Avoiding complementarity between primers when designing a PCR assay constitutes a central rule strongly anchored in the mind of the molecular scientist. 3’-complementarity will extend the primers during PCR elongation using one another as template, consequently disabling further possible involvement in traditional target amplification. However, a 5’-complementarity will leave the primers unchanged during PCR cycles, albeit sequestered to one another, therefore also suppressing target amplification. We show that 5’-complementarity between primers may be exploited in a new PCR method called COMplementary-Primer-Asymmetric (COMPAS)-PCR, using asymmetric primer concentrations to achieve target PCR amplification. Moreover, such a design may paradoxically reduce spurious non-target amplification by actively sequestering the limiting primer. The general principles were demonstrated using 5S rDNA direct repeats as target sequences to design a species-specific assay for identifying Salmo salar and Salmo trutta using almost fully complementary primers overlapping the same target sequence. Specificity was enhanced by using 3’-penultimate point mutations and the assay was further developed to enable identification of S. salar x S. trutta hybrids by High Resolution Melt analysis in a 35 min one-tube assay. This small paradigm shift, using highly complementary primers for PCR, should help develop robust assays that previously would not be considered.
Citation: Anglès d’Auriac MB (2016) COMplementary Primer ASymmetric PCR (COMPAS-PCR) Applied to the Identification of Salmo salar, Salmo trutta and Their Hybrids. PLoS ONE 11(10): e0165468. https://doi.org/10.1371/journal.pone.0165468
Editor: Ulrich Melcher, Oklahoma State University, UNITED STATES
Received: June 20, 2016; Accepted: October 12, 2016; Published: October 26, 2016
Copyright: © 2016 Marc B. Anglès d’Auriac. 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: All relevant data are within the paper and its Supporting Information files.
Funding: This work was funded by the Norwegian Institute for Water Research. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: I have read the journal's policy and the author of this manuscript has the following competing interest: part of this work is used in patent application WO 2014/168484 A1 entitled “COMPAS-PCR method and methods for detecting, identifying or monitoring salmonid species”. My employer, the Norwegian Institute for Water Research, is the sole applicant for this patent. This does not alter my adherence to PLOS ONE policies on sharing data and materials.
Since the Polymerase Chain Reaction (PCR) was invented in the mid-80s , Nucleic Acid amplification techniques have had an unprecedented development for molecular biology applications. A contributing factor to this success is its flexibility with the development of several modifications which expands the technical capabilities of PCR. For example, several methods have been developed for the detection of point mutations such as the Amplification Refractory Mutation System (ARMS)  and variants such as the PCR Amplification of Specific Alleles (PASA) [3, 4], bidirectional-PASA  or Mismatch Amplification Mutation Assay (MAMA) , Taq-MAMA  and Melt-MAMA . Detection of point mutations, also called Single Nucleotide Polymorphism (SNP) and Single Nucleotide Variants (SNV), may be relevant in various contexts spanning from medical applications for infectious disease, genetic and cancer diagnostics to population genetics and species identification. However, limitations inherent to DNA chemistry may reduce PCR specificity or sensitivity. For instance, non-target amplification and in particular primer complementarity leading to Primer Dimer (PD) formation is a well-known limiting factor for the design of PCR assays. PD formation may considerably reduce PCR reaction efficiency and is carefully avoided when designing an assay i.e. by using ad hoc software packages . A 3’ complementarity between primers may be detrimental during PCR as annealing between the primers will elicit DNA extension by the DNA polymerase, producing a non-target amplicon itself being a perfect match for further non-target amplification competing with target amplification. Moreover, it has emerged that PD formation appears to be incompletely understood . For instance dimer products may have lack of complementarity with the primers or show mismatches in the 3’ portion of the primers . Improvements to avoid non-target amplification include the development of hot-start PCR, adding nucleotide tags in 5’ of both primers for Tag-driven PCR , heat-activatable primers  and cooperative primers .
In this study we show it is possible to use highly complementary primers in 5’ and avoid PD formation and develop efficient amplification assays by using a new asymmetric PCR method, COMplementary Primer ASymmetric PCR (COMPAS-PCR), using different forward and reverse primer concentrations. This counterintuitive approach will sequester, hence also protect, the limiting primer PL, while the excess primer PX initiates linear amplification in presence of the target sequence. The reaction shifts towards exponential amplification when sufficient complementary amplicon strands are produced to serve as template material for PL. The PCR annealing temperature Ta is adjusted according to the lowest primer melt temperature Tm from PX, and the addition of short 3’ overhangs on the complementary primer improves the amplification efficiency. Asymmetric PCR, for which primer concentrations in a simplex reaction are unequal, is not a new concept and has been used for enrichment of one strand of the PCR amplicon with the purpose of improving probe detection. In particular, Linear-After-The-Exponential (LATE)-PCR improves such assay by compensating the decrease of melt temperature incurred to decreased concentrations of the limiting primer by extending it by a few nucleotides , further reaching optimum results when TmL–TmX ≥ 5°C . Opposite to LATE-PCR, COMPAS-PCR, by design, will begin by linear amplification before shifting to exponential amplification depending on sample target DNA concentration and PX strand amplicon accumulation.
This COMPAS method was used to develop a 35 min three-primer duplex PCR for simultaneous identification of S. salar, S. trutta and hybrids using High Resolution Melt (HRM) analysis by targeting 5S rDNA, a multigene family organized in tandem direct repeat units . Highly complementary primers were designed to have the same DNA target, and yet, structurally define an amplicon product due to the direct repeat structure of the target DNA (Fig 1 and Table 1). Specificity of the assay was enhanced by using 3’-penultimate point mutations in the reverse primers. Efficiency and specificity evaluation of variable elements such as degree of primer complementarity and concentration, Ta, and melt temperatures for PL and PX are presented and discussed.
Non Transcribed Sequence lengths are indicated according to sequence access numbers S73107 and LN835408-LN835422, varying from 137 and 138 bp for S. salar to 160 bp for S. trutta.
Materials and Methods
This study involved no endangered or protected species. Fish sampling was conducted according to the Norwegian Animal Research Authority (NARA) instructions and authorized by NARA approval ID 09/1723. Fish were sacrificed by a sharp blow to the head immediately after collection and all efforts were made to minimize suffering or distress. Salmonid sample information is shown in Table 2. The S. salar and S. trutta individuals used in this study for sequencing the 5S rDNA gene originated from 2 different areas in southern Norway: the Driva and the Lærdalselva river basins. Fins from fish individuals were clipped and preserved in 95% ethanol. DNA extraction was performed using Mole tissue kit on the Mole instrument (Mole Genetics, Lysaker, Norway; discontinued). Briefly, fin material was rinsed with distilled water and approximately 20 mg for each individual was transferred to a tube containing 100 μl Mole lysis buffer and 2 μl proteinase K from a 20 mg ml-1 stock solution (Merck, EC 188.8.131.52; www.merck.com). The samples were incubated at 65°C for 1 h and further processed using the Mole instrument according to the manufacturer’s instructions. The DNA concentration was measured using a NanoDrop ND-1000 spectrophotometer (www.nanodrop.com) and all samples were diluted to 2 ng μl−1 prior to performing qPCR.
All primers designed for this study are shown in Table 1 and primer names include length, overhang position into the NTS as well as presence, if any, of penultimate destabilizing point mutations, degenerate nucleotide positions and S. trutta specific mutations.
Results shown in Fig 2 were produced with an ABI 7500 qPCR machine (Life Technologies, Applied Biosystems) using Mesa Blue master mix (Eurogentec). The final PCR reaction volume of 25 μl contained 12.5 μl mastermix, 0.6 μM of either 5SNTS-23R+2 or 5SNTS-23R+3 reverse primer and 5SNTS-23F forward primer at concentrations varying from 0.6 to 0.05 μM, 2.5 μl sample (5 ng DNA), completed with sterile deionized water. Cycling conditions were as follows: 5 min denaturing step at 95°C, followed by 40 cycles at 95°C for 20 s, 62°C for 30 s and 72°C for 60 s.
Asymmetric concentration effect for 5S rDNA qPCR highly complementary primers tested on S. salar L235 and S. trutta T107. Concentration of the forward primer 5SNTS-23F in A and B ranges from 0.6 to 0.05 μM while a constant concentration of 0.6 μM was used for the reverse primer 5SNTS-22R+2 in A and 5SNTS-23R+3 in B.
For sequencing, PCR amplifications were carried out with a CFX96 BioRad thermocycler (Bio-Rad, Hercules, CA, USA) under the following conditions: a denaturing step for 30 s with iProof (BioRad) at 98°C, followed by 40 cycles of 98°C for 10 s, 65°C for 10 s and 72°C for 15 s.
Cycle sequencing was performed in both directions using amplification primers and BigDye Terminator v3.1 kit (Life Technologies, Applied Biosystems). PCR template was diluted 10 fold in ddH2O and 1 μl was used with 0.5 μl Terminator mix, 0.32 μl 10 μM forward or reverse primer, 1.75 μl Terminator 5X buffer in a final volume of 10 μl. Cycle sequencing was performed using an ABI 7500 qPCR machine as following: 96°C for 1 min followed by 28 cycles of 96°C for 10 s, 50°C for 5 s and 60°C for 4 min. Sequence purification was performed using BigDye XTerminator Purification kit (Life Technologies, Applied Biosystems) adding 10 μl XTermination solution and 45 μl Sam solution to each PCR sample well, final volume of 65 μl. The PCR plate was then sealed and vortexed for 30 min prior to being processed by an ABI3730XL DNA analyzer (Life Technologies, Applied Biosystems). Trace files analyses were performed using CodonCode Aligner v5.1.5 (CodonCode Corporation), sequence alignments were performed using MultAlin  and edited for presentation using GeneDoc v2.7 software. The two three primer duplex COMPAS-PCR for HRM identification of S. salar, S. trutta and hybrids were carried out under the following conditions: a denaturing step for 2 min (SsoFast EvaGreen) at 98°C, followed by 30 cycles of 98°C for 1 s and 70°C for 1 s. Primers 5SNTS-23F-W1 100 nM and 5SNTS-23R+3-mamT 300 nM were combined with either 5SNTS-23R+3-mamG-m2 500 nM or 5SNTS-21R+57 2000 nM. Melt curve analysis was performed from 69°C to 92°C using 0.5°C increments and HRM analysis was performed using Precision Melt analysis software (Bio-Rad) by setting the difference curve analysis between 78 and 82°C. Oligo7 v7.60  was used for calculating Tm and predicting dimer and hairpin formation for primers. PCR products were electrophoresed on a 1.4% agarose gel (Agarose I biotechnology grade, VWR) in 2 x TAE buffer (VWR), with a 100 bp ladder (NEB) and visualized with GelRed (Biotium; www.biosciences.co.uk) staining.
Results and Discussion
Choice of target DNA for designing PCR assays will depend on the purpose of the application. Taxonomic group identification or genetic diseases diagnostic will often have distinct requirements, in particular to achieve specificity and required sensitivity. High copy number target genes are useful as they help improve sensitivity of the assay although they may lack sufficient sequence variability to insure specificity. This shortcoming may be mitigated when a non-coding sequence is associated in the immediate proximity of the targeted conserved transcripted target DNA gene. This is the case with rDNA genes present in multiple copy number which display conserved sequences homogenized though concerted evolution . As expected, the degree of sequence variability is highest for the non-coding sections such as the non-transcribed spacer (NTS) of 5S rDNA . Hence, several methods have been developed targeting 5S rDNA for molecular diagnostic of parasites [21, 22], squids , and fish [24–31]. The genetic organization of direct repeat multi-copy gene families gives the theoretical possibility of designing a pair of primers targeting the same locus and yet amplifying a distinct product as shown in Fig 1. However, such a design would transgress the conventional practice of avoiding primer complementarity when developing PCR assays [32, 33]. In this study we show that COMPAS-PCR enables such a design to be successfully used for the development of efficient PCR assays primarily by using asymmetric primer concentrations. The choice of short length repeat unit targets, such as the 5S rDNA genes, further enables the amplification of short amplicons e.g. around 200bp, which are better suited when analyzing possibly degraded samples .
DNA based diagnosis for salmonids, and in particular identification of the closely related S. salar and S. trutta species, has previously been performed by 5S rDNA “universal” PCR targeting the conserved 120bp Coding DNA Section (CDS). The corresponding amplification products comprise the length variable NTS, used in the method for species identification by gel analysis , as well as for S. salar x S. trutta hybrid identification . Simplex PCR species specific amplification was later developed by targeting the NTS section of the 5S rRNA gene, albeit still requiring gel analysis . Other methods have been developed for salmonid identification such as PCR-RFLP applied to the p53 and mitochondrial tRNAGlu/cytochrome b genes [35, 36] or COI gene very short amplicon simplex PCR  and COI multiplex probe qPCR . However, most of these methods require time consuming post PCR product analysis and none of them include S. trutta identification. Hence, COMPAS-PCR principles were initially developed to provide a user-friendly rapid single tube qPCR assay for unambiguous identification of S. salar, S. trutta and hybrids without the need to run post amplification analysis. The primers were designed at the start of the 120 bp CDS of the 5S rDNA with a short part extending over the non-transcribed sequence (NTS) section. This design over the CDS/NTS intersection aimed at strengthening the robustness of the assay by increasing primer stability over the conserved CDS section, to avoid false negatives, and seek for specificity over the NTS section. The forward primer starts at position 1 of the CDS extending into the CDS, and the reverse primers initiate in the start region of the CDS extending into the NTS section with up to 3 nucleotides overhang in 3’. The organization of the target in tandem direct repeats insures that at least 1 unit of each section may be amplified. Hence, depending on how many direct repeats are present, several products consisting of 2 or more sections may also be amplified as previously reported using standard PCR . The COMPAS-PCR primers purposely overlap the same target section and are highly complementary to each other (Fig 1). This primers’ self-complementarity is expected to compete with target priming, hence strongly inhibit target amplification, the reason for which this configuration is avoided when designing PCR assays [32, 33].
In order to favor priming to target DNA, primers’ self-priming was unlocked by using asymmetric primer concentrations by decreasing either the forward or the reverse primer concentration until optimal PCR amplification was reached. As shown in Fig 2A, a strong and equal amplification was progressively generated for both S. salar and S. trutta as the forward primer concentration was decreased. Asymmetric PCR has been previously described for enhancing probe based detection during which the PCR shifts from exponential to linear amplification to favor probe hybridization to its target single stranded sequence using LATE-PCR [14, 39]. With COMPAS-PCR the primers are highly complementary and the asymmetric PCR has an opposite pattern shifting from linear to exponential amplification, effectively alleviating the target amplification inhibition otherwise observed with complementary primers. During the first amplification cycles the concentration-limited primer PL will be mainly sequestered by the excess primer PX such that mostly PX initiated linear amplification will take place. As linear products complementary to PL accumulate while sequestering PX complementary primer concentration decreases, PL target priming and subsequent amplification will be favored.
Forward and reverse primers in Fig 2 have an overlapping complementary perfect match of 20 nucleotides. Primers were designed based on S73107 sequence information. Testing of reverse primer overhang extension into the NTS section showed that position +3 gave a sharp differentiation between S. salar and S. trutta (Fig 2B). The reverse primer in Fig 2B has an additional nucleotide in 3’ compared with the reverse primer used in Fig 2A. Sequencing showed the presence of a point mutation at the corresponding 3’ reverse primer terminal position differentiating S. salar from S. trutta in Fig 2B. Amplification products were sequenced in order to identify species specific variations and use them for further developing a one-tube assay for simultaneous identification of S. salar, S. trutta and hybrids as detailed in the next sections.
Primer dimer formation is typically described as resulting from the association in 3’ of 2 primers during a PCR reaction, followed with DNA extension resulting in the production of a non-target amplicon shorter than the sum of the length of the two primers. Sequencing of such primer dimers have shown that primer mismatches in 3’ may be present and that unknown short nucleotide sequences may also be present in its center [10, 11] showing a more complex situation than first thought. A possible explanation for incorporation of non-primer sequences in primer dimers may be the involvement of genomic DNA in the non-target annealing of the primers close to each other . COMPAS-PCR will effectively reduce the development of “genomic” primer dimers as the limiting primer is sequestered by the excess primer dimer during the linear phase. After target sequence has accumulated and excess primer concentration has decreased sufficiently, the limiting primer will be released resulting in exponential target amplification. When applied to tandem direct repeat targets such as the 5S rDNA used in this study, primer complementarity and extension in 3’ would theoretically not hinder complementarity to the target as the extended primers would still find a perfect match on the target sequence. However, the resulting 100% self-primer match produces a less efficient amplification (Fig 3A and 3B).
Effect of length variations in the reverse excess primer (PX) with a 23 bp complementary forward limiting primer (PL) using 5 ng genomic S. salar DNA and SsoFast Evagreen mastermix. PL = 5NTS-23F at a concentration of 50 (A & C) or 200 nM (B & D) and PX at 600 nM (A, B, C & D). In each experiment PX 3’ end is unchanged, either with no overhang (A & B) or with a 3 nucleotide overhang (C & D) after the forward PL 5’ complementary end. PX length is incremented in 5’ from 18 nucleotides until it reaches the 3’ end of PL at 23 nucleotides resulting in a 100% complementarity between PX and PL (A & B), or 26 nucleotides (C & D). A gradient PCR was run varying the annealing temperature (Ta) from 62 to 72°C. The PX nucleotide length increase is shown on the lower horizontal axis. The difference between melt temperature of the limiting primer (TmL) and melt temperature of the excess primer (TmX) is reported on the left-hand vertical axis as TmL—TmX and plotted as triangles. For each PX, the corresponding optimal Ta is reported on the upper horizontal axis. The resulting Cycle Threshold CT is reported on the right-hand vertical axis and plotted as circles.
Effect of Primer Length and Complementarity Positioning
Primer length and degree of complementarity was tested by using the forward 23 bp PL 5NTS-23F paired with a complementary reverse PX varying in length from 18 bp up to 26 bp. Two groups of reverse PX were tested forming either a 3 nucleotide overhang or a blunt end in 3’ when paired with the forward PL. The length of the reverse PX was increased in 5’ from 18 bp length to reach either 26 bp with the 3 nucleotide 3’ overhang group or 23 bp for the 3’ blunt end therefore forming 100% complementarity when paired to the forward PL. Two concentrations, 50 and 200 nM, were tested for PL whereas PX always had a concentration of 600 nM. Melting temperatures for both PL and PX were calculated taking into account primer length, composition and concentration, and displayed as TmL–TmX in Fig 3. Finally, a gradient qPCR was performed, amplification specificity was checked by melt curve analysis and the resulting optimal annealing temperatures as well as cycle threshold values were reported in Fig 3 and plotted together with TmL–TmX and PX length. As expected, the melt temperature difference between PL and PX decreases as PX length increases and becomes negative before PX length matches PL length at 23bp (as expected since PX has a higher concentration than PL). Best CT values are obtained with the highest TmL–TmX values, up to + 6.9°C difference (Fig 3B), and remain similar when PX is increased by up to two nucleotides. This best CT value corresponds to the smallest tested PX at 18bp. In general, CT values increased moderately and regularly as PX length increased, showing reduced PCR efficiency, except for reverse PX primer 5SNTS-21R+3 (Fig 3C and 3D) characterized by a CT value increased by approximately 5 cycles. This exception was consistently observed whether using a concentration of 50 or 200 nM for the forward PL primer. As both reverse primers with either one less nucleotide or one more, 20 and 22 nucleotides in length respectively, fitted the general trend, the reduced efficiency for the 21 nucleotide reverse primer must be associated to its 5’ end nucleotide. Oligo7 showed that no hairpin structure was present and that dimer formations were similar to those found for 5SNTS-20R+3 and 5SNTS-22R+3. Terminal dangling ends in 5’ , with 5SNTS-21R+3 either associated to the forward primer or to the target DNA, could possibly partly explain this increased CT value. However, primer 5SNTS-18R which has the same 5’ terminal end, showed no reduced efficiency, indicating that the 3’ overhang present with 5SNTS-21R+3 seems also involved when associated to the 5’ specific terminal position for reducing the efficiency of the PCR.
As expected, optimal annealing temperature is found to generally increase as the tested PX is extended. Moreover, and in particular for PX without any overhang, robustness of the assay, as defined by the range of suitable Ta for the assay, decreases as PX increases in size (data not shown). When an overhang is present, limits of the assay seem to have been reached at 26 bp when PL concentration is 50 nM (Fig 3C).
Testing the 100% complementary primer pair 5NTS-23F / 5NTS-23R required using asymmetric primer concentrations to produce target results whereas the presence of a short overhang of one to three nucleotides on at least one side enabled target amplification without requiring asymmetric concentrations when using SsoFast EvaGreen kit. However, important variations were observed when comparing PCR mastermix kits and assays using 100% complementary primers had low sensitivity. PCR efficiency was evaluated by establishing standard curves using tenfold serial dilutions of S. salar genomic DNA in duplicates. A dynamic range over 5 logs was obtained starting from 5ng template DNA producing a PCR efficiency and correlation values of 97.0%– 101.8% and 0.993 respectively with primers 5NTS-23F at 50 or 200 nM and 5NTS-18R+3 at 600 nM.
The S. salar and S. trutta 5S rDNA sequences from this study, accession numbers LN835408 to LN835422 shown in Table 2, are available at the European Nucleotide Archive. The primers used for COMPAS-PCR were initially designed based on the published S. salar 5S rDNA sequence S73107 . The primers 5SNTS-23F and 5SNTS-22R+2 were used for amplifying 5S rDNA from S. salar and S. trutta by COMPAS-PCR using asymmetric concentrations (Fig 2), and for sequencing. The primary objective of sequencing the produced amplicons was to identify the 3’ terminal SNP deduced from the S. salar specificity shown by 5SNTS-23R+3 compared with 5SNTS-22R+2 (Fig 2). All 8 S. trutta produced identical sequences confirming the presence of nucleotide A instead of C in position 279 (Fig 4) and showed an insertion of 23 bp in the NTS at position 204. Additionally, the S. trutta samples showed the presence of an ambiguity in position 2 of the 120 bp coding DNA sequence (CDS). Both nucleotides, C, also present in S73107, and T were found in this position. This ambiguity was consistently observed in this position for both repeated CDS parts present in the amplicon. New forward and reverse sequencing primers, respectively 5SNTS-23F-m1 and 5SNTS-23R+3-m2, using T instead of C for CDS position 2 unambiguously showed the presence of a T for all 8 sequenced S. trutta. Moreover, 4 additional SNPs were observed in all S. trutta sequences compared with the S. salar sequences (Fig 4 and Figs A-H in S1 File).
Coding DNA sequence is indicated by the dotted boxing. Non-sequenced positions are shown (N) and gaps (-) are inserted for alignment purposes. Product length is indicated at the end of each sequence while sequence numbering along the sequences is performed according to the alignment. 1, Salmo salar S73107; 2, Salmo salar LN835408 to LN835414, all 7 sequences are identical; 3, Salmo trutta LN835408 to LN835414, all 8 sequences are identical. Positioning of the primers is shown on the figure and have the following specificity: “universal” forward primer 5SNTS-23F-W1 + “universal” reverse primer 5SNTS-22R+2-W1 for amplifying both S. salar, S. trutta and S. salar X S. trutta hybrids; forward primer 5SNTS-23F-W1 & Reverse primer 5SNTS-23R+3-mamT for amplifying S. salar, and S. salar X S. trutta hybrids; “universal” forward primer 5SNTS-23F-W1 & Reverse primer 5SNTS-23R+3-mamG-m2 for amplifying S. trutta, and S. salar X S. trutta hybrids; “universal” forward primer 5SNTS-23F-W1 & Reverse primer 5SNTS-21R+57 for amplifying specifically S. trutta, and S. salar X S. trutta hybrids.
All 7 S. salar individuals produced identical sequences which showed 4 discrepancies compared with S73107 (Fig 4 and Figs A-H in S1 File) including an insertion in the NTS (position 234 in Fig 4) as well as an intra-individual variation at position 174 in the NTS (Fig 4 and Figs E and F in S1 File). Nucleotides T and G were identified at position 174, corresponding to the nucleotides reported in S. salar S73107 and S. trutta (this study) respectively. Direct sequencing from PCR products used in the present study takes advantage of the electropherograms quantitative properties which show the presence of different nucleotides at a given position when analyzing PCR products from multi-copy target DNA. In particular this has been exploited in the field of epigenetics with the development of direct bisulfite PCR sequencing [42, 43]. Direct PCR product sequencing can also be used to uncover heteroplasmy, an intra-individual multi-copy gene variation found for example in plastids such as mitochondria, for which heteroplasmy may have been under-reported . Although not reported in S73107 5S rDNA sequence, intra-individual variation may have gone unnoticed as only 2 clones were sequenced for determining this sequence . This intra-individual variation was identified in all 7 S. salar individuals originating from 2 different Norwegian river basins and therefore shows stability within the species in this geographic area. Analyses of individuals from new localities would be necessary to evaluate the extent of the presence of this intra-individual variation across the species.
One-Tube S. salar and S. trutta Specific Assay
The additional sequence information showing differences between the 2 species was exploited for designing and testing additional species specific primers for developing a single tube COMPAS-qPCR identification assay for S. salar, S. trutta and their hybrids (Table 1).
In particular the 23 bp S. trutta specific insert in position 204–226 and the SNP in position 279 (Fig 4) were exploited for developing two separate S. trutta specific assays. A single common forward primer was used for both species using the first 23 bp of the CDS. To take into account the SNP identified in position 2 (and 283 in the following CDS), both A & G nucleotide found in this position were included in the degenerate “universal” primer 5SNTS-23F-W1. However, a mismatch would have had little effect since the SNP is positioned at the 5’ end of the forward primer. Conversely, the same SNP is positioned at the 3’ end of the reverse COMPAS primers where a mismatch will have a higher impact with increased miss priming effect. This SNP was used together with SNP position 279 placed at the 3’ terminal end of reverse primer 5SNTS-23R+3-m2 for increased S. trutta specificity. Assay specificity robustness may further be improved by strategies using penultimate mutations to strengthen the effect of a primer 3’ terminal specific mutation [2, 6] and was used for enhancing this assay. All three mutation possibilities were tested for both species showing T best for S. salar specific assay implemented in 5SNTS-23R+3-mamT reverse primer and G best for S. trutta specific assay implemented in 5SNTS-23R+3-mamG-m2 reverse primer (Table 1 and Fig 5). Finally, a second S. trutta specific assay was developed based on the specific 23 bp insert using primer 5SNTS-21R+57 amplifying a 225 bp product when used with 5SNTS-23F-W1. Discrimination between S. salar and S. trutta was achieved with all 3 assays while hybrids were also detected as expected in all 3 assays, each assay producing a size specific amplicon (Fig A in S2 File).
Reverse complement of the primers are shown in the alignment, the 5S rDNA coding sequence is indicated by the dotted box. 1, Salmo salar S73107; 2, Salmo salar LN835408 to LN835414, all 7 sequences are identical; 3, Salmo trutta LN835408 to LN835414, all 8 sequences are identical; 4, Reverse primer 5SNTS-22R+2-W1 for amplifying both S. salar, S. trutta and S. salar X S. trutta hybrids; 5, Reverse primer 5SNTS-23R+3-mamT for amplifying specifically S. salar, and S. salar X S. trutta hybrids; 6, Reverse primer 5SNTS-23R+3-mamG-m2 for amplifying specifically S. trutta, and S. salar X S. trutta hybrids.
The species specific reverse primers of the simplex assays were combined with the same forward primer in order to develop a one-tube assay for discrimination of both S. salar, S. trutta and hybrids. The “universal” forward primer was associated with the penultimate mutation specific S. salar reverse primer and the penultimate mutation specific S. trutta reverse primer in a three primer duplex COMPAS-PCR assay. Finally, a second three primer duplex assay was developed by replacing the penultimate mutation specific S. trutta reverse primer with the S. trutta insert specific primer. The same assay stringency conditions used for the COMPAS-PCR salmo simplex using a 2-step PCR, 1 s annealing and 1 s amplification, was successfully applied to the duplex assays achieving amplification and melt analysis within 35 min. Both assays showed species specific products as well as the presence of both products for hybrid individuals when run on a gel (Fig B in S2 File).
In order to avoid the necessity to run a gel, a High Resolution Melt Analysis was successfully implemented for discrimination of the 3 groups (Fig 6). The specificity and sensitivity of these two assays will depend on the conservation of the DNA variations used to characterize and identify each species. The fish individuals used in this study for sequencing the 5S rDNA gene originated from 2 different river basins in southern Norway. Hence, additional testing is required to assess the validity and efficiency of these assays for target individuals originating from other geographic areas. Non-target amplification, other than differentiating between the three targets, was assessed by testing two Oncorhynchus tshawytscha individuals (Table 2), a salmonid species belonging to the sub-family Salmoninae along with S. salar and S. trutta. DNA quality of the O. tshawytscha individuals had been previously successfully tested  and gave negative results when used with the S. salar and S. trutta specific assays (Fig B in S2 File). However, additional testing with other species would be required to validate these assays.
Primers 5SNTS-23F-W1 100 nM and 5SNTS-23R+3-mamT 300 nM were combined with either 5SNTS-23R+3-mamG-m2 500 nM (A) or 5SNTS-21R+57 2000 nM (B). Color code: In both (A) and (B) the lower blue cluster shows all analyzed S. salar with a 278bp PCR product. The top green cluster shows all analyzed S. trutta, with a specific PCR product in A and B, respectively 300bp and 225bp. The central red cluster shows all analyzed hybrids with mixed PCR products, 278bp + 300bp in A and 278bp + 225bp in B. The hybrid cluster has been chosen as the reference cluster in both (A) and (B).
The COMPAS-PCR method was demonstrated for, but is not restricted to the identification of fish species. Using almost fully complementary primers targeting the same sequence may apply to any tandem direct repeats DNA motifs of interest as target sequences. Ribosomal genes and in particular the 5S r-DNA tandem direct repeats are found in all eukaryotic cells [46, 47] and are therefore suitable for developing specific complementary-primer assays for other taxon and species than salmonids. DNA repeat sequences are common in Eukaryote genomes and reported composing more than 50% of the human genome . Hence, the general COMPAS-PCR principles will help develop new DNA amplification strategies taking advantage of these repeated DNA structures.
S1 File. Sequencing electropherograms showing sequence variations, both single nucleotide polymorphisms (SNPs) and indels, between S. salar and S. trutta.
4 individuals are shown for each species: S4829, S4826, L235 and L237 for S. salar and T4809, T4815, T107 and T124 for S. trutta. Primers 5SNTS-23F and 5SNTS-23R+3 are used for S. salar and primers 5SNTS-23F-m1 and 5SNTS-23R+3-m2 are used for S. trutta. Coding DNA sequence is indicated by the dotted boxing.
Both H. A. Urke and K. O’Malley are acknowledged and thanked for kindly providing the Salmo salar + Salmo trutta samples and the Oncorhynchus tshawytscha samples respectively.
- Conceptualization: MAD.
- Data curation: MAD.
- Formal analysis: MAD.
- Funding acquisition: MAD.
- Investigation: MAD.
- Methodology: MAD.
- Project administration: MAD.
- Supervision: MAD.
- Validation: MAD.
- Visualization: MAD.
- Writing – original draft: MAD.
- Writing – review & editing: MAD.
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