Melt Analysis of Mismatch Amplification Mutation Assays (Melt-MAMA): A Functional Study of a Cost-Effective SNP Genotyping Assay in Bacterial Models

被引:81
作者
Birdsell, Dawn N. [1 ]
Pearson, Talima [1 ]
Price, Erin P. [1 ]
Hornstra, Heidie M. [1 ]
Nera, Roxanne D. [1 ]
Stone, Nathan [1 ]
Gruendike, Jeffrey [1 ]
Kaufman, Emily L. [1 ]
Pettus, Amanda H. [1 ]
Hurbon, Audriana N. [1 ]
Buchhagen, Jordan L. [1 ]
Harms, N. Jane [6 ]
Chanturia, Gvantsa [2 ,3 ]
Gyuranecz, Miklos [5 ]
Wagner, David M. [1 ]
Keim, Paul S. [1 ,4 ]
机构
[1] No Arizona Univ, Ctr Microbial Genet & Genom, Flagstaff, AZ 86011 USA
[2] Natl Ctr Dis Control & Publ Hlth, Tbilisi, Georgia
[3] Ilia State Univ, Tbilisi, Georgia
[4] Translat Genom Res Inst, Phoenix, AZ USA
[5] Hungarian Acad Sci, Vet Med Res Inst, H-1581 Budapest, Hungary
[6] Univ Saskatchewan, Western Coll Vet Med, Dept Vet Pathol, Saskatoon, SK S7N 0W0, Canada
来源
PLOS ONE | 2012年 / 7卷 / 03期
基金
美国国家卫生研究院;
关键词
SINGLE-NUCLEOTIDE POLYMORPHISMS; ALLELE-SPECIFIC PCR; POLYMERASE-CHAIN-REACTION; SYBR-GREEN-I; FRANCISELLA-TULARENSIS; LARGE-SCALE; DNA; DISCRIMINATION; IDENTIFICATION; FLUORESCENCE;
D O I
10.1371/journal.pone.0032866
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 similar to 50% to similar to 80%. We observed that Melt-MAMA accurately genotypes across a broad DNA range (similar to 100 ng to similar 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.
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页数:18
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