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Review
. 2023 Jun 15;136(12):jcs260682.
doi: 10.1242/jcs.260682. Epub 2023 Jun 21.

Viral evasion of the interferon response at a glance

Affiliations
Review

Viral evasion of the interferon response at a glance

Junji Zhu et al. J Cell Sci. .

Abstract

Re-emerging and new viral pathogens have caused significant morbidity and mortality around the world, as evidenced by the recent monkeypox, Ebola and Zika virus outbreaks and the ongoing COVID-19 pandemic. Successful viral infection relies on tactical viral strategies to derail or antagonize host innate immune defenses, in particular the production of type I interferons (IFNs) by infected cells. Viruses can thwart intracellular sensing systems that elicit IFN gene expression (that is, RIG-I-like receptors and the cGAS-STING axis) or obstruct signaling elicited by IFNs. In this Cell Science at a Glance article and the accompanying poster, we review the current knowledge about the major mechanisms employed by viruses to inhibit the activity of intracellular pattern-recognition receptors and their downstream signaling cascades leading to IFN-based antiviral host defenses. Advancing our understanding of viral immune evasion might spur unprecedented opportunities to develop new antiviral compounds or vaccines to prevent viral infectious diseases.

Keywords: Innate immunity; Interferon; Intracellular sensors; Viral evasion.

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Conflict of interest statement

Competing interests The authors declare no competing or financial interests.

References

    1. Ablasser, A., Bauernfeind, F., Hartmann, G., Latz, E., Fitzgerald, K. A. and Hornung, V. (2009). RIG-I-dependent sensing of poly(dA:dT) through the induction of an RNA polymerase III-transcribed RNA intermediate. Nat. Immunol. 10, 1065-1072. 10.1038/ni.1779 - DOI - PMC - PubMed
    1. Acharya, D., Reis, R., Volcic, M., Liu, G., Wang, M. K., Chia, B. S., Nchioua, R., Gross, R., Munch, J., Kirchhoff, F.et al. (2022). Actin cytoskeleton remodeling primes RIG-I-like receptor activation. Cell 185, 3588-3602.e21. 10.1016/j.cell.2022.08.011 - DOI - PMC - PubMed
    1. Aguirre, S., Maestre, A. M., Pagni, S., Patel, J. R., Savage, T., Gutman, D., Maringer, K., Bernal-Rubio, D., Shabman, R. S., Simon, V.et al. (2012). DENV inhibits type I IFN production in infected cells by cleaving human STING. PLoS Pathog. 8, e1002934. 10.1371/journal.ppat.1002934 - DOI - PMC - PubMed
    1. Aguirre, S., Luthra, P., Sanchez-Aparicio, M. T., Maestre, A. M., Patel, J., Lamothe, F., Fredericks, A. C., Tripathi, S., Zhu, T., Pintado-Silva, J.et al. (2017). Dengue virus NS2B protein targets cGAS for degradation and prevents mitochondrial DNA sensing during infection. Nat. Microbiol. 2, 17037. 10.1038/nmicrobiol.2017.37 - DOI - PMC - PubMed
    1. Andrejeva, J., Childs, K. S., Young, D. F., Carlos, T. S., Stock, N., Goodbourn, S. and Randall, R. E. (2004). The V proteins of paramyxoviruses bind the IFN-inducible RNA helicase, mda-5, and inhibit its activation of the IFN-beta promoter. Proc. Natl. Acad. Sci. USA 101, 17264-17269. 10.1073/pnas.0407639101 - DOI - PMC - PubMed

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