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Introduction

In the last decade, genetic approaches to answering evolutionary and ecological questions have become less expensive and more easily applied to non-model species (Allendorf, Hohenlohe & Luikart, 2010; Guichoux et al., 2011). Microsatellites, or tandem repeats of two to six nucleotides, are popular molecular markers due to their resolution in distinguishing individual genotypes (Selkoe & Toonen, 2006) and their ability to describe patterns of population connectivity across landscapes (Manel et al., 2003) and seascapes (Galindo, Olson & Palumbi, 2006). Much of the literature focuses on organisms with single free-living diploid stages (i.e., animals and higher plants). Yet, there are many species with both haploid and diploid stages in the same life cycle in which both ploidies undergo somatic development and live as independent, functional organisms.

While theory predicts that selection should favor either diploidy or haploidy (Mable & Otto, 1998), Hughes & Otto (1999) demonstrated the maintenance of both haploid and diploid stages when the two stages occupy different ecological niches. However, there are relatively few empirical tests of these alternative hypotheses (but see Destombe et al., 1992; Thornber & Gaines, 2004; Guillemin et al., 2013), and for isomorphic species in which ploidy is not easily identified through morphological traits, molecular markers will be essential to advance research in this field. These same markers can additionally be used to understand connectivity and demographic history in haploid–diploid populations. Among marine haploid–diploid macroalgae, relatively few microsatellites have been developed to address any of these issues (but see Table 1).

Table 1:
Studies in which both the haploid and diploid stages of seaweeds and mosses were investigated to reveal patterns in genetic structure and mating system.
Phylum Species Marker Type of study
Sosa et al. (1998) Rhodophyta Gelidium arbuscula Isozymes Genetic structure and mating system
Sosa et al. (1998) Rhodophyta Gelidium canariensis Isozymes Genetic structure and mating system
Engel et al. (1999) Rhodophyta Gracilaria gracilis Microsatellites Paternity analyses and dispersal
van der Velde et al. (2001) Bryophyta Polytrichum formosum Microsatellites Paternity analyses and dispersal
van der Strate et al. (2002) Chlorophyta Cladophoropsis membranacea Microsatellites Shorescape structure and mating system
Engel, Destombe & Valero (2004) Rhodophyta Gracilaria gracilis Microsatellites Shorescape structure and mating system
Guillemin et al. (2008a) and Guillemin et al. (2008b) Rhodophyta Gracilaria chilensis Microsatellites Genetic structure, mating system and comparisons between natural and farmed populations
Szövényi, Ricca & Shaw (2009) Bryophyta Sphagnum lescurii Microsatellites Paternity analyses and dispersal
Alström-Rapaport, Leskinen & Pamilo (2010) Chlorophyta Ulva intenstinalis Microsatellites Genetic structure and mating system
Krueger-Hadfield et al. (2011) Rhodophyta Chondrus crispus Microsatellites Genetic structure and mating system
Krueger-Hadfield et al. (2013) Rhodophyta Chondrus crispus Microsatellites Shorescape structure and mating system
Couceiro et al. (2015) Ochrophyta Ecotcarpus crouaniorum Microsatellites Genetic structure and mating system
Couceiro et al. (2015) Ochrophyta Ectocarpus siliculosus Microsatellites Genetic structure and mating system
Krueger-Hadfield et al. (2015) Rhodophyta Chondrus crispus Microsatellites Paternity analyses and dispersal
DOI: 10.7717/peerj.1159/table-1

Understanding the consequences of biphasic life cycles and land- or seascape features on population structure is particularly relevant in light of the increasing frequency of biological introductions. There are numerous examples of widespread, and putatively invasive species, that have free-living haploid and diploid stages, including macroalgae (e.g., Asparagopsis spp.; Andreakis et al., 2007), ferns (e.g., Lygodium spp.; Lott et al., 2003) and mosses (e.g., Campylopus introflexus; Schirmel, Timler & Buchholz, 2010). Macroalgae, or seaweeds, account for approximately 20% of the world’s introduced marine species (Andreakis & Schaffelke, 2012) and a subset of these invasions are by species that are exploited in their native range, either for the phycocolloid industry or as food products (Williams & Smith, 2007).

The red seaweed Gracilaria vermiculophylla (Omhi) Papenfuss is native to the northwest Pacific and, in the last 30–40 years, has spread throughout high to medium salinity estuaries of the eastern North Pacific (Saunders, 2009), the western North Atlantic (Byers et al., 2012) and the eastern North Atlantic (Weinberger et al., 2008; Guillemin et al., 2008a). G. vermiculophylla transforms the ecosystems into which it is introduced through negative impacts on native species (e.g., direct competition, Hammann et al., 2013), the addition of structural complexity to soft-bottom systems (e.g., Nyberg, Thomsen & Wallentinus, 2009; Wright et al., 2014) and the alteration of community structure, species interactions and detrital pathways (e.g., Byers et al., 2012). Previous studies of the population genetics of G. vermiculophylla focused on the mitochondrial gene cytochrome b oxidase I (Kim, Weinberger & Boo, 2010; Gulbransen et al., 2012), but mitochondrial genetics do not necessarily predict the population genetics of the nuclear genome and cannot assess patterns of ploidy and mating system. Thus, we developed nine polymorphic microsatellite loci for G. vermiculophylla.

Table 2:
Characteristics of nine polymorphic microsatellite loci developed for Gracilaria vermiculophylla.
Acc. No., GenBank accession number; locus; motif; primer sequences; allele range; avg. error: TANDEM (Matschiner & Saltzburger, 2009) rounding errors for each microsatellite locus (the authors of TANDEM suggest that good loci have an average rounding error which is below 10% of the repeat size); Ntall, total number of alleles. All loci showed one-locus genetic determinism.
Locus Acc. No. Motif Primer sequence Allele range Avg. Error N tall
Gverm_5276 KT232089 (AC)10 F: GGAGAGCAGCACGTTTTAGG R: CTGCTTAGTTCCACGATCGAC 282–316 0.14 11
Gverm_6311 KT232090 (AG)9 F: GCGTCATTCCACTGAATGTG R: GATGAACCTCAATGCCTCGT 203–223 0.17 6
Gverm_8036 KT232091 (AC)12 F: GCCCTTTTAAGGATGCAACA R: GGGGTAAACGACCACAGAGA 213–251 0.14 5
Gverm_3003 KT232092 (AG)11 F: CATCTTGCTTCCTTGCTTCC R: TTGAAAGCCGGAATTTATCG 198–230 0.11 4
Gverm_1203 KT232093 (AAG)8 F: CTCCTGGTGCACAAGCAATA R: ACATTCTGCGCACCTTTCTT 284–308 0.12 4
Gverm_1803 KT232094 (AC)11 F: GCGTGCACGATGTCTACACT R: GACAGCAACAAGTGGGGTTT 352–356 0.07 3
Gverm_804 KT232095 (AAG)8 F: TGTAGGATTGCTCTCCTGGTG R: CAGGCTGGCCAAAATAACAT 182–188 0.16 3
Gverm_10367 KT232096 (AG)8 F: GCTGAGAAATGAAGCGAAGG R: GCAAACCTGCCTTGTTTGTT 198–200 0.07 2
Gverm_2790 KT232097 (AATGC)5 F: GAACAATGCGGGAAAACATT R: GGAAGAGGCTCAAAAGCAGA 262–267 0.16 2
DOI: 10.7717/peerj.1159/table-2

Materials and Methods

A library of contigs for G. vermiculophylla was generated using the 454 next-generation sequencing platform (Cornell University Life Sciences Core Laboratory Center) from a single individual collected from Charleston, South Carolina, USA. For library preparation, DNA was extracted using CTAB (Eichenberger, Gugerli & Schneller, 2000) and library construction followed Hamilton et al. (1999). Dimeric to hexameric microsatellite repeats were identified with the program MSATCOMMANDER, ver 1.0.8 (Faircloth, 2008) and primers were designed using PRIMER 3 (Rozen & Skalesty, 2000) for contigs with at least four sequences present in the library. Bioinformatics of these sequences was facilitated by the APE package (Paradis, Claude & Strimmer, 2004) in R (R Development Core Team, 2014).

Total genomic DNA was isolated using 120 µL of a 10% Chelex solution (BioRad Laboratories, Hercules, California, USA) in which approximately 1 cm of dried algal tissue was heated at 95 °C for 30 min and vortexed intermittently (Walsh, Metzger & Higuchi, 1991). Loci were amplified on a thermocycler (BioRad) as follows: 10 µL final volume, 2 µL of stock DNA template, 0.5 units of GoTAQ Flexi-DNA Polymerase (Promega, Madison, Wisconsin, USA), 1X buffer, 250 µM of each dNTP, 1.5 nM of MgCl2, 150 nM of fluorescently-labeled forward primer, 100 nM of unlabeled forward primer and 250 nM of unlabeled reverse primer. The PCR program included 2 min at 95 °C, 30 cycles of 30 s at 95 °C, 30 s at 55 °C and 30 s at 72 °C, and a final 5 min at 72 °C. One µL of each PCR product was added to 10 µL of loading buffer containing 0.35 µL of size standard (GeneScan500 Liz; Applied Biosystems, Foster City, California, USA). Samples were electrophoresed on an ABI 3130xL genetic analyzer equipped with 36 cm capillaries (Applied Biosystems). Alleles were scored manually using GENEMAPPER ver. 4 (Applied Biosystems) and allele sizes were binned with TANDEM ver. 1.08 software (Matschiner & Saltzburger, 2009; Krueger-Hadfield et al., 2013).

We screened a total of 42 primer pairs for amplification and polymorphism in G. vermiculophylla (Table 2, Table S1). For the amplifiable loci that also showed polymorphism (nine total, see “Results and Discussion”), we verified single locus genetic determinism (SGLD). Loci were in SLGD if known haploids produced a single allele and diploids produced either one or two alleles in their homozygous or heterozygous state, respectively. We verified SGLD in a subset of known haploid gametophytes (n = 28) and diploid tetrasporophytes (n = 30) collected at Elkhorn Slough, California, USA (Table 3, Fig. S1). Elkhorn Slough was the only population for which ploidy was determined by reproductive structures and for which we had known haploids and diploids for genotyping.

Table 3:
Location of the four populations used to test for polymorphism in newly characterized microsatellite loci in Gracilaria vermiculophylla.
The region, range (native or non-native), latitude, longitude, sampling date, collector* and ploidy determination (using reproductive phenology or microsatellite genotype) are provided.
Population Region Range Latitude Longitude Date Collector Ploidy determination
Akkeshi, Japan NW Pacific Native 43.04774 144.9498 25 Aug 10, 31 Jul 12 NMK, KH, KM, AP, MS Genotype
Elkhorn Slough California, USA NE Pacific Non-native 36.50447 −121.4513 3 Nov 13 SAKH, BFK, TDK, BH Genotype, phenology
Fort Johnson SC, USA NW Atlantic Non-native 32.7513 −79.900 11 Dec 13 CEG Genotype
Nordstrand, Germany North Sea Non-native 54.454571 8.874846 24 Mar 10 MH Genotype
DOI: 10.7717/peerj.1159/table-3

Notes:

Collector abbreviations
NMK

NM Kollars

KH

K Honda

KM

K Momota

AP

A Pansch

MS

M Sato

SAKH

SA Krueger-Hadfield

BFK

BF Krueger

TDK

TD Krueger

BH

B Hughes

CEG

CE Gerstenmaier

MH:

M Hammann

The frequency of null alleles was estimated in the haploid subpopulation from Elkhorn Slough as well as diploid tetrasporophytes for each of the four populations (Table 3). It is possible to calculate the null allele frequency directly in the haploids based on the number of non-amplification events, after discounting technical errors. For diploid tetrasporophytes, we used a maximum likelihood estimator (ML-NullFreq: Kalinowski & Taper, 2006).

Next, we screened loci for short allele dominance (Wattier et al., 1998). The presence of short allele dominance is rarely tested during microsatellite development, even though it can result in artificial heterozygote deficiencies. In contrast to null alleles, primer binding is successful, but the larger allele is not amplified due to the preferential amplification of the smaller allele. Wattier et al. (1998) demonstrated an analytical method to detect short allele dominance using linear models. If a regression of allele-specific Fis (inbreeding coefficient) statistics on allele size reveals a significant negative slope, then short allele dominance may be expected. We determined three to four allele size classes per locus and performed linear regressions using the STATS package in R (R Development Core Team, 2014).

To provide preliminary assessment of the genotypic and genetic diversity one can gain from these loci, we genotyped diploid tetrasporophytes from one native and three non-native populations of G. vermiculophylla (Table 3). Diploids were identified based either on reproductive phenology (Elkhorn) or microsatellite genotype (after assuring SGLD) if at least one locus was heterozygous (Akkeshi, Fort Johnson and Nordstrand, Table 3).

We calculated expected allelic richness using rarefaction in order to account for differences in sample size (HP-Rare; Kalinowski, 2005). Observed (HO) and expected heterozygosities (HE) were calculated using GenAlEx, ver. 6.501 (Peakall & Smouse, 2006; Peakall & Smouse, 2012). Tests for Hardy–Weinberg equilibrium and F-statistics were performed in FSTAT, ver. 2.9.3.2 (Goudet, 1995). Fis was calculated for each locus and over all loci according to Weir & Cockerham (1984) and significance (at the adjusted nominal level of 0.001) was tested by running 1,000 permutations of alleles among individuals within samples. We also tested for linkage disequilibrium in each population using GENEPOP, ver. 4.2.2 (Rousset, 2008), with 1,000 permutations followed by Bonferroni correction for multiple comparisons (Sokal & Rohlf, 1995).

Results and Discussion

Of the 42 loci screened, 16 did not amplify for G. vermiculophylla even after several PCR modifications (Table S1). Of the remaining 26 loci, four loci exhibited multi-peak profiles and were discarded from further use, 13 loci were considered monomorphic (Table S1), and nine loci showed polymorphism (Table 2). The nine polymorphic loci exhibited SLGD in which known haploids always exhibited one allele. The low number of polymorphic loci revealed from this screening process is consistent with previous efforts to develop microsatellite loci for some seaweeds (e.g., Varlea-Álvarez et al., 2011; Arnaud-Haond et al., 2013).

The frequency of null alleles was zero at all loci except Gverm_1803 and Gverm_2790 in which the frequencies were both 0.019 in the haploids at Elkhorn Slough (Table S2). The only evidence of null alleles in the diploids from Elkhorn Slough was at locus Gverm_1803, with a maximum likelihood estimated frequency of 0.115. The discrepancy between the haploid and diploid estimates is likely due to assumptions underlying the maximum likelihood estimators implemented in software like HP-Rare (Kalinowski, 2005), such as random mating. Krueger-Hadfield et al. (2013) demonstrated a strong bias in the estimates of null allele frequency when using these maximum likelihood estimators in macroalgal populations that have undergone non-random mating. The higher frequencies of null alleles (0.115–0.207) in the Akkeshi diploid subpopulation were most likely driven by a violation of these assumptions as well, though empirical estimates in haploid subpopulations are warranted. Nevertheless, the low frequency of null alleles and lack of evidence for short-allele dominance (all regression p-values were >0.2, Table S3), suggest that observed heterozygote deficiencies using these loci will be due to the mating system or spatial substructuring (Guillemin et al., 2008b; Krueger-Hadfield et al., 2011; Krueger-Hadfield et al., 2013).

Previous studies have used microsatellite loci to distinguish among individual clones and to describe the genetic diversity and the mating systems of seaweed populations despite low levels of polymorphism (e.g., Guillemin et al., 2008b; Arnaud-Haond et al., 2013). In the current study, the nine polymorphic markers described genetic variability in four populations sampled across the extant distribution of G. vermiculophylla. Overall, there was little evidence for linkage disequilibrium after Bonferroni correction (Table S4). Additionally, allelic diversity was comparable among the one native and three non-native sites we sampled, but Fis varied considerably (summary in Table 4; per locus statistics in Table S5). Together, these results suggest that unique demographic and evolutionary processes could be operating between native and non-native ranges and within each population, but more detailed sampling is needed to address these patterns.

Table 4:
Genetic features of four populations of Gracilaria vermicuolphylla.
These include: the sample size, N; the diploid genotypic richness, NA, + standard error (SE); mean allelic richness, AE, based on the smallest sample size of 46 alleles (23 diploid individuals) + SE; mean observed heterozygosity, HO, + SE; mean expected heterozygosity, HE, + SE; inbreeding oefficient, Fis, multilocus and per locus estimates.
Statistics Akkeshi Elkhorn slough Fort Johnson Nordstrand
N 31 30 38 23
NA 3.2 ± 0.5 2.2 ± 0.4 2.0 ± 0.2 1.9 ± 0.2
AE 3.1 ± 0.4 2.2 ± 0.3 2.0 ± 0.2 1.9 ± 0.2
HO 0.265 ± 0.060 0.311 ± 0.089 0.520 ± 0.110 0.527 ± 0.125
HE 0.374 ± 0.079 0.317 ± 0.084 0.387 ± 0.077 0.352 ± 0.079
Fis 0.294 * 0.017 −0.350 * −0.512 *
Fis per locus
Gverm_5276 0.484 * 0.120 −0.209 −0.492
Gverm_6311 0.435 * 0.140 −0.267 −0.048
Gverm_8036 0.334 NA −0.445 * −0.217
Gverm_3003 0.529 −0.121 −0.138 −0.553
Gverm_1203 −0.15 −0.206 −0.310 −0.508
Gverm_1803 0.569 * 0.460 −0.696 * NA
Gverm_804 −0.278 −0.206 −0.310 −0.508
Gverm_10367 −0.017 NA NA NA
Gverm_2790 NA NA NA −0.913*
DOI: 10.7717/peerj.1159/table-4

Notes:

p < 0.001, adjusted nominal value.

In summary, we have developed and characterized microsatellite markers for the haploid–diploid red seaweed G. vermiculophylla. These loci have the resolution to distinguish individual thalli and will aid studies on the invasive history of G. vermiculophylla, as well as the evolutionary ecology of rapidly spreading populations and mating system shifts in organisms that have biphasic life cycles with free-living haploid and diploid stages (i.e., macroalgae, ferns, mosses and some fungi).

Supplemental Information

Reproductive phenology of (A) haploid female gametophytes, (B) haploid male gametophytes (50x) and (C) diploid tetrasporophytes (50x)

Gracilaria vermiculophylla exhibits a complex haploid–diploid life cycle, including two free-living stages of different ploidy levels: the haploid dioecious gametophytes and the diploid tetrasporophytes. Fertilization takes place on the female gametophyte, and the female gametes, once fertilized, develop into cystocarps, an additional, though not a free-living, stage. The cystocarp is a macroscopic swelling on the surface of the female thallus, within which the zygote is mitotically copied producing thousands of diploid spores, called carpospores. Spores released from the cystocarps germinate into the diploid tetrasporophytes. (Photo credit: SA Krueger-Hadfield).

DOI: 10.7717/peerj.1159/supp-1

Characteristics of 33 microsatellite loci developed for Gracilaria vermiculophylla that showed monomorphism, non-amplification, or multi-locus genetic determinism

Acc. No., GenBank accession number; locus; motif; primer sequences; Profile: one- or multi-locus genetic determinism, no amp. indicates non-amplification; Ntall total number of alleles.

DOI: 10.7717/peerj.1159/supp-2

Null allele frequencies for the microsatellite loci developed for Gracilaria vermiculophylla

Frequencies were directly estimated in the haploid subpopulations, whereas frequencies in each of the diploid subpopulations at Akkeshi, Elkhorn Slough, Fort Johnson and Nordstrand were calculated using maximum likelihood and the software MLNullFreq (Kalinowski & Taper, 2006).

DOI: 10.7717/peerj.1159/supp-3

Short allele dominance analysis for microsatellite loci developed for Gracilaria vermiculophylla

This includes number of pooled size classes used in regression analysis (following Wattier et al., 1998), No. of classes, and linear regression statistics. Loci Gverm_10367 and Gverm_2790 only exhibited two alleles in our sampled populations and consequently, short allele dominance analysis was not applicable (NA).

DOI: 10.7717/peerj.1159/supp-4

Linkage disequilibrium analysis for microsatellite loci developed for Gracilaria vermiculophylla

Darkened cells indicate pairs of loci that show significant linkage disequilibrium after Bonferroni correction (p-value threshold < 0.006 at α = 0.05).

DOI: 10.7717/peerj.1159/supp-5

Genetic features per locus of four populations of Gracilaria vermiculophylla

This includes: number of alleles at each locus, NA, + standard error (SE); mean allelic richness, AE, based on the smallest global sample size of 46 alleles (23 diploid individuals) + SE; mean observed heterozygosity, HO, + SE; mean expected heterozygosity, HE, + SE.

DOI: 10.7717/peerj.1159/supp-6

Development and characterization of microsatellite loci for the haploid–diploid red seaweed Gracilaria vermiculophylla

DOI: 10.7717/peerj.1159/supp-7