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Virology. 2010 Mar 15;398(2):194-200. doi: 10.1016/j.virol.2009.11.037. Epub 2009 Dec 29.

An improved reverse genetics system for mammalian orthoreoviruses.

Author information

1
Department of Pediatrics, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.

Abstract

Mammalian orthoreoviruses (reoviruses) are highly useful models for studies of double-stranded RNA virus replication and pathogenesis. We previously developed a strategy to recover prototype reovirus strain T3D from cloned cDNAs transfected into murine L929 fibroblast cells. Here, we report the development of a second-generation reovirus reverse genetics system featuring several major improvements: (1) the capacity to rescue prototype reovirus strain T1L, (2) reduction of required plasmids from 10 to 4, and (3) isolation of recombinant viruses following transfection of baby hamster kidney cells engineered to express bacteriophage T7 RNA polymerase. The efficiency of virus rescue using the 4-plasmid strategy was substantially increased in comparison to the original 10-plasmid system. We observed full compatibility of T1L and T3D rescue vectors when intermixed to produce a panel of T1LxT3D monoreassortant viruses. Improvements to the reovirus reverse genetics system enhance its applicability for studies of reovirus biology and clinical use.

PMID:
20042210
PMCID:
PMC2823833
DOI:
10.1016/j.virol.2009.11.037
[Indexed for MEDLINE]
Free PMC Article

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