Female European corn borer, Ostrinia nubilalis, produce and males respond to sex pheromone blends with either E- or Z-Δ11-tetradecenyl acetate as the major component. E- and Z-race populations are sympatric in the Eastern United States, Southeastern Canada, and the Mediterranean region of Europe. The E- and Z-pheromone races of O. nubilalis are models for incipient species formation, but hybridization frequencies within natural populations remain obscure due to lack of a high-throughput phenotyping method. Lassance et al. previously identified a pheromone gland-expressed fatty-acyl reductase gene (pgfar) that controls the ratio of Δ11-tetradecenyl acetate stereoisomers. We identified three single nucleotide polymorphism (SNP) markers within pgfar that are differentially fixed between E- and Z-race females, and that are ≥98.2% correlated with female pheromone ratios measured by gas chromatography. Genotypic data from locations in the United States demonstrated that pgfar-z alleles were fixed within historically allopatric Z-pheromone race populations in the Midwest, and that hybrid frequency ranged from 0.00 to 0.42 within 11 sympatric sites where the two races co-occur in the Eastern United States (mean hybridization frequency or heterozygosity (HO) = 0.226 ± 0.279). Estimates of hybridization between the E- and Z-races are important for understanding the dynamics involved in maintaining race integrity, and are consistent with previous estimates of low levels of genetic divergence between E- and Z-races and the presence of weak prezygotic mating barriers.
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Biological traits that influence reproductive biology, chemical communication, and mate attraction can influence gene flow within a species, maintain phenotypic diversity among ecotypes, and may ultimately contribute to sympatric speciation. Key mutations that establish prezygotic mating barriers effectively decrease gene flow within previously panmictic populations and allow the subsequent accumulation of divergent life history traits (Roelofs and Rooney 2003). During the early stages of diversification, incipient species often maintain high levels of gene flow, such that introgression occurs in regions of the genome not linked to genes directly involved in speciation (Wu 2001; Lassance et al. 2010). Incipient species can retain genomic regions with shared ancestral polymorphisms, as well as regions with derived mutations at a few key loci that are fixed differentially among divergent lineages (Gentile et al. 2002; Machado et al. 2002; Roelofs and Rooney 2003). Incomplete barriers to gene flow and consequent introgression can lead to homogenization of genomic regions not linked to genes involved in speciation. Because genetic drift and selection can lead to divergent molecular signals and phenotypic traits unrelated to the mechanisms involved in speciation, analyses of incipient species provide not only opportunities, but unique challenges for the study of contemporary speciation.
The European corn borer, Ostrinia nubilalis, is a polyphagous lepidopteran insect native to Eastern Europe and Western Asia, but was inadvertently introduced to North America in the early 1900s (Vinal 1917). Phenotypic variation includes females that produce, and males that respond to, pheromone blends of 99:1 or 3:97 E-: Z-Δ11-tetradecenyl acetate (E11- and Z11-14:OAc) (Klun and Brindley 1970; Kochansky et al. 1975; Roelofs et al. 1972). The geographic distribution of O. nubilalis that dominantly use the Z11-14:OAc isomer for sexual communication (Z-race) extend across the eastern two thirds of the United States, southeastern Canada, and Europe (Klun and Cooperators 1975). In contrast, populations of the E-race are restricted to the Eastern United States (O'Rourke et al. 2010), southeastern Canada (J. Smith, unpubl. data), and the Mediterranean region of Europe (Anglade and Stockel 1984). Limited gene flow between O. nubilalis pheromone races has been suggested from molecular analyses (Harrison and Vawter 1977; Cardé et al. 1978; Cianchi et al. 1980; Glover et al. 1991; Dopman et al. 2005), laboratory choice tests (Liebherr and Roelofs 1975), and field collections of F1 hybrid females that produce a 65:35 E11- to Z11-14:OAc ratio (Klun and Maini 1979; Roelofs et al. 1985; Durant et al. 1995).
The female O. nubilalis pheromone gland is comprised of a single layer of epidermal cells located in the 8th and fused 9th/10th abdominal segments (Ma and Roelofs 2002). Both races produce an approximately equal proportion of E- and Z-11-tetradecenyl, the precursors of E11- and Z11-14:OAc (Roelofs et al. 1987, 2002). The specific E11 to Z11-14:OAc isomer ratios produced by female E- and Z-race O. nubilalis is controlled by a single codominant genetic locus (Klun and Maini 1979; Roelofs et al. 1987; Dopman et al. 2004), but are modified to a lesser degree by unlinked genetic loci that were revealed by analyses of backcross progeny (Löfstedt et al. 1989; Zhu et al. 1996). Subsequent genetic linkage analysis indicated that the major locus controlling production of the E- or Z-isomer mapped to the pheromone gland fatty-acyl reductase gene, pgfar (Lassance et al. 2010), and that two alleles, pgfar-e and pgfar-z, are differentially expressed in the pheromone gland of E- and Z-race females, respectively. Any barrier to gene flow between O. nubilalis E- and Z-race field populations may be reinforced by a reduced ability of F1 males to locate females of either race (Glover et al. 1991), which suggests a coevolution between male and female reproductive traits (Lassance 2010). Despite the known association between pgfar and pheromone isomer production, questions remain regarding this relationship in natural populations and the level of intrarace variation at the pgfar locus (Lassance 2010).
The degree of gene flow in a hybrid zone can be interpreted as a measure of species divergence, and can be important for understanding speciation mechanisms. Female O. nubilalis pheromones (phenotypes) can be determined via separation of pheromone gland-produced hydrocarbons by gas chromatography (GC) analysis and comparison to synthetic standards. GC analyses are often difficult to apply within large population studies because the pheromone gland must be dissected from virgin females during scotophase when the pheromone titer is highest (Smith et al. 1991). Male O. nubilalis can be collected in traps baited with either the synthetic E- or Z-pheromone blend, but the lures show reduced fidelity to race when imprecise formulations are used (Bartels et al. 1997; Mason et al. 1997; Pelozuelo and Frerot 2008). Furthermore, identifying hybrid males captured in traps baited with either kind of lure requires GC analysis of the pheromone produced by female offspring from controlled backcrosses, a slow and logistically challenging undertaking. A fast and accurate molecular diagnostic assay would be of great value to those seeking to phenotype an individual's race, not only in studies of race interactions and genetic isolation, but in any ecological or behavioral study of this species conducted in areas of sympatry.
A single nucleotide polymorphism (SNP) is a single base substitution at a genomic locus, and SNPs are useful tools for population and genetic mapping studies (Glaubitz et al. 2003). SNPs can be detected by automated genotyping assays (Tsuchihashi and Dracopoli 2002) or low-throughput methods (Vignal et al. 2003). Molecular genetic markers within or linked to genes affected by a recent selective sweep can be associated with divergent traits, and thus used to predict individual phenotypes in natural environments (Schulze and McMahon 2004). In this study, we identified SNP markers in O. nubilalis associated with pgfar-e and pgfar-z alleles previously provided by work by Lassance et al. (2010), and verified their pheromone race specificity by direct comparison to pheromone phenotypes determined by GC analyses. We then developed and applied a SNP assay to estimate rates of hybridization between E- and Z-pheromone races at several locations in the Eastern United States.
Material and Methods
Development of pheromone race-specific molecular genetic markers
GenBank nr database accessions GU808256 to GU808276 originally submitted by Lassance et al. (2010) which contain cDNA sequences derived from the O. nubilalis pgfar gene were downloaded in FASTA format, and aligned using the MEGA 5.0 DNA sequence alignment utility (Tamura et al. 2007) using the default parameters of the ClustalW algorithm (gap opening penalty 15, gap extension penalty 6.66, weight matrix IUB, and transition weight of 0.5). Nucleotide diversity (d) was estimated using MEGA 5.0 (Tamura et al. 2007), and 100-bp sliding windows were iterated across the aligned cDNA sequences in 25-bp increments using Python scripts of DNAux 3.0 (http://www.portugene.com/software.html), and Tajima's D was estimated from each window using MEGA 5.0 (Tamura et al. 2007). The sliding window analysis closely approximated that previously provided by Lassance et al. (2010), but was replicated within this study to accurately determine the position of SNPs.
Fixed sequence variation was identified between aligned pgfar cDNA sequences derived from E- and Z-pheromone races, and oligonucleotide primer pairs were designed from conserved flanking regions using Primer3Plus (Untergasser et al. 2007). Specifically, oligonucleotide primer pairs were designed to PCR-amplify products containing pgfar-e and pgfar-z specific SNPs. Adult O. nubilalis (Fig. 1.) were collected by light trap at Crawfordsville, IA (n = 24), located in the Midwest region of the United States, where only Z-race populations are present (Table 1; Fig. 2). Samples from a laboratory colony of bivoltine E-race O. nubilalis, BENY, were obtained from C. Linn (Cornell University, Ithaca, NY). All DNA was extracted from the thorax of individual O. nubilalis adults as described by Coates and Hellmich (2003), quantified on a NanoDrop 2000 (Thermo Scientific, Wilmington, DE), and diluted to 10 ng/μL with nuclease free water.
Table 1. Estimates of hybridization of Ostrinia nubilalis E- and Z-race within field populations in the United States
HO among SNP markers
HE (all SNPs)
P-value (all SNPs)
Observed and expected heterozygosity at diagnostic pgfar SNP loci assayed by PCR-RFLP from Ostrinia nubilalis adults collected by light traps at indicated locations. Site IDs correspond to those on the map in Figure 1. BENY colony adults are included as a control for monomorphic E-race. NA = not applicable.
SNPs within the pgfar gene were detected by three independent polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) assays. DNA samples were amplified in 10-μL PCR solutions that included 1× Thermal polymerase buffer (Promega, Madison, WI), 2.5 mmol/L MgCl2, 50 μmol/L dNTPs, 20 ng DNA, 1.5 pmol of each primer (Table 2), and 0.3125 U GoTaq DNA polymerase (Promega). PCR was conducted in a Tetrad2 thermocycler (BioRad, Hercules, CA) programmed for 96°C for 3 min, followed by seven initial touchdown (TD) cycles consisting of 96°C for 20 sec, 65°C for 30 sec (–2°C/cycle each subsequent cycle), and 72°C for 30 sec. Final PCR amplification took place with 32 cycles of 96°C for 20 sec, 52°C for 30 sec, and 72°C for 30 sec. PCR product in the entire reaction volume was digested with a restriction endonuclease (RE) by adding 2.0 μL 10× buffer and 0.5 U of MseI (New England BioLabs, Ipswich, MA), or NdeII or TaqI (Promega) in a 20-μL total reaction volume (Table 2), then incubated at 37°C (or 65°C for TaqI) for 14 h. Entire RE digest reaction volumes were loaded into 10-cm 3% agarose gels and separated at 80 V for 2 h. Resulting fragment sizes were estimated by comparison to a 50-bp ladder (Promega), and compared to those predicted for pgfar-e and pgfar-z alleles (Table 2). Differences between the number of observed and expected genotypes at Crawfordsville, IA (historically known to be Z-race) and BENY colony individuals (pure E-race colony provided by Dr. C. Linn) were tested for significance with Chi-square (χ2) tests. Expected heterozygote frequencies for the Crawfordsville, IA and BENY samples were calculated using Arlequin 184.108.40.206 (Excoffier and Lischer 2010), and were performed as an initial test of allelic variation among groups of individuals with an a priori known phenotype (E- or Z-race).
Table 2. Oligonucleotide primer pairs that anneal within the pheromone gland fatty-acyl reductase, pgfar, gene of Ostrinia nubilalis to prime the PCR amplification of regions that contain pheromone race-specific single nucleotide polymorphisms (SNPs)
The SNPs are indicated as the nucleotide position within the pgfar cDNA and alternate nucleotides present at the locus (nucleotide position), and the restriction enzyme (RE) used to detect each allele are indicated. G/T995 and G/T1005 are detected by PCR-RFLP of the same PCR-amplified fragment.
Correlation between genotype and pheromone production
To test the fidelity of the pgfar SNP markers for discriminating O. nubilalis females producing E-, Z-, and hybrid pheromone blends, both SNP genotype and GC-analyzed pheromone component data were collected from individual F4 females derived from six independent intercrossed families. Specifically, Families 1 to 6 were each initiated by pooling ~200 adults from a laboratory colony of pure bivoltine Z-race O. nubilalis maintained at the USDA-ARS, Corn Insects and Crop Genetics Research Unit, Ames, IA, and ~200 adults from the BENY colony (pure bivoltine E-race). The BENY and USDA colonies served as controls. All families were maintained as random mating populations of ≥1000 individuals until the F4 generation. Individual female F4 pupae were placed in 28-mL plastic cups along with a piece of moistened cotton dental wick and allowed to emerge as adults in growth chambers at 25°C and 16:8 (L:D). Pheromone glands were removed and volatile compounds extracted using methods similar to Durant et al. (1995). In brief, pheromone ring glands were excised with micro-scissors at the terminal segment just anterior of the ring gland, during the 6th hour of scotophase (time of peak pheromone recovery, C. Mason, pers. comm.) from adult females the second day after eclosion (24–48 h old). Each gland was placed into a 50-μL point-tipped auto-sampler vial containing 5 μL of heptane and an internal standard of 4.5 ng cis-7-tetradecenyl acetate (7-TDA). 0053amples were held for ≥30 min at room temperature or stored in a −20°C freezer before analysis. DNA was extracted from the thorax of the same females, quantified, and diluted as described above. DNA samples were processed for genotyping at the pgfar PCR-RFLP marker loci using the restriction endonucleases TaqI, NdeII, and MseI as described above.
A 10-μL Varian 8200 auto-sampler syringe using a sandwich technique with a 0.5 μL upper air gap was used to sample 3 μL of each pheromone extract and inject at a rate of 1.5 μL/sec into a Varian 3500 Gas Chromatograph (Agilent Technologies, Santa Clara, CA). The GC was equipped with a heated injector fitted with a 4 mm ID open-top glass uniliner (Restek Corp., Bellefonte, PA) containing glass wool, a fused silica capillary column 15 m × 0.25 mm with 0.25 μm Stabilwax® (Restek Corp.) film thickness, a 5 m × 0.25 mm fused silica guard column, and a flame ionization detector. The gas chromatograph was programmed for a 20 min run time as follows: injector temperature 200°C, splitless for 1.5 min, then split for the remainder of the run (split ratio 50:1 at 60°C); detector temperature 250°C, attenuation set at 32−11; column oven programmed at 80°C held for 2 min, temperature ramp from 60 to 240°C at 10°/min, held at 240°C for 5 min to end of the run. Hydrogen was used as the carrier gas at a flow rate of 20 cm/sec (6.5 psi head pressure) and nitrogen was used as makeup gas. Under these conditions, the 7-TDA internal standard and the two pheromone isomers (E- and Z-11-tetradecenyl acetate) eluted at ≈ 13.1–13.5 min with each of the three peaks separated by 0.2 to 0.4 min. Chromatograms were used to estimate the ratio of E- to Z-11-14:OAc isomers by comparing the area under the isomers’ peaks at the appropriate retention times. Samples containing insufficient quantity of pheromone for detection, as indicated by the lack of peaks at the appropriate retention times, were not classified and were indicated as unresolved (U).
Each F4 family (1–6) was treated as an independent replicate, and a Pearson product-moment correlation coefficient (PMCC) was estimated between phenotype and genotype within and across families using SAS 9.2 (SAS Institute, Cary, NC). Female phenotype determined from pheromone gland component separation on the GC (≥90% E11-14:OAc isomer = 1.0, ≤5% E11-14:OAc isomer = 3.0, and all remaining estimated ratios = 2.0) was paired with corresponding pgfar genotypes from the same female (pgfar-e/pgfar-e = 0.0, pgfar-e/pgfar-z = 0.5, and pgfar-z/pgfar-z = 1.0). Strength of the linear relationship between the dependent (pgfar genotype) and independent variables (female GC isomer designation) were evaluated within each colony and across all intercrossed lines and pure E- and Z-race laboratory control colonies.
Estimates of field hybridization among pheromone races
Adult O. nubilalis were collected using light traps at 16 locations from the Midwest and East Coast of the United States (Table 1; Fig. 2), where sites 1 to 5 were from geographic regions historically known to have pure Z-race populations. In contrast, collection sites 6 to 16 within the East Coast region of the United States were anticipated to have populations comprised of both E- and Z-race moths. The sex of each moth was determined visually, and DNA was extracted as described by Coates and Hellmich (2003). Individuals were genotyped at the three pgfar SNP markers assayed with TaqI, NdeII, and MseI as described above. Observed heterozygosity (HO) and expected heterozygosity (HE) and significance of the deviations from Hardy–Weinberg equilibrium (HWE) were tested for each pgfar SNP marker within all populations with Markov chain exact tests using the Arlequin 220.127.116.11 (Excoffier and Lischer 2010). Differences between male and female HO estimates were evaluated by Chi-square (χ2) tests using SAS 9.2 (SAS Institute). Hierarchical F-statistics and analysis of molecular variance (AMOVA) were also generated using Arlequin 18.104.22.168 (Excoffier and Lischer 2010) after subdividing populations into Midwest (sites 1 to 5) and East Coast (sites 7 to 16) groupings. Significance was evaluated based on 1000 permutations as described by Weir and Cockerham (1984). Pairwise FST estimates between sample sites were calculated by Arlequin 22.214.171.124 (Excoffier and Lischer 2010), and significance thresholds set at a modified α according to the B–Y method (Benjamini and Yekutieli 2001).
Development of pheromone race-specific molecular genetic markers
Alignment of cDNA sequences from the O. nubilalis pgfar gene produced a 1607-bp consensus sequence predicted to contain 1317-bp (439 aa) and 1326-bp (442 aa) coding regions for sequences derived from E- and Z-races, respectively (Fig. S1). Nucleotide diversity (d) (mean number of base substitutions per site) across all pgfar cDNAs was estimated as 0.013 ± 0.005. When partitioned within and between cDNAs derived from Z- and E- pheromone races, d was 0.002 ± 0.001 and 0.011 ± 0.005, respectively. The nucleotide diversity index (π) and Tajima's D estimate across the entire pgfar coding sequence was 0.020 and 1.614, respectively. Estimates of Tajima's D within 100-bp sliding windows across the pgfar coding sequence ranged from 1.514 to 2.778, and revealed four regions of significant sequence divergence between Z- and E-race O. nubilalis (significance threshold set at 2.0 as described for the same analysis performed by Lassance et al. 2010; Fig. 3). Three putative pgfar allele-specific polymorphisms (SNPs) were identified in these regions of significant Tajima's D estimates that were also within restriction endonuclease (RE) sites (Fig. 3). Nucleotide positions G857, T995, and T1005 were fixed among cDNA sequences from E-race (pgfar-e alleles), and T857, G995, and G1005 nucleotides were fixed among cDNAs derived from Z-race (pgfar-z alleles). Nucleotides T857, T995, and T1005 complete palindromes for TaqI (TCGA), NdeII (GATC), and MseI recognition sites (TTAA).
Oligonucleotide primers flanking the putative polymorphic pgfar RE sites were designed, and PCR-amplified fragments ranged from 145 to 150 bp. Restriction digest of the corresponding PCR-amplified products by TaqI, NdeII, and MseI generated 118 + 32-bp, 83 + 62-bp, and 93 + 52-bp PCR-RFLP fragments, respectively (Fig. S2). The fragment sizes estimated from electrophoretic RFLP patterns were approximately the same as predicted from DNA sequence data for each allele (Table 2 footnotes). A pure Z-race population from Crawfordsville, IA (n = 48) and samples from the pure E-race BENY colony (n = 44) were genotyped at the pgfar loci to provide preliminary validation of the PCR-RFLP assay. The results for the Crawfordsville, IA Z-race samples (Table 1) indicated fixation of the nucleotides T857, G995, and G1005 predicted for pgfar-z alleles (Fig. S1). In contrast, PCR-RFLP results from the BENY colony (Table 1) were fixed for G857, T995, and T1005 as predicted for pgfar-e alleles. Thus, the Crawfordsville, IA and BENY samples were fixed for alternate pgfar-z and pgfar-e alleles (HO = 0), and thus the genotypes were able to predict the phenotypes known to be fixed within both of these DNA sources (the pure Z-race population from Crawfordsville, IA was fixed for the pgfar-z allele, and the pure E-race BENY colony was fixed for the pgfar-e allele).
Correlation between genotype and pheromone production phenotype
The correspondence between PCR-RFLP defined pgfar-z and pgfar-e alleles and female pheromone gland-produced E11- and Z11-14:OAc ratios were determined for segregating F4 females from replicate lines generated by mass mating of E- and Z-races in the parental generation. Pheromone glands were dissected from a total of 269 female O. nubilalis from Families 1 to 6, of which 247 provided GC readings from Families 1 (n = 45), 2 (n = 46), 3 (n = 46), 4 (n = 30), 5 (n = 26), and 6 (n = 21), as well as control colonies for E-race (n = 17) and Z-race (n = 16). Pheromone gland-derived hydrocarbons from 251 females were detected by GC (Table S1), where the proportion of the E11-14:OAc isomer in extracts ranged from 2 to 99 across all samples and all replicate lines (Fig. 4). A total of 259 female samples were genotyped using TaqI, NdeII, and MseI PCR-RFLP assays, of which 244 samples had both genotypic and GC assay results. The proportions of E11-14:OAc among homozygous pgfar-e, heterozygous, and observed homozygous pgfar-z genotypes were 98.02 ± 4.24 (n = 42), 67.58 ± 8.92 (n = 59), and 2.74 ± 6.24 (n = 143), respectively. Among the seven female genotypes that showed potential discrepancies between SNP marker and GC data, five had E11-14:OAc ratios that ranged from 57 to 68 but were genotyped as homozygous pgfar-z at the TaqI-assayed SNP marker (T857/T857). The same five samples were genotyped as heterozygotes (pgfar-e/pgfar-z) for both NdeII- (G995/T995) and MseI-assayed (G1005/T1005) SNP markers (Table S1).
The Pearson product-moment correlation coefficient between the proportion of E11 and Z11-14:OAc pheromones produced by female O. nubilalis pheromone glands and the number of pgfar-e alleles from TaqI, NdeII, and MseI SNP marker assays showed a positive relationship. Specifically, the correlation coefficient (r) ranged from 0.8789 to 0.9942 across all markers (TaqI, NdeII, and MseI) and each replicated line (Family 1 to 6), and all were significant (P-values < 0.001; Fig. 5.). Mean correlation coefficients for data pooled across all lines were high for TaqI (r = 0.9699 ± 0.0321), NdeII (r = 0.9884 ±0.0182), and MseI-assayed SNP markers (r = 0.9884 ±0.0182) (P-values < 0.001).
Estimates of field hybridization among pheromone races
A total of 499 light trap-collected adult O. nubilalis were genotyped using the three pgfar SNP (PCR-RFLP) markers (Table 1; Fig. 2). The estimated mean pgfar-e allele frequencies at SNP loci G857, T995, and T1005 were 0.204 ± 0.100 (mean HO of 0.107 ± 0.105; range 0.000–0.419) across all populations and across both sexes. Sample sites from historically Z-race regions of the Midwest United States (Lexington, KY; Crawfordsville, IA; Kanawha, IA; Mead, NE; and Brookings, SD) were fixed for SNPs T857, G995, and G1005, and were fixed for the pgfar-z allele (HO = 0) as anticipated from historical data. In contrast, light trap samples from 11 East Coast locations (sites 6 through 16; Fig. 2) showed an estimated mean HO across sites of 0.154 ± 0.110, and confirmed the prediction that heterogeneous E- and Z-race populations were present within this geographic region. SNP genotypes from 9 of 11 East coast locations did not significantly deviate from HWE across all SNP marker loci (P ≥ 0.082), with significant deviations shown among genotypes from Cohansey, NJ (P-value < 0.001), and Newark, DE (P-value < 0.001; remaining data not shown). When partitioned into male and female samples, the mean HO did not deviate significantly between sexes at any location (P-values < 0.05; remaining data not shown). Global estimates of F-statistics indicated significant pgfar allele frequency variation among geographic regions (Midwest [sites 1 to 5] vs. East Coast [sites 7 to 16]; FST = 0.0782; P ≤ 0.001; Table S2). Pairwise FST estimates among light trap collection sites ranged from −0.02798 to 0.5156, and 17 of 55 comparisons (30.9%) were significant between Midwest and East Coast sample sites (P-values ≤ 0.009; B–Y significance threshold = 0.014) (Table S3). In contrast, seven of 65 pairwise FST estimates (10.8%) were significant among East Coast samples. Additionally, significant inbreeding was detected within Midwestern and within East Coast samples (FIS = 0.3133; P-value < 0.001; Table S2). The significant variation between population from the Midwest compared with the East Coast were expected due to historical geographic range of E-race populations within East Coast regions. Thus, these results could be considered complementary to the laboratory genotype–phenotype association studies performed above.
Development of pheromone race-specific molecular genetic markers
The two pheromone races of O. nubilalis show partial reproductive isolation when in sympatry, and may represent incipient species in the early stages of divergence (Dopman et al. 2010; Lassance et al. 2010). E- and Z-race individuals are morphologically indistinguishable, but females from each race can be identified by analysis of fatty acid derivatives produced in the pheromone gland (Klun and Brindley 1970; Kochansky et al. 1975; Roelofs et al. 1972). Correspondence of phenotype with genotypes (mutations) has been established for insecticide resistance traits (Ffrench-Constant et al. 1993), but population associations can be complicated by effects of inbreeding, population structure or selection (Berlocher and McPheron 1996; Baxter et al. 2010). The population association of the three molecular genetic markers developed in the current study was facilitated by prior knowledge that O. nubilalis pheromone production traits segregating in backcross pedigrees are linked to the pgfar locus (Lassance et al. 2010). Despite this association between pgfar alleles and female pheromone within pedigrees, marker association within populations requires linkage disequilibrium (LD) in the face of continued genetic recombination (Jorde 2000). The high levels of nucleotide diversity and lack of shared ancestral polymorphism between cDNAs derived from E- and Z-race O. nubilalis, along with significant Tajima's D estimates, suggested to Lassance et al. (2010) that directional selection is acting on the pgfar locus.
The three SNP markers within O. nubilalis pgfar that were assayed by PCR-RFLP in this study are positioned in regions that were significantly affected by directional selection (based on sliding window estimates of Tajima's D < 2.0). Although this analysis was replicated from that previously performed by Lassance et al. (2010), our similar analysis allowed positioning of the SNP markers within regions showing evidence of directional selection (Fig. 2). Furthermore, two of the three SNPs were at second codon positions and caused nonsynonymous (amino acid changing) mutations that were fixed differentially among E- and Z-race cDNAs. Specifically, the TaqI PCR-RFLP assay detected a G/T857 SNP that results in a deduced Cys to Phe change, and the NdeII PCR-RFLP assayed for a T/G995 SNP that predicts an Ile to Ser change. The T/G1005 SNP detected by the MseI PCR-RFLP assay is at a 3rd codon position, but is associated with a nonsynonymous Val to Met change that is due to mutation of the 1st codon position (Val [GTT] to Met [ATG]). Initial population screening of known E- and Z-race samples, followed by more broad population sampling and association studies, indicated that the three SNP markers are diagnostic for the differentiation of O. nubilalis pheromone races collected in the field. Focusing on amino acid changing SNPs in population association studies has been proposed, because significant associations may have a higher probability of being detected at nonsynonymous sites (Botstein and Risch 2003). The accumulation of mostly nonsynonymous changes within O. nubilalis pgfar suggests that divergent selection has resulted in enzymes with derived specificities for the production of E- and Z-stereoisomers.
Correlation between genotype and pheromone production
SNP markers consist of base substitutions at a single genomic locus, where individual mutations are generally biallelic and have lower allele diversities and provide less statistical power to discriminate unique genotypes compared to microsatellite loci (Xing et al. 2005). However, SNPs are increasingly being used for population genetics and mapping studies due to their abundance, and relative ease of discovery and development (Glaubitz et al. 2003; Morin et al. 2004). SNP markers were previously developed from O. nubilalis expressed sequence tags (ESTs; Coates et al. 2008, 2011a), and subsequently applied to detect significant levels of genetic differentiation among O. nubilalis populations (Coates et al. 2011a) and to determine linkage groups associated with Bacillus thuringiensis resistance traits (Coates et al. 2011b). SNPs have been used in other species of Lepidoptera to identify population genetic structure (Margam et al. 2011) and to detect genome regions that influence traits (Sreekumar et al. 2011). Our data show that the segregation of three SNP markers within the O. nubilalis pgfar gene are significantly correlated with the proportion of E11-14:OAc produced in the female pheromone gland. These results are consistent with previous analyses of backcross pedigree data (Lassance et al. 2010). This evidence also indicates that linkage disequilibrium in this genome region between O. nubilalis pheromone races may be maintained by disruptive selection. The size of the O. nubilalis genome region affected by LD remains unknown, but within other species where the level of LD is known haplotype blocks have been shown to span regions of ~500 kb (Hirschhorn and Daly 2005). Fourteen putative loci were identified and proposed to be involved in adaptive divergence between the species O. nubilalis and O. scapulalis (Midamegbe et al. 2011), but analogous genome wide studies have not been reported between E- and Z-race O. nubilalis.
Despite the strong correlation between pgfar genotype and female phenotype, estimated ratios of E11-14:OAc in F4 females with pgfar-e/pgfar-z genotypes ranged from 53 to 94 (mean 67.3 ± 9.0), and often deviated from the expected 65:35 E11- to Z11-14:OAc hybrid ratio (Klun and Maini 1979; Roelofs et al. 1985). Reciprocal crosses between E- and Z-race O. nubilalis in previous studies indicated that modifier loci may affect female pheromone production, causing shifts in heterozygote pheromone blend ratios, and were most noticeable in female F1 backcrosses to the Z-race (Löfstedt et al. 1989; Zhu et al. 1996). The effect of segregating modifier loci on female pheromone blend ratios may be responsible for the skewed ratios we observed among heterozygous F4 females, but additional experiments will be required to determine the genetic loci involved. The rate of mating success for F1 hybrid females from United States population that express intermediate pheromone blend ratios showed no significant difference in backcrosses to either E- or Z-race males in laboratory experiments (Pelozuelo et al. 2007), and suggest that these backcross individuals may also be present in natural populations.
Estimates of field hybridization among pheromone races
Mate attraction in O. nubilalis may be a function of independent genetic loci; the Pher (=pgfar) locus that determines female pheromone production, and Resp and Olf loci that influence male behavioral response and structure of the male antennae, respectively (Hansson et al. 1987; Roelofs et al. 1987; Dopman et al. 2004). The accumulation of genetic and phenotypic differences between E- and Z-race adults may lead to preferential mating within each race. Regardless, hybridization occurs in both the field and laboratory, where pairings of E-race male with Z-race females tend to be more frequent than the reciprocal cross (Liebherr and Roelofs 1975; Linn et al. 1997; Pelozuelo et al. 2007). Male attraction to females of the opposite pheromone race decreases significantly with increasing distances (Dopman et al. 2009), and successful mating may also depend upon recognition of a male courtship pheromone at close range as well as courtship behaviors and signaling (Lassance and Löfstedt 2009; Takanashi et al. 2010). Despite chemical and behavioral mechanisms of prereproductive isolation between E- and Z-races, accurate estimation of the strength of this reproductive barrier in natural populations has been elusive (see 'Introduction').
Limited gene flow has been detected between O. nubilalis pheromone races using anonymous genetic markers (Harrison and Vawter 1977; Cardè et al. 1978; Cianchi et al. 1980; Glover et al. 1991). Willett and Harrison (1999) concluded from analysis of variation in the pheromone binding protein gene that gene flow occurs between the E- and Z-races in New York. Hybrid female frequencies of 5%, 11%, and 12% were estimated at three locations in North Carolina (Durant et al. 1995), and 0–22% was observed among sites in New York (Roelofs et al. 1985), but estimates were based on GC analysis of a limited number of pheromone glands. Up to this point, estimation of hybrid formation within field populations has remained an impasse for population genetic studies due to difficulties in performing GC analysis upon dissected pheromone glands of wild caught virgin females. The novelty and utility of the current study is that molecular genetic markers developed herein discriminate pgfar-e and pgfar-z alleles within field populations, and for the first time offer a relatively high throughput method for identifying phenotypes for population genetic studies. The markers were applied to detect pgfar-e/pgfar-z heterozygotes, and subsequently to estimate hybridization frequency between E- and Z-race O. nubilalis. Genotyped individuals (n = 331) from light trap samples collected in regions of the United States with sympatric E- and Z-race populations indicated hybridization frequencies ranged from 0 to 41.9%. The assortative mating model assumes that attraction between E- and Z-race O. nubilalis is rare (Roelofs et al. 1987), but our genotype data suggest that intermating of E- and Z-races can occur at relatively high frequencies in natural populations in the Eastern United States. Given that mate attraction among pheromone races is weak at long distances (Dopman et al. 2009), the breakdown in assortative mating in the field may take place at close distances. Adults tend to concentrate in grassy “aggregation sites” during the night for mating (Showers et al. 1974, 1976), which perhaps would promote close-range encounters between E- and Z-race moths if temporal mating periods overlap.
Given the observed moderate to high levels of hybridization, assortative mating may not be the only factor reinforcing the genetic isolation between E- and Z-races. Females with 70, 72, and 73% E11-14:OAc were previously detected in New York, and may be evidence that backcross females are produced in natural populations (Roelofs et al. 1985), but genetic tests for backcross females remain undeveloped pending the identification of modifier loci (Löfstedt et al. 1989; Zhu et al. 1996). Furthermore, the reproductive fate of hybrid males remains obscure. Glover et al. (1991) showed that most heterozygous (F1 hybrid) males derived from reciprocal cross do not respond to pheromone blends produced by either E- or Z- race females. The infrequent hybrids that did respond showed no pheromone blend preference. Thus, F1 hybrid males might be a genetic dead end that are incapable of mating (Lassance 2010), and might impose a partial barrier to the introgression of genes between pheromone races. The development and application of markers for the male Resp locus (Dopman et al. 2005) as well as genes involved in the modification of female pheromone blend ratios among backcrosses in O. nubilalis (Löfstedt et al. 1989; Zhu et al. 1996) will likely be important in understanding direction of gene flow and the reproductive fate of hybrid within natural populations.
This research was a joint contribution from the United States Department of Agriculture – Agricultural Research Service (USDA-ARS; CRIS Project 3625-22000-017-00), and the Iowa Agriculture and Home Economics Experiment Station, Ames, IA (Project 3543). This article reports the results of research only. Mention of a proprietary product does not constitute an endorsement or a recommendation by USDA, Iowa State University or University of Delaware. The authors wish to thank Charlie Linn for providing females from the E-race laboratory, as well as USDA Technicians Bob Gunnarson and Jean Dyer for contributions to genotyping and insect rearing procedures. This study was a contribution to the NC-205 multistate regional research project, Ecology and Management of European Corn Borer and Other Lepidoptera.
B. S. C. designed assays and experimental approach, conducted analysis, interpreted results, and Primary person to write the manuscript. H. J. performed pheromone gland dissections. K. S. K. performed population genetic analyses. R. L. H. provided editorial remarks. C. A. A. managed funding and laboratory facilities. C. M. performed gas chromatograph analysis. T. W. S. provided critical interpretation of research results and write portions of the Discussion.