Skip the Alignment: Degenerate, Multiplex Primer and Probe Design Using K-mer Matching Instead of Alignments

PriMux is a new software package for selecting multiplex compatible, degenerate primers and probes to detect diverse targets such as viruses. It requires no multiple sequence alignment, instead applying k-mer algorithms, hence it scales well for large target sets and saves user effort from curating sequences into alignable groups. PriMux has the capability to predict degenerate primers as well as probes suitable for TaqMan or other primer/probe triplet assay formats, or simply probes for microarray or other single-oligo assay formats. PriMux employs suffix array methods for efficient calculations on oligos 10-∼100 nt in length. TaqMan® primers and probes for each segment of Rift Valley fever virus were designed using PriMux, and lab testing comparing signatures designed using PriMux versus those designed using traditional methods demonstrated equivalent or better sensitivity for the PriMux-designed signatures compared to traditional signatures. In addition, we used PriMux to design TaqMan® primers and probes for unalignable or poorly alignable groups of targets: that is, all segments of Rift Valley fever virus analyzed as a single target set of 198 sequences, or all 2863 Dengue virus genomes for all four serotypes available at the time of our analysis. The PriMux software is available as open source from http://sourceforge.net/projects/PriMux.

[1]  Peter L. Williams,et al.  Multiplex primer prediction software for divergent targets , 2009, Nucleic acids research.

[2]  S. Gardner,et al.  Annals of Clinical Microbiology and Antimicrobials Open Access Predicting the Sensitivity and Specificity of Published Real-time Pcr Assays , 2008 .

[3]  Michael Zuker,et al.  UNAFold: software for nucleic acid folding and hybridization. , 2008, Methods in molecular biology.

[4]  K. Hedlund,et al.  Quantitative analysis of particles, genomes and infectious particles in supernatants of haemorrhagic fever virus cell cultures , 2011, Virology Journal.

[5]  Ron Shamir,et al.  The Degenerate Primer Design Problem , 2002, ISMB.

[6]  Adam Zemla,et al.  Comparative Genomics Tools Applied to Bioterrorism Defence , 2003, Briefings Bioinform..

[7]  Shea N. Gardner,et al.  Sequencing Needs for Viral Diagnostics , 2004, Journal of Clinical Microbiology.

[8]  J B Moe,et al.  Plaque Assay for Ebola Virus , 1981, Journal of clinical microbiology.

[9]  Weixiong Zhang,et al.  Selecting Degenerate Multiplex PCR Primers , 2003, WABI.

[10]  W. Ian Lipkin,et al.  Greene SCPrimer: a rapid comprehensive tool for designing degenerate primers from multiple sequence alignments , 2006, Nucleic acids research.

[11]  Crystal Jaing,et al.  Viral Nucleic Acids in Live-Attenuated Vaccines: Detection of Minority Variants and an Adventitious Virus , 2010, Journal of Virology.

[12]  Thomas A. Kuczmarski,et al.  Limitations of TaqMan PCR for Detecting Divergent Viral Pathogens Illustrated by Hepatitis A, B, C, and E Viruses and Human Immunodeficiency Virus , 2003, Journal of Clinical Microbiology.

[13]  R. Mandell,et al.  Rift valley fever virus: a real bioterror threat. , 2011 .

[14]  Robert C. Edgar,et al.  MUSCLE: multiple sequence alignment with high accuracy and high throughput. , 2004, Nucleic acids research.

[15]  J. O'mahony,et al.  Rotavirus survival and stability in foods as determined by an optimised plaque assay procedure. , 2000, International journal of food microbiology.