Abstract

Rotaviruses are an important cause of severe gastroenteritis in children under two years of age. Two vaccines have become recently available, however, there are no specific pharmacological interventions of rotavirus disease. Recently, libraries of siRNAs or libraries of chemical compounds that can be tested for their ability to inhibit biological processes have been developed. To search these libraries for drugs or siRNAs that may prevent rotavirus replication it is necessary to have methods for high-throughput screening. In this study several methods to quantify rotavirus replication in cell culture were evaluated; the cell death and viral protein expression assays were compared, and an in-cell Western method based on infrared detection that allows the simultaneous quantification of viral antigen and total protein content in the same cell culture well was developed. This is an easy, inexpensive method for detection of viral replication, and it is compatible with high-throughput screening.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.