MultiPSQ: A Software Solution for the Analysis of Diagnostic n-Plexed Pyrosequencing Reactions

被引:2
作者
Dabrowski, Piotr Wojtek [1 ,2 ]
Schroeder, Kati [2 ]
Nitsche, Andreas [2 ]
机构
[1] Robert Koch Inst, Cent Adm IT 4, Berlin, Germany
[2] Robert Koch Inst, Ctr Biol Threats & Special Pathogens 1, Berlin, Germany
关键词
D O I
10.1371/journal.pone.0060055
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
Background: Pyrosequencing can be applied for Single-Nucleotide-Polymorphism (SNP)-based pathogen typing or for providing sequence information of short DNA stretches. However, for some pathogens molecular typing cannot be performed relying on a single SNP or short sequence stretch, necessitating the consideration of several genomic regions. A promising rapid approach is the simultaneous application of multiple sequencing primers, called multiplex pyrosequencing. These primers generate a fingerprint-pyrogram which is constituted by the sum of all individual pyrograms originating from each primer used. Methods: To improve pyrosequencing-based pathogen typing, we have developed the software tool MultiPSQ that expedites the analysis and evaluation of multiplex-pyrograms. As a proof of concept, a multiplex pyrosequencing assay for the typing of orthopoxviruses was developed to analyse clinical samples diagnosed in the German Consultant Laboratory for Poxviruses. Results: The software tool MultiPSQ enabled the analysis of multiplex-pyrograms originating from various pyrosequencing primers. Thus several target regions can be used for pathogen typing based on pyrosequencing. As shown with a proof of concept assay, SNPs present in different orthopoxvirus strains could be identified correctly with two primers by MultiPSQ. Conclusions: Software currently available is restricted to a fixed number of SNPs and sequencing primers, severely limiting the usefulness of this technique. In contrast, our novel software MultiPSQ allows analysis of data from multiplex pyrosequencing assays that contain any number of sequencing primers covering any number of polymorphisms.
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页数:6
相关论文
共 14 条
[1]   Single-nucleotide polymorphism analysis by pyrosequencing [J].
Ahmadian, A ;
Gharizadeh, B ;
Gustafsson, AC ;
Sterky, F ;
Nyrén, P ;
Uhlén, M ;
Lundeberg, J .
ANALYTICAL BIOCHEMISTRY, 2000, 280 (01) :103-110
[2]   mPSQed: A Software for the Design of Multiplex Pyrosequencing Assays [J].
Dabrowski, Piotr Wojtek ;
Nitsche, Andreas .
PLOS ONE, 2012, 7 (06)
[3]   High Throughput Automated Allele Frequency Estimation by Pyrosequencing [J].
Doostzadeh, Julie ;
Shokralla, Shadi ;
Absalan, Farnaz ;
Jalili, Roxana ;
Mohandessi, Sharareh ;
Langston, James W. ;
Davis, Ronald W. ;
Ronaghi, Mostafa ;
Gharizadeh, Baback .
PLOS ONE, 2008, 3 (07)
[4]  
Elahi Elahe, 2004, Methods Mol Biol, V255, P211
[5]   Pyrosequencing™:: An accurate detection platform for single nucleotide polymorphisms [J].
Fakhrai-Rad, H ;
Pourmand, N ;
Ronaghi, M .
HUMAN MUTATION, 2002, 19 (05) :479-485
[6]   Type-specific multiple sequencing primers -: A novel strategy for reliable and rapid genotyping of human papilloma viruses by pyrosequencing technology [J].
Gharizadeh, B ;
Oggionni, M ;
Zheng, BY ;
Akom, E ;
Pourmand, N ;
Ahmadian, A ;
Wallin, KL ;
Nyrén, P .
JOURNAL OF MOLECULAR DIAGNOSTICS, 2005, 7 (02) :198-205
[7]   Multiple-primer DNA sequencing method [J].
Gharizadeh, B ;
Ghaderi, M ;
Donnelly, D ;
Amini, B ;
Wallin, KL ;
Nyrén, P .
ELECTROPHORESIS, 2003, 24 (7-8) :1145-1151
[8]   Detection and typing of human pathogenic hantaviruses by real-time reverse transcription-PCR and pyrosequencing [J].
Kramski, Marit ;
Meisel, Helga ;
Klempa, Boris ;
Krueger, Etlev H. ;
Pauli, Georg ;
Nitsche, Andreas .
CLINICAL CHEMISTRY, 2007, 53 (11) :1899-1905
[9]  
Patel Pritesh, 2007, V373, P75
[10]   Multiplex pyrosequencing [J].
Pourmand, N ;
Elahi, E ;
Davis, RW ;
Ronaghi, M .
NUCLEIC ACIDS RESEARCH, 2002, 30 (07) :e31