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Genetic incompatibility drives mate choice in a parasitic wasp

Abstract

Introduction

Allelic incompatibility between individuals of the same species should select for mate choice based on the genetic make-up of both partners at loci that influence offspring fitness. As a consequence, mate choice may be an important driver of allelic diversity. A complementary sex determination (CSD) system is responsible for intraspecific allelic incompatibility in many species of ants, bees, and wasps. CSD may thus favour disassortative mating and in this, resembles the MHC of the vertebrate immune system, or the self-incompatibility (SI) system of higher plants.

Results

Here we show that in the monogamous parasitic wasp Bracon brevicornis (Wesmael), females are able to reject partners with incompatible alleles. Forcing females to accept initially rejected partners resulted in sex ratio distortion and partial infertility of offspring.

Conclusions

CSD-disassortative mating occurred independent of kin recognition and inbreeding avoidance in our experiment. The fitness consequences of mate choice are directly observable, not influenced by environmental effects, and more severe than in comparable systems (SI or MHC), on individuals as well as at the population level. Our results thus demonstrate the strong potential of female mate choice for maintaining high offspring fitness in this species.

Introduction

Mate choice, the non-random selection of mates, is extremely widespread in sexually reproducing animals. Sometimes, direct benefits such as resources are accrued, but often, females ‘shop’ for genetic benefits to increase the fitness of their offspring [1]. Mate choice may then be based on ‘good genes’ indicating the heritable quality of mates, or on ‘genetic compatibility’ [2, 3]. The latter concept implies that benefits gained by optimal mate choice are conditional on the genetic makeup of both partners at loci that influence offspring fitness. Some of the best-studied examples of mate choice based on genetic compatibility concern the major histocompatibility complex (MHC) in vertebrates. Diversity at MHC loci can enhance immunity against parasites and pathogens (e.g. [4]) and a preference for MHC-dissimilar mates exists in a variety of animals such as fish, birds, and mammals including humans (e.g. [57]). Mate choice is discussed as an important driver of allelic diversity within species [2, 7], even though the evidence is often inconsistent across studies [610]. That might be because the fitness benefits of MHC-disassortative mating depend on environmental factors, e.g. the exposure to parasites, and may thus vary between species and with experimental conditions [11, 12].

While genetic compatibility may enhance fitness in vertebrates, it is essential for offspring development in plants with a self-incompatibility (SI) system [13]. Genetic compatibility is also critical in hymenopteran insects exhibiting either single-locus or multiple-locus complementary sex determination (sl-CSD or ml-CSD, respectively). In those species, heterozygosity at the sex locus (or loci) is directly linked to offspring fitness because it initiates the pathway to female development in fertilized, diploid eggs [14]: Sons normally develop from unfertilized eggs and are haploid. However, diploid males are produced when eggs are fertilized with sperm with matching sex allele(s) so that they become homozygous at the sex locus (sl-CSD, Figure 1) or the sex loci (ml-CSD). In the majority of species diploid males are developmentally unviable or effectively sterile [15, 16]. Because sterile diploid males are produced at the expense of fertile females, the fitness consequences of mating a partner with a matching sex allele may be severe.

Figure 1
figure 1

Bracon brevicornis reproductive biology. Matched matings in parental generation P result in three kinds of offspring: diploid homozygous males (F1 on the left; identical colour bands on chromosomes), diploid heterozygous females (F1 centre; different colour bands), or haploid hemizygous males, from unfertilized eggs (F1 on the right).

Results and discussion

The parasitic wasp Bracon (Habrobracon) brevicornis Wesmael (Hymenoptera: Braconidae) (Figure 2), provides an excellent system to evaluate the hypothesis that genetic incompatibility drives mate choice because: a) parental care or resource transfer are absent and benefits of mate choice are purely genetic, b) females usually mate only once [Weeda & Thiel, unpublished observation], and c) genetic incompatibility leads to directly measurable fitness consequences via diploid male production [17, 18].

Figure 2
figure 2

Bracon brevicornis habitus. A female with inserted ovipositor sitting on a paralyzed host (photo: Nils Linek).

We used two populations that we assume to partially overlap in the sex alleles present. Individual females of one population were offered a male from the other population and vice versa, and a female could either accept this male (“accepted” mating) or reject it. If rejection occurred, we got the female to accept a second mating attempt of the same male by cooling her on ice (“rejected” mating). From “rejected” matings, a significantly higher proportion of fertilized eggs developed as diploid sons, at the expense of daughters (Χ2df=1, n=20 = 13.1, P < 0.001; error distribution (ED) = binomial, Figure 3). Genetic matching (Table 1) occurred significantly more often in “rejected” than in “accepted” matings (Fisher’s exact test, one-sided P = 0.009). However, since not all “rejected” matings have been matched, the females may have had additional mate choice criteria. When looking for alternative explanations for the increased diploid male production in “rejected” matings, we found that neither female fecundity (Χ21,20 = 0.007, P = 0.93, Table 1) nor offspring mortality (Χ21,20 = 1.02, P = 0.31) differed significantly between wasps of the different mating regimes.

Figure 3
figure 3

Mate choice consequences. The proportion (± SE) of all diploid offspring produced that is male and thus, costly (***P < 0.001).

Table 1 Numbers of eggs produced, haploid male (HM), diploid male (DM), female (F), undetermined male (UM) offspring, and the probability that a matched mating by chance did not result in diploid male production (matching probability, calculated as 0.5 (n diploid offspring) )

Even though only females from “rejected” mating had been cooled for a short time, an effect of cooling on the proportion of diploid males produced by females with a matched “rejected” mating is unlikely to have occurred. 1) Cooling occurred at a point in time that did neither correlate with egg production, nor sperm storage, nor fertilization. 2) Control females that were mated without cooling to one of their own sons, and thus had a guaranteed matched mating, produced equal proportions of diploid males (Χ21,15 = 0.14, P = 0.71, Table 1).

Females thus showed the ability to decrease the production of diploid males to approximately 1/4 of what was to be expected at random mating in our experiment. Since diploid sons are produced at the expense of fertile daughters and are effectively sterile in this species [Thiel & Weeda, unpublished observation], this clearly demonstrates the selective advantage of mate choice driven by genetic incompatibility.

Conclusions

Our results show that in an insect with sl-CSD, recognition of specific alleles can occur even among unrelated mating partners. CSD thus facilitates outcrossing analogous to the self-incompatibility (SI) system found in plants [12] and the MHC system in vertebrates [18]. Yet, fitness consequences of allelic matching are more severe under CSD, compared to MHC or SI, because homozygosity at the CSD-locus invariably increases post-zygotic mortality and the production of infertile offspring [19]. Kin recognition by olfactory cues has been described in a few insect species (e.g. [2022]) and inbreeding avoidance is certainly an important measure in reducing the probability with which a matched mating is likely to occur [16]. In bottlenecked populations however, even unrelated individuals become likely to share a sex determining allele. As a consequence, a rapid decline of effective population size and a high probability for extinction have been predicted from theoretical models [23, 24]. Female choice based on ‘genetic compatibility’, as described in our study, can thus be considered as an important mechanism for increasing population survival as well as individual wasp fitness.

Materials and methods

We used specimens from two laboratory populations of the gregarious, larval ectoparasitoid Bracon (Habrobracon) brevicornis Wesmael (Hymenoptera: Braconidae) established from collections in two different years (2006 and 2008) from the same field site near Leipzig, Germany. At the time of the experiment, the two populations had been separated for approximately 60 generations and their respective members were thus likely to overlap in the sex determining alleles present, but did not represent close kinships. Larvae of Ephestia kuehniella Zeller (Lepidoptera: Pyralidae) served as hosts. Experiments and rearing took place at 25°C, 55% r.h. and 16:8 h light:dark.

We worked with 14-18-day-old virgin females, which had previously parasitized one host. To avoid interference with kin-based mate choice, individual females of one population were placed with a male from the other population, and vice versa, in an empty Petri dish (ø 3.5 cm). A female could either accept the courting male, resulting in copulation usually within five minutes (“accepted” mating), or reject it by bending down the abdomen, kicking with the hind legs, or running away upon contact. If rejection occurred, the female was carefully transferred into a 250 μl plastic tube and placed on ice for eight minutes, until she stopped moving. The non-moving female was transferred back into the Petri dish with the same male she had at first rejected. The male usually approached her immediately and copulation took place before she regained full movement (“rejected” mating; method adapted from [25]). To check for a possible effect of cooling, we used a control group of females that were mated without cooling to one of their own sons, which they had produced as virgins. These females were of the same age than experimental females and had also had one oviposition experience before being mated. Because haploid sons inherit one of their mother’s sex alleles, mother-son matings are by definition matched in terms of sex alleles and should thus result in approximately half of the diploid offspring becoming homozygous at the sex determining locus (diploid males). Interestingly, about 1/2 of those females confronted with the own son mated without hesitation (and could thus be used as a control for effects of cooling), despite the allelic matching. Mating the own son is not contradictory to the idea of avoiding allelic matching if we consider the idea of mate acceptance changing with experience (i.e. [26, 27]): if a son is the only potential mate a female encounters, it may well be that there are no conspecifics around and that chances for meeting an unrelated male are really low.

After mating, each female parasitized a total of five host larvae within three days. Host larvae were immediately examined after removing the female to determine the number of eggs laid. After 10 days, we examined developing offspring daily; emerging wasps were sexed and counted. Ploidy levels of male offspring were determined using flow cytometry: individual wasp heads were homogenized in Galbraith buffer (21 mM MgCl2, 30 mM trisodium citrate dihydrate, 20 mM MOPS, 0.1% Triton X-100, 1 mg/l RNase [28]), filtered (40 μm), stained for 10 min with 15 μl propidium iodide (1.25 mg/ml) and loaded on a Coulter Epics XL-MCL flow cytometer (Beckman Coulter, Miami, FL, USA). We used an excitation wave length of 488 nm and a band pass filter of 585 nm to detect propidium iodide fluorescence. Samples were measured in an FSlog/FL2-log and FSlog/FL3-log gated region until 2500–3000 counts had been achieved, using Expo 32 ADC XL 4 Color (Beckman Coulter, USA). A threshold was applied to exclude very small debris. Known diploids (females) and haploids (males produced by virgin mothers) provided the reference histograms (Figure 4) used for assigning ploidy level to the male offspring produced. Males for which we could not determine ploidy level (Table 1), e.g. because either no definite haploid peak appeared or because the absence of a haploid peak could not be verified, were used only in the analysis of offspring survival.

Figure 4
figure 4

Flow cytometry reference histograms. Since DNA duplication is common in Hymenoptera, a haploid individual (right side) is recognized by the presence of a haploid peak, in addition to diploid and tetraploid peaks. A diploid individual is defined by the absence of a haploid peak, while at the same time, diploid and tetraploid peaks are present (left side).

Generalized linear models (GLMs, [29]) were fitted to the data, unless stated otherwise, using statistical procedures in “R 2.15.2” [30], with package “car” [31]. For analysing the proportions of fertilized eggs developing as diploid males, we used the “cbind” command to account for the different numbers of offspring produced by each female. The error distribution in this test was quasibinomial, with a logit link function. Female fecundity and offspring mortality were analysed with quasipoisson error distributions and log link functions.

Our results show that female choice can reduce the probability of a matched mating to approximately 1/4 of what was to be expected at random mating in our experiment. This calculation is based on those 18 couples for which we could define the matching status with their randomly assigned partners (Table 1): 0.4 of these matings had been matched. Among females that had an “accepted” mating, only a proportion of 0.1 was matched.

Abbreviations

CSD:

Complementary sex determination

F1:

First offspring generation

GLM:

Generalized linear model

MHC:

Major histocompatibility complex

MOPS:

3-(N-morpholino) propanesulfonic acid

P:

Parental generation

SI:

Self-incompatibility

References

  1. Partridge L: Mate choice increases a component of offspring fitness in fruit flies. Nature. 1980, 283: 290-291.

    Article  Google Scholar 

  2. Tregenza T, Wedell N: Genetic compatibility, mate choice and patterns of parentage: invited review. Mol Ecol. 2000, 9: 1013-1027.

    Article  CAS  PubMed  Google Scholar 

  3. Mays HL, Hill GE: Choosing mates: good genes versus genes that are a good fit. Trends Ecol Evol. 2004, 19: 554-559.

    Article  PubMed  Google Scholar 

  4. Wegner KM, Kalbe M, Kurtz J, Reusch TBH, Milinski M: Parasite selection for immunogenetic optimality. Science. 2003, 301: 1343-1343.

    Article  CAS  PubMed  Google Scholar 

  5. Wedekind C, Seebeck T, Bettens F, Paepke AJ: MHC-dependent mate preferences in humans. Proc R Soc London B. 1995, 260: 245-249.

    Article  CAS  Google Scholar 

  6. Lie HC, Simmons LW, Rhodes G: Genetic dissimilarity, genetic diversity, and mate preferences in humans. Evol Behav. 2010, 31: 48-58.

    Article  Google Scholar 

  7. Kempenaers B: Mate choice and genetic quality: a review of the heterozygosity theory. Ad Stud Behav. 2007, 37: 189-278.

    Article  Google Scholar 

  8. Mays HL, Albrecht T, Liu M, Hill GE: Female choice for genetic complementarity in birds: a review. Genetica. 2008, 134: 147-158.

    Article  PubMed  Google Scholar 

  9. Bos DH, Williams RN, Gopurenko D, Bulut Z, Dewoody JA: Condition-dependent mate choice and a reproductive disadvantage for MHC-divergent male tiger salamanders. Mol Ecol. 2009, 18: 3307-3315.

    Article  PubMed  Google Scholar 

  10. Havlicek J, Roberts SC: MHC-correlated mate choice in humans: a review. Psychoneuroendocrinology. 2009, 34: 497-512.

    Article  CAS  PubMed  Google Scholar 

  11. Hunt J, Bussiere LF, Jennions MD, Brooks R: What is genetic quality?. Trends Ecol Evol. 2004, 19: 329-333.

    Article  PubMed  Google Scholar 

  12. Neff BD, Pitcher TE: Genetic quality and sexual selection: an integrated framework for good genes and compatible genes. Mol Ecol. 2005, 14: 19-38.

    Article  CAS  PubMed  Google Scholar 

  13. Goldberg EE, Kohn JR, Lande R, Robertson KA, Smith SA, Igic B: Species selection maintains self-incompatibility. Science. 2010, 330: 493-495.

    Article  CAS  PubMed  Google Scholar 

  14. Beye M, Hasselmann M, Fondrk MK, Page RE, Omholt SW: The gene csd is the primary signal for sexual development in the honeybee and encodes an SR-type protein. Cell. 2003, 114: 419-429.

    Article  CAS  PubMed  Google Scholar 

  15. Heimpel GE, de Boer JG: Sex determination in the Hymenoptera. Ann Rev Entomol. 2008, 53: 209-230.

    Article  CAS  Google Scholar 

  16. van Wilgenburg E, Driessen G, Beukeboom LW: Single locus complementary sex determination in Hymenoptera: an "unintelligent" design?. Front Zool. 2006, 3: 1-10.1186/1742-9994-3-1.

    Article  PubMed Central  PubMed  Google Scholar 

  17. Speicher BR, Speicher KG: The occurence of diploid males in Habrobracon brevicornis. Am Nat. 1940, 74: 379-382.

    Article  Google Scholar 

  18. Bernatchez L, Landry C: MHC studies in nonmodel vertebrates: what have we learned about natural selection in 15 years?. J Evol Biol. 2003, 16: 363-377.

    Article  CAS  PubMed  Google Scholar 

  19. Hedrick PW, Gadau J, Page RE: Genetic sex determination and extinction. Trends Ecol Evol. 2006, 21: 55-57.

    Article  PubMed  Google Scholar 

  20. Simmons LW: Pheromonal cues for the recognition of kin by female field crickets, Gryllus bimaculatus. Anim Behav. 1990, 40: 192-195.

    Article  Google Scholar 

  21. Herzner G, Schmitt T, Heckel F, Schreier P, Strohm E: Brothers smell similar: variation in the sex pheromone of male European Beewolves Philanthus triangulum F. (Hymenoptera: Crabronidae) and its implications for inbreeding avoidance. Biol J Linn Soc. 2006, 89: 433-442.

    Article  Google Scholar 

  22. Metzger M, Bernstein C, Hoffmeister TS, Desouhant E: Does kin recognition and sib-mating avoidance limit the risk of genetic incompatibility in a parasitic wasp?. PLoS One. 2010, 5: e13505-10.1371/journal.pone.0013505.

    Article  PubMed Central  PubMed  Google Scholar 

  23. Zayed A, Packer L: Complementary sex determination substantially increases extinction proneness of haplodiploid populations. Proc Nat Acad Sci USA. 2005, 102: 10742-10746.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  24. Hein S, Poethke HJ, Dorn S: What stops the 'diploid male vortex'?-a simulation study for species with single locus complementary sex determination. Ecol Mod. 2009, 220: 1663-1669.

    Article  Google Scholar 

  25. Kitthawee S: Forced-contact mating: a technique for crossing experiments with the fruit fly parasitoid, Diachasmimorpha longicaudata (Ashmead) (Hymenoptera: Braconidae). Biol Con. 2008, 44: 73-78.

    Article  Google Scholar 

  26. Bailey NW, Zuk M: Field crickets change mating preferences using remembered social information. Biol Let. 2009, 5: 449-451.

    Article  Google Scholar 

  27. Fowler-Finn KD, Rodriguez RL: Experience-mediated plasticity in mate preferences: mating assurance in a variable environment. Evolution. 2012, 66: 459-468.

    Article  PubMed  Google Scholar 

  28. Galbraith DW, Harkins KR, Maddox JM, Ayres NM, Sharma DP, Firoozabady E: Rapid flow cytometric analysis of the cell cycle in intact plant tissues. Science. 1983, 220: 1049-1051.

    Article  CAS  PubMed  Google Scholar 

  29. Nelder JA, Wedderburn RWM: Generalized linear models. J R Stat Soc A. 1972, 135: 370-384.

    Article  Google Scholar 

  30. R Development Core Team: R: a language and environment for statistical computing. 2011, Vienna, Austria: R Foundation for Statistical Computing, 2140

    Google Scholar 

  31. Fox J, Weisberg S: An (R) companion to applied regression. 2011, Thousand Oaks, CA: Sage, 2

    Google Scholar 

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Acknowledgments

The study was funded by ESF (BEPAR) with a short visit grant to AT, the German Federal Ministry of Economy and Technology (BMWi) (KF 2152901MD8 to TSH), and the Netherlands Organization for Scientific Research (ALW 863.07.010 to JGdB). We thank B. Wührer and O. Zimmermann (AMW Nützlinge GmbH) for insects, W. van de Poll (Marine Biology, RUG) for help with flow cytometry, and R. Amann, L.W. Beukeboom, M. Dicke, and B.D. Roitberg for discussion.

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Correspondence to Andra Thiel.

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The authors declare that they have no competing interests.

Authors’ contributions

AT initiated and supervised the project, ACW performed the experiments, JGdB directed the flow cytometry. AT and TSH performed the statistics. AT wrote the first draft and all authors contributed to interpreting results, and improvement of the paper. All authors read and approved the final manuscript.

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Thiel, A., Weeda, A.C., de Boer, J.G. et al. Genetic incompatibility drives mate choice in a parasitic wasp. Front Zool 10, 43 (2013). https://0-doi-org.brum.beds.ac.uk/10.1186/1742-9994-10-43

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