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Evol Appl. Jul 2012; 5(5): 481–488.
Published online Jun 7, 2012. doi:  10.1111/j.1752-4571.2012.00274.x
PMCID: PMC3407866

Evolution in biocontrol strains: insight from the harlequin ladybird Harmonia axyridis

Abstract

After being used as a biocontrol agent against aphids for decades without harmful consequences, the Asian harlequin ladybird Harmonia axyridis has suddenly become an invasive pest on a worldwide scale. We investigate the impact of captive breeding on several traits of this ladybird such as genetic diversity, fecundity, survival and pathogen resistance. We conducted an experiment in the laboratory to compare the fecundity and the susceptibility to the entomopathogenic fungus Beauveria bassiana of wild and biocontrol adults of H. axyridis. We compiled these new findings with already published data. Altogether, our findings suggest that mass rearing of biological control agents may strongly impact genetic diversity and life-history traits. We discuss how such changes may subsequently affect the fitness of biological control strains in natural environments.

Keywords: biological control, biological invasion, fungal entomopathogen, genetic drift, Harmonia axyridis, inadvertent selection, laboratory adaptation, life-history traits

Introduction

Biological control agents can be viewed as a type of domesticated species (Diamond 2002; Savolainen et al. 2002; Ross-Ibarra et al. 2007), particularly when they are reared in captivity prior to release. As such, they may experience the same types of phenotypic and genetic changes experienced by other domesticated species (Burke et al. 2007; O'Neill et al. 2010; Rubin et al. 2010).

As such, it is important to document and understand the evolutionary changes that occur in captive populations of biological control agents. Three major mechanisms may cause genetic changes under laboratory rearing conditions: random drift, inbreeding and selection (Hopper et al. 1993). The first two mechanisms can be related to small population size. Indeed, drift arises from taking a finite sample from a population: by chance, some individuals, and thus genotypes, contribute more and some less in each generation. This process can be substantial and induces a high initial loss of genetic variability when only few founders are used to start laboratory populations and/or when such populations include a low number of effective parents at each generation (Wajnberg 1991; Fiumera et al. 2000). Inbreeding, the mating of close relatives, increases the frequency of homozygotes and can lead to changes in gene frequencies by exposing deleterious recessive alleles to selection. Deleterious effects of inbreeding could deter the successful field colonization of exotic species in classical biological control programs. For instance, Kuriwada et al. (2011) reported higher inbreeding depression in a mass-reared strain of Cylas formicarius than in a wild strain, suggesting that mass-reared weevils suffer serious inbreeding depression.

Because captive environments differ from wild ones, selection can favour some peculiar genetic variants. In agreement with this, genetic adaptations to captivity have been documented in various species (see for instance, Zouros et al. 1982; Allard 1988; Levin et al. 2001; Lewis and Thomas 2001; Heath et al. 2003). It is worth stressing that selection can be intentional or not. On the one hand, humans can alter deliberately the genetic composition of a set of individuals to suit their needs, a process called genetic improvement (Hopper et al. 1993). Such intentional selection has allowed improving the efficiency of several biological control agents, especially in relation to host acceptance/suitability, temperature tolerance, diapause induction and insecticide resistance (Hoy 1985). For instance, two greenhouse populations of Amblyseius fallacis have shown a 64-fold increase in resistance against permethrin insecticide after 12 rounds of selection. On the other hand, continued laboratory breeding may result in relaxed selection for some life-history characteristics (Sgro and Partridge 2000; Mack et al. 2001). Such characteristics selected under captivity conditions can sometimes be disadvantageous in the natural environment (Waples 1999; McGinnity et al. 2003; Kraaijeveld-Smit et al. 2006; Araki et al. 2007; Frankham 2008). For instance, a hatchery stock of chinook salmon (Oncorhynchus tshawytscha) in Canada evolved smaller eggs and supplementation of wild populations using this stock reduced egg size in introgressed wild populations, resulting in reduced fitness in nature (Heath et al. 2003). Such inadvertent selection may also occur for biological control agents during laboratory culture and maintenance of captive populations, favouring laboratory-adapted genotypes that are maladapted to the field (Hopper et al. 1993).

Given its use for biological control and invasive history (reviewed in Brown et al. 2011), the Asian harlequin ladybird Harmonia axyridis is a good biological model to examine the evolutionary impact of conditions in captivity and its potential consequences in the field. Native to Asia, the coccinellid H. axyridis has been introduced repeatedly in North America as a biocontrol agent against aphids since 1916 (Tedders and Schaefer 1994; Krafsur et al. 1997) and in Europe and South America since 1980s (Ongagna et al. 1993; Poutsma et al. 2008). Despite recurrent intentional releases, the species did not establish for decades. However, it suddenly became invasive in eastern and western North America in 1988 and 1991 (Chapin and Brou 1991; LaMana and Miller 1996), in Europe in 2001 (Belgium, Adriaens et al. 2003), South America in 2001 (Argentina, Saini 2004) and in Africa in 2004 (South Africa, Stals and Prinsloo 2007). The species has spread widely in these areas where it consumes nontarget arthropods, invades households and is a pest of fruit production (Koch 2003; Koch and Galvan 2008). Based on the analysis of neutral genetic variation, Lombaert et al. (2010, 2011) recently retraced the routes of all five worldwide H. axyridis invasions. Eastern and western North American invasive populations originate from two independent introductions from the native Asian range. Surprisingly, eastern North America is the source of colonists for all other successfully invaded areas. In South America and South Africa, invasive populations bear no trace of genetic admixture with other sources. In Europe, however, Lombaert et al. (2010) found evidence for genetic admixture between eastern North American founders and individuals from the laboratory European biocontrol population used locally to manage aphid populations (with a contribution of biocontrol genes estimated around 43%).

In the present study, we took advantage of this context to investigate the impact of captive breeding on several characteristics (such as fecundity, larval survival, resistance to a pathogen or genetic diversity) by comparing different sources of H. axyridis, i.e. the laboratory mass-reared population used for biological control in Europe, as well as wild populations (invasive alien and native ones). To this end, we first conducted an experiment in the laboratory to compare the fecundity and the susceptibility to the entomopathogenic fungus Beauveria bassiana of wild and biocontrol adults of H. axyridis. We then compiled these new findings with already published data by our research group and close collaborators to test for several predictions regarding the impact of captive breeding practices on H. axyridis.

First, we expect a lower genetic diversity in European biocontrol population compared to wild ones owing to genetic drift. It is likely that only a few founders would have been used to start laboratory population and/or the number of effective parents at each generation was most likely lower than in a wild population.

Second, the laboratory environment strongly differs from the wild ones. Notably, lab-rearing conditions do not display seasonal variations of temperatures and cultures are maintained as free of pathogen as possible. Owing to the absence of these selective pressures in captivity, we could hypothesize that biocontrol individuals should exhibit a lower survival rate at low temperatures and a lower resistance to a pathogen such as B. bassiana, the latter being present on both the native and introduced ranges of H. axyridis. It has to be noted that a decrease of both traits upon relaxation of selection requires the additional assumption of a cost, either a quantitative cost or a trade-off with some other trait (Hufbauer 2002).

Third, similar selection in different environments might not be equally effective in leading to adaptation (Wilson et al. 2006). Notably, lab-rearing conditions being less multifaceted and more constant than field conditions, directional selection on particular traits maximizing fitness in captivity may be more effective in biocontrol population. For instance, we might predict that biocontrol individuals would display higher larval survival, higher male reproductive success and an earlier and higher fecundity. Obviously, these four traits may also boost invasive success. By specifically comparing biocontrol population, European invasive and American invasive ones, we could assess whether the traits with higher values in the biocontrol population have been preserved or not in the field (i.e. in the European invasive population, the latter being the result of an admixture between American population and biocontrol one).

Materials and methods

Description of published data

Our research group and close collaborators have previously produced data comparing biocontrol-type H. axyridis with field collected ones for several characteristics. Lombaert et al. (2011) estimated genetic diversity at 18 microsatellites in the European biocontrol populations and in several native and invasive populations. Three other studies have compared, using experiments in controlled conditions, the performances of European biocontrol individuals and field collected ones. First, Lombaert et al. (2008) measured the survival rate during quiescence at low temperatures for biocontrol and invasive European adults. Second, Facon et al. (2011) estimated the male reproductive success of biocontrol and invasive European adults. Third, Turgeon et al. (2011) assessed larval survival, age at first reproduction and fecundity for individuals coming from biocontrol, American and European invasive populations. We compiled these published data with those obtained in our new study (see above), to test for predictions described in Introduction regarding the impact of captive breeding practices on H. axyridis.

New experiments: susceptibility to B. bassiana and fecundity

Population sampling and rearing conditions

Five H. axyridis populations of three different types were used in this study, i.e. a laboratory-reared type commonly used for biological control purposes as well as invasive and native types. Two populations were collected from the native range of H. axyridis in 2009 (Beijing in China and Fuchuk in Japan). Two invasive populations were collected in North America and Europe between 2008 and 2009 (Quebec City in Canada and Bataszek in Hungary). One population was obtained from a laboratory population of a biocontrol agent producer (winged strain of H. axyridis; Biotop company, Valbonne, France) in 2007. This biocontrol population has been reared in laboratory conditions since 1982; this is for a minimum of 70 generations (assuming 2.5 generations per year; Koch 2003; Koch et al. 2006). This population was commercialized and used for the biocontrol of aphids between 1995 and 1999 throughout Europe (Ferran et al. 1997; Tourniaire et al. 2000). We reared the five populations for two generations under controlled conditions (24°C; L: D 14:10; 60% relative humidity) to minimize potential biases owing to maternal effects until the third generation was used for experiments. All populations were fed ad libitum with irradiated eggs of Ephestia kuehniella (Lepidoptera: Pyralidae) for these generations as well as for the following experiment.

Experimental procedures

A total of 40 females and 40 males of the third laboratory-standardized generation of each of the five test populations were placed into a large box during 10 days to allow copulations. After this period, females were transferred individually into 9-cm-diameter Petri dishes and kept at 24°C; L: D 14:10; 60% relative humidity. Each female was presented to a single male for a period of 24 h. This was repeated three times with three different males per week. This procedure minimized density effects (e.g., delayed growth or reduced fecundity in paired individuals owing to competition) whilst allowing multiple copulations.

For each fertilized female, the number of eggs laid during seven consecutive days following the first clutch were counted and averaged to estimate the mean daily fecundity prior treatment. Females of each population were then infected with B. bassiana or remained untreated. It is known to be a natural mortality agent among overwintering adult coccinellids (Steenberg and Harding 2009). This result has led some authors to suggest that B. bassiana could be a potential candidate for the biological control of invasive populations of H. axyridis (Shah and Pell 2003; Kenis et al. 2008; Roy et al. 2011). The strain of B. bassiana used in this study corresponded to a commercial preparation (BotaniGardES®, strain GHA 2.2 × 1013 conidia per kg; Laverlam International Corporation, Butte, USA) that was already used in an experiment with H. axyridis (Roy et al. 2008). The concentration of viable conidia was 6.4 × 108 per g. Infected females were singly held in a B. bassiana solution in plastic cups (2 cm×3 cm) for 5 s (2.2 × 108 conidia per ml). The exposures have been made during four consecutive days with an equal representation of each population each day. It has to be noted that no significant differences were found between exposure days. The control females were held singly in sterile distilled water for the same duration. A total of 89 females were infected with the fungus and 48 females were used in controls. After exposures to fungus or sterile distilled water, all females were transferred individually into 9-cm-diameter Petri dishes and kept at 24°C; L: D 14:10; 80% relative humidity. Subsequently, eggs were counted per female and removed on a daily basis during 15 days to estimate the mean daily fecundity after treatment. Mortality was recorded daily until 15 days after treatment. Dead individuals were transferred to 1.5-mL Eppendorf tubes with moistened cotton to observe external fungal growth and hence to confirm B. bassiana as likely cause of death. External fungal growth has been recorded for around 60% (with no differences between populations) of treated females, as it is classically observed with this kind of bioassay.

Statistical analyses

All data were analysed using the software JMP 8.01 (SAS Institute Inc., Cary, NC, USA). First, we calculated the proportional reduction in daily mean egg production for each female as follows: ReductionFecundity = (Daily fecundity prior treatmentDaily fecundity after treatment)/Daily fecundity prior treatment. This trait was then analysed using anova with population type (biocontrol, native or invasive), treatment (infected or control) and population nested in population type, as well as the interaction between population type and treatment as fixed factors. Second, we analysed the mortality using GLM (binomial distribution) with population type (biocontrol, native or invasive) and population nested in population type as fixed factors. We excluded the control females from this analysis because none of them died during the experiment. Therefore, the factor treatment was removed from the full model. For the dead infected females, the date of death (i.e. survival time) was analysed using anova with population type (biocontrol, native or invasive) and population nested in population type as fixed factors. Finally, we used control females to analyse the fecundity apart from the effect of the fungus using anova with population type (biocontrol, native or invasive) and population nested in population type as fixed factors.

For the response variables analysed using anova, we performed two analyses, one with the original data and one with the traditional transformations (square root for fecundity, log for survival time and Box-Cox for ReductionFecundity; Sokal and Rohlf 1995). As similar results were obtained, only results from untransformed data will be reported.

Results and discussion

This study supports the predictions that laboratory conditions have significantly impacted several characteristics of H. axyridis (Table 1). We detailed these results in three parts: neutral genetic diversity, traits counter-selected in the laboratory and traits under positive selection in the laboratory.

Table 1
Predictions and compilations of results regarding the impact of captive breeding practices in H. axyridis on various traits (for details, see Introduction and Results). Symbols + and − indicate relatively high and low values of these traits, respectively, ...

Neutral genetic diversity

Genetic drift is the most important of the random processes that influence the gene frequencies in a laboratory colony (Joslyn 1984). To avoid a substantial loss of genetic diversity, Wajnberg (1991) recommended that laboratory cultures should be started with the maximal effective population size, and maintaining a maximum number, within the limitations imposed, during the entire rearing process.

In the case of H. axyridis, the European biocontrol population exhibits evidence of substantial genetic drift, as it harbours significantly lower genetic diversity (2.4 alleles per locus) than native (5.3–6.6 alleles per locus) or invasive (4.1–6.5 alleles per locus; Lombaert et al. 2011) populations. Because the European invasive population originated from a genetic admixture between eastern North American founders and individuals from the laboratory European biocontrol population (Lombaert et al. 2010), the level of genetic diversity is also significantly lower in the European biocontrol population than in the European invasive population (6.0 alleles per locus).

Traits counter-selected in the laboratory

In agreement with our predictions, the European biocontrol population exhibits lower performance than natural populations (Table 1). It has a significantly lower survival rate (41%) during quiescence at low temperatures compared to invasive European population (86%). Similarly, European biocontrol individuals are significantly more susceptible to B. bassiana infection than individuals collected from native or invasive populations. In the biocontrol population, there are twice as many deaths as in the natural native and invasive populations (93% vs 38% and 46%, respectively; P = 0.0007) owing to B. bassiana infection, whereas no significant differences in mortality are found between invasive and native females (Table 2 and Fig. 1). On the contrary, the decrease of fecundity and the survival time of the infected females owing to fungus infection are not influenced by the population type (i.e. biocontrol, native or invasive; Table 2 and Fig. 2).

Figure 1
Mean values for (A) mortality and (B) survival time owing to fungus infection, depending on the population type, i.e. biocontrol, invasive and native.
Figure 2
Mean values for (A) fecundity without fungus infection and (B) fecundity reduction owing to fungus infection, depending on the population type, i.e. biocontrol, invasive and native.
Table 2
Results of statistical analyses for reduction of fecundity, mortality and survival time owing to fungus infection and for fecundity without fungus infection

We suggest that both mortality during quiescence and mortality because of fungal infection can be viewed as examples of adverse genetic changes as a result of captive rearing. An important issue raised by such adverse genetic changes is how selection for laboratory-adapted genotypes may induce maladaptation to the field when laboratory-reared individuals are introduced into the wild and reproduce among wild individuals. According to the literature, characteristics selected under captive conditions are often disadvantageous in natural environments (see for instance Frankham et al. 1986; Fleming and Gross 1993; Reisenbichler and Rubin 1999; Chilcote 2003; Heath et al. 2003; Kraaijeveld-Smit et al. 2006). The most emblematic examples come from fishes where selection in hatcheries causes highly deleterious effects. For instance, lifetime reproductive success of hatchery fish stocks, once returned to the field, was found to be only 5–15% of that for the wild fish populations (Leider et al. 1990). In the case of H. axyridis, the decrease of survival during quiescence and pathogen resistance upon relaxation of selection suggests that there exists a cost for both traits, either a quantitative cost or a trade-off with some other trait that has been selected in laboratory conditions. The very poor survival rate at low temperatures of the biocontrol strain seems to be counter-selected in the field as the invasive European populations show a much higher survival rate. Regarding the susceptibility to B. bassiana, the invasive European population displays the same mortality owing to this fungus as the invasive American population, which is twofold lower than the biocontrol population. This result indicates that this higher susceptibility of biocontrol population seems also to be counter-selected in the field. Both results are, at least intuitively, not surprising as survival during quiescence and resistance to pathogens are certainly important parts of the fitness of H. axyridis individuals during the invasion process of natural habitats.

Traits under positive selection in the laboratory

The European biocontrol population displays higher values for several traits suggesting a higher efficiency of directional selection in the less multifaceted laboratory environment (Table 1). Indeed, it has a significant higher male reproductive success than the European invasive population (Facon et al. 2011). When competing with European invasive males, biocontrol males sire around 75% of offspring produced by females. Biocontrol females display also higher fecundity (average = 40.0 eggs per day) than native (average = 28.6 eggs per day) and invasive ones (28.2 eggs per day; Fig. 2 and Table 2). This trend is confirmed by Turgeon et al. (2011), who showed that biocontrol females lay significantly more eggs (38.9 eggs per day) than females from the American (25.4 eggs per day) and European (29.5 eggs per day) invasive populations. For two other traits, biocontrol individuals performed better than American invasive individuals but not compared to European invasive ones. Biocontrol individuals survive at significantly higher rates in the larval period (91%) and reproduce significantly earlier (11.1 days after emergence on average) than the American invasive population (73% and 13.3 days, respectively) but not compared to European invasive population (92% and 12.1 days).

A number of genetic adaptations to captivity have been previously suggested in a variety of taxa (Frankham 2008). Most of these cases also correspond to an increase of fecundity and a reduction of development time (Hopper et al. 1993; Frankham 2008). For instance, a threefold increase in reproductive fitness has been reported over 84 generations in the dipteran fly Drosophila (Gilligan and Frankham 2003). The butterfly Pieris brassicae laid many more eggs in cage experiments and had a higher ovary mass when laboratory reared for 100-150 generations than females from a stock recently obtained from the wild (Lewis and Thomas 2001). For this kind of traits, we could envisage that adaptation to laboratory conditions may also inadvertently select for values favouring establishment and range expansion in the field. With respect to H. axyridis, it seems to be the case for larval survival and age at first clutch as European invasive population has retained the biocontrol genetic background associated to higher fitness. On the other hand, European invasive population displays lower fecundity than biocontrol individuals. It is more difficult to envision how lower fecundity may be advantageous for the invasive European beetles. This result suggests that it may exist a trade-off between fecundity and unknown trait(s) not considered in the study that could be selected in the field.

Conclusions

A weakness of our study lies in the absence of replicate biocontrol populations. Unfortunately, to our knowledge, there remain only two biocontrol strains of H. axyridis (Biotop and Biobest; Turgeon et al. 2011). Furthermore, the Biobest strain was derived from the Biotop strain used in this study and thus even was it available to us, it would be somewhat problematic as a replicate. Given this limitation, we cannot rule out with certainty that the differences of life-history trait values observed in the biocontrol-type H. axyridis only stem from genetic drift, more especially as we demonstrated that the European biocontrol population exhibits evidence of substantial genetic drift. However, this would imply that only individuals with these trait values were sampled in the creation of this laboratory mass-reared biocontrol population. It seems unlikely that genetic drift alone can explain all the changes of trait values along our predictions on the impact of captive breeding and the action of selection seems more parsimonious. Ruling out this alternative hypothesis more definitively would require experimental selection, which would provide a better understanding of the genetic architecture of the traits, and would give us information about the relative likelihood of drift versus selection.

This study hence supports the predictions that biological control agents can undergo drastic genetic and phenotypic changes as a consequence of laboratory conditions. However, we are still at an early stage in understanding how mass rearing of biological control agents can induce genetic changes of life-history traits important for the success of field releases or for evolutionary trajectories of wild populations. We hope that our study will stimulate new research on this topic.

Acknowledgments

We thank D. Bourguet and N. Ris for comments and discussions. This work was supported by grants from the French Agropolis Foundation (RTRA – Montpellier, BIOFIS project number 1001-001) and from the INRA department SPE.

Data archiving statement

Raw data used to generate the main results of the paper are available as Online Supplementary Material.

Supporting Information

Additional Supporting Information may be found in the online version of this article:

Data S1. Raw data concerning the experiment of susceptibility to Beauveria bassiana.

Please note: Wiley-Blackwell are not responsible for the content or functionality of any supporting materials supplied by the authors. Any queries (other than missing material) should be directed to the corresponding author for the article.

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