A New Target for Preventing Dicistroviridae–mediated Agricultural Loss
UAB Research Foundation
posted on 10/26/2011
Protein synthesis is a highly regulated process whereby messenger RNA (mRNA) is translated by ribosomes to create proteins. Certain viral infections result in a global shut-down of cellular translation and subvert the host ribosomes to translate the viral RNA by a mechanism known as cap-independent translation. These viruses include the Dicistroviridae family, which cause Honey Bee Colony Collapse Disorder and Taura Syndrome in shrimp. Researchers at the University of Alabama at Birmingham (UAB) have identified Rps25, a non-essential host protein that is required for cap-independent translation and infectivity of these viruses. This discovery could lead to new approaches for preventing these devastating diseases and loss of billions of dollars to the honey bee and shrimp industries.
Suggested Uses
Advantages
Rps25-mediated translation initiation
- A molecular, host-derived target, Rps25, implicated in Dicistroviridae-mediated agricultural loss has been identified.
- A host-derived target will decrease the likelihood of the virus generating treatment-resistant variants.
- A method for screening for inhibitors of Rps25-mediated translation has been developed.
- Small-molecule-based inhibitors of Rps25-mediated translation have already been identified.
Detailed Description
File Number: U2009-0049, Agriculture
Web site: http://www.uab.edu/uabrf
Other Information:
| Patent Number(s): | 13/259503, PCT/US2010/028917 |
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This innovation currently is not available for online licensing. Please contact Deborah Powe at UAB Research Foundation for more information.
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