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Virology. 2009 Apr 25;387(1):157-67. doi: 10.1016/j.virol.2009.02.017. Epub 2009 Mar 9.

Murine Polyomavirus encodes a microRNA that cleaves early RNA transcripts but is not essential for experimental infection.

Author information

1
The University of Texas at Austin, Institute for Cellular and Molecular Biology, Section of Molecular Genetics and Microbiology, 1 University Station A5000, Austin TX 78712-0162, USA. chris_sullivan@mail.utexas.edu

Abstract

MicroRNAs are small regulatory RNAs that post-transcriptionally regulate gene expression and can be encoded by viral as well as cellular genomes. The functions of most viral miRNAs are unknown and few have been studied in an in vivo context. Here we show that the murine polyomavirus (PyV) encodes a precursor microRNA that is processed into two mature microRNAs, both of which are active at directing the cleavage of the early PyV mRNAs. Furthermore, we identify a deletion mutant of polyomavirus that is defective in encoding the microRNAs. This mutant replicates normally and transforms cultured cells with efficiencies comparable to wildtype PyV. The miRNA mutant is competent to establish a transient infection of mice following parenteral inoculation, and is cleared post infection at approximately the same rate as the wildtype virus. In addition, under these laboratory conditions, we observe no differences in anti-viral CD8 T cell responses. These results indicate that PyV miRNA expression is not essential for infection of cultured cells or experimentally inoculated mice, and raise the possibility that its role in natural infection might involve aspects of acquisition or spread that are not recapitulated by experimental inoculation.

PMID:
19272626
PMCID:
PMC2722155
DOI:
10.1016/j.virol.2009.02.017
[Indexed for MEDLINE]
Free PMC Article

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