Abstract：
:PRRSV is a positive-sense RNA virus with a high degree of genetic variability among isolates. For diagnostic sensitivity and vaccine design it is essential to monitor PRRSV genetic diversity. However, to date only a few full genome sequences of PRRSV isolates have been made publicly available. In the present study, fast and robust methods for long range RT-PCR amplification and subsequent next generation sequencing (NGS) were developed and validated on nine Type 1 and nine Type 2 PRRSV viruses. The methods generated robust and reliable sequences both on primary material and cell culture adapted viruses and the protocols performed well on all three NGS platforms tested (Roche 454 FLX, Illumina HiSeq2000, and Ion Torrent PGM™ Sequencer). These methods will greatly facilitate the generation of more full genome PRRSV sequences globally.
journal_name
J Virol Methodsjournal_title
Journal of virological methodsauthors
Kvisgaard LK,Hjulsager CK,Fahnøe U,Breum SØ,Ait-Ali T,Larsen LEdoi
10.1016/j.jviromet.2013.07.019subject
Has Abstractpub_date
2013-11-01 00:00:00pages
697-705issue
2eissn
0166-0934issn
1879-0984pii
S0166-0934(13)00273-5journal_volume
193pub_type
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