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Significant inhibition of two different genotypes of grass carp reovirus in vitro using multiple shRNAs expression vectors.

Virus Res. 2014; 
Ma J, Zeng L, Fan Y, Zhou Y, Jiang N, Chen Q.
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Polyclonal Antibody Services The primary antibodies used in this experimental were rabbit polyclonal antibodies (at a 1:500 for anti-GCRV-JX0901 Vp2 and anti-GCRV-JX0901 Vp7 antibody; at a 1:300 dilution for anti- HGDRV Vp2 and anti-HGDRV Vp6 antibody), and a rabbit polyclonal anti-GAPDH for loading control (GenScript, Piscataway, NJ, USA, 1:500 dilution).... Color development was performed by incubat- ing with alkaline horseradish peroxidase-conjugated anti-rabbit IgG, and followed by adding diaminobenzidine (DAB) (GenScript) substrate. Get A Quote

摘要

The hemorrhagic disease of grass carp (Ctenopharyngodon idellus), caused by grass carp reovirus (GCRV), is the most severe disease of the fish that leads to huge economic losses. GCRV, belonging to the genus Aquareovirus of the family Reoviridae, has been classified into three genotypes based on their phylogenetic relationship. It is essential to develop an effective method to inhibit the replication of different genotypes of GCRV simultaneously. In this report, two multiple-shRNAs expression vectors, named pMultishVP2/2 and pMultishVP6/7, were generated and investigated. pMultishVP2/2 targeted the VP2 gene of GCRV-JX0901 (genotype I) and the VP2 gene of HGDRV (Hubei grass carp disease reovirus; genotype III). ... More

关键词

GCRV; Inhibition; Multiple-shRNAs; Viral replication
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