Abstract
The pathogenicity of Saffold virus (SAFV) among humans still remains unclear, although it was identified as a novel human cardiovirus in 2007. In order to encourage the molecular pathogenetic studies of SAFV, we generated an infectious cDNA clone of SAFV type 3 (SAFV-3). The present study demonstrated that the synthesis of the full-length infectious RNA by T7 RNA polymerase was terminated by a homologous sequence motif with the human preproparathyroid hormone (PTH) signal in the SAFV-3 genome. To obtain the infectious RNA using T7 promoter, a variant of T7 RNA polymerase, which fails to recognize the PTH signal, was useful. This study will provide a valuable technical insight into the reverse genetics of SAFV. © 2011 Himeda et al; licensee BioMed Central Ltd.
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CITATION STYLE
Himeda, T., Hosomi, T., Asif, N., Shimizu, H., Okuwa, T., Muraki, Y., & Ohara, Y. (2011). The preparation of an infectious full-length cDNA clone of Saffold virus. Virology Journal, 8. https://doi.org/10.1186/1743-422X-8-110
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