Journal article

Processing of Genome 5′ Termini as a Strategy of Negative-Strand RNA Viruses to Avoid RIG-I-Dependent Interferon Induction


Authors listHabjan, M; Andersson, I; Klingström, J; Schümann, M; Martin, A; Zimmermann, P; Wagner, V; Pichlmair, A; Schneider, U; Mühlberger, E; Mirazimi, A; Weber, F

Publication year2008

JournalPLoS ONE

Volume number3

Issue number4

ISSN1932-6203

DOI Linkhttps://doi.org/10.1371/journal.pone.0002032

PublisherPublic Library of Science


Abstract
Innate immunity is critically dependent on the rapid production of interferon in response to intruding viruses. The intracellular pathogen recognition receptors RIG-I and MDA5 are essential for interferon induction by viral RNAs containing 59 triphosphates or double-stranded structures, respectively. Viruses with a negative-stranded RNA genome are an important group of pathogens causing emerging and re-emerging diseases. We investigated the ability of genomic RNAs from substantial representatives of this virus group to induce interferon via RIG-I or MDA5. RNAs isolated from particles of Ebola virus, Nipah virus, Lassa virus, and Rift Valley fever virus strongly activated the interferon-beta promoter. Knockdown experiments demonstrated that interferon induction depended on RIG-I, but not MDA5, and phosphatase treatment revealed a requirement for the RNA 59 triphosphate group. In contrast, genomic RNAs of Hantaan virus, Crimean-Congo hemorrhagic fever virus and Borna disease virus did not trigger interferon induction. Sensitivity of these RNAs to a 59 monophosphate-specific exonuclease indicates that the RIG-I-activating 59 triphosphate group was removed posttranscriptionally by a viral function. Consequently, RIG-I is unable to bind the RNAs of Hantaan virus, Crimean-Congo hemorrhagic fever virus and Borna disease virus. These results establish RIG-I as a major intracellular recognition receptor for the genome of most negative-strand RNA viruses and define the cleavage of triphosphates at the RNA 59 end as a strategy of viruses to evade the innate immune response.



Citation Styles

Harvard Citation styleHabjan, M., Andersson, I., Klingström, J., Schümann, M., Martin, A., Zimmermann, P., et al. (2008) Processing of Genome 5′ Termini as a Strategy of Negative-Strand RNA Viruses to Avoid RIG-I-Dependent Interferon Induction, PLoS ONE, 3(4), Article e2032. https://doi.org/10.1371/journal.pone.0002032

APA Citation styleHabjan, M., Andersson, I., Klingström, J., Schümann, M., Martin, A., Zimmermann, P., Wagner, V., Pichlmair, A., Schneider, U., Mühlberger, E., Mirazimi, A., & Weber, F. (2008). Processing of Genome 5′ Termini as a Strategy of Negative-Strand RNA Viruses to Avoid RIG-I-Dependent Interferon Induction. PLoS ONE. 3(4), Article e2032. https://doi.org/10.1371/journal.pone.0002032


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