- Research article
- Open Access
Influence of the length of target DNA overhang proximal to the array surface on discrimination of single-base mismatches on a 25-mer oligonucleotide array
© Tomlinson et al.; licensee BioMed Central Ltd. 2014
- Received: 13 July 2013
- Accepted: 9 April 2014
- Published: 17 April 2014
The performance of probes on an oligonucleotide microarray can be characterised in terms of hybridisation signal strength and the ability to discriminate sequence mismatches between the probe and the hybridising target strand, such as those resulting from SNPs. Various properties of the probe affect mismatch discrimination, such as probe length and the position of mismatched bases, and the effects of these factors have been well characterised in a variety of array formats.
A low-density microarray was developed to systematically investigate the effect of a probe’s position within hybridised target PCR products on the tolerance and discrimination of single-nucleotide mismatches between the probe and target. In line with previous reports, hybridisation signals were attenuated by different degrees depending on the identity of the mismatch, the position of the mismatch within the probe, and the length of the PCR product. However, the same mismatch caused different degrees of attenuation depending on the position of the probe within the hybridising product, such that improved mismatch discrimination was observed for PCR products where a greater proportion of the total length was proximal to the array surface.
These results suggest that the degree of mismatch discrimination can be influenced by the choice of PCR primers, providing a means by which array performance could be fine-tuned in addition to manipulation of the properties of the probes themselves.
- Oligonucleotide microarray
- Mismatch discrimination
High-density microarrays in a conventional glass slide format with fluorescence detection, such as those used for gene expression studies, pose a relatively high operational burden due to time-consuming protocols and the cost of the equipment required for high-resolution fluorescence detection. In the context of pathogen detection, however, the requirement is more likely to be for a method which allows large numbers of samples to be tested efficiently at one time. Low-density microarrays, such as those using the ArrayTube (AT) platform [1–3] allow the detection of a smaller number of targets (typically < 100) with improved simplicity of handling and low-cost scanning instrumentation.
A typical low-density array protocol involves subjecting sample DNA to multiplex PCR with labelled nucleotides or primers, followed by application of the labelled products to the array and identification of the probes to which the products have hybridised. A frequently used approach is to select conserved target genes, enabling amplification using broad-range PCR primers followed by discrimination of different products by hybridisation to specific probes . Conversely, in order to reliably detect sequence variants (for example, different viral strains or novel viruses) it can be necessary to tolerate sequence differences both in the PCR primers and the probes on the array . In order to detect diverse targets (for example, bacterial and viral pathogens) on a single array, it may therefore be necessary to maximise mismatch discrimination for some targets while tolerating mismatches for others.
The performance of probes on an array is affected by factors including probe length [6, 7], number and distribution of mismatches between the probe and target [8–10], orientation of attachment to the array surface and presence or absence of spacers [11, 12]. The effects of mismatched bases on probe-target hybridisation have been studied in great detail, using microarrays in a variety of formats [10, 13]. Greater specificity is achieved by using shorter probes , but longer probes are associated with higher hybridisation signals . Furthermore, mismatches located at the centre of the probe have a greater effect on hybridisation signals than mismatches close to the ends of the probe [8, 13, 14]. Hybridisation is also dependent on the properties of the target nucleic acid; in particular, relatively long targets are associated with secondary structure which can significantly hinder hybridisation [15–17]. The performance of the array is therefore also influenced by the PCR primers used, in terms of the specificity they confer, their general suitability for PCR (since array sensitivity is largely determined by the sensitivity of the PCR) and the secondary structure of the amplified product. Generalisations can be made about favourable properties of the PCR products, such as length  and labelling method, for optimal performance of an array in terms of signal strength, specificity and limit of detection. The location of the PCR primers within the target sequence will also determine the position of the probe within the amplified product. Peytavi et al.  reported that the position of the probe can affect hybridisation signal strength; while Stedtfeld at al  found that false positive signals can be caused by interaction between overhanging target nucleic acid and labelled background DNA. We hypothesise that the position of the probe within the PCR product (i.e. it’s proximity to the 5′ or 3′ end of the hybridising strand) could also influence its performance in terms of the tolerance or discrimination of mismatches. A 25-mer oligonucleotide array in an AT format was designed to investigate this hypothesis.
Sequence (5′ to 3′)
5 AC 1
3 AC 1
5 AC 2
3 AC 2
PCR primer design
Primers used for biotin-labelled PCR
Forward primer sequence (5′ to 3′)
Reverse primer sequence (5′ to 3′)
Amplicon length (bases)
Length of 5′ segment (bases)
Burkholderia pseudomallei CLO2 DNA was prepared and quanitified by the Defence Science and Technology Organisation (DSTO) in Melbourne, Australia. The DNA extract was sterility checked to enable work under Biological Safety Level 2 (BSL2) conditions.
PCR with biotin labelling
PCR was carried out in 50 μl reactions containing 1× GoTaq Flexi Colourless Buffer (Promega, Madison, WI, USA); 1.5 mM MgCl2; 80 μM each dATP, dCTP and dGTP; 52 μM dTTP; 28 μM biotin-11-dUTP (Thermo Scientific, Waltham, MA, USA); 300 nM forward primer; 300 nM reverse primer; 1.25 units Go Taq polymerase (Promega) and 1 ng B. pseudomallei DNA. Primer combinations were as shown in Table 2. Cycling conditions were 95°C for 2 min, followed by 30 three-step cycles of 95°C for 30 s 58°C for 30 s and 72°C for 1 min, with a final extension step at 72°C for 5 min. After amplification, reactions were purified using the QIAquick PCR Purification kit (Qiagen, Hilden, Germany) according to the manufacturer’s instructions and eluted in nuclease-free water. Approximate DNA concentrations of the purified PCR products were determined using a Qubit fluorometer and dsDNA HS Assay Kit (Life Technologies, Foster City, CA, USA) according to the manufacturer’s instructions. Approximate copy numbers were estimated on the basis of DNA concentration and the molecular weight of the predicted product. Each primer combination was initially tested in unlabelled PCR with dNTPs at 80 μM each and the products analysed by agarose gel electrophoresis to confirm the approximate size of the product and absence of primer dimers or other amplification artifacts (data not shown).
Asymmetric PCR with biotin labelling
Asymmetric PCR is often used to generate predominantly single-stranded PCR products for hybridisation to microarrays, and the presence of the complementary, non-hybridising strand has been shown to influence hybridisation efficiency and other factors [18, 20]. In order to investigate the effect on tolerance and discrimination of mismatches, forward primer for4 was modified for asymmetric PCR taking into account design considerations for Linear-After-The-Exponential (LATE) PCR  as shown in Table 2. PCR reactions and cycling conditions were the same as those used for symmetric PCR, except that the concentration of the reverse (excess) primer was increased to 500 nM and the concentration of the modified forward (limiting) primer was reduced to 25, 50 or 100 nM to give primer ratios of 20:1, 10:1 and 5:1, respectively. Approximate total DNA concentrations (single- and double-stranded DNA) were determined for symmetrical and asymmetrical PCR products using a Qubit fluorometer and ssDNA Assay Kit (Life Technologies) according to the manufacturer’s instructions, and concentrations were adjusted to give approximately equal total DNA concentrations. The symmetrical and asymmetrical PCR products were treated with S1 nuclease and subjected to agarose gel electrophoresis to determine the presence or absence of single-stranded amplification products . For treatment with S1 nuclease, 10 μl PCR product was combined with 20 units S1 nuclease and 4 μl 5× S1 nuclease reaction buffer (Thermo Scientific) in a final reaction volume of 20 μl and incubated at 37°C for 30 min. Treated and untreated PCR products (10 μl and 5 μl, respectively) were analysed by electrophoresis in 1.2% agarose gels containing GelRed nucleic acid stain (Biotium, Hayward, CA) at a final concentration of 0.5×.
Array hybridisation and analysis
Biotin-labelled PCR products were made up to a volume of 40 μl in nuclease-free water and mixed with 70 μl Nexterion Hybridisation Buffer (Schott, Mainz, Germany), then heated to 95°C for 4 min and cooled to 55°C. ArrayTubes were conditioned by applying 500 μl nuclease-free water and incubating at 55°C with shaking at approx. 500 rpm for 5 min, after which the water was removed and 500 μl Nexterion Hybridisation Buffer was added and incubated at 55°C for 5 min with shaking. The buffer was removed and the pre-heated PCR products were applied to the ArrayTubes and incubated at 55°C for 1 h with shaking at approx. 500 rpm. The ArrayTubes were washed three times: first in 2× SSC containing 0.01% Triton X-100 (Sigma-Aldrich, St Louis, MO, USA), then 2× SSC and finally in 0.2× SSC; for each wash step, the previous solution was removed, 500 μl relevant wash buffer was added and the ArrayTubes were incubated for 5 min at room temperature with shaking at approx. 500 rpm. The final wash buffer was removed and 100 μl blocking solution containing 1× phosphate buffered saline (PBS), 2% dried milk powder and 0.05% Triton X-100 was applied to each ArrayTube and incubated at 30°C for 15 min, then removed. HRP-linked anti-biotin antibody (New England Biolabs, Ipswich, MA, USA) was diluted 1 in 100 in blocking solution and 100 μl diluted antibody was applied to each array and incubated for 15 min at room temperature. Finally, the ArrayTubes were washed three times as described above in 1x PBS containing 0.1% Tween 20 (Sigma) (500 μl for each wash step). The final wash buffer was removed and 100 μl SeramunGrün Chip substrate (Seramun Diagnostica, Wolzig, Germany) was added to each ArrayTube. The ArrayTubes were scanned after approx. 15 – 20 min using an ATR-03 ArrayTube Reader (Alere), and images were analysed using the Iconoclust software package (Alere) as described by Cannon et al. .
Effect of probe position on single base mismatch discrimination
Effect of probe position on limit of detection
Limit of detection of PCR products with similar total lengths but different 5′ segment lengths
Signal intensity (mean ± sd)*
Total length (bases)
5′ segment length (bases)
Approx. 8 × 109copies
Approx. 8 × 108copies
Approx. 8 × 107copies
0.63 ± 0.03
0.23 ± 0.03
0.62 ± 0.01
0.22 ± 0.02
0.66 ± 0.06
0.28 ± 0.05
0.57 ± 0.03
0.24 ± 0.00
Combined effect of total product length and probe position
Effect of primer ratio
The ArrayTube hybridisation architecture in the format used here contains around 200 locations for the deposition of DNA probes depending on the spacing between spots. With two replicates of each probe and an appropriate multiplexed PCR this allows the detection/discrimination of around 80–90 targets and subtyping of panels of associated agents along with appropriate controls such as for DNA extraction. Since this is an open platform, the user has control over the number of targets and the specific properties of the probes being used. The technology can also be used in a strip format for the simultaneous processing of up to 96 arrays, potentially allowing the development of higher throughput screening capabilities than other multiplex PCR-based platforms .
Clinical diagnostic applications require methods with high sensitivity and robustness. By using an array format it is possible to screen a sample for multiple targets from the same agent (for example, plasmid and chromosomal sequences) [3, 24] and this redundancy has the potential to increase the robustness of detection in terms of the avoidance of both false positives and false negatives . The ability to discriminate small sequence differences is crucial for some purposes, such as the discrimination of SNPs in the identification of antimicrobial resistance  or differentiation of bacterial genotypes . Microarrays for pathogen detection are often designed to detect a relatively narrowly defined group of targets (for example, a particular bacterial taxon in a specified clinical matrix). More versatile arrays may be developed to perform a set of related functions, such as detection of a range of organisms and identification of the presence of antimicrobial resistance markers , or simultaneous detection of diverse agents, for example, bacteria and viruses, in the same sample. For the effective detection of viruses it may be necessary to tolerate multiple sequence differences, while for the detection of bacteria there may be a need to accurately discriminate between targets on the basis of minor sequence differences. While sensitivity will be largely influenced by PCR efficiency, our results indicate that it could be possible to leverage the specificity (or conversely, inclusivity) of detection by manipulating the length of the target’s PCR amplicon, positioning the probe with respect to the 5′ end of the hybridising strand and changing the primer ratio to generate double-stranded or partially single-stranded products.
In line with previous reports, we observed that different mismatches were tolerated to different degrees, with the greatest effect when the mismatch was located close to the centre of the probe [8, 27, 28]. In the limited probe sets that we used, a GT mismatch was tolerated (little or no attenuation of the hybridisation signal) while CC, AC and CT mismatches caused significant signal attenuation. However, we also observed that the same mismatched probe was observed to give different signal intensities when approximately equal numbers of copies of PCR products differing in terms of probe position were hybridised to the array. The maximum effect of single mismatches (and in particular CC, AC and CT mismatches) was observed for PCR products where a greater proportion of the total length was at the 5′ end relative to the probe (and therefore proximal to the array surface). A reduction in the discrimination of individual mismatches was observed if PCR primers were used at unequal concentrations resulting in generation of some single-stranded product, presumably because the complementary non-target strand competes with the shorter mismatched probe for hybridisation to the target strand. This is consistent with the proposal of Peytavi et al.  that the complementary strand destabilises the target-probe duplex, particularly in relation to the length of the distal segment of the hybridised target. We did not observe a reduction in signal strength with a longer 3′ segment of the PCR product (distal to the array surface) as was reported by Peytavi et al. (in fact, as shown in Figure 4, signal strength decreased with a shorter 3′ segment length); however, there are differences between the two experimental systems, including the probe orientation and hybridisation conditions, which could partially explain this difference. Our results suggest that in the experimental set-up used here, mismatch discrimination is most likely to be achieved using equal primer concentrations, while inclusive detection of sequence variants would be enhanced by the use of asymmetrical primer concentrations.
It should be noted that the results presented are for PCR using single primer pairs, and factors such as product length and primer ratio may impact on the performance of a primer pair in a multiplex reaction in terms of sensitivity. For example, shorter PCR amplicons may generally be preferable due to the likelihood of higher yields  and reduced formation of intra- and intermolecular structures which are reported to hinder hybridisation [15, 18, 19].
Our results suggest a strategy for the rational design of PCR primers in order to leverage the exclusivity (specificity) or inclusivity of detection of individual targets on the array. Specifically, positioning a probe within the PCR product such that there is a longer section proximal to the array surface may increase the discrimination of single mismatches. As these primer design strategies could be applied independently to each target as required, this presents a means of fine-tuning an array for detection of potentially diverse targets. Optimisation of array performance by adjustment of the primers used for multiplex PCR has the potential to increase flexibility and cost effectiveness in comparison with redesigning the probes themselves.
This study was funded by the UK Ministry of Defence (Programme Office). The funding body approved submission of the manuscript for publication but had no role in study design, data collection and analysis, or preparation of the manuscript. The authors thank Lois Blackman and Matthias Dorsch of Defence Science Technology Organisation, Melbourne, Australia for the B. pseudomallei DNA used in this study.
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