feed on more than one plant species during their development has been neglected. We executed a quantitative genetic analysis of performance with larvae of the leaf beetle Oreinaelongata, raised on each of two sympatric host plants or on a mixture of them. Growth rate was higher for larvae feeding on Adenostylesalliariae, intermediate on the mixed diet and lowest on Cirsium spinosissimum. Development time was shortest on A. alliariae, intermediate on mixed diet and longest on C. spinosissimum. Survival was higher on the mixed diet than on both pure hosts. Genetic variation was present for all three performance traits but a genotype by host interaction was found only for growth rate. However, the reaction norms for growth rate are unlikely to evolve towards an optimal shape because of a lack of heritability of growth rate in each single environment. We found no negative genetic correlations for performance traits among hosts. Therefore, our results do not support a hypothesis predicting the existence of between‐host trade‐offs in performance when both hosts are sympatric with an insect population. We conclude that the evolution of host specialized genotypes is unlikely in the study population.     

Local adaptation and ecological genetics of host-plant specialization in a leaf beetle

The tendency of insect species to evolve specialization to one or a few plant species is probably a major reason for the remarkable diversity of herbivorous insects. The suggested explanations for this general trend toward specialization include a range of evolutionary mechanisms, whose relative importance is debated. Here we address two potentially important mechanisms: (i) how variation in the geographic distribution of host use may lead to the evolution of local adaptation and specialization; (ii) how selection for specialization may lead to the evolution of trade‐offs in performance between different hosts. We performed a quantitative genetic experiment of larval performance in three different populations of the alpine leaf beetle Oreina elongata reared on two of its main host plants. Due to differences in host availability, each population represents a distinctly different selective regime in terms of host use including selection for specialization on one or the other host as well as selection for utilizing both hosts during the larval stage. The results suggest that selection for specialization has lead to some degree of local adaptations in host use: both single‐host population had higher larval growth rate on their respective native host plant genus, while there was no difference between plant treatments in the two‐host population. However, differences between host plant treatments within populations were generally small and the degree of local adaptation in performance traits seems to be relatively limited. Genetic correlations in performance traits between the hosts ranged from zero in the two‐host population to significantly positive in the single‐host populations. This suggests that selection for specialization in single host populations typically also increased performance on the alternative host that is not naturally encountered. Moreover, the lack of a positive genetic correlation in the two host‐population give support for the hypothesis that performance trade‐offs between two host plants may typically evolve when a population have adapted to both these plants. We conclude that although there is selection for specialization in larval performance traits it seems as if the genetic architecture of these traits have limited the divergence between populations in relative performance on the two hosts.     

Effects of pathogen exposure on life‐history variation in the gypsy moth (Lymantria dispar)

Investment in host defences against pathogens may lead to trade‐offs with host fecundity. When such trade‐offs arise from genetic correlations, rates of phenotypic change by natural selection may be affected. However, genetic correlations between host survival and fecundity are rarely quantified. To understand trade‐offs between immune responses to baculovirus exposure and fecundity in the gypsy moth (Lymantria dispar), we estimated genetic correlations between survival probability and traits related to fecundity, such as pupal weight. In addition, we tested whether different virus isolates have different effects on male and female pupal weight. To estimate genetic correlations, we exposed individuals of known relatedness to a single baculovirus isolate. To then evaluate the effect of virus isolate on pupal weight, we exposed a single gypsy moth strain to 16 baculovirus isolates. We found a negative genetic correlation between survival and pupal weight. In addition, virus exposure caused late‐pupating females to be identical in weight to males, whereas unexposed females were 2–3 times as large as unexposed males. Finally, we found that female pupal weight is a quadratic function of host mortality across virus isolates, which is likely due to trade‐offs and compensatory growth processes acting at high and low mortality levels, respectively. Overall, our results suggest that fecundity costs may strongly affect the response to selection for disease resistance. In nature, baculoviruses contribute to the regulation of gypsy moth outbreaks, as pathogens often do in forest‐defoliating insects. We therefore argue that trade‐offs between host life‐history traits may help explain outbreak dynamics.     

Trade-offs in responses to host plants within a population of a generalist herbivore,Christoneura rosaceana

Evolutionary constraints on the ability of herbivores to efficiently use a set of phytochemically similar hosts, while maintaining a high performance on phytochemically different hosts, are central in explaining the predominance of host specialization in phytophagous insects. Such feeding trade-offs could be manifested within insect populations as negative genetic correlations in fitness on different host species. We tested the hypothesis that feeding trade-offs were present within a population of the obliquebanded leafroller,Choristoneura rosaceana (Harris). Components of fitness were measured in families originating from an apple orchard that were fed on four host-plant species in the laboratory. Under the conditions of this experiment, all across-host genetic correlations were strongly positive, suggesting that this population comprised true generalists. With the exception of diapausing propensity, the heritability of the fitness components tended to be lower in caterpillars fed on apple leaves than in insects fed other hosts. This suggests a constraint on the selective response of the fitness components in the orchard environment.     

Genetic variation and covariation of aphid life-history traits across unrelated host plants

A central paradigm of life-history theory is the existence of resource mediated trade-offs among different traits that contribute to fitness, yet observations inconsistent with this tenet are not uncommon. We previously found a clonal population of the aphid Myzus persicae to exhibit positive genetic correlations among major components of fitness, resulting in strong heritable fitness differences on a common host. This raises the question of how this genetic variation is maintained. One hypothesis states that variation for resource acquisition on different hosts may override variation for allocation, predicting strong fitness differences within hosts as a rule, but changes in fitness hierarchies across hosts due to trade-offs. Therefore, we carried out a life-table experiment with 17 clones of M. persicae, reared on three unrelated host plants: radish, common lambsquarters and black nightshade. We estimated the broad-sense heritabilities of six life-history traits on each host, the genetic correlations among traits within hosts, and the genetic correlations among traits on different hosts (cross-environment genetic correlations). The three plants represented radically different environments with strong effects on performance of M. persicae, yet we detected little evidence for trade-offs. Fitness components were positively correlated within hosts but also between the two more benign hosts (radish and lambsquarters), as well as between those and another host tested earlier. The comparison with the most stressful host, nightshade, was hampered by low survival. Survival on nightshade also exhibited genetic variation but was unrelated to fitness on other hosts. Acknowledging that the number of environments was necessarily limited in a quantitative genetic experiment, we suggest that the rather consistent fitness hierarchies across very different plants provided little evidence to support the idea that the clonal variation for life-history traits and their covariance structure are maintained by strong genotypexenvironment interactions with respect to hosts. Alternative explanations are discussed.     

Phylogenetic analysis reveals positive correlations between adaptations to diverse hosts in a group of pathogen‐like herbivores

A jack of all trades can be master of none—this intuitive idea underlies most theoretical models of host‐use evolution in plant‐feeding insects, yet empirical support for trade‐offs in performance on distinct host plants is weak. Trade‐offs may influence the long‐term evolution of host use while being difficult to detect in extant populations, but host‐use evolution may also be driven by adaptations for generalism. Here we used host‐use data from insect collection records to parameterize a phylogenetic model of host‐use evolution in armored scale insects, a large family of plant‐feeding insects with a simple, pathogen‐like life history. We found that a model incorporating positive correlations between evolutionary changes in host performance best fit the observed patterns of diaspidid presence and absence on nearly all focal host taxa, suggesting that adaptations to particular hosts also enhance performance on other hosts. In contrast to the widely invoked trade‐off model, we advocate a “toolbox” model of host‐use evolution in which armored scale insects accumulate a set of independent genetic tools, each of which is under selection for a single function but may be useful on multiple hosts.     

Trade-offs and the evolution of host specialization

Summary Trade-offs in performance on different hosts are thought to promote the evolution of host specificity by blocking host shifts. Yet, in contrast, most experiments using phytophagous insects have shown performance on alternative hosts to be uncorrelated or positively correlated. Recent quantitative genetic models based on mutation—selection balance indicate that underlying constraints on the simultaneous maximization of different components of fitness may not always generate negative genetic correlations. We suggest an alternative or additional explanation for the lack of observed negative genetic correlations. If performance is polygenically controlled and some performance loci possess only antagonistically pleiotropic alleles, then the expression of trade-offs in performance will vary over time in populations. Consequently, a trade-off will be seen only in populations that have adapted to two hosts and are at or close to genetic equilibrium. Therefore, studies testing performance on a novel as compared with a normal host will generally yield non-negative genetic correlations between performance on the two hosts. The results of published studies are consistent with the predictions of this hypothesis.     

Genetic and phenotypic variation in diet breadth in a generalist herbivore

Summary The genetic and plastic components of polyphagy were investigated in a population ofLymantria dispar, the gypsy moth. A simple genetic experiment assessed the expression of (1) genetic variability in life history traits within each of four environments, (2) genetic variability in diet breadth, expressed as a change in the ranks of family performance across hosts, and (3) homeostasis (equivalent performance by a family across hosts) versus phenotypic plasticity (variable performance by a family across hosts). Sibs from each of 14 families, randomly selected from a single population, were reared on four diets: two natural hosts — chestnut and red oak, and two synthetic hosts — a standard laboratory diet and a low-protein version of this diet. Average population performance, measured in terms of development time and pupal weight, was better on standard laboratory diet than on low-protein diet, and was equal on chestnut and red oak for pupal weight, but better on chestnut oak for development time. Average population performance provided no information about the genetic component of host use ability. The gypsy moth expressed genetic variation in development time within each host environment and in pupal weight within natural host environments. Phenotypic plasticity was expressed by a significant number of families in development time and pupal weight across synthetic hosts and, to a lesser extent, across natural hosts. It was only across natural hosts that genetic variation in diet breadth was expressed, and this was confined to females. Genetic variability in diet breadth may be maintained in this species as a consequence of the unpredictability of its food sources.     

Performance of two monophagous leaf feeding beetles (Coleoptera: Chrysomelidae) on each other's host plant: Do intrinsic factors determine host plant specialization?

There has been much recent debate on whether physiological tradeoffs in performance across hosts or ecological factors such as predation are the primary determinants of host plant specialization in plant-herbivore interactions. This paper examines the relative role of intrinsic behavioral and physiological factors in host specialization of two species of leaf-feeding beetles (Coleoptera: Chrysomelidae). Ophraella notulata and Ophraella slobodkini are sister taxa that feed exclusively on the asteraceous plants Iva frutescens and Ambrosia artemisiifolia, respectively. Ambrosia is the ancestral host plant for this pair of beetles. I performed full-sib breeding experiments in both the laboratory and the field to assess mean responses of each species to both its native host and the host of its congener, genetic variation within each species for traits associated with using each host, and tradeoffs in performance across hosts. I reared each beetle species on each host plant and measured larval consumption, survival, development time and growth. I measured only survival and growth in the field. Genetic correlations were calculated to assess tradeoffs in performance across hosts. In the laboratory experiment, larval survival of O. slobodkini on I. frutescens was lower and development time longer than on A. artemisiifolia. Survival of O. notulata on A. artemisiifolia was marginally lower than on I. frutescens while development time did not differ. There was little genetic variation among families in host use traits for either species. None of the estimates of genetic correlations were negative. The results of the field experiment support the results of the laboratory experiment. I conclude that O. notulata, the species with the derived host association, retains considerable ability to utilize the ancestral host plant, while O. slobodkini, the species witht he ancestral host association, does not show a similar ability to ut ilize the derived host. Tradeoffs in performance across hosts were not documented for either species of Ophraella. That notulata performs so well on A. artemissifolia suggests that intrinsic factors may not provide a sufficient explanation for the host specialization of this species on I. frutescens.     

Host use of a hemiparasitic plant: no trade-offs in performance on different hosts

To examine putative specialization of a hemiparasitic plant to the most beneficial host species, we studied genetic variation in performance and trade-offs between performance on different host species in the generalist hemiparasite, Rhinanthus serotinus. We grew 25 maternal half-sib families of the parasite on Agrostis capillaris and Trifolium pratense and without a host in a greenhouse. Biomass and number of flowers of the parasite were the highest when grown on T. pratense. There were significant interactions between host species and R. serotinus seed-family indicating that the differences in performance on the two hosts and without a host varied among the families. However, we found no significant negative correlations between performance of R. serotinus on the host species or between performance on the two hosts and autotrophic performance. Thus, the genetic factors studied here are not likely to affect the evolution of specialization of R. serotinus to the most beneficial host.     

GENETIC VARIATION AND COVARIATION IN RESPONSES TO HOST PLANTS BY ALSOPHILA POMETARIA (LEPIDOPTERA: GEOMETRIDAE)

Progeny of uncommon parthenogenetic genotypes of the polyphagous geometric Alsophila pometaria were reared on four host plant species representing the same genus, different confamilial genera, and different families. On the supposition that uncommon asexual genotypes have arisen recently from the sympatric sexual population, they may be viewed as a representation of variation in the sexual population that has been captured by parthenogenesis. In both the laboratory and the field, significant effects of genotype, host, and their interaction were found for survival. Live weight displayed significant effects of genotype, host, and genotype x host interaction in the laboratory, and significant main effects in the field. The broad heritability of live weight within hosts was significantly greater than zero in all cases, ranging from 0.18 to 0.33. Heritability values in the field were similar to those in the laboratory. Genetic correlations between weight attained on pairs of host plants, calculated from uncorrected family means, were all positive and many were statistically significant. When the data were corrected for differences in generalized vigor by taking the deviations from genotype means on a standard host plant, one of nine genetic correlations was significant and positive, and one was significant and negative. Within their limits of precision, these data suggest that genetic factors enhancing performance on one host do not generally have strong antagonistic pleiotropic effects on performance on the other hosts in this population. The relevance of these observations to the evolution of resource specialization in general and host specialization by phytophagous insects in particular is discussed. The common assumption that trade-offs in efficiency of utilization cause the evolution of specialized resource use requires more empirical evidence than seems to exist.     

Life‐history trade‐offs vary with resource availability across the geographic range of a widespread plant

• Trade‐offs between reproduction, growth and survival arise from limited resource availability in plants. Environmental stress is expected to exacerbate these negative correlations, but no studies have evaluated variation in life‐history trade‐offs throughout species geographic ranges. Here we analyse the costs of growth and reproduction across the latitudinal range of the widespread herb Plantago coronopus in Europe.
• We monitored the performance of thousands of individuals in 11 populations of P. coronopus, and tested whether the effects of growth and reproduction on a set of vital rates (growth, probability of survival, probability of reproduction and fecundity) varied with local precipitation and soil fertility. To account for variation in internal resources among individuals, we analysed trade‐offs correcting for differences in size.
• Growth was negatively affected by previous growth and reproduction. We also found costs of growth and reproduction on survival, reproduction probability and fecundity, but only in populations with low soil fertility. Costs also increased with precipitation, possibly due to flooding‐related stress. In contrast, growth was positively correlated with subsequent survival, and there was a positive covariation in reproduction between consecutive years under certain environments, a potential strategy to exploit temporary benign conditions.
• Overall, we found both negative and positive correlations among vital rates across P. coronopus geographic range. Trade‐offs predominated under stressful conditions, and positive correlations arose particularly between related traits like reproduction investment across years. By analysing multiple and diverse fitness components along stress gradients, we can better understand life‐history evolution across species’ ranges, and their responses to environmental change.

     

Genetic structure and host–parasite co‐divergence: evidence for trait‐specific local adaptation

Host–parasite co‐evolution can lead to genetic differentiation among isolated host–parasite populations and local adaptation between parasites and their hosts. However, tests of local adaptation rarely consider multiple fitness‐related traits although focus on a single component of fitness can be misleading. Here, we concomitantly examined genetic structure and co‐divergence patterns of the trematode Coitocaecum parvum and its crustacean host Paracalliope fluviatilis among isolated populations using the mitochondrial cytochrome oxidase I gene (COI). We then performed experimental cross‐infections between two genetically divergent host–parasite populations. Both hosts and parasites displayed genetic differentiation among populations, although genetic structure was less pronounced in the parasite. Data also supported a co‐divergence scenario between C. parvum and P. fluviatilis potentially related to local co‐adaptation. Results from cross‐infections indicated that some parasite lineages seemed to be locally adapted to their sympatric (home) hosts in which they achieved higher infection and survival rates than in allopatric (away) amphipods. However, local, intrinsic host and parasite characteristics (host behavioural or immunological resistance to infections, parasite infectivity or growth rate) also influenced patterns of host–parasite interactions. For example, overall host vulnerability to C. parvum varied between populations, regardless of parasite origin (local vs. foreign), potentially swamping apparent local co‐adaptation effects. Furthermore, local adaptation effects seemed trait specific; different components of parasite fitness (infection and survival rates, growth) responded differently to cross‐infections. Overall, data show that genetic differentiation is not inevitably coupled with local adaptation, and that the latter must be interpreted with caution in a multi‐trait context.     

Genetic basis for established and novel host plant use in a herbivorous ladybird beetle, Epilachna vigintioctomaculata

Genetic trade-offs in host plant use are thought to promote the evolution of host specificity. Experiments on a range of herbivorous insects, however, have found negative genetic correlation in host plant use in only a limited number of species. To account for the general lack of negative genetic correlation, recent hypotheses advocate that different stages in evolution of host use must be distinguished: initial performance on a novel host in comparison with the established host, and performance on both hosts after the insect population has interacted with both hosts for a long time. The hypotheses suggest that genetic correlation may not necessarily be negative at the initial stage. The present study examines growth performance on both the established and a novel host in a herbivorous ladybird beetle, Epilachna vigintioctomaculata Motschulsky (Coccinellidae, Epilachninae). The results show that traits of growth performance across hosts were positively or neutrally correlated, but there was no evidence of a negative genetic correlation. In addition, significant genetic variance of growth performance on each host was detected, suggesting that E. vigintioctomaculata can potentially respond to selection for increased performance on both plant species. These results and similar results from experiments on other herbivores suggest that host expansion may not be constrained genetically, at least at the initial stage of host range evolution.     

Loss of adaptation following reversion suggests trade‐offs in host use by a seed beetle

Experimental evolution has provided little support for the hypothesis that the narrow diets of herbivorous insects reflect trade‐offs in performance across hosts; selection lines can sometimes adapt to an inferior novel host without a decline in performance on the ancestral host. An alternative approach for detecting trade‐offs would be to measure adaptation decay after selection is relaxed, that is, when populations newly adapted to a novel host are reverted to the ancestral one. Lines of the seed beetle Callosobruchus maculatus rapidly adapted to a poor host (lentil); survival in lentil seeds increased from 2% to > 90% in < 30 generations. After the lines had reached a plateau with respect to survival in lentil, sublines were reverted to the ancestral host, mung bean. Twelve generations of reversion had little effect on performance in lentil, but after 25–35 generations, the reverted lines exhibited lower survival, slower development and smaller size. The most divergent pair of lines was then assayed on both lentil and mung bean. Performance on lentil was again much poorer in the reverted line than in the nonreverted one, but the lines performed equally well on mung bean. Moreover, the performance of the nonreverted line on mung bean remained comparable to that of the original mung‐bean population. Our results thus present a paradox: loss of adaptation to lentil following reversion implies a trade‐off, but the continued strong performance of lentil‐adapted lines on mung bean does not. Genomic comparisons of the reverted, nonreverted and ancestral lines may resolve this paradox and determine the importance of selection vs. drift in causing a loss of adaptation following reversion.     

Jack of all trades masters novel host plants: positive genetic correlations in specialist and generalist insect herbivores expanding their diets to novel hosts

One explanation for the widespread host specialization of insect herbivores is the 'Jack of all trades-master of none' principle, which states that genotypes with high performance on one host will perform poorly on other hosts. This principle predicts that cross-host correlation in performance of genotypes will be negative. In this study, we experimentally explored cross-host correlations and performance among families in four species (two generalist and two specialist) of leaf beetles (Cephaloleia spp.) that are currently expanding their diets from native to exotic plants. All four species displayed similar responses in body size, developmental rates and mortality rates to experimentally controlled diets. When raised on novel hosts, body size of larvae, pupae and adults were reduced. Development times were longer, and larval mortality was higher on novel hosts. Genotype × host-plant interactions were not detected for most traits. All significant cross-host correlations were positive. These results indicate very different ecological and evolutionary dynamics than those predicted by the 'Jack of all trades-master of none' principle.     

Parallel evolution in sympatric, hybridizing species: performance of Colias butterflies on their introduced host plants

Shared ancestry and introgression can contribute to genetic similarity between hybridizing species, and it is generally difficult to disentangle these causes. However, shared ancestry plays a more limited role in traits that have recently undergone parallel directional selection in the two species, permitting the role of introgression to be better understood. The butterflies Colias eurytheme (Boisduval) and Colias philodice (Godart) (Lepidoptera, Pieridae) are native to North America and have shifted their host ranges in parallel onto several introduced weedy and agricultural legumes. These butterflies hybridize at moderate rates throughout their range, and there is a strong possibility that they could be sharing host‐associated adaptations. We split families of each species among nine introduced, prospective hosts and measured survivorship, larval duration, pupal weight, and a new variable, effective daily growth rate (DGR), analogous to a compound daily interest rate in economics. We found strong effects of host, sex, and family (species), but negligible effects of the host*species interaction that would indicate species‐specific differences in performance on different hosts. We found species‐specific life‐history differences: C. eurytheme matured significantly later and reached a significantly larger body size than C. philodice while growing at the same DGR. Protandry was strong, and males, in addition to pupating sooner than females, grew significantly faster than females as measured by DGR. We measured broad‐sense heritabilities and genetic correlations for host‐associated performance variables. Most pairwise comparisons of performance among hosts and most pairwise comparisons between performance variables showed positive genetic correlations, except survivorship where little heritability was found. Nevertheless, a factorial multivariate analysis of variance of G‐matrices showed highly significant species, host, and host*species interactions, suggesting differentially evolving genetic architectures underlying host adaptation in these two species, despite the small differences in overall performance. At least some of the genes affecting host performance in Colias are likely to be in the small, species‐diagnostic regions and not shared via introgression between these hybridizing species. For biologists interested in the evolutionary ecology of their host associations, including applied biologists managing their agricultural pest potential, C. eurytheme and C. philodice are most usefully studied as if they were a single polymorphic species wherever they co‐exist. In studying species that hybridize readily with a sympatric congener, it may often be necessary to include the second species in the experimental design.     

Trade-offs in larval performance on normal and novel hosts

The evolution of host specialization in phytophagous insects is generally thought to involve genetic trade-offs that prevent individuals from maximizing fitness simultaneously on two or more hosts. Several hypotheses, however, have suggested that trade-offs may not be evident in experiments comparing larval performance on normal and novel hosts. Tests on survivorship, growth rate, and pupal mass among families of the swallowtail butterfly Papilio oregonius on its normal host and on a novel host provide support for these hypotheses, although they do not discriminate among them. Families differed in their relative performance on the hosts, but there was no evidence of a negative genetic correlation between hosts for any of the measures of performance. In addition, there were no correlations among the different measures, corroborating an earlier result suggesting that these different components of performance in the P. machaon species group are under at least partially separate genetic control. These results and similar results published for other insects have now produced a body of studies indicating that genetic trade-offs in individual components of larval performance may not be a major factor preventing shifts onto novel host plants. Trade-offs leading to the evolution of host specialization are more likely to involve coordination among the various components of performance together with ecological factors that allow higher fitness on one host than on others.     

Genotype‐by‐genotype interactions between an insect and its pathogen

Genotype‐by‐genotype (G×G) interactions are an essential requirement for the coevolution of hosts and parasites, but have only been documented in a small number of animal model systems. G×G effects arise from interactions between host and pathogen genotypes, such that some pathogen strains are more infectious in certain hosts and some hosts are more susceptible to certain pathogen strains. We tested for G×G interactions in the gypsy moth (Lymantria dispar) and its baculovirus. We infected 21 full‐sib families of gypsy moths with each of 16 isolates of baculovirus and measured the between‐isolate correlations of infection rate across host families for all pairwise combinations of isolates. Mean infectiousness varied among isolates and disease susceptibility varied among host families. Between‐isolate correlations of infection rate were generally less than one, indicating nonadditive effects of host and pathogen type consistent with G×G interactions. Our results support the presence of G×G effects in the gypsy moth–baculovirus interaction and provide empirical evidence that correlations in infection rates between field‐collected isolates are consistent with values that mathematical models have previously shown to increase the likelihood of pathogen polymorphism.