Abstract Inbreeding depression is a major concern in almost all human activities relating to plant and animal breeding. The biological control of pests with natural enemies is no exception, because populations of biocontrol agents experience a series of bottlenecks during importation, rearing, and introduction. A classical biological control program for the Comstock mealybug Pseudococcus comstocki (Hemiptera: Pseudococcidae) was initiated in France in 2008, based on the introduction of an exotic parasitoid, Allotropa burrelli Mues. (Hymenoptera: Platygastridae), a haplodiploid parasitoid imported from Japan. We evaluated the sensitivity of A. burrelli to inbreeding, to optimize rearing and release strategies. We compared several morphological and life‐history traits between the offspring of siblings and the offspring of unrelated parents. We took into account the low level of genetic variability due to the relatively small size of laboratory‐reared populations by contrasting two types of pedigree: one for individuals from a strain founded from a single field population, and the other generated by hybridizing individuals from two strains founded from two highly differentiated populations. Despite this careful design, we obtained no evidence for a negative impact of inbreeding on laboratory‐reared A. burrelli. We discussed the results in light of haplodiploid sex determination and parasitoid mating systems, and classical biological control practices.
We performed no-choice tests to study the host range of the parasitoid Allotropa burrelli (Muesebeck) (Hymenoptera: Platygastridae) for use against the Comstock mealybug, Pseudococcus comstocki (Kuwana) (Hemiptera: Pseudococcidae), in Southern France. We tested three Pseudococcidae species as potential non-target hosts: two species from the same genus (Pseudococcus longispinus and Pseudococcus viburni) and Planococcus citri. Allotropa burrelli did not parasitize any of the non-target mealybug species tested. No attempt of oviposition was recorded for the three species tested during the first 20min of parasitoid release and no parasitism occurred in 6-8hr of exposure of the mealybugs to the parasitoid.
Thomas Mathers (The Genome Analysis Centre UK) Evidence for ancient expansions of gene families in aphids and genome streamlining in M. persicae. [Mathers T., Chen Y., Mugford S., Van Oosterhout C., Swarbreck D., Hogenhout S.] Grit Kunert (Max-Planck Institute for Chemical Ecology Germany) Who is manipulating whom? The relationship between pea aphid biotypes and their host plants. [Kunert G.] Jens Joschinski (University of Würzburg Germany) Day length constraints and diurnal activity of the pea aphid. [Joschinski J., Krauss J.] Freddy Tjallingii (EPG systems Netherlands) Early sieve element interactions during stylet penetration. [Tjallingii W.F.] Yazhou Chen (John Innes Centre UK) Transcription plasticity of specific gene families are involved in Myzus persicae adaptation to diverse plant species. [Chen Y., Mathers T., Mugford S., Van Oosterhout C., Swarbreck D., Hogenhout S.]
Inbreeding and inbreeding depression are key processes in small or isolated populations and are therefore central concerns for the management of threatened or (re)introduced organisms. Haplodiploid species of the order Hymenoptera have a particular status with regard to inbreeding depression. Although recessive deleterious alleles that are expressed in males should be purged, an alternative form of inbreeding depression exists in species with single-locus complementary sex determination (sl-CSD). Under sl-CSD, genetically-related parents have a high probability of producing sterile sons instead of fertile daughters. In this article, we study inbreeding depression in Venturia canescens (Hymenoptera: Ichneumonidae), a parasitoid wasp with sl-CSD. We used a crossing design to manipulate relatedness according to three levels: within-family, between-family and between-population. For each level, several fitness components were measured on parents and female offspring. We found a 20% reduction in egg load at emergence for inbred crosses. Inbred crosses also yielded a higher proportion of males, as expected in a species with sl-CSD. Mating probability, presence of daughters among offspring, body size, symmetry and longevity were unaffected by inbreeding.
Summary1. Host plant quality affects herbivorous insect performance and consequently their susceptibility to natural enemies. Recently, it has been hypothesized that the immune function of herbivorous insects can be altered by their host plant, thus generating variation in their susceptibility to entomopathogens. Previous studies testing this hypothesis provided contradictory outcomes, mainly as a result of the differences in methodology such as measuring a single‐immune parameter rather than considering trade‐off‐mediated interactions between immune defence systems of the insect. Here, we hypothesized that plant‐mediated changes in insect immunity could result from the alteration of physiological immune effectors of the herbivore evident as trade‐offs.2. Larvae of an inbred strain of the European grape berry moth Eupoecilia ambiguella were reared on five artificial diets each based on a different grape variety (Chardonnay, Chasselas, Gewurztraminer, Merlot, Riesling) and tested for changes in the baseline concentration of haemocytes, activities of the prophenoloxidase (PPO) system and of antimicrobial peptides of their haemolymph. Immune responsiveness of larvae across diets was also assessed by measuring changes in haemocyte concentration and activity of the PPO system after a bacterial immune challenge.3. We found that variation among diets significantly affected immune defences of larvae. The alteration of the E. ambiguella immune system appears plastic and partly mediated by existing physiological trade‐offs between immune pathways, at least between induced antibacterial defences and the PPO system.4. These results clearly show that host plant quality can affect immune defences and potentially disease resistance of E. ambiguella and that these changes in immunity may also result from intrinsic trade‐offs between immune defence systems in insects.