tetano
Editor, Senior Moderator
High resolution melting analysis: rapid and precise characterisation of recombinant influenza A genomes
Donata Kalthoff, Martin Beer and Bernd Hoffmann
For all author emails, please log on.
Virology Journal 2013, 10:284 doi:10.1186/1743-422X-10-284
Published: 12 September 2013
Abstract (provisional)
Background
High resolution melting analysis (HRM) is a rapid and cost-effective technique for the characterisation of PCR amplicons. Because the reverse genetics of segmented influenza A viruses allows the generation of numerous influenza A virus reassortants within a short time, methods for the rapid selection of the correct recombinants are very useful.
Methods
PCR primer pairs covering the single nucleotide polymorphism (SNP) positions of two different influenza A H5N1 strains were designed. Reassortants of the two different H5N1 isolates were used as a model to prove the suitability of HRM for the selection of the correct recombinants. Furthermore, two different cycler instruments were compared.
Results
Both cycler instruments generated comparable average melting peaks, which allowed the easy identification and selection of the correct cloned segments or reassorted viruses.
Conclusions
HRM is a highly suitable method for the rapid and precise characterisation of cloned influenza A genomes
full article
http://www.virologyj.com/content/pdf/1743-422X-10-284.pdf
Donata Kalthoff, Martin Beer and Bernd Hoffmann
For all author emails, please log on.
Virology Journal 2013, 10:284 doi:10.1186/1743-422X-10-284
Published: 12 September 2013
Abstract (provisional)
Background
High resolution melting analysis (HRM) is a rapid and cost-effective technique for the characterisation of PCR amplicons. Because the reverse genetics of segmented influenza A viruses allows the generation of numerous influenza A virus reassortants within a short time, methods for the rapid selection of the correct recombinants are very useful.
Methods
PCR primer pairs covering the single nucleotide polymorphism (SNP) positions of two different influenza A H5N1 strains were designed. Reassortants of the two different H5N1 isolates were used as a model to prove the suitability of HRM for the selection of the correct recombinants. Furthermore, two different cycler instruments were compared.
Results
Both cycler instruments generated comparable average melting peaks, which allowed the easy identification and selection of the correct cloned segments or reassorted viruses.
Conclusions
HRM is a highly suitable method for the rapid and precise characterisation of cloned influenza A genomes
full article
http://www.virologyj.com/content/pdf/1743-422X-10-284.pdf