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Antiviral activities of ISG20 in positive-strand RNA virus infections
Journal article   Open access   Peer reviewed

Antiviral activities of ISG20 in positive-strand RNA virus infections

Zhi Zhou, Nan Wang, Sara E. Woodson, Qingming Dong, Jie Wang, Yuqiong Liang, Rene Rijnbrand, Lai Wei, Joan E. Nichols, Ju-Tao Guo, …
Virology (New York, N.Y.), v 409(2), pp 175-188
2011
PMID: 21036379
url
https://doi.org/10.1016/j.virol.2010.10.008View
Published, Version of Record (VoR)Open Access (Publisher-Specific) Open

Abstract

Antiviral Bovine viral diarrhea virus Hepatitis A virus Hepatitis C virus Innate immunity Interferon ISG20 ISG20L1 ISG20L2 Severe acute respiratory syndrome coronavirus Yellow fever virus
ISG20 is an interferon-inducible 3′–5′ exonuclease that inhibits replication of several human and animal RNA viruses. However, the specificities of ISG20's antiviral action remain poorly defined. Here we determine the impact of ectopic expression of ISG20 on replication of several positive-strand RNA viruses from distinct viral families. ISG20 inhibited infections by cell culture-derived hepatitis C virus (HCV) and a pestivirus, bovine viral diarrhea virus and a picornavirus, hepatitis A virus. Moreover, ISG20 demonstrated cell-type specific antiviral activity against yellow fever virus, a classical flavivirus. Overexpression of ISG20, however, did not inhibit propagation of severe acute respiratory syndrome coronavirus, a highly-pathogenic human coronavirus in Huh7.5 cells. The antiviral effects of ISG20 were all dependent on its exonuclease activity. The closely related cellular exonucleases, ISG20L1 and ISG20L2, did not inhibit HCV replication. Together, these data may help better understand the antiviral specificity and action of ISG20.

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Virology
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