Abstract

Single nucleotide polymorphisms (SNPs) are abundant in genomes of all species and biologically informative markers extensively used across broad scientific disciplines. Newly identified SNP markers are publicly available at an ever-increasing rate due to advancements in sequencing technologies. Efficient, cost-effective SNP genotyping methods to screen sample populations are in great demand in well-equipped laboratories, but also in developing world situations. Dual Probe TaqMan assays are robust but can be cost-prohibitive and require specialized equipment. The Mismatch Amplification Mutation Assay, coupled with melt analysis (Melt-MAMA), is flexible, efficient and cost-effective. However, Melt-MAMA traditionally suffers from high rates of assay design failures and knowledge gaps on assay robustness and sensitivity. In this study, we identified strategies that improved the success of Melt-MAMA. We examined the performance of 185 Melt-MAMAs across eight different pathogens using various optimization parameters. We evaluated the effects of genome size and %GC content on assay development. When used collectively, specific strategies markedly improved the rate of successful assays at the first design attempt from ∼50% to ∼80%. We observed that Melt-MAMA accurately genotypes across a broad DNA range (∼100 ng to ∼0.1 pg). Genomic size and %GC content influence the rate of successful assay design in an independent manner. Finally, we demonstrated the versatility of these assays by the creation of a duplex Melt-MAMA real-time PCR (two SNPs) and conversion to a size-based genotyping system, which uses agarose gel electrophoresis. Melt-MAMA is comparable to Dual Probe TaqMan assays in terms of design success rate and accuracy. Although sensitivity is less robust than Dual Probe TaqMan assays, Melt-MAMA is superior in terms of cost-effectiveness, speed of development and versatility. We detail the parameters most important for the successful application of Melt-MAMA, which should prove useful to the wider scientific community.

Highlights

  • Single nucleotide polymorphisms (SNPs) are point mutations with biological significance across diverse scientific disciplines ranging from medicine to agriculture

  • We summarize our efforts in employing Melt-MAMA across multiple pathogenic bacterial species for SNP interrogation and the positive effects of specific strategies that maximized the successful application of this cost-effective technique

  • We conclude that Melt-MAMA is a highly effective and robust SNP genotyping approach applicable to laboratories with varying economic resources

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Summary

Introduction

Single nucleotide polymorphisms (SNPs) are point mutations with biological significance across diverse scientific disciplines ranging from medicine to agriculture. Over the course of multiple studies, 185 SNPs from eight bacterial pathogen species, differing greatly with respect to sequence, genome size and %GC content (Table 1), were developed into Melt-MAMA genotyping assays.

Results
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