Key result
Deep sequencing of HIV-1-infected T lymphocytes identified numerous HIV-1-derived small RNAs, including vmiRNAs and vsiRNAs, which can potently repress HIV-1 production.
HIV-1 infection in mammalian cells triggers the production of viral small RNAs (vmiRNAs and vsiRNAs) that can modulate viral gene expression.
Small virus-derived interfering RNAs (viRNAs) play an important role in antiviral defence in plants, insects and nematodes by triggering the RNA interference (RNAi) pathway. The role of RNAi as an antiviral defence mechanism in mammalian cells has been obscure due to the lack of viRNA detection. Although viRNAs from different mammalian viruses have recently been identified, their functions and possible impact on viral replication remain unknown. To identify viRNAs derived from HIV-1, we used the extremely sensitive SOLiD(TM) 3 Plus System to analyse viRNA accumulation in HIV-1-infected T lymphocytes. We detected numerous small RNAs that correspond to the HIV-1 RNA genome. The majority of these sequences have a positive polarity (98.1%) and could be derived from miRNAs encoded by structured segments of the HIV-1 RNA genome (vmiRNAs). A small portion of the viRNAs is of negative polarity and most of them are encoded within the 3'-UTR, which may represent viral siRNAs (vsiRNAs). The identified vsiRNAs can potently repress HIV-1 production, whereas suppression of the vsiRNAs by antagomirs stimulate virus production. These results suggest that HIV-1 triggers the production of vsiRNAs and vmiRNAs to modulate cellular and/or viral gene expression.
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Schopman et al. (2011) studied HIV-1 infection. HIV-1 infection vs. Uninfected cells was evaluated on Detection and characterization of HIV-1-derived small RNAs (viRNAs). Deep sequencing of HIV-1-infected T lymphocytes identified numerous HIV-1-derived small RNAs, including vmiRNAs and vsiRNAs, which can potently repress HIV-1 production.
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