Conflict between the sexes over reproductive interests can drive rapid evolution of reproductive traits and promote speciation. Here we show that inter-species mating between Caenorhabditis nematodes sterilizes maternal individuals. The principal effectors of male-induced harm are sperm cells, which induce sterility and shorten lifespan by displacing conspecific sperm, invading the ovary, and sometimes breaching the gonad to infiltrate other tissues. This sperm-mediated harm is pervasive across species, but idiosyncrasies in its magnitude implicate both independent histories of sexually antagonistic coevolution within species and differences in reproductive mode (self-fertilizing hermaphrodites versus females) in determining its severity. Consistent with this conclusion, in androdioecious species the hermaphrodites are more vulnerable, the males more benign, or both. Patterns of assortative mating and a low incidence of invasive sperm occurring with conspecific mating are indicative of ongoing intra-specific sexual conflict that results in inter-species reproductive incompatibility.
The sexes have divergent reproductive interests, and conflict arising from this disparity can drive the rapid evolution of reproductive traits and promote speciation. Here we describe a unique reproductive barrier in Caenorhabditis nematodes that is induced by sperm. We found that mating between species can sterilize maternal worms and even cause premature death, and we were able to attribute this phenomenon directly to the sperm themselves. Sperm from other species can displace sperm from the same species and, in some cases, can invade inappropriate parts of the maternal reproductive system and even their non-reproductive tissues. We find that mating to males of another species harms females far more than does within-species mating. Overall, our observations are consistent with ongoing sexual conflict between the sexes within species, arising as a byproduct of sperm competition among the gametes of different males. Finally, patterns of assortative mating indicate that mating behaviours that reduce the likelihood of costly inter-species mating have evolved in this group of animals. These findings support an important role of sexual selection and gametic interactions contributing to reproductive boundaries between species, as predicted by evolutionary theory.
Citation: Ting JJ, Woodruff GC, Leung G, Shin N-R, Cutter AD, Haag ES (2014) Intense Sperm-Mediated Sexual Conflict Promotes Reproductive Isolation in Caenorhabditis Nematodes. PLoS Biol 12(7): e1001915. doi:10.1371/journal.pbio.1001915
Academic Editor: Mariana Federica Wolfner, Cornell University, United States of America
Received: December 6, 2013; Accepted: June 19, 2014; Published: July 29, 2014
Copyright: © 2014 Ting et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by grants from NSERC and NIH to ADC, NIH award GM79414 to ESH, a Canada Research Chair to ADC, an NSERC Post-Graduate Scholarship to JJT, and an Anne G. Wylie Dissertation Fellowship to GCW. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Abbreviations: df, degree of freedom; DIC, differential interference contrast; Fog, feminization of germline; XX animals, females and hermaphrodites
Rarely do reproductive interests of males and females perfectly align. Sexual selection can accelerate the evolution of the traits and molecules mediating reproductive encounters, and this can lead to sexual conflict ,. Components of the reproductive system that mediate male-female interactions, such as reproductive tract morphology, sperm and egg traits, and molecular components of seminal fluid all diverge rapidly between many species ,. The particularly forceful process of sexual antagonism drives co-evolutionary arms races between sex-limited traits that exact or counteract harmful, but self-serving, effects on the other sex ,,. Ongoing sexually antagonistic coevolution that operates within a species might generate mismatched interactions between gametes or other reproductive tract components when mating occurs between species. When such mismatches interfere with normal conspecific reproduction ,, they have the potential to instigate or magnify reproductive isolation between species ,. Selection for traits that prevent the deleterious consequences of inter-species mating for the parents or hybrid offspring may result in further trait evolution . Though pre-mating reinforcement behaviours have received much attention and debate –, post-mating mechanisms of gametic isolation, such as conspecific sperm precedence, also can play key roles in pre-zygotic reproductive isolation ,.
The prevailing view of gametic isolation between species is that fertilization precedence of conspecific sperm can provide a potent reproductive barrier, mediated by cryptic female choice, sperm competition, or incompatibilities between female reproductive tracts and heterospecific ejaculates –. Conspecific sperm precedence occurs both in species with internal and external fertilization, governed by a broad variety of proximate mechanisms ,,.
Alternatively, Drosophila provide examples of inter-species mating harm, for example, owing to an overly engorged “insemination reaction mass” that exacts a fitness cost on females ,, and female Carabus beetles suffer ruptured reproductive tracts from physical damage upon inter-species matings . Within species, male seminal proteins can manipulate female physiology in a manner sub-optimal for females but beneficial to males . While coevolution between the sexes may obscure the traces of such sexual antagonism (as for other forms of genetic conflict ), interactions between divergent populations and species can unmask the underlying conflicts by revealing mismatched male and female traits .
Caenorhabditis nematodes provide a powerful system to examine both sexual antagonism and its modulation by reproductive mode. Males, females, and hermaphrodites will mate readily and promiscuously in lab culture, and mechanical harm incurred from multiple mating reduces longevity and survival in C. elegans hermaphrodites  and C. remanei females . Male-derived chemical cues also are thought to accelerate female and hermaphrodite aging . Following copulation, C. elegans hermaphrodites can expel male ejaculates , and males deposit copulatory plugs that inhibit re-mating , and induce larger brood sizes in their partners . In response to experimentally elevated sperm competition, C. elegans evolve larger sperm . Though anatomical evolution in Caenorhabditis is conservative, these intra-specific dynamics suggest there may be substantial inter-species divergence in cryptic reproductive traits.
Evolutionary transitions in reproductive mode from highly outbreeding to highly self-fertilizing are expected to reduce intra- and inter-sexual conflict ,. Three species of Caenorhabditis have independently evolved androdioecy (hermaphrodites and males) from dioecy (females and males), such that hermaphrodites are capable of self-fertilization in addition to being fertilized by males . These androdioecious species manifest a “selfing syndrome” analogous to plants that includes reduced sperm size and low mating vigor ,. Hermaphrodites from such species with relaxed sexual selection might be particularly susceptible to adverse effects of mating to vigorous males from closely related species that have a recent history of strong sexual selection (the “weak inbreeder, strong outbreeder” or WISO hypothesis ,). Despite the generally limited understanding of Caenorhabditis ecology and inter-species interactions in their rotting fruit and vegetal habitats, some species are sympatric ,, putting them at risk for inter-species encounters. Species readily mate with one another in the laboratory, and the animals' transparent bodies provide literal windows into postmating-prezygotic, and postzygotic, reproductive interactions and barriers –.
Here we describe an unprecedented postmating-prezygotic reproductive barrier in Caenorhabditis nematodes, induced directly by sperm cells, that imposes potent fitness costs to females and hermaphrodites. Theory predicts species with selfing hermaphrodites to be more susceptible to inter-species harm and less capable of inducing harm ,. Theory also predicts that rapid divergence in sexually selected traits will produce heterogeneity in harmful effects between species pairs and consequently may fail to yield phylogenetic signal in the magnitudes of effect ,. In this counterpoint to mechanisms of conspecific sperm precedence, we affirm a potent role for sexual conflict as a pre-zygotic isolating barrier between species.
Mating to Males of a Different Species Is Harmful
In no-choice mating arenas, Caenorhabditis copulate repeatedly (Figure S1; Text S1), and will readily mate with different species –. We first examined the impact of mating the self-fertile hermaphrodites of C. briggsae, C. elegans, and C. tropicalis  with males of other species (Figure 1A–1C; Text S1). Despite the presence of abundant self-sperm, offspring production was invariably compromised. By contrast, mating to conspecific males leads to increased reproductive output, because hermaphrodite sperm stores are supplemented by the male sperm (Figure S2) . The extremity of reduced reproductive output upon inter-species mating, however, depends in part on the identity of maternal and paternal partners. For example, C. briggsae and C. elegans hermaphrodites produced <5% and <30% of their normal brood, respectively, when mated with any of seven dioecious species of Caenorhabditis tested (Figure 1A and 1B). C. tropicalis hermaphrodites, however, showed similarly striking sensitivity to males of C. brenneri, but were resistant or less sensitive to males of other species (Figure 1C).
Hermaphrodites of each selfing species were mated to males of dioecious (A–C) or another androdioecious (D, E) species and reproductive output was quantified as the number of self-progeny produced two days post mating treatment. (A) C. briggsae and (B) C. elegans produced significantly fewer progeny after heterospecific matings to males of all species tested (white) compared to selfing or “no mating” (blue). (C) C. tropicalis also produced fewer progeny after heterospecific matings, but only to a subset of the species tested. (D) A single heterospecific mating event was sufficient to induce progeny loss for C. briggsae hermaphrodites crossed to C. nigoni males (Mann-Whitney U = 37.0, p≤0.001). (E, F) Males from hermaphroditic species also reduced hermaphrodite self-progeny production following heterospecific mating (C. briggsae U = 65.0, p = 0.001; C. elegans U = 178.0, p = 0.008). However, males from hermaphroditic species were less effective at reducing progeny compared to dioecious males (C. briggsae U = 122.0, p≤0.001; C. elegans U = 631.0, p≤0.001). (G) C. briggsae hermaphrodites mated to C. nigoni males (solid blue line) suffer higher mortality than when mated to C. briggsae males (dashed black line; Kaplan-Meier log-rank test: χ2 = 5.218, df = 1, p = 0.022). Asterisks in (A–F) indicate significant difference from selfing control (Mann-Whitney U test p<0.05; Bonferroni correction applied in (A–C); (A, C) corrected α = 0.007; (B) corrected α = 0.008; Table S1). In (A–F), boxplot whiskers indicate 1.5× (interquartile range) and dotted horizontal lines indicate median of viable progeny produced by the selfing control for reference. Dagger (†) in (C) indicates that no successful matings occurred between C. portoensis males and C. tropicalis hermaphrodites. Sample sizes are shown in parentheses. Phylogeny in (A–C) adapted from .
In crosses between C. briggsae hermaphrodites and C. nigoni males, a single heterospecific mating event is sufficient to strongly depress reproductive output (Figure 1D), and prolonged exposure accelerates hermaphrodite mortality beyond that seen in conspecific or reciprocal crosses (Figure 1G). Increasing the abundance of conspecific sperm in hermaphrodites by mating them with conspecific males immediately before or after the heterospecific matings was insufficient to prevent or rescue sterilization of C. briggsae hermaphrodites by C. nigoni males (Figure S2). Males from androdioecious species of both C. elegans and C. briggsae were markedly less able to reduce the reproductive output of heterospecific hermaphrodites compared to the effect of dioecious males (Figure 1E and 1F). However, there is no clear association between degree of sterilization and phylogenetic distance (Figure S3A), although notably C. tropicalis is most sensitive to males of its closest tested relative, C. brenneri.
The above observations demonstrate that (i) hermaphrodites of all three self-fertile species are susceptible to adverse effects of mating with males of at least some other species and (ii) males of all species are capable of adversely affecting the reproductive output of hermaphrodites of at least some species. Such disparities among species in gametic isolation are predicted to be a common outcome of sexual selection on sperm competition . Consistent with intense intra-species sperm competition, multiple mating is readily observed in laboratory populations of outbreeding species (Figure S1; Text S1), while the rarity of males in self-fertile populations , suggests that multiple mating in these lineages is rare. Additionally, males from highly selfing species are less harmful to heterospecific mates, consistent with weak inbreeder, strong outbreeder (WISO) dynamics ,.
To assess the generality of heterospecific sterilization, we also examined male effects on females of dioecious species (Figure 2). Despite their similar sperm sizes ,, heterospecific mating of dioecious males from C. remanei, C. nigoni, and C. brenneri reduced the reproductive output of females of C. remanei and C. nigoni (Figure 2A and 2B). However, males from highly selfing species lacked the capacity to compromise the fecundity of heterospecific females (Figure 2A and 2B).
Females from dioecious species (A: C. nigoni, B: C. remanei) were initially mated overnight to conspecific males, followed by overnight mating of treatment females (white) to heterospecific males from either dioecious (C. nigoni, C. remanei, C. brenneri) or androdioecious (C. briggsae, C. elegans) species; control females (red) did not receive a second mating. Reproductive output was then quantified as the number of progeny produced two days post mating treatment. (A, B) Females often became sterilized upon a subsequent mating with heterospecific males from dioecious species compared to controls: (A) C. nigoni females (C. remanei males U = 385.5, p = 0.001; C. brenneri males U = 206.5, p≤0.001), (B) C. remanei females (C. nigoni males U = 239.5, p≤0.001; C. brenneri males U = 259.5, p≤0.001). However, females were resistant to harm induced by males of androdioecious species: (A) C. nigoni (C. briggsae males U = 409.5, p = 0.020; C. elegans males U = 577.0, p = 0.291), (B) C. remanei (C. briggsae males U = 887.0, p = 0.886; C. elegans males U = 863.0, p = 0.731). (C) C. nigoni females mated to heterospecific C. briggsae males (solid red line) did not incur a statistically significant survival cost relative to conspecific mating (dashed black line; Kaplan-Meier log-rank test: χ2 = 0.203, df = 1, p = 0.652; ns not significant). Asterisks in (A and B) indicate significant difference from controls (Bonferroni correction for multiple tests were applied; corrected α = 0.0125). Boxplot whiskers in (A and B) indicate 1.5× (interquartile range) and dotted horizontal lines indicate median of viable progeny produced by the controls (females mated with conspecifics); sample sizes are shown in parentheses.
In Drosophila, different levels of sexual antagonism can lead to reduced female survivorship in inter-strain matings . To explore whether heterospecific Caenorhabditis matings exert negative effects beyond reproductive output, we quantified maternal survival in the four cross combinations involving C. briggsae and its outbreeding sister species, C. nigoni. Mating with C. nigoni males significantly reduced the lifespan of C. briggsae hermaphrodites relative to conspecific mating (Figure 1G), but did not adversely affect conspecific C. nigoni female survival in our assay (Figure 2C), consistent with additional harmful effects of heterospecific mating beyond sterilization. Matings between another closely related selfer-outbreeder pair produced a different pattern, in which males from the selfing C. tropicalis exerted a much weaker effect on C. wallacei female longevity than did the other three cross combinations (Figure S4A). Matings between dioecious species yielded heterogeneous impacts on maternal survival. C. nigoni and C. sp. 5 males produced no significant reduction in female survival beyond that seen for conspecific matings (Figure S4B), whereas C. nigoni asymmetrically harmed C. remanei survival (Figure S4C). Similar to sterilization, then, inter-species mating affects maternal survival with species-pair dependencies in both outbreeding and selfing species. This observation is consistent with distinct evolutionary resolutions of sexual conflicts in different lineages. Additionally, we see a compelling effect of reproductive mode: in selfing species, hermaphrodites are more vulnerable, the males more benign, or both (as for C. briggsae).
One possible mechanism of reduced female fitness is competitive displacement of conspecific sperm by heterospecific sperm. Hermaphrodite Caenorhabditis make relatively small sperm that compete poorly with even conspecific male sperm, and their conspecific males make sperm that are smaller than those of dioecious species' males ,,,. Thus, the sterilization of hermaphrodites could result from the displacement of self-sperm by larger, yet ineffectual, heterospecific sperm . To address this issue, we labeled C. elegans and C. nigoni males with vital dyes, mated them to phenotypically female C. elegans fog-2 animals, and observed the transferred sperm from each male in live animals. Indeed, within a few hours of mating, we observed strong displacement of the smaller C. elegans male sperm from the spermathecae by the larger C. nigoni sperm (Figures 3A and S6C). However, sperm displacement does not explain the adverse effects of heterospecific mating on survivorship nor does it account for the seeming irreversibility of sterility induced by males upon their mating partners.
(A) Shortly after mating, the smaller C. elegans male sperm (red) are displaced from the spermatheca by larger C. nigoni sperm (green) in C. elegans fog-2 “females” doubly mated to vitally dyed males. sth, spermatheca; u, uterus, v, vulva. This panel is a mosaic assembled from multiple overlapping images. (B) C. briggsae adult hermaphrodite after overnight mating with conspecific males. Abundant embryos (e) are restricted to the uterus and reliably laid through the vulva (v). Diakinesis stage oocytes (do) are seen distal to the uterus, but not beyond the bend in the reflexed gonad (asterisk). (C) When mated overnight with C. nigoni males, few embryos are produced despite abundant sperm (sp). Proximal oocytes are abnormal (ao), and diakinesis oocytes are pushed distal to the gonad bend. p, copulatory plug. (D) In hermaphrodites recently inseminated by heterospecific males, the germ line is generally well organized, but ectopic embryos (ece) can be observed distal to the oviduct (od), which is often distended by sperm that have breached it from the spermatheca (sth). Embryos are also seen in the normal uterine position, explaining how some cross progeny are laid . (E) Hoechst DNA staining of conspecifically mated C. briggsae reveals abundant punctate sperm nuclei (sp) that are always restricted to the uterus and spermatheca and multiple diakinesis-stage meiotic nuclei (do). (F) DNA staining of C. briggsae hermaphrodites mated overnight with C. nigoni (similar to B) reveal a zone of endomitotic oocytes (emo) in the proximal region of the ovary abutting a large mass of sperm (sp). (G) In some cases, embryos localized to the uterus (emb) are viable (as judged by their advanced state of development) but not laid through the vulva (v).
Invasive Sperm Are the Primary Cause of Male Harm
C. briggsae hermaphrodites mated to C. nigoni males display striking germ line abnormalities, including disorganized proximal germ cells and ectopic, distally localized diakinesis-stage oocytes (Figure 3C). In addition, embryos often formed distal to the oviduct (Figure 3D), and, more rarely, we observed egg-laying defects (Figures 3G and S5). The proximal mass of disorganized germ cells is reminiscent of ovulation-defective mutant phenotypes in C. elegans ,,. Consistent with this, DNA staining of C. briggsae hermaphrodites revealed extensive endomitotic oocyte accumulation after one day of mating with C. nigoni males (54%, n = 78; Figure 3F), which increased further after a second day (91%, n = 70). No endomitotic oocytes were observed among C. briggsae hermaphrodites mated to conspecific males (n = 51; Figure 3B), indicating that C. nigoni males promote oocyte maturation defects in C. briggsae hermaphrodites.
Males transfer both sperm and seminal fluid components to mates, and in principle, either might negatively affect their partner's reproduction and lifespan after heterospecific matings. To distinguish these possible mechanisms, we again applied a fluorescent vital dye to males, mated them to conspecific or heterospecific individuals, and observed transferred sperm in live animals. After six hours of mating to C. briggsae hermaphrodites, conspecific male sperm had localized to the spermathecae and uterus in all animals (n = 52), as expected (Figure 4A; Movie S1). In a striking contrast, we found that 90% of C. briggsae hermaphrodites mated heterospecifically to C. nigoni males had sperm present in ectopic locations in the distal and proximal gonad, whereas only 10% of animals had sperm properly localized exclusively to the spermathecae or uterus (n = 188; Figures 4F and S6A; Movies S1 and S2). This appears to begin when many sperm penetrate the distal spermathecal valve, which normally separates maturing oocytes from sperm. Further, 7% of the hermaphrodites showed invasion of sperm into the body cavity (n = 159; Figure 4F; see Movie S1).
(A–F) Paired images of DIC and vitally dyed sperm inside maternal animals after conspecific and heterospecific crosses. (A) In conspecific crosses with C. briggsae, sperm remain completely in the uterus and spermatheca (bracket). (B) Female from C. nigoni conspecific cross displaying sperm localization to the uterus and spermatheca. (C and D) In rare cases of conspecific crosses for C. nigoni (C; 5%) and C. remanei (D; 8%), we observe isolated sperm (arrows) breach the distal spermathecal valve, but this does not cause sterility. (F) When C. nigoni males are mated with C. briggsae hermaphrodites, ectopic sperm are seen in large numbers, and in some cases breach the gonad completely. Wedge, anterior end of ovary; arrowhead, sperm nuclei in head region. (G) Series of frames from time-lapse movie (Movie S2) depicting movement of an individual ectopic C. nigoni sperm in the distal gonad of a C. briggsae hermaphrodite. The yellow crescent outlines the cell body of a sessile sperm, which serves as a reference point to highlight the motion of a second sperm, whose body is outlined in red.
Sperm of C. nigoni males also commonly invaded the gonad past the spermatheca when mated to other species (C. elegans and C. remanei; Figures S5, S6A–S6C), but the effect was most extreme in C. briggsae hermaphrodites, consistent with its pronounced deficits in reproductive output. Just three hours after mating, more than 50% (n = 72) of C. briggsae hermaphrodites had C. nigoni sperm in the distal gonad (cf. 90% six hours post mating; Figure S6A and S6D), whereas ∼20% (n = 39) of C. elegans and 2.9% (n = 35) of C. tropicalis hermaphrodites were similarly afflicted (Figure S6B). Ectopic sperm also were very rarely observed in C. tropicalis hermaphrodites mated heterospecifically to C. brenneri and C. remanei (0.9%, n = 111 and 0%, n = 18, respectively; Figure S6B), consistent with the infrequency of sterilization observed for this species. The ability of C. nigoni sperm to overrun the spermatheca is greater than that of other species tested. C. remanei sperm were rarely found in ectopic locations in C. nigoni females (5%, n = 100; Figure S6A), and ectopic sperm originating from C. briggsae males were never observed (n = 70; Figure 4A and 4E). Notably, the distinctly stronger sterilization of C. tropicalis by males of C. brenneri than C. nigoni occurs in the face of similar sperm localization patterns three hours post-mating (Figures 1B and S6C), further supporting the idea that factors other than sperm displacement are important in heterospecific sterilization. Intriguingly, in conspecific matings with C. nigoni and C. remanei, 5%–8% of females had small numbers of sperm in ectopic gonad locations (Figures 4C, 4D, and S6A). This low but detectable incidence of mislocalized sperm in conspecific matings is indicative of ongoing sperm-driven sexual conflict within dioecious species.
Negative effects of seminal components contributed by somatic glands can potentially trigger harmful reactions in females and hermaphrodites –. We therefore tested for a direct role of sperm in causing harm to C. briggsae hermaphrodites by feminizing the germ line of C. nigoni males via fog-3(RNAi) (Figure 5A and 5B) . Treated males have a normal somatic testis, mate normally, and can deposit seminal components including the copulatory plug, but transfer no sperm. The reproductive output (Figure 5C) and survival (Figure 5D) of C. briggsae hermaphrodites mated to spermless C. nigoni fog-3(RNAi) males is strikingly higher than that of animals mated to wild-type C. nigoni males. These observations implicate sperm infiltration into the gonad arms (and potentially into the body cavity) as the principal cause of male-induced permanent harm in heterospecific matings.
(A) Wild-type C. nigoni male, with spermatocytes (spc) and sperm (sp) in the seminal vesicle. These are extruded through the vas deferens (vd) during copulation. (B) C. nigoni male treated with maternal Cni-fog-3(RNAi). Oocytes (o) develop instead of sperm, while the somatic testis, including the glandular vas deferens (vd), remain unaffected. (C) The number of viable progeny of C. briggsae hermaphrodites do not differ when unmated (blue) or mated (white) to germline-feminized (fog-3 (RNAi)) C. nigoni males (Mann-Whitney U = 51.5, p = 0.419; ns, not significant), unlike when unmated or mated to wild-type C. nigoni males (U = 26.5, p = 0.019). Boxplot whiskers indicate 1.5× (interquartile range). (D) C. briggsae hermaphrodites mated to Cni-fog-3 (RNAi) males (solid line) have significantly reduced mortality compared to when mated to wildtype C. nigoni males (dashed line; Kaplan-Meier log-rank test: χ2 = 23.7, df = 1, p≤0.001). Sample sizes are shown in parentheses.
Assortative Mating of Species
The extreme fitness costs to inter-species mating might select for behaviours that promote assortative mating ,,,. We first examined female avoidance of heterospecific males because Caenorhabditis males mate indiscriminately when given the opportunity, and mating pheromones produced by virgin females are strongly attractive to males across species ,; tests for assortative mating in choice experiments have not been reported previously between Caenorhabditis species. We created assay populations with an equal mixture of females from each of two species and males from one of them (reciprocally), and then quantified the incidence of avoidance behaviour and of mating success of each species, as evidenced by copulatory plugs placed onto the vulva. This assay design presumes that dioecious males mate indiscriminately  and thus that female and hermaphrodite behaviour will dominate mating outcomes (Text S1).
Owing to their aggressive sperm, we first focused on copulatory responses to C. nigoni males. Overall, we observed that C. nigoni females exhibit a conspecific mating bias (Figure 6A–6C). We introduced C. nigoni females and males to either C. briggsae hermaphrodites (Figure 6A), C. elegans hermaphrodites (Figure 6B), or C. remanei females (Figure 6C). C. nigoni males were favoured by conspecific females over all heterospecific mating partners. When C. remanei and C. nigoni females (Figure 6C) were presented with C. remanei males, the females of both species showed no mating biases and were equally likely to mate with the males. This contrasts with the conspecific mating bias we observed when these females were presented with C. nigoni males (Figure 6C). This discrepancy suggests stronger assortative mating bias in favour of conspecifics by C. nigoni females compared to C. remanei females.
In assay arenas containing a mixture of females from two species and males from one species, (A) C. nigoni females are more likely than C. briggsae hermaphrodites to mate with C. briggsae males (t = 2.828, df = 24, p = 0.009) and C. nigoni males (t = 8.988, df = 24, p≤0.001). (B) A similar female mating bias was also observed when C. elegans hermaphrodites and C. nigoni females were presented to C. elegans males (t = 2.939, df = 19, p = 0.008) and to C. nigoni males (t = 28.996, df = 19, p≤0.001). (C) Mixtures of C. remanei and C. nigoni females show a mating bias toward C. nigoni females over C. remanei females when they are presented with C. nigoni males (t = 2.683, df = 24, p = 0.013), but not when presented with C. remanei males (t = 1.365, df = 24, p = 0.185). Positive values indicate that C. nigoni females mated more readily than the other female (or hermaphrodite) species that they were paired with; negative values indicate the reciprocal, while zero indicate no mating bias. Error bars represent ±1 standard error (SE); sample sizes are shown in parentheses.
We also tested C. nigoni females in the presence of either C. brigggsae hermaphrodites and males (Figure 6A) or C. elegans hermaphrodites and males (Figure 6B). Interestingly, C. nigoni females mated more readily with the heterospecific males than did the hermaphrodites to males of their own species (Figure 6A and 6B). The insensitivity of C. nigoni female reproductive output to having mated with androdioecious males (Figure 2A) could partially contribute to a lack of mate avoidance towards this class of heterospecific males (Figure 6A and 6B), although female sex pheromones  and hermaphrodite mating avoidance behaviours  also could contribute to this outcome. In addition to the mating outcomes, C. briggsae hermaphrodites were distinct in that they crawled away from the mating area when in the presence of C. nigoni males (t = −2.449, degree of freedom [df] = 44.672, p = 0.018). We interpret leaving the mating area as avoiding copulatory attempts by males.
Here we show that sperm transferred from matings between species of Caenorhabditis nematodes induce severe damage to females, compromising their reproduction and longevity. This phenomenon is the antithesis of the conspecific sperm precedence observed in diverse organisms, but still yields a form of gametic isolation owing to sperm displacement and ectopic sperm migration by heterospecific sperm. Caenorhabditis females commonly mate with multiple males (Figure S1; Text S1), and sperm competition selects for more aggressive sperm within species . Attracted to oocyte-secreted chemical cues, sperm must repeatedly crawl to the spermatheca (the site of fertilization) as embryos push them into the uterus (Figure 7) ,. We propose that intra-specific sperm competition between males within the reproductive tracts of multiply mated females acts to select for aggressive sperm in an evolutionary intra-species arms race. Sperm migration into distal portions of the gonad would represent a byproduct of sperm competition with harmful consequences for females, that in turn leads to counter-selection for female resistance ,,. While co-evolution within a species largely keeps these interactions matched, male and female changes can fail to complement one another in an inter-species context. Although such divergence need not have precipitated the initial isolating events, they nevertheless contribute to extant reproductive isolation among species. It remains to be tested whether heterospecific sterilization by sperm could also be co-opted as a weapon in inter-species resource competition when multiple Caenorhabditis species inhabit the same resource patch.
(A) Diagram of the reproductive tract of a XX nematode animal, magnified in (B) to illustrate the typical movement of gametes near the site of fertilization. Sperm must repeatedly crawl from the uterus to the spermatheca via the proximal spermathecal valve (psv) after being pushed out by fertilized eggs, migrating toward attractants secreted by the most proximal oocytes; red arrows indicate direction of sperm movement. Oocytes in the oviduct enter the spermatheca through the distal spermathecal valve (dsv) to be fertilized, then move into the uterus and exit the animal through the vulva; black arrows indicate direction of oocyte and embryo movement. (C) The normal process of self-fertilization in hermaphrodites (adapted from ) becomes disrupted upon heterospecific mating. (D) Heterospecific male sperm inhibit ovulation, invade the proximal gonad, induce premature oocyte maturation and ectopic fertilization, and in some cases invade somatic tissues.
This model of sperm competition (Figure 7D) and sexual conflict predicts sexual antagonism as an ongoing selective pressure within species of Caenorhabditis. We find evidence supporting this idea in the low incidence of ectopic sperm migration observed in conspecific matings for C. remanei and C. nigoni (Figure S6A). This model also could explain fertility patterns reported for crosses between parthenogenic and amphimictic Aphelenchus nematodes , suggesting applicability of this mode of gametic isolation across diverse taxa. Interactions between species with overlapping geographic ranges, as occurs for some Caenorhabditis including C. briggsae with C. nigoni  and C. tropicalis with several species , could select for behavioural or gametic strengthening of species boundaries or yield reproductive character displacement ,, consistent with some patterns of assortative mating and sperm migration observed in our experiments (Figures 6, S6A, and S6B). However, further tests comparing sympatric and allopatric genotypes are needed ,. This model further predicts the evolution of distinct cellular and molecular mechanisms mediating male sperm vigor and female resistance in different species, and relaxation of selection in some highly self-fertilizing hermaphrodite species ,. Consistent with what we observe empirically, differences among species in the mechanisms of evolutionary response to intra-species sexual conflict will create phylogenetic heterogeneity in how strongly the inter-species mismatches manifest as harm to females and hermaphrodites.
We addressed several other potential mechanisms that could contribute to the compromised maternal fecundity and longevity upon inter-species mating. (i) Trauma through copulation may occur in Caenorhabditis , and repeated matings in Drosophila melanogaster can induce female sterility and mortality . We can rule out this possibility because germline-feminized males with normal copulatory behaviours do not affect maternal reproductive output or longevity (Figure 5C and 5D). We also exclude repeated matings as an explanation for reduced reproduction because a single inter-species mating event also severely diminishes hermaphrodite reproductive output (Figure 1D). (ii) We can rule out insufficient sperm or oocytes as the cause of sterilization, as hermaphrodites cease laying embryos despite the abundance of oocytes and sperm in the reproductive tract (Figure 3) . (iii) The reduction in progeny production after heterospecific mating could result from superior fertilization capability of heterospecific sperm, leading to mortality of hybrid embryos, as post-zygotic reproductive isolation is nearly complete between most species studied here. However, we and others have observed insufficient numbers of dead eggs to account for the overall reduction in reproductive output –. (iv) Larger sperm from males of another species also could potentially outcompete and displace the conspecific sperm from the spermatheca, yielding fewer progeny . Indeed, such displacement occurs initially following heterospecific matings to males of a species with larger sperm (Figure 3A). However, hermaphrodite sperm for C. briggsae, C. elegans, and C. tropicalis all are similarly small ,, and yet these species differ starkly in susceptibility to the negative effects of mating to heterospecific males (Figure 1A–1C). Likewise, the disparity in sperm size of males from different dioecious species does not correlate with the extremity of reduced progeny production (Figure S3), and would not be expected to shorten lifespan. These observations reinforce the direct effects of sperm mislocalization in the maternal reproductive tract as the primary mechanism of male-induced permanent harm in inter-species matings.
Although our experiments demonstrate the key role of sperm cells in heterospecific harm upon mating, non-sperm components also could contribute. For example, upon maturation, C. elegans sperm cells release by exocytosis the contents of their lysosome-like membranous organelles (MOs) , and it is conceivable that molecules from this sperm cell-derived component of the seminal fluid could interact with female tissues. Indeed, the nematode major sperm proteins (MSPs) act as hormone-like signaling molecules to oocytes and gonad sheath cells, delivered in sperm-derived vesicles, in addition to MSP performing cytoskeletal functions ,. Additionally, components of the seminal fluid that derive from cells of the male somatic gonad play important roles in reproduction ,. Such seminal factors might compromise female tissue in some way that makes it more susceptible to adverse effects of heterospecific sperm, perhaps by inducing dilation of the gonadal sheath cells bordering the distal end of the spermatheca. In C. elegans, gst-4 and daf-2 mutants show defects in dilation of the spermathecal valve  and many proteins affect sheath contraction , suggesting potential pathway targets for compounds transferred by males during mating.
In C. elegans, oocyte-derived chemical cues guide sperm migration to the spermathecae . The attractant comprises a complex mixture of F-series prostaglandins derived from poly-unsaturated fatty acid (PUFA) precursors, whose synthesis and modulation depends on a suite of fatty acid desaturases, glutathione S-transferases, cytochrome P450s, insulin-like signaling, and communication between the somatic gonad and germ cells –. In C. elegans mutants of these genes, conspecific sperm fail to localize efficiently to the spermathecae, instead occurring more readily in the uterus ,. Heterospecific sperm migrate to the spermathecae efficiently in C. elegans and C. briggsae hermaphrodite reproductive tracts (Figure S6A–S6D) , indicating conservation of the sperm attractants and their detection between species. The high density of aggressive heterospecific sperm in their spermathecae then sets the stage for invasion of sperm into ectopic locations. However, sperm localization patterns for C. tropicalis suggests that its oocytes might secrete a sperm cue that is only weakly attractive, or a chemical mixture that attracts sperm efficiently only for some species (Figure S6B). Consequently, heterospecific sperm occur with lower density in the spermathecae, with correspondingly reduced likelihood of invasion into the distal gonad (Figure S6B). This hypothesis could underlie the limited adverse effects of heterospecific mating on C. tropicalis hermaphrodites. It might even implicate the weak sperm attractants as an evolutionary response through gametic reinforcement  if negative effects of inter-species mating in sympatry occurred in C. tropicalis' past . Finally, it is conceivable that differences among species in sperm attraction to distinct prostaglandins, or other compounds, coupled with secretion of them by more distally developing oocytes could encourage ectopic sperm migration.
The mechanism by which sperm migrate ectopically past the spermathecal boundary remains a key unsolved problem. Moreover, the breaching of the ovary basement membrane and migration of sperm into the body cavity through amoeboid movement, bearing a striking resemblance to features of metastasis in cancer –, motivates further investigation of the molecular basis of tissue integrity and resistance to cellular invasion .
Materials and Methods
Animals were maintained according to standard C. elegans procedures , with the exception of increased agar concentration in NGM plates to 2.2% in order to discourage animals from burrowing underneath the surface of the plate. Cultures were maintained at 20°C and 25°C. See Text S1 for strains of each species used for experiments: C. afra (sp. 7), C. brenneri, C. briggsae, C. elegans, C. latens (sp. 23), C. nigoni (sp. 9), C. portoensis (sp. 6), C. remanei, C. tropicalis (sp. 11), C. wallacei (sp. 16), C. sp. 5 .
Quantification of Reduced Reproductive Output
Crosses consisted of placing one hermaphrodite at the fourth larval stage (L4, penultimate stage of development) with six heterospecific males overnight (18–24 hours) on a 35 mm diameter Petri dish with a 10 mm diameter bacteria spot (E. coli OP50). Hermaphrodites (Figure 1A–1F) that successfully mated (presence of a copulatory plug) were transferred daily and we measured reproductive output as the yield of viable adult progeny from two days of egg laying following the final mating event (representing >90% of lifetime brood size). Control hermaphrodites were individuals allowed to produce self-progeny.
For matings involving females (Figure 2A and 2B), we first mated them to conspecific males overnight and the subsequent day we mated treatment females to heterospecific males. In all cases except one (C. briggsae×C. nigoni), matings are incapable of yielding viable hybrid progeny (few hybrids are produced by C. briggsae×C. nigoni ,). Therefore, reproductive output measures the number of conspecific progeny of females (or, equivalently, self-progeny of hermaphrodites).
The single mating treatment (Figure 1D) consisted of placing ten young adult hermaphrodites (C. briggsae) with 40 young adult males (C. nigoni) on a 35 mm Petri dish with a 10 mm diameter bacteria spot. After an hour, mated hermaphrodites were isolated to individual 35 mm diameter Petri dishes, transferred daily, and allowed to lay eggs in order to measure progeny production.
In situations when both female and hermaphrodites are used, they will be referred to as XX animals as they both have two X chromosomes. Seven L4 XX animals, depending on the species, were placed with ten heterospecific or conspecific males per plate and left overnight. The next day, XX animals were assayed for mortality by being touched on the head with an eyebrow hair glued to a toothpick. If the animal performed a backwards locomotive response to the touch, it was scored as alive. If it did not, it was scored as dead. This was performed every day for at least seven days. Every two days, XX animals and males were transferred to new plates in order to prevent the confusion of progeny with parents. Additionally, in these assays, XX animals were kept under continuous mating conditions: when males died or crawled off the plate, they were replaced with new males. XX animals that crawled off the plate were excluded from the lifespan measurements.
DNA Staining and Vital Staining of Sperm
The nuclei of animals were visualized using Hoechst 33258 staining. Seven XX animals were mated with ten heterospecific or conspecific males per plate for 1–3 days, and then XX animals were fixed in 100% methanol overnight at 4°C. The animals were then washed three times in M9 buffer and incubated in 1 µg/ml Hoechst in M9 buffer for 5 minutes, followed by mounting for fluorescent microscopy and imaging.
Male sperm were fluorescently labeled in vivo with MitoTracker Red CMXRos (Invitrogen) . Males were incubated in 1 mM dye for 2–3 hours, and then left on a plate to recover overnight. Subsequently, these males were mated with virgin young adult XX animals for 1–4 hours (matings with C. elegans males were allowed to run overnight). Virginity was assured by isolating XX L4 animals from males before reaching adulthood. Mated XX animals were then mounted on 10% agarose pads  or 2% agarose pads and immobilized with 50 mM sodium azide for differential interference contrast (DIC) and fluorescence imaging. Automated time-lapse photography (1–10 frames per second) was performed with the Open Lab software package and a Zeiss Axioskop 2 equipped with DIC and fluorescence microscopy.
C. nigoni-fog-3(RNAi) and Scoring Germ Line Feminization Phenotypes
A 929 base pair fragment including coding sequence homologous to fog-3 was PCR amplified from C. nigoni genomic DNA using primers flanked with 5′ T7 promoters. The reaction was gel purified using the QIAquick kit (Qiagen), and the resultant template was then used for in vitro transcription using the MAXIscript kit (Ambion) to make dsRNA. The dsRNA was recovered using phenol-chloroform extraction and isopropanol precipitation, and the dsRNA was then introduced into the animals via maternal microinjection. The male progeny of injected animals were scored for the feminization of germline (Fog) phenotype using DIC microscopy via standard methods . The worms were mounted on 2% agarose pads and immobilized with 50 mM sodium azide. Only males with clearly defined oocytes and no observable sperm were used for sterilization and lethality experiments. Fog males were allowed to recover for 30 minutes on a plate in a drop of M9 buffer. These males were capable of performing the mating behaviour and of depositing copulatory plugs (and presumably other seminal fluids). These males were then assayed for their ability to sterilize and prematurely kill C. briggsae hermaphrodites. These males were then used for experiments as described above. Control wild-type males were mounted, immobilized, and allowed to recover for the same amount of time in order to remove these as confounding factors.
We focused our assortative mating assays on C. nigoni males, as their aggressive sperm results in sterility and increased mortality (Figure 1). We expect males to mate indiscriminately ,; therefore, XX animal behaviours (preference or avoidance) should account for the majority of mating biases observed.
Assortative mating assays consisted of placing ten virgin C. nigoni males with ten virgin conspecific and/or heterospecific mating partners on a 35 mm diameter Petri dish. The three treatments involved presenting males to (i) ten conspecific, (ii) ten heterospecific (C. remanei, C. elegans, or C. briggsae), or (iii) a mixture of five conspecific and five heterospecific mating partners. See Text S1 for results of (i) conspecific and (ii) heterospecific treatment. Control assays consisted of males (C. remanei, C. elegans, or C. briggsae) following the same treatments as above with C. nigoni females as the heterospecific species.
We recorded successful mating by the presence of a copulatory plug deposited by a male onto an XX animal's vulva. We also recorded whether any XX animals left the 3 mm diameter (5 µl) bacterial spot mating area, which, we reasoned, was effective in avoiding copulation. We limited the mating period to 10 minutes to ensure males only mated once (male∶female ratio >1 was used to more easily observe successful copulations with inefficient males of androdioecious species). This 10 minute mating period was determined by preliminary experiments with a male placed with multiple conspecific females. In order to visually distinguish the two female/hermaphrodite species from one another, strains with pharyngially expressed GFP (C. briggsae PS9391) or RFP (C. nigoni VX0092) markers were used, which we presume exerts no direct effect on mate choice. See Text S1 for observed mating frequencies.
All statistical analyses were performed using IBM SPSS Statistics v.20, unless otherwise noted. We conducted non-parametric tests for measures of reproductive output, owing to non-normal distributions and heterogeneous variances. To assess the effect of heterospecific matings on reproductive output (i.e., extent of sterilization), we compared the control (selfing for hermaphrodites and conspecific matings for females) to each treatment (heterospecific mating) using Mann-Whitney U tests with Bonferroni correction for multiple testing. We used Kaplan-Meier survival analysis to test for an effect of mating on survival of females or hermaphrodites. The survival analyses were performed with the OASIS online application  and SPSS.
In experiments that explored assortative mating with a mixed species treatment (five conspecific and five heterospecific mating partners; Figure 6), an index of mating bias was calculated as the difference between the number of mated C. nigoni females and the number of mated individuals of the other maternal species present in the arena, divided by the number of C. nigoni females present in the arena (five). Positive values indicate a mating bias towards C. nigoni females over the female (or hermaphrodite) species that they were paired with, negative values indicate the reciprocal, and a value of zero indicates no mating bias (a lack of preference or avoidance). Negative values were not observed in our experiments. We then tested for a significant difference from zero with two-tailed one sample t-tests.
C. nigoni females mate multiply. (A) DIC image of a C. nigoni adult hermaphrodite after a two hour mating period with conspecific males labeled with vital dyes (red or green). Diakinesis stage oocytes (do) are seen distal to the uterus, but not beyond the bend in the reflexed gonad (asterisk). (B, C) Sperm (sp) from males stained with red and green are localized in the spermatheca. Also denoted is the vulva (v), and embryos localized to the uterus (emb). (D) A merged image of (A–C). (C, D) Auto fluorescence of the gut is visible. Each panel is a mosaic assembled from multiple overlapping images; all scale bars are 100 microns. See Text S1 for quantification of multiple mating experiments.
Inter-species mating harm is neither prevented nor substantially rescued by conspecific mating. C. briggsae hermaphrodites were left unmated (selfing only), treated to one mating period with one set of males (Con only: conspecific C. briggsae or Het only: heterospecific C. nigoni), or treated to two mating periods with two sets of males (Het-Het, Het-Con, Con-Het, Con-Con). A conspecific mating taking place one day after a heterospecific mating does not strongly rescue C. briggsae progeny production (Het-Het versus Het-Con: Mann-Whitney U = 126.5, p = 0.043: not significant after multiple tests corrections). Additionally, a conspecific mating does not prevent sterilization from a subsequent heterospecific mating (Con-Con versus Con-Het: U = 5.5, p≤0.001). Finally, C. briggsae hermaphrodites mated with heterospecific males, regardless of order, experience the same decrease in reproductive output (Het-Con versus Con-Het: U = 208.0, p = 0.599). Dotted line indicates the median of the selfing control for reference; samples sizes are in parentheses. Boxplot whiskers indicate 1.5× (interquartile range). For all mating treatments reproductive output is quantified by adult progeny produced two days following the second mating period. Multiple Mann-Whitney U tests were conducted and Bonferroni correction for multiple tests were applied (corrected α = 0.0125). Asterisk indicate statistical significance and (ns) indicate non-significance following Bonferroni correction.
No correlation between severity of harm by heterospecific males and phylogenetic distance or disparity in sperm size. We constructed an ordinal scale of severity of harm to females (or hermaphrodites) as: 1 = no sterilization and/or ectopic sperm; 2 = weak progeny reduction and/or no ectopic sperm; 3 = moderate progeny reduction and/or some ectopic sperm detected; 4 = strong sterilization and/or ectopic sperm present; 5 = near complete sterilization and/or extensive ectopic sperm. (A) We plotted the metric of severity of harm as a function of discretized evolutionary distance of hermaphrodites to heterospecific males mates, on the basis of the phylogenetic topology among species (see Figure 1). We observed no significant relation between phylogenetic distance and severity of harm, either for all hermaphrodite species pooled (Spearman's ρ = −0.15, p = 0.52) or considered separately (all distances have identical harm index for C. briggsae; C. elegans ρ = −0.54, p = 0.28, C. tropicalis ρ = −0.17, p = 0.74). Although this analysis is crude and is based on only a modest number of species comparisons, a more sophisticated analysis of phylogenetic contrasts is undermined by the topology of phylogenetic relationships among the species included in our study. (B) On the basis of sperm size values for the subset of species available in , we computed the difference in sperm cross-sectional area between conspecific and heterospecific males. In the case of matings to hermaphrodites, size of hermaphrodite sperm was used in calculations. Spearman rank correlation between these phylogenetically uncorrected metrics was not significant for matings to heterospecific males from dioecious species (p = 0.32). In the case of matings to androdioecious males, we detected a significant association (p = 0.012) owing to the weak sensitivity of hermaphrodites and no sensitivity of females to heterospecific androdioecious males.
Patterns of maternal survival in different Caenorhabditis crosses. Maternal survival in conspecific and heterospecific crosses of (A) C. tropicalis (hermaphrodite/male) with C. wallacei (female/male); (B) C. sp. 5 (female/male) with C. nigoni (female/male); and (C). C. remanei (female/male) with C. nigoni (female/male). (A) C. wallacei maternal survival was statistically greater in the presence of C. tropicalis males (Kaplan-Meier log-rank test: χ2 = 49.57, df = 1, p≤0.001). However, C. tropicalis maternal survival was not affected by C. wallacei males (χ2 = 0.45, df = 1, p = 0.503). (B) The presence of heterospecific males had no statistically significant effect on survival of C. sp. 5 females (χ2 = 0.002, df = 1, p = 0.961) or C. nigoni females (χ2 = 0.16, df = 1, p = 0.688). (C) C. remanei maternal lifespan over eight days was significantly reduced in the presence of C. nigoni males (χ2 = 8.81, df = 1, p = 0.003). C. nigoni maternal survival was not decreased by C. remanei males (χ2 = 1.65, df = 1, p = 0.199). Sample sizes are in parentheses, asterisks indicate significant difference in survival (p≤0.05), and ns indicate non-significant difference in survival. In all panels, dashed lines represent conspecific crosses and solid lines represent heterospecific crosses, while colours correspond to the maternal species.
C. nigoni sperm can ectopically localize and fertilize oocytes in C. elegans hermaphrodites. (A–D) Two C. elegans hermaphrodites mated for 2–6 hours with vitally stained C. nigoni males. Panels display images under DIC (A, C) and fluorescence microscopy (B, D). Indicated is the presence of ectopically localized C. nigoni sperm (esp). (E) A different focal plane of the animal in panels (C, D) reveals the presence of an ectopic embryo (ece) distal to the spermatheca. Also denoted are sperm (sp), the vulva (v), and a properly localized embryo (emb). The bend of the gonad is noted by an asterisk. All scale bars are 100 microns.
Mislocalization of sperm in different Caenorhabditis crosses. The percent of mated females/hermaphrodites observed to contain fluorescently labeled male sperm that localize outside of the spermatheca and uterus (ectopic, purple), in the uterus (orange), and/or in the spermathecae (blue). (A, B) Species names in black boxes below the x-axis indicate dioecious species; white boxes indicate androdioecious species. (C) C. elegans fog-2 “females” doubly mated to vitally stained males (red or green) show that the smaller C. elegans male sperm are displaced from the spermatheca by larger C. nigoni sperm. (D) The percent of observed C. briggsae hermaphrodites with ectopic C. nigoni male sperm increases with time since mating. The dotted horizontal line denotes a 50% reference line; sample sizes are in parentheses.
Statistical results of multiple Mann-Whitney U tests corresponding to Figure 1A–1C.
Male sperm localization in mated C. briggsae hermaphrodites. (A) Labeled C. briggsae male sperm localize to the spermatheca and uterus of a C. briggsae hermaphrodite. Time-lapse video of a C. briggsae hermaphrodite that has been mated with a fluorescently labeled C. briggsae male. (B) Labeled C. nigoni male sperm ectopically migrate in a C. briggsae hermaphrodite. Time-lapse video of a C. briggsae hermaphrodite that has been mated with a fluorescently labeled C. nigoni male. Numerous sperm are located outside of the hermaphrodite's gonad. The spermatheca and uterus have been outlined in yellow, whereas the proximal and distal gonad have been labeled in white. Scale bar represents 100 microns. Images were taken every 10 seconds and the video is sped up 10×.
Ectopic migration of an individual C. nigoni sperm in a C. briggsae hermaphrodite. Differential interference contrast time-lapse video of a C. briggsae hermaphrodite that has been mated with a C. nigoni male. Three ectopic sperm are visible (indicated by the white arrowheads in the opening frames). One ectopic sperm is observed crawling transversely around the distal gonad (lone arrowhead in subsequent frames). Each frame step represents one second.
Supplementary methods and results. Strains used in each experiment. Results of mating frequencies observed from assortative mating assays. Additional experiments examining sperm competition within species, effects of conspecific matings to heterospecifically mated hermaphrodites, and sperm localization in different species of Caenorhabditis.
We thank S. Baird, M.A. Félix, and the Caenorhabditis Genetics Center (funded by the NIH Research Infrastructure award P40 OD010440)) for strains, C. Braendle for sharing unpublished data on C. tropicalis sperm size, and G. Wilkinson, H. Rodd, J. Levine, H. Rundle, and L. Rowe for useful discussions.
The author(s) have made the following declarations about their contributions: Conceived and designed the experiments: JJT GCW ADC ESH. Performed the experiments: JJT GCW GL NRS. Analyzed the data: JJT GCW ADC ESH. Contributed reagents/materials/analysis tools: JJT GCW. Wrote the paper: JJT GCW ADC ESH.
- 1. Swanson WJ, Vacquier VD (2002) The rapid evolution of reproductive proteins. Nat Rev Genet 3: 137–144. doi: 10.1038/nrg733
- 2. Chapman T, Arnqvist G, Bangham J, Rowe L (2003) Sexual conflict. Trends Ecol Evol 18: 41–47. doi: 10.1016/s0169-5347(02)00004-6
- 3. Arnqvist G, Edvardsson M, Friberg U, Nilsson T (2000) Sexual conflict promotes speciation in insects. Proc Natl Acad Sci U S A 97: 10460–10464. doi: 10.1073/pnas.97.19.10460
- 4. Arnqvist G, Rowe L (2005) Sexual conflict. Princeton (New Jersey): Princeton University Press.
- 5. Rice WR, Holland B (1997) The enemies within: intergenomic conflict, interlocus contest evolution (ICE), and the intraspecific Red Queen. Behav Ecol Sociobiol 41: 1–10. doi: 10.1007/s002650050357
- 6. Knowles LL, Markow TA (2001) Sexually antagonistic coevolution of a postmating-prezygotic reproductive character in desert Drosophila. Proc Natl Acad Sci U S A 98: 8692–8696. doi: 10.1073/pnas.151123998
- 7. Matute DR, Coyne JA (2010) Intrinsic reproductive isolation between two sister species of Drosophila. Evolution 64: 903–920. doi: 10.1111/j.1558-5646.2009.00879.x
- 8. Parker G, Partridge L (1998) Sexual conflict and speciation. Philos T Roy Soc B 353: 261–274. doi: 10.1098/rstb.1998.0208
- 9. Rice WR (1998) Intergenomic conflict, interlocus antagonistic coevolution, and the evolution of reproductive isolation. Howard DJ, Berlocher SH, editors. Endless forms: species and speciation. New York: Oxford University Press. pp. 261–270.
- 10. Servedio MR, Noor MA (2003) The role of reinforcement in speciation: theory and data. Annu Rev Ecol Syst 34: 339–364. doi: 10.1146/annurev.ecolsys.34.011802.132412
- 11. Coyne JA, Orr HA (2004) Speciation. Sunderland (Massachusetts): Sinauer.
- 12. Butlin R (1987) Speciation by reinforcement. Trends Ecol Evol 2: 8–13. doi: 10.1016/0169-5347(87)90193-5
- 13. Howard DJ, Palumbi SR, Birge LM, Manier MK (2009) Sperm and speciation. Birkhead TR, Hosken DJ, Pitnick S, editors. Sperm biology: an evolutionary perspective. Boston: Academic Press. pp. 367–403.
- 14. Palumbi SR (2009) Speciation and the evolution of gamete recognition genes: pattern and process. Heredity 102: 66–76. doi: 10.1038/hdy.2008.104
- 15. Price CSC (1997) Conspecific sperm precedence in Drosophila. Nature 388: 663–666.
- 16. Chang AS (2004) Conspecific sperm precedence in sister species of Drosophila with overlapping ranges. Evolution 58: 781–789. doi: 10.1111/j.0014-3820.2004.tb00411.x
- 17. Eberhard WG, Cordero C (1995) Sexual selection by cryptic female choice on male seminal products - a new bridge between sexual selection and reproductive physiology. Trends Ecol Evol 10: 493–496. doi: 10.1016/s0169-5347(00)89205-8
- 18. Gregory PG, Howard DJ (1994) A postinsemination barrier to fertilization isolates two closely-related ground crickets. Evolution 48: 705–710. doi: 10.2307/2410480
- 19. Howard DJ (1999) Conspecific sperm and pollen precedence and speciation. Annu Rev Ecol Syst 30: 109–132. doi: 10.1146/annurev.ecolsys.30.1.109
- 20. Lorch PD, Servedio MR (2007) The evolution of conspecific gamete precedence and its effect on reinforcement. J Evolution Biol 20: 937–949. doi: 10.1111/j.1420-9101.2007.01306.x
- 21. Sota T, Kubota K (1998) Genital lock-and-key as a selective agent against hybridization. Evolution 52: 1507–1513. doi: 10.2307/2411321
- 22. Avila FW, Sirot LK, LaFlamme BA, Rubinstein CD, Wolfner MF (2011) Insect seminal fluid proteins: identification and function. Annu Rev Entomol 56: 21–40. doi: 10.1146/annurev-ento-120709-144823
- 23. Werren JH (2011) Selfish genetic elements, genetic conflict, and evolutionary innovation. Proc Natl Acad Sci U S A 108: 10863–10870. doi: 10.1073/pnas.1102343108
- 24. Gems D, Riddle DL (1996) Longevity in Caenorhabditis elegans reduced by mating but not gamete production. Nature 379: 723–725. doi: 10.1038/379723a0
- 25. Diaz SA, Haydon DT, Lindström J (2010) Sperm-limited fecundity and polyandry-induced mortality in female nematodes Caenorhabditis remanei. Biol J Linn Soc 99: 362–369. doi: 10.1111/j.1095-8312.2009.01352.x
- 26. Maures TJ, Booth LN, Benayoun BA, Izrayelit Y, Schroeder FC, et al. (2014) Males shorten the life span of C. elegans hermaphrodites via secreted compounds. Science 343: 541–544. doi: 10.1126/science.1244160
- 27. Kleemann GA, Basolo AL (2007) Facultative decrease in mating resistance in hermaphroditic Caenorhabditis elegans with self-sperm depletion. Anim Behav 74: 1339–1347. doi: 10.1016/j.anbehav.2007.02.031
- 28. Palopoli MF, Rockman MV, TinMaung A, Ramsay C, Curwen S, et al. (2008) Molecular basis of the copulatory plug polymorphism in Caenorhabditis elegans. Nature 454: 1019–1022. doi: 10.1038/nature07171
- 29. Barker DM (1994) Copulatory plugs and paternity assurance in the nematode Caenorhabditis elegans. Anim Behav 48: 147–156. doi: 10.1006/anbe.1994.1221
- 30. Timmermeyer N, Gerlach T, Guempel C, Knoche J, Pfann J, et al. (2010) The function of copulatory plugs in Caenorhabditis remanei: hints for female benefits. Front Zool 7: 28. doi: 10.1186/1742-9994-7-28
- 31. LaMunyon CW, Ward S (2002) Evolution of larger sperm in response to experimentally increased sperm competition in Caenorhabditis elegans. P Roy Soc Lond B Bio 269: 1125–1128. doi: 10.1098/rspb.2002.1996
- 32. Greeff JM, Michiels NK (1999) Low potential for sexual selection in simultaneously hermaphroditic animals. P Roy Soc Lond B Bio 266: 1671–1676. doi: 10.1098/rspb.1999.0830
- 33. Brandvain Y, Haig D (2005) Divergent mating systems and parental conflict as a barrier to hybridization in flowering plants. Am Nat 166: 330–338. doi: 10.1086/432036
- 34. Kiontke K, Felix M-A, Ailion M, Rockman M, Braendle C, et al. (2011) A phylogeny and molecular barcodes for Caenorhabditis, with numerous new species from rotting fruits. BMC Evol Biol 11: 339. doi: 10.1186/1471-2148-11-339
- 35. Cutter AD (2008) Reproductive evolution: symptom of a selfing syndrome. Curr Biol 18: R1056–R1058. doi: 10.1016/j.cub.2008.09.008
- 36. Thomas CG, Woodruff GC, Haag ES (2012) Causes and consequences of the evolution of reproductive mode in Caenorhabditis nematodes. Trends Genet 28: 213–220. doi: 10.1016/j.tig.2012.02.007
- 37. Martín-Coello J, Benavent-Corai J, Roldan ER, Gomendio M (2009) Sperm competition promotes asymmetries in reproductive barriers between closely related species. Evolution 63: 613–623. doi: 10.1111/j.1558-5646.2008.00585.x
- 38. Felix M-A, Jovelin R, Ferrari C, Han S, Cho YR, et al. (2013) Species richness, distribution and genetic diversity of Caenorhabditis nematodes in a remote tropical rainforest. BMC Evol Biol 13: 10. doi: 10.1186/1471-2148-13-10
- 39. Baird SE, Seibert SR (2013) Reproductive isolation in the Elegans-Group of Caenorhabditis. Natural Sciences 5: 18–25. doi: 10.4236/ns.2013.54a004
- 40. Woodruff GC, Eke O, Baird SE, Félix M-A, Haag ES (2010) Insights into species divergence and the evolution of hermaphroditism from fertile interspecies hybrids of Caenorhabditis nematodes. Genetics 186: 997–1012. doi: 10.1534/genetics.110.120550
- 41. Hill KL, L'Hernault SW (2001) Analyses of reproductive interactions that occur after heterospecific matings within the genus Caenorhabditis. Dev Biol 232: 105–114. doi: 10.1006/dbio.2000.0136
- 42. Baird SE, Sutherlin ME, Emmons SW (1992) Reproductive isolation in Rhabditidae (Nematoda: Secernentea): mechanisms that isolate six species of three genera. Evolution 46: 585–594. doi: 10.2307/2409629
- 43. Garcia LR, LeBoeuf B, Koo P (2007) Diversity in mating behavior of hermaphroditic and male-female Caenorhabditis nematodes. Genetics 175: 1761–1771. doi: 10.1534/genetics.106.068304
- 44. Felix MA, Braendle C, Cutter AD (2014) A streamlined system for species diagnosis in Caenorhabditis (Nematoda: Rhabditidae) with name designations for 15 distinct biological species. PLoS ONE 9: e94723. doi: 10.1371/journal.pone.0094723
- 45. Ward S, Carrel JS (1979) Fertilization and sperm competition in the nematode Caenorhabditis elegans. Dev Biol 73: 304–321. doi: 10.1016/0012-1606(79)90069-1
- 46. Barrière A, Félix M-A (2005) High local genetic diversity and low outcrossing rate in Caenorhabditis elegans natural populations. Curr Biol 15: 1176–1184. doi: 10.1016/j.cub.2005.06.022
- 47. Félix M-A, Duveau F (2012) Population dynamics and habitat sharing of natural populations of Caenorhabditis elegans and C. briggsae. BMC Biol 10: 59. doi: 10.1186/1741-7007-10-59
- 48. Baldi C, Viviano J, Ellis RE (2011) A bias caused by ectopic development produces sexually dimorphic sperm in nematodes. Curr Biol 21: 1416–1420. doi: 10.1016/j.cub.2011.07.034
- 49. LaMunyon CW, Ward S (1999) Evolution of sperm size in nematodes: sperm competition favours larger sperm. P Roy Soc Lond B Bio 266: 263–267. doi: 10.1098/rspb.1999.0631
- 50. Rice WR (1996) Sexually antagonistic male adaptation triggered by experimental arrest of female evolution. Nature 381: 232–234. doi: 10.1038/381232a0
- 51. Murray RL, Kozlowska JL, Cutter AD (2011) Heritable determinants of male fertilization success in the nematode Caenorhabditis elegans. BMC Evol Biol 11: 99. doi: 10.1186/1471-2148-11-99
- 52. Iwasaki K, McCarter J, Francis R, Schedl T (1996) emo-1, a Caenorhabditis elegans Sec61p gamma homologue, is required for oocyte development and ovulation. J Cell Biol 134: 699–714. doi: 10.1083/jcb.134.3.699
- 53. Kim S, Spike C, Greenstein D (2013) Control of oocyte growth and meiotic maturation in Caenorhabditis elegans. Germ cell development in C elegans. New York: Springer. pp. 277–320.
- 54. Chapman T, Liddle LF, Kalb JM, Wolfner MF, Partridge L (1995) Cost of mating in Drosophila melanogaster females is mediated by male accessory gland products. Nature 373: 241–244. doi: 10.1038/373241a0
- 55. Fowler K, Partridge L (1989) A cost of mating in female fruitflies. Nature 338: 760–761. doi: 10.1038/338760a0
- 56. Markow TA (2013) Sterilization by copulation in Drosophila. Entomol Exp Appl 146: 195–198. doi: 10.1111/eea.12020
- 57. Chen P-J, Cho S, Jin S-W, Ellis RE (2001) Specification of germ cell fates by FOG-3 has been conserved during nematode evolution. Genetics 158: 1513–1525.
- 58. Chasnov J, So W, Chan C, Chow K (2007) The species, sex, and stage specificity of a Caenorhabditis sex pheromone. Proc Natl Acad Sci U S A 104: 6730–6735. doi: 10.1073/pnas.0608050104
- 59. Han SM, Cottee PA, Miller MA (2010) Sperm and oocyte communication mechanisms controlling C. elegans fertility. Dev Dynam 239: 1265–1281. doi: 10.1002/dvdy.22202
- 60. Gavrilets S, Arnqvist G, Friberg U (2001) The evolution of female mate choice by sexual conflict. P Roy Soc Lond B Bio 268: 531–539. doi: 10.1098/rspb.2000.1382
- 61. Parker GA (1979) Sexual selection and sexual conflict. Sexual selection and reproductive competition in insects. New York: Academic Press. pp. 166.
- 62. Fisher JM (1972) Observations on the effect of males on reproduction and fecundity of Aphelenchus avenae. Nematologica 18: 179–189. doi: 10.1163/187529272x00421
- 63. Matute DR (2010) Reinforcement of gametic isolation in Drosophila. PLoS Biol 8: e1000341. doi: 10.1371/journal.pbio.1000341
- 64. Singson A, Hill KL, L'Hernault SW (1999) Sperm competition in the absence of fertilization in Caenorhabditis elegans. Genetics 152: 201–208.
- 65. Ward S, Argon Y, Nelson GA (1981) Sperm morphogenesis in wild-type and fertilization-defective mutants of Caenorhabditis elegans. J Cell Biol 91: 26–44. doi: 10.1083/jcb.91.1.26
- 66. Miller MA, Nguyen VQ, Lee M-H, Kosinski M, Schedl T, et al. (2001) A sperm cytoskeletal protein that signals oocyte meiotic maturation and ovulation. Science 291: 2144–2147. doi: 10.1126/science.1057586
- 67. Kosinski M, McDonald K, Schwartz J, Yamamoto I, Greenstein D (2005) C. elegans sperm bud vesicles to deliver a meiotic maturation signal to distant oocytes. Development 132: 3357–3369. doi: 10.1242/dev.01916
- 68. Smith JR, Stanfield GM (2011) TRY-5 is a sperm-activating protease in Caenorhabditis elegans seminal fluid. PLoS Genet 7: e1002375. doi: 10.1371/journal.pgen.1002375
- 69. Edmonds JW, Prasain JK, Dorand D, Yang Y, Hoang HD, et al. (2010) Insulin/FOXO signaling regulates ovarian prostaglandins critical for reproduction. Dev Cell 19: 858–871. doi: 10.1016/j.devcel.2010.11.005
- 70. Hoang HD, Prasain JK, Dorand D, Miller MA (2013) A heterogeneous mixture of F-series prostaglandins promotes sperm guidance in the Caenorhabditis elegans reproductive tract. PLoS Genet 9: e1003271. doi: 10.1371/journal.pgen.1003271
- 71. Kubagawa HM, Watts JL, Corrigan C, Edmonds JW, Sztul E (2006) Oocyte signals derived from polyunsaturated fatty acids control sperm recruitment in vivo. Nat Cell Biol 8: 1143–1148. doi: 10.1038/ncb1476
- 72. Edmonds JW, McKinney SL, Prasain JK, Miller MA (2011) The gap junctional protein INX-14 functions in oocyte precursors to promote C. elegans sperm guidance. Dev Biol 359: 47–58. doi: 10.1016/j.ydbio.2011.08.014
- 73. Hanahan D, Weinberg RA (2011) Hallmarks of cancer: the next generation. Cell 144: 646–674. doi: 10.1016/j.cell.2011.02.013
- 74. Kirienko NV, Mani K, Fay DS (2010) Cancer models in Caenorhabditis elegans. Dev Dynam 239: 1413–1448. doi: 10.1002/dvdy.22247
- 75. Podsypanina K, Du Y-CN, Jechlinger M, Beverly LJ, Hambardzumyan D, et al. (2008) Seeding and propagation of untransformed mouse mammary cells in the lung. Science 321: 1841–1844. doi: 10.1126/science.1161621
- 76. Kelley LC, Lohmer LL, Hagedorn EJ, Sherwood DR (2014) Traversing the basement membrane in vivo: a diversity of strategies. J Cell Biol 204: 291–302. doi: 10.1083/jcb.201311112
- 77. Wood WB (1988) The nematode Caenorhabditis elegans. Cold Spring Harbor (New York): CSHL Press.
- 78. Kozlowska JL, Ahmad AR, Jahesh E, Cutter AD (2012) Genetic variation for post-zygotic reproductive isolation between Caenorhabditis briggsae and Caenorhabditis sp. 9. Evolution 66: 1180–1195. doi: 10.1111/j.1558-5646.2011.01514.x
- 79. Fang-Yen C, Wasserman S, Sengupta P, Samuel AD (2009) Agarose immobilization of C. elegans. Worm Breeder's Gazette 18: 32.
- 80. Yang J-S, Nam H-J, Seo M, Han SK, Choi Y, et al. (2011) OASIS: Online application for the survival analysis of lifespan assays performed in aging research. PLoS ONE 6: e23525. doi: 10.1371/journal.pone.0023525