Male-benefit sexually antagonistic genotypes show elevated vulnerability to inbreeding
© The Author(s). 2017
Received: 21 March 2017
Accepted: 25 May 2017
Published: 12 June 2017
There is theoretical and empirical evidence for strong sexual selection in males having positive effects on population viability by serving to purify the genome of its mutation load at a low demographic cost. However, there is also theoretical and empirical evidence for negative effects of sexual selection on female fitness, and therefore population viability, known as the gender load. This can take the form of sexually antagonistic (SA) genetic variation where alleles with a selective advantage in males pose a detriment to female fitness, and vice versa. Here, using seed beetles, we shed light on a previously unexplored manifestation of the gender load: the effect of SA genetic variation on tolerance to inbreeding.
We found that genotypes encoding high male, but low female fitness exhibited significantly greater rates of extinction upon enforced inbreeding relative to genotypes encoding high female but low male fitness. Also, genotypes encoding low fitness in both sexes exhibited greater rates of extinction relative to generally high-fitness genotypes (though marginally non-significant), an expected finding attributable to variation in mutation load across genotypes. Despite follow-up investigations aiming to identify the mechanism(s) underlying these findings, it remains unclear whether the gender load and the mutation load have independent consequences for tolerance to inbreeding, or whether these two types of genetic architecture interact epistatically to render male-benefit genetic variation relatively intolerant to inbreeding.
Regardless of the underlying mechanism(s), our results show that male-benefit/female-detriment SA genetic variation poses a previously unseen detriment to population viability due to its elevated vulnerability to inbreeding/homozygosity. This suggests that sexual selection in the context of SA genetic variance for fitness may enhance the gender load on population viability more than previously appreciated, due to selecting for male-benefit SA genetic variation that engenders lineages to extinction upon inbreeding. We note that our results imply that SA alleles that are sexually selected for in males may be underrepresented or even lacking in panels of inbred lines.
KeywordsAntagonistic pleiotropy Balancing selection Fitness Genetic variation Inbreeding depression Intralocus sexual conflict Mutation load Sexually antagonistic selection
Sexual selection can purge the genome of its mutation load on population viability, and at low demographic costs when via males [1–6]. This requires that deleterious mutations have sexually concordant (SC) effects, affecting both sexes similarly, such that the mutations that are selectively sieved out of a population due to the detriments they pose to male fitness are the same mutations that would harm population viability by causing reductions in female offspring production and/or juvenile survival . If sexual selection is strong enough, this process poses a population-level viability advantage over asexual invaders . In theory, this can counter the two-fold transmission advantage of asexual genomes, offering a population-level adaptive explanation for the prevalence and maintenance of sexual reproduction in eukaryotes . This explanation for the maintenance of sex  and some supporting empirical evidence (e.g. [7–11]) has caused sexual selection to become viewed as a phenomenon that, if anything, likely elevates population viability.
However, as SC genetic variation for fitness is eroded by purifying selection, we expect populations to become dominated by sexually antagonistic (SA) genetic variance for fitness . SA genetic variation is characterized by genotypes encoding high fitness in one sex but low fitness in the other [13–18] and is expected to contribute disproportionately to genetic variance for fitness in well-adapted populations [12, 19–21]. Because female offspring production is a crucial aspect of population viability, a paradox emerges: while sexual selection in males may promote population viability by purifying the genome of its SC mutation load , the SA genetic variation left behind  can pose a severe gender load on the population [15, 22–24]. For example, in a wild-caught population of the seed beetle Callosobruchus maculatus dominated by SA genetic variance for fitness , we have shown that genotypes exhibiting high male fitness exhibit low potential to contribute positively to population growth rate . Indeed, Whitlock and Agrawal  point out that the capacity for strong sexual selection in males to purge a population’s mutation load will depend critically on what proportion of the genetic variance for fitness is SA (as well as the degree of phenotypic sexual conflict), where a strong enough gender load could nullify or even reverse the population-level benefits of sexual selection in males.
Here, using that same population of seed beetle described above, we evaluate the potential for SA genetic variation for fitness to pose population-level detriments via another important component of population viability: tolerance to inbreeding depression. Inbreeding depression occurs due to increasing homozygosity for weakly deleterious mutations throughout the genome, which are (partially) shielded from purging by virtue of being rare and partially recessive [27–30]. Indeed, Jarzebowska and Radwan  showed that while sexual selection in males can act to remove large-effect mutations, posing short-term tolerance to inbreeding depression, it may be ineffective at removing much of the small-effect mutations that contribute to a mutation load on population viability. Thus, even populations dominated by SA genetic variance for fitness will exhibit a SC mutation load on population viability, despite their presumed history of purifying sexual selection, and this mutation load is expected to cause inbreeding depression upon increasing homozygosity [28–30]. However, it is currently not clear how this SC mutation load will interact with SA genetic variation upon increasing homozygosity.
Because female offspring production plays an obvious role in buffering the population-level detriments of inbreeding depression, one general prediction is that male-benefit/female-detriment genotypes will contribute greater detriments to populations upon increasing homozygosity relative to female-benefit/male-detriment genotypes. Here, we test this prediction by measuring lineage extinction under enforced inbreeding among SA genotypes. The population of seed beetle used for this experiment exhibits predominantly SA genetic variance for fitness [25, 26] and we have demonstrated strong sexual selection in males against an induced mutation load on female/population offspring production in this population . We therefore expect that this population has experienced a history of strong sexual selection in males that has contributed to purging some of its SC mutation load, and therefore also contributed to generating its predominantly SA genetic variance for fitness.
We subjected 20 replicate lineages from each of 41 isofemale lines (~800 lineages at the start) to single-pair full-sib inbreeding for 10 consecutive generations or until lineage extinction. We predicted that lineages originating from isofemale lines enriched for male-benefit/female-detriment alleles would exhibit greater rates of extinction relative to lineages originating from female-benefit/male-detriment isofemale lines. Further, if lineage extinction results from increased homozygosity, then variation in deleterious recessives should cause lineages from generally low-fitness isofemale lines (i.e. low-male and low-female fitness) to likewise exhibit greater extinction rates relative to lineages from generally high-fitness isofemale lines [28–30]. Our findings support these predictions, demonstrating an additional mechanism by which sexual antagonism can impose a gender load on population viability.
C. maculatus (Coleoptera: Bruchidae) is a pest of leguminous crops that has colonized most of the tropical and subtropical regions of the world . Males and females are sexually mature upon adult eclosion, and exhibit a polyandrous mating system . The eggs are glued onto the surface of dry beans and hatched larvae bore into the beans, where they complete their life cycle. C. maculatus are facultatively aphagous; adults require neither food nor water to reproduce successfully.
The population of 41 isofemale lines used in our inbreeding experiment (below) was previously shown to exhibit significant SA genetic variance for fitness under normal environmental conditions [25, 26]. The population was isolated from Vigna unguiculata seed pods collected at a small-scale agricultural field close to Lomé, Togo (06°10'N 01°13'E) during October and November, 2010. Seed pods were stripped in the laboratory and beans isolated individually. Virgin males and females hatching out of these beans were paired randomly and each pair founded an isofemale line (n = 41), each of which was thus derived from a single maternal and a single paternal genome. The F1 offspring from each of these pairs/isofemale lines were allowed to breed with their siblings in order to expand the isofemale lines. The isofemale lines were cultured at a population size of 200–300 adults each generation on 150 ml. of V. unguiculata seeds at 29° C, 55% RH and a 12 L:12D light regime until the start of experiments. Thus, inbreeding upon the establishment of the isofemale lines, as well throughout their maintenance until the start of experimentation, was limited to that one original F1 generation. Our isofemale lines thus exhibit segregating genetic variation that can be driven to fixation upon inbreeding. We note that no isofemale line went extinct during the establishment phase.
The inbreeding experiment began after the completion of the sex-specific fitness assays (see above ). 20 replicate lineages of each of the 41 isofemale lines (with minor exceptions, see Additional file 1: S1) were initiated by a single virgin mating pair placed in a petri dish (90 mm ∅) containing ad libitum V. unguiculata seeds, for a starting total of 804 lineages. These lineages were placed in incubators with the same abiotic conditions described above. After these parents died, egg-laden seeds were selected and isolated to harvest virgin offspring. Upon emergence, a random selection of virgin full-sib offspring were placed in a small empty petri dish (30 mm ∅) until copulating pairs formed (typically several formed in < 1 min), and a single pair (while still in copula) was gently transferred to a fresh petri dish (90 mm ∅) containing ad libitum V. unguiculata seeds. Thus, a single virgin full-sib mating pair from each lineage was used to parent the next generation. This was repeated for 10 consecutive generations or until the lineage went extinct. Extinctions were never attributable to the absence of copulation, as all copulations were witnessed (but see Additional file 1: S2).
Causes of extinction
Determining the proximate causes of extinction is, for rather obvious reasons, very difficult . Yet, we conducted a follow-up experiment to shed light on the extent to which patterns of extinction could be attributed to variation in female fecundity or male fertility per se across the different isofemale lines of origin. After 10 generations of inbreeding, the 3 isofemale lines with the most positive, and 3 with the most negative, score along the first principle component extracted from the bivariate regression of ‘antagonism’ on ‘extinction risk’ (see Fig. 2a and Statistical analysis, below) were identified as the 3 most male-benefit/high-extinction isofemale lines and 3 most female-benefit/low-extinction isofemale lines, respectively. We note that all 20 replicate lineages of three of the most male-benefit/high-extinction isofemale lines had gone extinct after 10 generations of inbreeding; thus this follow-up experiment lacks representation from some of the most extremely male-benefit/high-extinction isofemale lines. In these cases, the isofemale lines with the next-most positive score along the principle component describe above were used instead. Two representative extant lineages from each of these extreme 6 (i.e. 3 ‘male-benefit’ and 3 ‘female-benefit’) isofemale lines were randomly selected for use in assays of female fecundity and male fertility—for some extreme isofemale lines, the 1 or 2 extant lineages remaining were the only available option.
Representative lineages selected for this follow-up experiment were expanded to a population size of approximately 200–300 adults that were then kept on 150 ml. of V. unguiculata seeds at the same abiotic conditions described above. Parents of these populations were allowed to oviposit for 2 days, at which point egg-laden seeds were isolated to harvest virgin offspring. Virgin male and female focal individuals from representative lineages were mated to virgin individuals from an outbred base population established at the same time, and from the same population, as the isofemale lines (see above). For logistic purposes, the base population was cultured in temporally staggered cohorts. The base population cohort to which focal individuals were mated was recorded. Mated pairs (i.e. focal females crossed to base population males, and focal males crossed to base population females) were placed in a petri dish (90 mm ∅) containing ad libitum V. unguiculata seeds and these assays were placed in an incubator exhibiting the same abiotic conditions described above, thus mimicking the protocol for the inbreeding experiment but in a fashion capable of revealing differences in lifetime offspring production attributable to either female fecundity or male fertility within extreme lineages.
In addition to this follow up experiment, three additional efforts were made to provide further insight regarding extinction patterns across isofemale lines. First, we performed a demographic simulation based solely on estimates of female fecundity from Berger et al. . This simulation provided an expected proportion of lineage extinction per isofemale line attributable to females having little or no fecundity (in which either no offspring, or offspring of only one sex, emerged) at any point during 10 consecutive generations of single-pair matings (see Additional file 1: S3 for details). Second, we calculated the expected proportion of lineage extinction per isofemale line based solely on linear projections of their extinction rates exhibited in the first generation (i.e. upon the establishment of their ~20 replicate lineages). This calculation provides the expected proportion of lineages going extinct for each isofemale line after 10 consecutive generations of single-pair matings without any further inbreeding (see Additional file 1: S4 for details). Lastly, the apparent mode of extinction (e.g. no eggs laid, unhatched eggs, only one sex emerging, etc.) for each lineage going extinct was recorded and later converted to quantitative data that were analyzed in a variety of ways aiming to gain mechanistic insight to patterns of extinction (see Additional file 1: S5 for details). These analyses on the mode of extinction were inconclusive regarding any mechanistic insight to the observed patterns of extinction beyond that reported in the Results section below. Thus, we report and discuss the results of the mode of extinction analyses in Additional file 1: S5.
In order to acquire the derived variables, antagonism and concordance (see Fig. 1), we rotated the coordinate system of the intersexual genetic correlation clockwise 45° as in Berger et al. . This rotation was performed on log-transformed mean fitness for males and females of each isofemale line (collected by ), which was variance-standardized (and thus zero-centered) within each sex separately. The resultant antagonism and concordance variables pass through the origin with slopes of −1 and 1 on the original coordinate system, respectively (Fig. 1).
A mixed effects Cox regression was used to analyze variation in extinction risk across isofemale lines (a random effect) in relation to isofemale line values for antagonism and concordance. We also present an alternative mixed effects Cox regression using isofemale line values for female fitness and male fitness (rather than antagonism and concordance) to aid the interpretation of our results. Analyses were performed using the ‘coxme’ package (v.2.2-5, ) in R (v.3.2.1, ). One extremely male-benefit isofemale line, > 3 SD from the mean for antagonism (Additional file 1: Figure S1a), was a potential outlier in our analyses. There is currently no way, in theory or in practice, to extract residuals or similar from mixed-effects Cox regressions , making the assessment of outliers difficult. Thus, the potential outlier was assessed by examining the frequency distribution of differences in fit for the beta coefficients attributable to each datum’s exclusion from a standard Cox proportional hazards model using the ‘survival’ package (v.2.38 ) in R  (Additional file 1: Figure S1b). Note that the ‘survival’ package’s cluster argument does not properly incorporate random effects [34, 36]. Nevertheless, this approach revealed a cluster of observations from the isofemale line in question with a disproportionate influence on the model (Additional file 1: Figure S1b). In the proper mixed effects Cox regressions (from ‘coxme’), removal of this isofemale line provided a superior improvement of models’ fits relative to their respective null models. Whether it was for the antagonism/concordance model or the male-fitness/female-fitness model (since they are the exact same data distributed onto different variables), when the outlier line was included the AIC difference between the fitted and null models was 50.39, whereas without the outlier line the AIC difference was 54.38—the latter being a substantially better fit (i.e. greater reduction in AIC) relative to their respective null models. Thus, this outlier isofemale line was excluded from all analyses (including the follow-up investigations) and derived variables were recalculated in its absence (see Additional file 1: Table S1 and S2 for Cox regressions including this outlier line). Model comparison by log-likelihood ratio tests were used to evaluate whether or not an interaction term should be included in these models (i.e. antagonism*concordance, or male*female). Neither model’s fit was significantly improved by the inclusion of an interaction term (antagonism/concordance: χ 2 = 0.001, P = 0.97; male-/female-fitness: χ 2 = 0.23, P = 0.63).
Female fecundity and male fertility data showed a number of zeros, but were otherwise normally distributed. The likelihood of producing zero eggs did not differ between male-benefit/high-extinction and female-benefit/low-extinction categories in the female fecundity assays (χ 2 = 0.03, P = 0.87) or the male fertility assays (χ 2 = 0.12, P = 0.73). Zero-data were therefore excluded, and general linear mixed models (producing normally distributed residuals) were used to analyze differences in female fecundity (n = 153 male-benefit, n = 109 female-benefit) and male fertility (n = 157 male-benefit, n = 126 female-benefit) between individuals descended from the three most female-benefit/low-extinction isofemale lines and the three most male-benefit/high-extinction isofemale lines. Here, lifetime offspring production was the response variable and random effects included isofemale line, lineage nested within isofemale line, and date of the assay. Fixed effects included category (i.e. male-benefit or female-benefit) and base population cohort. These analyses were performed using the ‘lme4’ package (v.1.1-8, ) in R .
Results of a mixed effects Cox regression of extinction risk, with antagonism and concordance as fixed effects, and isofemale line as a random effect
Results of a mixed effects Cox regression of extinction risk, with female and male fitness as fixed effects, and isofemale line as a random effect
Causes of extinction
There were no significant differences in female fecundity (χ2 1 = 0.55, P = 0.46) or male fertility (χ2 1 = 1.50, P = 0.22) between female-benefit and male-benefit categories. There were also no differences between categories in the likelihood of producing zero eggs (female fecundity assays: χ 2 = 0.03, P = 0.87; male fertility assays: χ 2 = 0.12, P = 0.73).
Simulations of the expected proportion of extinction across isofemale lines, based solely on the female fecundity of each isofemale line, revealed a pattern of extinction across isofemale lines that was qualitatively similar to that observed (Additional file 1: Figure S2). However, the simulation predicted that only 18.2% of the ~800 lineages would have gone extinct after 10 generations of single pair matings, whereas 77.8% of the lineages actually went extinct. Similarly, calculating the proportion of lineages per isofemale line expected to go extinct based on linear projections of their extinction rates exhibited in the first generation of single-pair (but not full-sib) matings predicted only 19.9% of lineages going extinct (Additional file 1: Figure S2). Both of these efforts to forecast the pattern of extinction that would ensue during this experiment in the absence of continued inbreeding leave ~75% of the observed extinction unaccounted for. These efforts show that inbreeding per se must have played a major role in generating the observed patterns of extinction across isofemale lines.
The last decade has seen a renewed interest in the effects of sexual selection on population viability, a long-standing issue . While it is currently clear that sexual selection may in theory have both positive [1–6, 39, 40] and negative [22, 41–47] effects, the net effect on a population and whether different effects might interact is much less clear. Our work shows that although strong sexual selection in males may act to purify the genome of SC mutation load, the overall load on population viability may be greater than currently anticipated due to the interaction between the SA gender load and residual SC mutation load, both of which are expected to be left in the wake of strong purifying sexual selection [6, 9, 12]. Specifically, we have shown that male-benefit SA genotypes (isofemale lines) are at greater risk of extinction under inbreeding. Thus, sexual selection may pose two related and interacting costs to populations: (1) the gender load, expected to cause a general depression of population fitness [15, 22–24], and (2) the interaction between gender load and mutation load, for which the present study provides the first empirical insights. There are potentially two reasons for the latter cost being (at least partly) attributable to sexual selection in conventional mating systems : (1) if sexual selection in males does purify some of the SC mutation load and leave behind mostly SA genetic variance for fitness as well as some residual SC mutation load, an evolutionary history of strong sexual selection in males would set the stage for the present findings, and (2) continued sexual selection in males in the context of SA genetic variance for fitness will enrich populations for male-benefit/female-detriment alleles, which, as suggested by the present findings, would render populations more prone to extinction from inbreeding. By this process, sexual selection would tend to prevent the population-level detriments of male-benefit/female-detriment alleles from being canceled out by the population-level benefits of female-benefit/male-detriment alleles. However, even if alternative allelic variants at SA loci across the genome were typically in near equal frequencies and their effects on inbreeding depression might cancel out, (small) sub-populations owing to fragmentation or founder effects may still sometimes be enriched for male-benefit/female-detriment allelic variation by chance and therefore suffer enhanced vulnerability to extinction from inbreeding. The mechanistic explanation of how this type of genetic variation may elevate vulnerability to inbreeding remains unclear, but below we discuss some non-mutually exclusive possibilities, and their implications.
Potential causes of extinction
Female fecundity is a major contributor to population viability in most species with separate sexes  and seed beetles are no exception to this rule [24, 50]. At first it may seem that our findings reinforce this notion in that female fitness, but not male fitness, significantly explains variation in extinction from inbreeding (Table 2). However, this difference may be due to the marked environmental variance in male fitness (see Methods). With male and female fitness being highly correlated, our model is likely biased toward finding covariation between extinction and female (rather than male) fitness as it was measured with less error (see Methods and ). Nevertheless, one intuitive explanation would be that our results were generated by the demographic consequence of low fecundity exhibited by females from male-benefit/female-detriment genotypes. That is, the risk of lineage extinction should increase with decreasing female fecundity simply due to the risk in low numbers of offspring being all the same sex. However, our simulation of this effect, based solely on fecundity differences across isofemale lines (i.e. without the effects of inbreeding), showed that this would only have generated about one quarter of the extinction we observed. Likewise, a linear continuation of the extinction observed in the first generation of inbreeding (i.e. with very little input from inbreeding yet), would also have generated only about one quarter of the extinction we observed. Even if these two efforts to forecast the expected extinction rates among isofemale lines over 10 consecutive generations of single-pair (but not full-sib) matings represent entirely different mechanisms, then their combined/additive effects would still only have generated about half of the observed extinction, indicating that inbreeding must have played a major role in generating the pattern of extinction we observed. It would of course seem plausible that a risk of extinction posed by the demographic consequences of low fecundity could become exaggerated with increasing homozygosity for SA loci and/or deleterious recessives, and we address this in our explanations below. However, if that were the case, one might expect that extant lineages from the most female-detriment/high-extinction isofemale lines would have lower fecundity than the extant lineages from the most female-benefit/low-extinction isofemale lines after 10 consecutive generations of inbreeding, but this prediction was not supported by our follow-up experiment. Note that our follow-up experiment suffered from a complete lack of estimates from some of the most female-detriment/high-extinction isofemale lines, as all 20 of their replicate lineages were extinct after 10 generations of inbreeding, a testament to the difficulty of identifying the proximate causes of extinction . We suggest three additional effects that may have contributed to the increased risk of extinction seen in male-benefit/female-detriment genotypes.
First, our isofemale lines were genetically diverse and male-benefit/female-detriment isofemale lines should, across many loci, harbor higher allele frequencies of male-benefit/female-detriment alleles at SA loci (and the opposite case for female-benefit/male-detriment isofemale lines). This implies that the risk of fixation of male-benefit/female-detriment alleles during inbreeding is higher in male-benefit/female-detriment isofemale lines, and the opposite for female-benefit/male-detriment isofemale lines. With the male-benefit SA isofemale lines of this population already having relatively low female fecundity and population productivity , fixation of such alleles via inbreeding would likely further depress female-specific fitness and increase the risk of extinction. We note that this effect would not involve a conventional genetic load maintained by mutation-selection balance [29, 30] but rather a gender load maintained by balancing selection at SA loci. Under this scenario, our analyses (Table 1) would be interpreted as showing independent effects of a SC mutation load, as revealed by the ‘concordance’ dimension, and a SA gender load, as revealed by the ‘antagonism’ dimension, upon the increasing homozygosity that follows from inbreeding. The relative contribution of these different sources of inbreeding depression (mutation load versus loci under balancing selection) has fundamental implications for the classic evolutionary paradox of what maintains genetic variance for fitness . If inbreeding depression is attributable more so to homozygosity for mutation load than to homozygosity for loci under balancing selection, the implication would be that mutation selection balance (a constant influx of mutations and weak selection against them) plays a greater role in maintaining genetic variance for fitness relative to balancing selection at loci of major effect . Oppositely, if inbreeding depression is attributable more so to homozygosity for loci under balancing selection, such loci would be implicated as greater contributors to the maintenance of genetic variance for fitness . Granted our population’s genetic variance for fitness was already known to be dominated by balancing selection at SA loci (recall that this is the theoretical expectation for well-adapted populations at equilibrium, [12, 21]), our analyses would imply that inbreeding depression (and therefore genetic variance for fitness) may to a relatively large extent be attributed to (homozygosity at) loci under balancing selection, a possibility acknowledged early on [51, 52] due the relatively large fitness effects of such loci.
Second, the effective genetic load may differ between the sexes, and this may interact epistatically with SA genetic variation for fitness. Sex differences in the effective genetic load could result from, for example, differences in the number or types of genes that contribute to sex-specific fitness. Immonen et al.  recently showed that more than 50% of all genes are differentially expressed in the abdomen of male and female C. maculatus, so sex-specificity in the genetic architecture of inbreeding depression is certainly possible. Remarkably, females have previously been shown to be much more affected by inbreeding than males in this species, both in terms of reduced body size  and life span [55, 56], congruent with recent findings in Drosophila . This suggests that the genetic load across loci encoding for male-specific fitness may be lower, perhaps due to more efficient purging via stronger selection [11, 48] and/or sex-linked mutations being exposed unconditionally in the heterogametic sex . If there is a greater effective load on female-specific function relative to male-specific function, then females with male-benefit SA genotypes (i.e. those starting out with already lower female-specific function) might suffer greater detriments upon inbreeding/homozygosity relative to males with female-benefit genotypes. This sort of epistatic interaction between sex-specific effective mutation load and SA genetic variation could have generated the asymmetric pattern of extinction we observed along the ‘antagonism’ dimension.
Lastly, there could actually be more mutation load linked to male-benefit SA genetic variation than to female-benefit SA genetic variation. Connallon and Jordan  have recently shown that, in theory, SA selection should generate female-harming mutations near male-benefit SA alleles, and vice versa. This process would generate a similar mutation load linked to male- and female-benefit SA genetic variation, and would therefore not explain the asymmetric pattern of extinction we observed along the ‘antagonism’ dimension. However, Connallon and Jordan  also showed that male-biased mutation rates (a common and widespread phenomenon) should interact with SA selection to generate an increased mutation load on male-benefit haplotypes relative to female-benefit haplotypes. If there is a greater mutation load linked to male-benefit (relative to female-benefit) SA genetic variation in our population, this could explain our observation that male-benefit SA genotypes exhibited greater extinction rates upon inbreeding/homozygosity relative to female-benefit genotypes.
Independent of the precise causes of extinction, our experiments reveal a previously unappreciated manifestation of the gender load that may result from sexual selection. Whether strong sexual selection in males will tend to increase the relative frequency of SA genotypes in a population depends critically on the extent to which sexual selection favors SC or SA genotypes [6, 12]. Nevertheless, whether due to the purifying capacity of sexual selection  or other forms of SC purifying selection, we expect well-adapted populations to exhibit predominantly SA genetic variance for fitness [12, 21], in which case continued sexual selection would favor male-benefit/female-detriment alleles [6, 16]. We have shown here that this male-benefit/female-detriment genetic variation favored by sexual selection in males incites greater inbreeding depression than female-benefit/male-detriment genetic variation. Depending on the underlying mechanism (see above), this means that male-benefit SA genetic architecture, its phenotypic effects, or both pose an additional threat to population viability that has not yet been recognized. Further, in addition to selecting for female-detriment alleles that are sensitive to inbreeding depression, strong sexual selection in males should also decrease effective population size [22, 28, 59]. Thus, under certain conditions, sexual selection may set off an extinction vortex whereby these mechanisms reinforce one another.
Whether strong sexual selection in males poses greater net benefits or detriments to population viability will depend on many interacting factors [6, 59]. Our findings add resolution to the role of SA genetic variation for fitness in determining that outcome. Although we expect natural populations to exhibit mostly SA genetic variance for fitness [12, 19–21], such as the population we used here, we note that other populations of C. maculatus show less SA genetic variance . Empirical evidence suggests that natural populations exhibit variable but potentially abundant levels of SA genetic variance for fitness [15, 23, 25, 56, 60–66]. Perhaps owing to these varying levels sexual antagonism, or to the varying methodologies across studies, empirical estimates of the effects of sexual selection on populations show a range of effects, from positive (e.g. [7–11]), to ineffectual (e.g. [67, 68]), and even negative (e.g. [47, 68, 69]; reviewed in [6, 19]). Indeed, Whitlock and Agrawal , among others, warn that strong sexual selection in males in the context of SA genetic variance for fitness could have neutral or even negative effects on populations. Our findings add merit to this possibility, showing that in a population exhibiting SA genetic variance for fitness, continued sexual selection for male-benefit/female-detriment genotypes could enhance a population’s risk of extinction under inbreeding depression. This may weaken the general potential for strong sexual selection in males to account for the two-fold cost of sex [1–6].
As a final cautionary note, we have shown here that when constructing inbred lines, a non-random pattern of extinction occurs with regard to sex-specific fitness. Thus, a panel of inbred lines will exhibit a non-random representation of segregating genetic variation for fitness. Specifically, SA alleles that are sexually selected in males may be underrepresented or even lacking from panels of inbred lines, such as the Drosophila genetic reference panel (DGRP ). It remains unclear how far this result can be extrapolated, especially with reference to loci under other forms of balancing selection. Nevertheless, this raises the issue of what types of questions regarding genetic architecture we can expect to validly address using inbred lines. At the very least, our results suggest that we should exercise caution when drawing conclusions based on such panels. One strategy to combat this issue, of course, would be to characterize how populations’ genetic variance for fitness is distributed across genotypes prior to inbreeding them, so as to detect the type of genetic architecture expected to be underrepresented or lacking in a resultant panel of inbred lines.
We thank Johanna Liljestrand Rönn for help with experiments.
This research was supported by the European Research Council (GENCON AdG-294333; to GA), the Swedish Research Council (621-2010-5266; 621-2014-4523; to GA), the Stiftelsen för Zoologisk Forskning (to KG), and the Liljewalch's Resestipendier (to KG).
Availability of data and materials
All authors contributed to the experiment design. KG carried out all experiments, analyses and writing, with the guidance and supervision of DB and GA. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Not applicable for invertebrate animals.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Manning JT. Males and the advantage of sex. J Theor Biol. 1984;108:215–20.View ArticlePubMedGoogle Scholar
- Agrawal AF. Sexual selection and the maintenance of sexual reproduction. Nature. 2001;411:692–5.View ArticlePubMedGoogle Scholar
- Siller S. Sexual selection and the maintenance of sex. Nature. 2001;411:689–92.View ArticlePubMedGoogle Scholar
- Whitlock MC. Selection, load and inbreeding depression in a large metapopulation. Genetics. 2002;160:1191–202.PubMedPubMed CentralGoogle Scholar
- Lorch PD, Proulx S, Rowe L, Day T. Condition-dependent sexual selection can accelerate adaptation. Evol Ecol Res. 2003;5:867–81.Google Scholar
- Whitlock MC, Agrawal AF. Purging the genome with sexual selection: reducing mutation load through selection on males. Evolution. 2009;63:569–82.View ArticlePubMedGoogle Scholar
- Radwan J. Effectiveness of sexual selection in removing mutations induced with ionizing radiation. Ecol Lett. 2004;7:1149–54.View ArticleGoogle Scholar
- Hollis B, Fierst JL, Houle D. Sexual selection accelerates the elimination of a deleterious mutant in Drosophila melanogaster. Evolution. 2009;63:324–33.View ArticlePubMedGoogle Scholar
- Jarzebowska M, Radwan J. Sexual selection counteracts extinction of small populations of the bulb mites. Evolution. 2010;64:1283–9.PubMedGoogle Scholar
- Lumley AJ, Michalczyk Ł, Kitson JJ, Spurgin LG, Morrison CA, Godwin JL, Dickinson ME, Martin OY, Emerson BC, Chapman T, Gage MJ. Sexual selection protects against extinction. Nature. 2015;522:470–3.View ArticlePubMedGoogle Scholar
- Grieshop K, Stångberg J, Martinossi‐Allibert I, Arnqvist G, Berger D. Strong sexual selection in males against a mutation load that reduces offspring production in seed beetles. J Evol Biol. 2016;29:1201–10.View ArticlePubMedGoogle Scholar
- Connallon T, Clark AG. A general population genetic framework for antagonistic selection that accounts for demography and recurrent mutation. Genetics. 2012;190:1477–89.View ArticlePubMedPubMed CentralGoogle Scholar
- Lande R. Sexual dimorphism, sexual selection, and adaptation in polygenic characters. Evolution. 1980;34:292–305.View ArticlePubMedGoogle Scholar
- Rice WR, Chippindale AK. Intersexual ontogenetic conflict. J Evol Biol. 2001;14:685–93.View ArticleGoogle Scholar
- Chippindale AK, Gibson JR, Rice WR. Negative genetic correlation for adult fitness between sexes reveals ontogenetic conflict in Drosophila. Proc Natl Acad Sci. 2001;98:1671–5.View ArticlePubMedPubMed CentralGoogle Scholar
- Arnqvist G, Rowe L. Sexual conflict. Princeton: Princeton University Press; 2005.View ArticleGoogle Scholar
- Bonduriansky R, Chenoweth SF. Intralocus sexual conflict. Trends Ecol Evol. 2009;24:280–8.View ArticlePubMedGoogle Scholar
- Van Doorn GS. Intralocus sexual conflict. Ann N Y Acad Sci. 2009;1168:52–71.View ArticlePubMedGoogle Scholar
- Connallon T, Cox RM, Calsbeek R. Fitness consequences of sex-specific selection. Evolution. 2010;64:1671–82.View ArticlePubMedGoogle Scholar
- Stewart AD, Pischedda A, Rice WR. Resolving intralocus sexual conflict: genetic mechanisms and time frame. J Hered. 2010;101 Suppl 1:S94–9.View ArticlePubMedPubMed CentralGoogle Scholar
- Connallon T, Clark AG. Evolutionary inevitability of sexual antagonism. Proc R Soc Lond B Biol Sci. 2014;281:20132123.View ArticleGoogle Scholar
- Kokko H, Brooks R. Sexy to die for? Sexual selection and the risk of extinction. Ann Zool Fenn. 2003;40:207–19. Finnish Zoological and Botanical Publishing Board.Google Scholar
- Pischedda A, Chippindale AK. Intralocus sexual conflict diminishes the benefits of sexual selection. Plos Biol. 2006;4:2099–103.View ArticleGoogle Scholar
- Arnqvist G, Tuda M. Sexual conflict and the gender load: correlated evolution between population fitness and sexual dimorphism in seed beetles. Proc R Soc Lond B Biol Sci. 2009;277:1345–52.View ArticleGoogle Scholar
- Berger D, Grieshop K, Lind MI, Goenaga J, Maklakov AA, Arnqvist G. Intralocus sexual conflict and environmental stress. Evolution. 2014;68:2184–96.View ArticlePubMedGoogle Scholar
- Berger D, Martinossi-Allibert I, Grieshop K, Lind MI, Maklakov AA, Arnqvist G. Intralocus sexual conflict and the tragedy of the commons in seed beetles. Am Nat. 2016;188:E98–E112.View ArticlePubMedGoogle Scholar
- Hartl DL, Clark AG, Clark AG. Principles of population genetics. Sunderland: Sinauer Associates; 1997.Google Scholar
- Lynch M, Walsh B. Genetics and analysis of quantitative traits. Sunderland: Sinauer associates; 1998.Google Scholar
- Charlesworth B, Charlesworth D. The genetic basis of inbreeding depression. Genet Res. 1999;74:329–40.View ArticlePubMedGoogle Scholar
- Charlesworth D, Willis JH. The genetics of inbreeding depression. Nat Rev Genet. 2009;10:783–96.View ArticlePubMedGoogle Scholar
- Southgate BJ. Biology of the Bruchidae. Annu Rev Entomol. 1979;24:449–73.View ArticleGoogle Scholar
- Miyatake T, Matsumura F. Intra-specific variation in female remating in Callosobruchus chinensis and C. maculatus. J Insect Physiol. 2004;50:403–8.View ArticlePubMedGoogle Scholar
- Simberloff D. The proximate causes of extinction. In: Fisher DC, editor. Patterns and processes in the history of life. Berlin: Springer; 1986. p. 259–76.View ArticleGoogle Scholar
- Therneau T. Mixed effects Cox models. R package version 2.2-5. 2015. http://CRAN.R-project.org/package=coxme.
- R Core Team. R: a language and environment for statistical computing. Vienna: R Foundation for Statistical Computation; 2015. http://www.R-project.org/.Google Scholar
- Therneau T. A package for survival analysis in S. R package version 2.38. 2014. http://CRAN.R-project.org/package=survival.
- Bates D, Maechler M, Bolker B, Walker S. Fitting linear mixed-effects models using lme4. J Stat Soft. 2015;67:1–48.View ArticleGoogle Scholar
- Huxley JS. The present standing of the theory of sexual selection. In: deBeer, GR, editor. Evolution. Oxford: Clarendon Press; 1938. p. 11-42.Google Scholar
- Rowe L, Houle D. The lek paradox and the capture of genetic variance by condition dependent traits. Proc R Soc Lond B Biol Sci. 1996;263:1415–21.View ArticleGoogle Scholar
- Houle D, Kondrashov AS. Coevolution of costly mate choice and condition-dependent display of good genes. Proc R Soc Lond B Biol Sci. 2002;269:97–104.View ArticleGoogle Scholar
- Holland B, Rice WR. Experimental removal of sexual selection reverses intersexual antagonistic coevolution and removes a reproductive load. Proc Natl Acad Sci. 1999;96:5083–8.View ArticlePubMedPubMed CentralGoogle Scholar
- Rankin DJ, López‐Sepulcre A. Can adaptation lead to extinction? Oikos. 2005;111:616–9.View ArticleGoogle Scholar
- Eldakar OT, Wilson DS, Dlugos MJ, Pepper JW. The role of multilevel selection in the evolution of sexual conflict in the water strider Aquarius remigis. Evolution. 2010;64:3183–9.View ArticlePubMedPubMed CentralGoogle Scholar
- Rankin DJ, Dieckmann U, Kokko H. Sexual conflict and the tragedy of the commons. Am Nat. 2011;177:780–91.View ArticlePubMedGoogle Scholar
- Plesnar-Bielak A, Skrzynecka AM, Prokop ZM, Radwan J. Mating system affects population performance and extinction risk under environmental challenge. Proc R Soc Lond B Biol Sci. 2012;279:4661–7.View ArticleGoogle Scholar
- Takahashi Y, Kagawa K, Svensson EI, Kawata M. Evolution of increased phenotypic diversity enhances population performance by reducing sexual harassment in damselflies. Nat Commun. 2014; doi:https://doi.org/10.1038/ncomms5468.
- Chenoweth SF, Appleton NC, Allen SL, Rundle HD. Genomic evidence that sexual selection impedes adaptation to a novel environment. Curr Biol. 2015;25:1860–6.View ArticlePubMedGoogle Scholar
- Janicke T, Häderer IK, Lajeunesse MJ, Anthes N. Darwinian sex roles confirmed across the animal kingdom. Sci Adv. 2016; doi:https://doi.org/10.1126/sciadv.1500983.
- Stearns SC. The evolution of life histories. Oxford: Oxford University Press; 1992.Google Scholar
- Rankin DJ, Arnqvist G. Sexual dimorphism is associated with population fitness in the seed beetle Callosobruchus maculatus. Evolution. 2008;62:622–30.View ArticlePubMedGoogle Scholar
- Crow JF. Alternative hypotheses of hybrid vigor. Genetics. 1948;33:477–87.PubMedPubMed CentralGoogle Scholar
- Crow JF. Dominance and overdominance. In: Gowen JE, editor. Heterosis. Ames: Iowa State College Press; 1952. p. 282–97.Google Scholar
- Immonen E, Sayadi A, Bayram H, Arnqvist G. Mating changes sexually dimorphic gene expression in the seed beetle Callosobruchus maculatus. Genome Biol Evol. 2017; doi:https://doi.org/10.1093/GBE/evx029.
- Tran B, Credland PF. Consequences of inbreeding for the cowpea seed beetle, Callosobruchus maculatus (F.)(Coleoptera: Bruchidae). Biol J Linn Soc. 1995;56:483–503.Google Scholar
- Fox CW, Scheibly KL, Wallin WG, Hitchcock LJ, Stillwell RC, Smith BP. The genetic architecture of life span and mortality rates: gender and species differences in inbreeding load of two seed-feeding beetles. Genetics. 2006;174:763–73.View ArticlePubMedPubMed CentralGoogle Scholar
- Bilde T, Maklakov AA, Meisner K, la Guardia L, Friberg U. Sex differences in the genetic architecture of lifespan in a seed beetle: extreme inbreeding extends male lifespan. BMC Evol Biol. 2009;9:33.View ArticlePubMedPubMed CentralGoogle Scholar
- Carazo P, Green J, Sepil I, Pizzari T, Wigby S. Inbreeding removes sex differences in lifespan in a population of Drosophila melanogaster. Biol Lett. 2016; doi:https://doi.org/10.1098/rsbl.2016.0337.
- Connallon T, Jordan CY. Accumulation of deleterious mutations near sexually antagonistic genes. G3: Genes| Genomes|. Genetics. 2016;6:2273–84.Google Scholar
- Martínez‐Ruiz C, Knell RJ. Sexual selection can both increase and decrease extinction probability: reconciling demographic and evolutionary factors. J Anim Ecol. 2017;86:117–27.View ArticlePubMedGoogle Scholar
- Fedorka KM, Mousseau TA. Female mating bias results in conflicting sex-specific offspring fitness. Nature. 2004;429:65–7.View ArticlePubMedGoogle Scholar
- Brommer JE, Kirkpatrick M, Qvarnström A, Gustafsson L. The intersexual genetic correlation for lifetime fitness in the wild and its implications for sexual selection. Plos One. 2007. doi:https://doi.org/10.1371/journal.pone.0000744.
- Foerster K, Coulson T, Sheldon BC, Pemberton JM, Clutton-Brock TH, Kruuk LE. Sexually antagonistic genetic variation for fitness in red deer. Nature. 2007;447:1107–10.View ArticlePubMedGoogle Scholar
- Mainguy J, Côté SD, Festa-Bianchet M, Coltman DW. Father–offspring phenotypic correlations suggest intralocus sexual conflict for a fitness-linked trait in a wild sexually dimorphic mammal. Proc R Soc Lond B Biol Sci. 2009;276:4067–75.View ArticleGoogle Scholar
- Svensson EI, McAdam AG, Sinervo B. Intralocus sexual conflict over immune defense, gender load, and sex‐specific signaling in a natural lizard population. Evolution. 2009;63:3124–35.View ArticlePubMedGoogle Scholar
- Tarka M, Åkesson M, Hasselquist D, Hansson B. Intralocus sexual conflict over wing length in a wild migratory bird. Am Nat. 2013;183:62–73.View ArticlePubMedGoogle Scholar
- Barson NJ, Aykanat T, Hindar K, Baranski M, Bolstad GH, Fiske P, Jacq C, Jensen AJ, Johnston SE, Karlsson S, Kent M. Sex-dependent dominance at a single locus maintains variation in age at maturity in salmon. Nature. 2015; doi:https://doi.org/10.1038/nature16062.
- Mcguigan K, Petfield D, Blows MW. Reducing mutation load through sexual selection on males. Evolution. 2011;65:2816–29.View ArticlePubMedGoogle Scholar
- Arbuthnott D, Rundle HD. Sexual selection is ineffectual or inhibits the purging of deleterious mutations in Drosophila melanogaster. Evolution. 2012;66:2127–37.View ArticlePubMedGoogle Scholar
- Hollis B, Houle D. Populations with elevated mutation load do not benefit from the operation of sexual selection. J Evol Biol. 2011;24:1918–26.Google Scholar
- MacKay TF, Richards S, Stone EA, Barbadilla A, Ayroles JF, Zhu D, Casillas S, Han Y, Magwire MM, Cridland JM, Richardson MF. The Drosophila melanogaster genetic reference panel. Nature. 2012;482:173–8.View ArticlePubMedPubMed CentralGoogle Scholar
- Grieshop K, Berger D, Arnqvist G. (2017) Data from: Male-benefit sexually antagonistic genotypes show elevated vulnerability to inbreeding. Dryad Digital Repository. http://dx.doi.org/10.5061/dryad.cv4h2.