PLoS Neglected Tropical Diseases (Jul 2017)

Lineage-dependent differences in the disease progression of Zika virus infection in type-I interferon receptor knockout (A129) mice.

  • Stuart D Dowall,
  • Victoria A Graham,
  • Emma Rayner,
  • Laura Hunter,
  • Barry Atkinson,
  • Geoff Pearson,
  • Mike Dennis,
  • Roger Hewson

DOI
https://doi.org/10.1371/journal.pntd.0005704
Journal volume & issue
Vol. 11, no. 7
p. e0005704

Abstract

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Zika virus (ZIKV) falls into two lineages: African (ZIKVAF) and Asian (ZIKVAS). These lineages have not been tested comprehensively in parallel for disease progression using an animal model system. Here, using the established type-I interferon receptor knockout (A129) mouse model, it is first demonstrated that ZIKVAF causes lethal infection, with different kinetics of disease manifestations according to the challenge dose. Animals challenged with a low dose of 10 plaque-forming units (pfu) developed more neurological symptoms than those challenged with 5-log higher doses. By contrast, animals challenged with ZIKVAS displayed no clinical signs or mortality, even at doses of 106 pfu. However, viral RNA was detected in the tissues of animals infected with ZIKV strains from both lineages and similar histological changes were observed. The present study highlights strain specific virulence differences between the African and Asian lineages in a ZIKV mouse model.