Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6135341 | Journal of Virological Methods | 2011 | 8 Pages |
Abstract
The 3â² and 5â² untranslated regions (UTRs) of the gene segments of orthomyxoviruses interact closely with the polymerase complex and are important for viral replication and transcription regulation. Despite this, the 3â² and 5â² RNA UTRs of the infectious salmon anaemia virus (ISAV) genome have only been partially characterized and little is known about the level of conservation between different virus subtypes. This report details for the first time, the adaptation of a rapid method for the simultaneous characterization of the 3â² and 5â² UTRs of each viral segment of ISAV. This was achieved through self circularization of segments using T4 RNA ligase, followed by PCR and sequencing. Dephosphorylation of 5â² ends using tobacco acid pyrophosphatase (TAP) proved to be a specific requirement for ligation of ISAV ends which was not essential for characterization of influenza virus in a similar manner. The development of universal primers facilitated the characterization of 4 genetically distinct ISAV isolates from Canada, Norway and Scotland. Comparison of the UTR regions revealed a similarity in organization and presence of conserved terminal sequences as reported for other orthomyxoviruses. Interestingly, the 3â² ends of ISAV segments including segments 1, 5 and 6, were shorter and 5â² UTRs generally longer than in their influenza counterparts.
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Authors
Mickael Fourrier, Sandra Heuser, Eann Munro, Mike Snow,