Knockdown of piRNA pathway proteins results in enhanced Semliki Forest virus production in mosquito cells

Esther Schnettler(Roslin Institute), Claire L. Donald(Roslin Institute), Stacey Human(The Pirbright Institute), Mick Watson(Roslin Institute), Ricky W. C. Siu(Roslin Institute), Melanie McFarlane(MRC University of Glasgow Centre for Virus Research), John K. Fazakerley(The Pirbright Institute), Alain Kohl(Roslin Institute), Rennos Fragkoudis(The Pirbright Institute)
Journal of General Virology
April 5, 2013
Cited by 235Open Access
Full Text

Abstract

The exogenous siRNA pathway is important in restricting arbovirus infection in mosquitoes. Less is known about the role of the PIWI-interacting RNA pathway, or piRNA pathway, in antiviral responses. Viral piRNA-like molecules have recently been described following infection of mosquitoes and derived cell lines with several arboviruses. The piRNA pathway has thus been suggested to function as an additional small RNA-mediated antiviral response to the known infection-induced siRNA response. Here we show that piRNA-like molecules are produced following infection with the naturally mosquito-borne Semliki Forest virus in mosquito cell lines. We show that knockdown of piRNA pathway proteins enhances the replication of this arbovirus and defines the contribution of piRNA pathway effectors, thus characterizing the antiviral properties of the piRNA pathway. In conclusion, arbovirus infection can trigger the piRNA pathway in mosquito cells, and knockdown of piRNA proteins enhances virus production.


Related Papers

No related papers found

Powered by citation graph analysis