The maternally transmitted bacterium Wolbachia pipientis is well known for spreading and persisting in insect populations through manipulation of the fitness of its host. Here, we identify three new Wolbachia pipientis strains, wHho, wHho2 and wHho3, infecting Hyposoter horticola, a specialist wasp parasitoid of the Glanville fritillary butterfly. The wHho strain (ST435) infects about 50% of the individuals in the Åland islands in Finland, with a different infection rate in the two mitochondrial (COI) haplotypes of the wasp. The vertical transmission rate of Wolbachia is imperfect, and lower in the haplotype with lower infection rate, suggesting a fitness trade-off. We found no association of the wHho infection with fecundity, longevity or dispersal ability of the parasitoid host. However, preliminary results convey spatial associations between Wolbachia infection, host mitochondrial haplotype and parasitism of H. horticola by its hyperparasitoid, Mesochorus cf. stigmaticus. We discuss the possibility that Wolbachia infection protects H. horticola against hyperparasitism.
Citation: Duplouy A, Couchoux C, Hanski I, van Nouhuys S (2015) Wolbachia Infection in a Natural Parasitoid Wasp Population. PLoS ONE 10(8): e0134843. doi:10.1371/journal.pone.0134843
Editor: Kostas Bourtzis, International Atomic Energy Agency, AUSTRIA
Received: March 3, 2015; Accepted: July 15, 2015; Published: August 5, 2015
Copyright: © 2015 Duplouy 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
Data Availability: Data files are available from Dryad under the doi:10.5061/dryad.34sv3.
Funding: The project was funded by the Academy of Finland (grant #255553 to SvN, 213547 and 250444 to SvN and IH, and 266021 to AD) and the Otto Malm foundation (grant to AD).
Competing interests: The authors have declared that no competing interests exist.
Wolbachia pipientis is estimated to infect up to 60% of all insect species [1–4]. The maternally inherited bacterial endosymbiont often manipulates host reproduction to increase the frequency of infected host individuals in the population . Moreover, Wolbachia can manipulate other aspects of host biology via interactions ranging from parasitism to mutualism. In parasitic interactions, Wolbachia infection decreases host fecundity [6–10], longevity , and other comparable physiological traits [12, 13], while in mutualistic interactions Wolbachia increases fitness components of the host, such as resistance to pathogens (reviewed in ). In parasitoid wasps, Wolbachia has been shown to impose physiological cost to the host (as in Leptopilina heterotoma ) and to manipulate host reproduction, such as thelytokous parthenogenesis in Trichogramma [16, 17] and Asobara japonica  or cytoplasmic incompatibility in the wasps Leptopilina  and Nasonia . In contrast, some Asobara wasps have a strong mutualistic relationship with their Wolbachia, which plays an essential role in the development of the host ovaries . In many cases, exactly how Wolbachia affects host biology and persists in the host population is unknown.
Prevalence of Wolbachia infection varies from 100% to extremely low between host species and among populations within a host species [21, 22]. This range of prevalence comes about because host-symbiont associations either occur under different environmental conditions [23–25]; are at different stages of infection history ; or are affected by variable genetic factors of either the symbiont or the host [27, 28]. Furthermore, through manipulation of its host reproductive system Wolbachia have the potential to persist in their host population despite obvious costs to host fecundity. CI inducing-Wolbachia do this by causing total or partial reproductive failure between males and females with a different infection status, providing a reproductive advantage to female hosts, which can produce viable offspring regardless of whether they mate with infected or uninfected males. Wolbachia that distort population sex-ratio (male-killing, parthenogenesis and feminization) promote the production and fitness of infected females, ensuring the transmission of infection through generations . Finally, the coexistence of infected and uninfected individuals in a population is possible if there is perfect vertical transmission of the symbiont [29–32].
In the Åland islands in Southwest Finland, the population dynamics of the Glanville fritillary butterfly, Melitaea cinxia, and its specialized parasitoid wasp, Hyposoter horticola, are closely linked. The butterfly lives as a metapopulation in a landscape consisting of ~4000 small habitat patches (dry meadows), of which 500 to 800 are occupied yearly. The habitat patches are clustered into ~100 semi-independent networks (SINs)  with little gene flow of the butterfly between the networks. In contrast, H. horticola is highly dispersive among local butterfly populations resulting in high gene flow and low isolation by distance . Hyposoter horticola is itself parasitized by a similarly dispersive specialist hyperparasitoid, Mesochorus c.f. stigmaticus . Of the three species, H. horticola is the only one yet found to be infected with Wolbachia (Duplouy pers. obs.). In such a spatially and trophically structured system, Wolbachia epidemiology depends both on the effects of the bacterium on the wasp host, as well as on the demography and population dynamics of its host.
Here, we report three new Wolbachia strains, and describe one, wHho, which is present in the Åland islands, at intermediate prevalence. In an attempt to explain the intermediate level of infection, we measured the rate of vertical transmission and the association of infection with several life-history traits. We report spatial associations suggesting that Wolbachia infection may influence the resistance of H. horticola to its common larval specialist hyperparasitoid M. c.f. stigmaticus.
Materials and Methods
Hyposoter horticola (Gravenhorst)(Hymenoptera: Ichneumonidae: Campoplaginae) is a solitary egg-larval parasitoid of the Glanville fritillary butterfly, Melitaea cinxia (L.)(Lepidoptera: Nymphalidae) . The wasp parasitizes about a third of the host caterpillars in the Åland islands . We used H. horticola reared from naturally parasitized host caterpillars that were systematically sampled in the Åland islands (60°07’N, 19°54’E) between 2008 and 2013 as a part of the long-term ecological study of the Glanville fritillary . To document Wolbachia infection over a longer period, we also screened individuals sampled less systematically between 1993 and 2005 and preserved frozen (-20°C) in ethanol. Moreover, to place the samples in a geographical context, we analysed the infection status of H. horticola collected from Estonia (58°41’N, 22°50’E & 59°35’N, 24°05’E), France (43°61’N, 3°87’E), Spain (37°38’N, 5°98’E) and Sweden (60°00’N, 18°00’E & 56°73’N, 16°67’E). Altogether 751 wasps were screened (Table 1, S1–S3 Tables). The butterfly and its parasitoid are not classified as threatened species and hence no permits are required for their collection in Europe.
Wolbachia strains and Hyposoter horticola mitotype diversity
DNA was extracted from the wasp abdomen using a Qiagen DNeasy blood and tissues extraction kit, following the manufacturer’s protocol (Qiagen, USA). The DNA quality was tested by PCR amplifying the mitochondrial COI gene (primer pair LCO/HCO ). Any sample with no amplification for COI was removed. The COI locus was sequenced from 514 samples (422, 45, 6, 6 and 35 from Finland, Estonia, France, Spain and Sweden, respectively, S2 Table). Wolbachia infection was assessed through the amplification of two to seven Wolbachia loci, including the wsp gene (primer pair 81F/691R ), the 16S-RNA gene (553F_W/1334R_W ) and the five MLST loci (MultiLocus Sequence Typing genes: CoxA, FbpA, HCpA, GatB and FtSZ using respective primers from ). We also sequenced two to seven Wolbachia loci (MLST, wsp and 16s loci) from 249 (218, 5 and 26 from Finland, France and Sweden, respectively) of the 340 wasps infected with Wolbachia. The Fst values, based on the COI sequences, were calculated using Arlequin 3  (S5 Table). Each consensus sequence was submitted to GenBank (KF722987–94, KJ150624, KM598264–68 & KR185318–21).
Phylogenies (Fig 1, S1 Fig and S1 File) were built using the online tree-building program Phylogeny.fr [43, 44] in the One-click mode with default settings. For Wolbachia, we used the concatenated wsp, 16S and MLST consensus sequences from our three strains and eight additional Wolbachia strains (GenBank AM999887, CP001391, CP003883, AE017321, AE017196, EF025179 to -183, EF078895, AB474245 to -249, AB094382, AB052745). We rooted the tree using wBm as an outgroup. For H. horticola mtDNA, we used the seven mitotypes obtained from our samples together with sequences from five other species of Hyposoter (GenBank JF963449, JQ576453, JQ576979 & DQ538855 to -58) and two Campoletis sonorensis (Ichneumonidae, GenBank DQ538849 & -50). We rooted the tree using two Cotesia melitaearum (Braconidae, GenBank KM598269 & -70) as outgroups.
Mapping of the infection in the Åland island population
Each wasp was collected from a known geographic location, allowing us to analyse Wolbachia prevalence at the levels of local butterfly populations, semi-independent patch network (SIN), and in the landscape as a whole. We used log-linear models to investigate temporal variation in prevalence from 2008 until 2012 in the pooled material for the Åland islands (variables: year & infected versus uninfected) and variation in prevalence among the five SINs with the largest sample sizes (variables: SIN & infected versus uninfected). Finally, we compared infection levels between Sweden and the Åland islands using Fisher’s exact test using pooled data from 2008 to 2012 (categories compared were infected and uninfected individuals from Sweden and Finland).
Wolbachia transmission rate
The vertical transmission of Wolbachia is not always perfect . We measured the proportion of Wolbachia-infected progeny from 15 female wasps from the Åland islands, eight infected and seven uninfected. Each female parasitized a butterfly host egg-clutch in the laboratory (see  for methods). The caterpillars were reared until the 4th instar (15 caterpillars per female) or until wasps emerged as adults. We detected parasitism in the 4th instar caterpillars by amplifying both the parasitoid wasp DNA (microsatellite region Hho10 ) and a section of the repeat element protein-b11 from the wasp-integrated ichnovirus (length: 429bp, PCR annealing temperature: 50°C, primers: 34F 5’-GGCGTATGCARTAGTGRTGAA and 463R 5’-GATTATCGGAACCTGRTYGAA, this article). Additionally, because most H. horticola emerging from the same family group of Glanville fritillary larvae are full siblings , we estimated transmission rate in a larger sample using the infection status of wasps emerging from samples of two or three host individual taken from each of 51 host family groups during the field survey (S4 Table). The rate of transmission associated with the two wasp mitotypes was compared using a Fisher’s exact test.
Hyposoter horticola sex ratio
In some systems, Wolbachia skews the sex ratio of the host population toward females (through killing or feminization of males, or via parthenogenesis) . As each parasitized M. cinxia larval group contains primarily offspring of a single H. horticola female , we determined the per-mother allocation to male and female progeny, and the population-level sex ratio, by recording the sex of each individual reared from 53 larval groups parasitized naturally in the Åland islands between 2007 and 2010. Their infection-status is not known. However yearly random collections show that half of all collected wasps carry wHho in the Åland islands (S1 Table), so we assume that around half of these 53 larval groups originate from infected wasps. The mean brood sex ratio (fraction male) was compared with an equal (0.5) sex ratio using t-test. The distribution of brood sex ratios was compared with a normal distribution using the Shapiro-Wilk goodness of fit test.
Hyposoter horticola egg-load
Wolbachia is known to affect host fecundity [7, 9]. We tested for an association between the infection status and egg-load (as proxy for fecundity) of 213 females (including 111 infected and 102 uninfected) ranging from age 0 (day of emergence) to 51 days (maximum lifespan in the laboratory). The wasps were reared from naturally parasitized caterpillars and randomly killed at different ages, yielding a similar sample of infected and uninfected individuals at each age point. The ovaries were dissected in sterile conditions and mature eggs in the oviduct and calyx organs were counted as part of another study . The infection status of each wasp was determined upon death. The egg load was then analysed using a linear model, with the infection status and age of the wasp as explanatory variables.
Hyposoter horticola longevity
Presence of Wolbachia can decrease host longevity . Fifteen females and 33 males, reared under laboratory conditions from caterpillars naturally parasitized in the Åland islands in 2010 and 2011, were kept in individual vials (V = 100 ml) in an incubator at 12:12 L/D and 18/10°C day/night temperature. Wasps were fed 30% honey solution every other day until natural death (as described in ), and later assessed for Wolbachia infection. We tested the association of longevity with infection status using a linear model, with sex included as an extra explanatory variable.
Association of Wolbachia infection with habitat connectivity
If Wolbachia infection decreases dispersal ability of wasps, we would expect low prevalence of the bacterium where local butterfly populations are sparse in the landscape (low connectivity) , as the chances for Wolbachia-infected wasps to reach the surrounding habitat patches would be reduced. Alternatively, if the bacterium increased dispersal ability , we might expect prevalence to be lower in highly connected habitat patches. For each year (2008–2013), we calculated an index of connectivity of each local butterfly population from which wasps were reared, accounting for the distance from each local butterfly population to all other populations, the sizes of the populations and the dispersal ability of the butterfly [50, 51]. Using a linear model we tested possible association of the infection rate of H. horticola in a local butterfly population in year t with the connectivity of the population in year t-1, as wasps collected in the current year were the progeny of adults from the previous summer.
Wolbachia infection and host metabolic rate
Wolbachia can influence basic physiological and metabolic functions of its host. This would be especially relevant for the dispersal ability of the wasp, as flight is metabolically expensive [52, 53]. We compared the active and resting metabolic rates (AMR and RMR, respectively) of 33 Wolbachia-infected and 29 uninfected wasps reared from caterpillars collected from the wild in 2013. The metabolic rates were measured using flow-through respirometry at the constant temperature of 30°C . The AMR was measured as the maximum rate of CO2 emission under a bright light during 7 min of forced activity induced by flicking the 100 ml metabolic chamber each time the wasp’s wings were still (H. horticola may fly for more than 30 min without exhaustion, Duplouy, pers. obs.). We used the average CO2 emission rate during 60 sec preceding the active period, under a cover to block light, as a measure of the of the baseline RMR. Measures of AMR and RMR were corrected for variation in body mass by using residuals from linear regression between the metabolic rate and the weight. Linear models were used to analyse associations of CO2 emission rate with the infection status and sex of individuals.
Prevalence of Wolbachia and the rate of hyperparasitism
If Wolbachia confers resistance against parasitoids, we might expect the bacterial infection to be high where the risk of parasitism is high . We used linear regression to compare the prevalence of Wolbachia infection in H. horticola and the rate of hyperparasitism by Mesochorus c.f. stigmaticus using data from ten semi-independent patch networks (SINs) in the Åland islands. For each SIN, we calculated the relative abundance of the hyperparasitoid as the number of hyperparasitoids in the sample divided by the sum of the parasitoids and hyperparasitoids.
Wolbachia infection in Hyposoter horticola
The Finnish and Swedish populations of H. horticola carry a common Wolbachia strain that belongs to the Wolbachia B-supergroup (Fig 1), and which we name wHho (ST435). A single specimen from the Åland islands (sampled in 1998) was infected by an A-supergroup strain, wHho3. Samples from Estonia (n = 43) and Spain (n = 6) were uninfected, while samples from France (n = 6) carried a third strain, called wHho2, also in the A-supergroup.
In the Åland islands and Sweden, Wolbachia infection rate is related to the mitochondrial haplotype (mitotype) of the host. Based on the COI sequence, there are two common mitotypes, which differ by a single base pair substitution (synonymous substitution between C and T at the nucleotide position 364, the codon encoding for Leucine at position 121). Individuals with mitotype T are more likely to be infected by Wolbachia than individuals with mitotype C (Åland: 87% vs. 30%; Sweden: 100% vs. 56%, Fisher’s exact tests P = 0.0001 and P = 0.0068, respectively, Fig 2). The overall infection rate is significantly higher in samples from Sweden than from the Åland islands (P = 0.012). Within the Åland islands, from where we have samples from 2008 until 2013, the overall infection rate has remained stable (non-significant interaction between year and infection rate, df = 4, P = 0.21). However, there are highly significant differences in the infection rate between SINs (df = 16, P<0.001, Fig 2), and the overall infection rate is correlated with the frequencies of the two mitotypes (df = 1, P = 0.039, Fig 3).
The data includes samples collected between 2008 and 2013. Large circles show the infection rate in the T mitotype and small circles in the C mitotype. When one mitotype is absent, the respective circle is also absent (e.g. only the C mitotype occurs in Estonia).
The data were collected from 2008 to 2013. Panel (A) shows the association between Wolbachia infection rate and the relative abundance of the T mitotype in H. horticola (P = 0.01). The next two panels show the relationships between the relative abundance of the hyperparasitoid and (B) the relative abundance of the T mitotype (P = 0.039) and (C) Wolbachia infection rate (P = 0.11).
Of the fifteen female wasps used in the transmission experiment, eight were infected by Wolbachia. Five of the eight showed high Wolbachia transmission (>85%), while the remaining three showed lower transmission (between 33 and 66%). None of the offspring of the seven uninfected mothers were infected (S4 Table). As only one of the eight infected females had mitotype C, this material cannot be used on its own to compare the two mitotypes. We therefore augmented the lab-reared material with the field-collected samples. Among the presumed sibling groups produced by an infected individual of the C mitotype, nine out of 17 (53%) included one uninfected offspring (two to seven offspring per mother). In contrast, among the presumed siblings groups from infected females with mitotype T, only five out of 30 (17%) sibling groups had at least one uninfected individual. These results suggest that transmission is less efficient in the C mitotype (Fisher’s exact test, P = 0.018). The absolute values of uninfected individuals are likely to be biased, as some infected females of either mitotype may have had only uninfected offspring, and hence the female was wrongly scored as uninfected. However, comparison of the two mitotypes suggests more efficient transmission in the T mitotype.
Life-history and fitness consequences of Wolbachia infection
In the Åland islands, H. horticola has an equal population-level sex ratio (0.54, SD = 0.24), which does not differ from 0.5 (t = 1.01, P>0.05). Moreover, the brood level sex ratio was normally distributed around the mean in wasps from 53 host larval family groups (Shapiro-Wilk Goodness-of-fit test, W = 0.9827, P = 0.78). There is thus no evidence for extreme sex ratio distortion. However, these results do not rule out the possibility of other reproductive manipulations apart from sex ratio distortion, such as CI.
We found no association of Wolbachia infection with fitness-related traits in H. horticola. Infected and uninfected females had similar egg-load (520 and 522, df = 1, P>0.05, Fig 4). Females lived longer than males (37 versus 31 days, df = 1, P = 0.036), and Wolbachia infection was unrelated to longevity in either sex (df = 1, P>0.05, S2 Fig).
We found no association of Wolbachia infection with habitat connectivity in the previous year (Fig A in S2 File), suggesting that the infection does not influence wasp mobility. Consistent with this negative result, there was no association of Wolbachia infection with active or resting metabolic rate (Figs B and C in S2 File).
Parasitoid-hyperparasitoid interaction and Wolbachia infection
We analysed the relative abundances of H. horticola and its hyperparasitoid Mesochorus c.f. stigmaticus, as well as Wolbachia infection rate, in ten regions in the Åland islands (Fig 2B). The hyperparasitoid had greater relative abundance where the prevalence of the host T mitotype was lower (P = 0.039). Recalling that Wolbachia infection rate is higher among T- than C-mitotype wasps (above), this result suggests the hypothesis that wHho infection protects H. horticola against the hyperparasitoid. Indeed, in these data Wolbachia infection rate is low where hyperparasitism is high, though the association is not statistically significant (P = 0.11, Fig 3C). In Estonia, where Wolbachia is entirely absent, all the wasps are of mitotype C and the hyperparasitoid is absent. Under the hypothesis that Wolbachia protects against hyperparasitism, we would expect Wolbachia to be absent where there is no hyperparasitoid because, as it would be no advantage to its host, it would not spread.
We describe three Wolbachia strains in the ichneumonid wasp Hyposoter horticola, a parasitoid of the Glanville fritillary butterfly: two A-group strains, wHho2 and wHho3, detected from French samples and a unique Finnish sample, respectively, and a B-group strain, wHho (ST435), which is widespread in the Åland islands in Finland and in Sweden. No Wolbachia was identified in samples from Estonia (n = 47). The host H. horticola has seven COI mitotypes in our material, of which the two common ones (mitotypes C and T) occur in Finland and Sweden, one rare mitotype occurs in Estonia, and four other divergent mitotypes came from France and Spain. The post-glacial range expansion of H. horticola is unclear, but it may have spread to northern Europe, possibly with different Wolbachia strains, from both Asian and southern European refugia, as has its host butterfly  and another specialist parasitoid Cotesia melitaearum .
Rate of transmission and association of Wolbachia infection with host mitotype
We found that in the Åland islands the rate of vertical transmission of Wolbachia is imperfect, suggesting that the infection persists in an intermediate state, in balance between fitness benefits and costs [58, 59]. Moreover, the two H. horticola mitotypes are not equally infected. In the Finnish and Swedish populations, Wolbachia is common in the host mitotype T (92%) but much less common in the C mitotype (43%). In Estonia, all wasps had the C mitotype and were uninfected.
Both mitochondria and Wolbachia are transmitted maternally. Hence patterns of mtDNA-Wolbachia association reflect infection biogeography, strength of transmission, and history of Wolbachia spread in host populations [60, 61]. When vertical transmission is efficient, Wolbachia infection may result in a selective sweep leading to distinct infected and uninfected matrilines ([26, 62] e.g. in butterflies  and fig wasps ). When transmission is imperfect or when there is horizontal transfer, infected and uninfected individuals may share the same mitotypes . Infection rate of the wHho strain in Finland and Sweden may be higher in the T than the C mitotype because wHho infected the common ancestral matriline of both mitotypes, but transmission rate is higher in the T mitotype. Alternatively, the wHho strain may have first arisen in the T mitotype and later colonized the C mitotype by lateral transfer. Such lateral transmission could occur if two individuals parasitize the same host (superparasitism), which can occasionally happen in H. horticola . Alternatively the hyperparasitoid M. c.f. stigmaticus could transmit the bacterium between hosts (e.g. in aphids ). Finally, it is also possible that the mitotype diversity is higher than what the COI gene alone indicates, which would increase the complexity of the system.
Wolbachia infection and host fitness
Wolbachia is known to influence host fitness, reproductive system and behaviour to improve its transmission . In this study the prevalence of wHho differed geographically between the study regions, from 0 to 74%, at the scale of several hundred km (Fig 2A), as well as at a smaller spatial scale within the Åland islands, where infection rate varies from 8 to 100% regionally (Fig 2B). With efficient transmission, as appears to happen in the T mitotype, the bacterium would need to enhance host fitness only little, or to induce a strong CI, to persist. In the C mitotype with less efficient vertical transmission, the fitness benefit would need to be greater to compensate for the lower transmission rate.
Models predict that high variation in prevalence among populations may occur when there is high spatial population dynamics [59, 68]. Environmental heterogeneity in the Åland islands leading to large variation and fluctuation of local host population sizes  and prevalence of the hyperparasitoid M. c.f. stigmaticus , may interact with the effects of Wolbachia on its host, leading to spatial variation in prevalence.
Longevity and fecundity are correlated with fitness in parasitoids , and are often affected by Wolbachia [15, 71]. Wolbachia infection can also influence behavioural traits, such as dispersal in mosquitos . However, we found no evidence for wHho influencing host wasp longevity, fecundity or dispersal in the field. The lack of an association of infection with life history or behaviour suggests that the pattern of Wolbachia infection in the Åland islands may simply be in a transitional state, on its way toward fixation or extinction (e.g. in butterflies ). However, the spread of a CI-inducing or a beneficial strain could also show such heterogeneity between local populations [72, 73].
Alternatively, Wolbachia may have a less commonly studied association with fitness. One interesting hypothesis, suggested by our results, is that Wolbachia confers resistance to hyperparasitism. Several symbionts, including Wolbachia ( but see [75, 76]) have been found to protect their hosts against parasitoids (e.g. in aphids [77, 78] and fruit flies ). The specialist hyperparasitoid M. c.f. stigmaticus is ubiquitous in the Åland islands and Sweden , where Wolbachia prevalence is greater than 50%, while M. c.f. stigmaticus is absent from Estonia , where Wolbachia is also absent. Furthermore, within the Åland islands, the relative abundance of the hyperparasitoid decreased with increasing prevalence of the host T mitotype. As the T mitotype is also more often associated with Wolbachia than the C mitotype, we suggest that the presence of Wolbachia may improve resistance to hyperparasitism. Thus, wHho could be maintained because the infection reduces the likelihood of successful hyperparasitism.
To conclude, in this comprehensive landscape-level study of Wolbachia prevalence in a large spatially structured wasp population, there is a stable intermediate Wolbachia infection rate, which is significantly different in two host mitochondrial haplotypes (mitotypes). This pattern has several possible explanations, including imperfect but dissimilar vertical transmission rate in the two mitotypes. Second, we found no direct effect of infection, positive or negative, on fitness-related traits of the host, including egg-load (fecundity), adult longevity, metabolic rate and a measure reflecting dispersal rate in the field. Third, we have no evidence of sex-ratio distortion in the host, though we cannot rule out the expression of CI and its consequences for the spread of the bacterium in the population. The lack of a positive association with host fitness may indicate that Wolbachia is in a transitional state in the landscape, or that it is maintained via some other mechanism. One such mechanism is protection against hyperparasitism. We do not have direct experimental evidence for this hypothesis, but it is supported by the distributional data showing association of infection with the occurrence of the hyperparasitoid across the study landscape.
S1 Fig. Rooted phylogram based on the COI gene sequences from several Hyposoter species including H. horticola, and two specimens of a second ichneumonidae wasp, Campoletis sonorensis.
COI sequences of two specimens of the Braconidae Cotesia melitaearum were used as outgroups. The mitotypes associated with wHho are shown in grey, and those associated with wHho2 are encircled by a dashed-line.
S2 Fig. Longevity of wHho-infected (grey, NwHho = 27) and uninfected (white, NU = 21) male and female Hyposoter horticola from the Åland islands.
S1 File. Rooted phylograms based on the sequences of (Fig A) wsp, (Fig B) 16sRNA and (Figs C-G) each MLST gene from several Wolbachia strains, including wHho.
(Figs A and B): The wHho2 and wHho3 are only included in the trees built on wsp and 16s gene sequences, respectively. The wBm strain is used as an outgroup in each phylogeny. The phylogenies resemble each other and the phylogeny constructed with the concatenated sequence of each gene (Fig 1), suggesting absence of recombination.
S2 File. (Fig A) Presence/absence of Wolbachia in Hyposoter horticola samples from local host butterfly populations in the Åland islands between 2008 and 2013 (time t), and the mean butterfly population connectivity in the previous year (t-1).
Connectivity differs significantly between the years (P = 7.06e-7), but is not related to Wolbachia infection status. Weight-corrected (Fig B) active and (Fig C) resting metabolic rates of H. horticola infected or not with Wolbachia.
S1 Table. Sample size and wHho infection status for each year.
(*) indicates samples infected by a less commonly found Wolbachia strain, wHho2 or wHho3. SA: Estonian island of Saaremaa, VÄ: mainland Sweden, Väddö, ÖL: Swedish island of Öland.
S2 Table. Year-specific Wolbachia infection status and associated Hyposoter horticola mitotype.
S3 Table. Sample sizes for the studies.
Sample size in the transmission experiment is presented in S4 Table. The mapping study includes an additional 28 uninfected samples for which sex is unknown.
S4 Table. Transmission rate of Wolbachia, wHho, in the two matrilines of Hyposoter horticola collected from the Åland islands.
In the laboratory experiment, females with less than 3 offspring were not included in the analysis.
S5 Table. Population pairwise Fst values for Hyposoter horticola (below diagonal), average number of pairwise differences within population (πx, diagonal bold elements), and average number of pairwise differences between populations (πxy, above diagonal).
We thank T. Nyman, S. Ikonen, T. Lahtinen, M. Brunfeldt and M.C. Singer for help with the molecular work, collecting or rearing of the material. We thank A-N. Volkoff for providing the H. didymator COI sequence, A. Miraldo and T. Fountain for help with phylogeny and pairwise distance analyses. The project was funded by the Academy of Finland (grant #255553 to SvN, 213547 and 250444 to SvN and IH, and 266021 to AD) and the Otto Malm foundation (grant to AD).
Conceived and designed the experiments: AD. Performed the experiments: AD CC SvN. Analyzed the data: AD IH SvN. Wrote the paper: AD IH SvN.
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