Tula hantavirus infection of Vero E6 cells induces apoptosis involving caspase 8 activation

Xiao Dong Li, Sami Kukkonen, Olli Vapalahti, Alexander Plyusnin, Hilkka Lankinen, Antti Vaheri

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42 Scopus citations

Abstract

Hantaviruses are known to cause two severe human diseases: haemorrhagic fever with renal syndrome and hantavirus pulmonary syndrome. The mechanisms of pathogenesis of these two diseases are progressively becoming understood. Recently, two hantaviruses, Hantaan and Prospect Hill were reported to cause programmed cell death of Vero E6 cells. This study shows that Tula hantavirus (TULV) infection efficiently triggers an apoptotic programme in infected Vero E6 cells, and that the replication of TULV is required for the activation of caspase 3 and the cleavage of poly (ADP-ribose) polymerase, two molecular hallmarks of apoptosis. The enforced treatment of infected Vero E6 cells with tumour necrosis factor alpha (TNF-α), but not interferon alpha (IFN-α), advanced the time course of apoptosis. Furthermore, caspase 8 was activated on day 4 post-infection, the same day when caspase 3 was activated. TNF receptor 1 was induced during a late stage of TULV infection. These data suggest that, unlike during influenza A virus infection, TNF-α, but not type I IFN-α/β, may contribute significantly to apoptosis in a synergistic manner with TULV propagation. Interestingly, pretreatment with a broad-spectrum caspase inhibitor, z-VAD-fmk, efficiently inhibited apoptosis of TULV-infected Vero E6 cells. Taken together, these results suggest that TULV replication initiates a typical apoptotic programme involving caspase 8 activation.

Original languageEnglish (US)
Pages (from-to)3261-3268
Number of pages8
JournalJournal of General Virology
Volume85
Issue number11
DOIs
StatePublished - Nov 1 2004

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ASJC Scopus subject areas

  • Virology

Cite this

Li, X. D., Kukkonen, S., Vapalahti, O., Plyusnin, A., Lankinen, H., & Vaheri, A. (2004). Tula hantavirus infection of Vero E6 cells induces apoptosis involving caspase 8 activation. Journal of General Virology, 85(11), 3261-3268. https://doi.org/10.1099/vir.0.80243-0