Abstract

The economic impact of non-lethal human and equine West Nile virus (WNV) disease is substantial, since it is the most common presentation of the infection. Experimental infection with virulent WNV strains in the mouse and hamster models frequently results in severe neural infection and moderate to high mortality, both of which are not representative features of most human and equine infections. We have established a rabbit model for investigating pathogenesis and immune response of non-lethal WNV infection. Two species of rabbits, New Zealand White (Oryctolagus cuniculus) and North American cottontail (Sylvilagus sp.), were experimentally infected with virulent WNV and Murray Valley encephalitis virus strains. Infected rabbits exhibited a consistently resistant phenotype, with evidence of low viremia, minimal-absent neural infection, mild-moderate neuropathology, and the lack of mortality, even though productive virus replication occurred in the draining lymph node. The kinetics of anti-WNV neutralizing antibody response was comparable to that commonly seen in infected horses and humans. This may be explained by the early IFNα/β and/or γ response evident in the draining popliteal lymph node. Given this similarity to the human and equine disease, immunocompetent rabbits are, therefore, a valuable animal model for investigating various aspects of non-lethal WNV infections.

Highlights

  • West Nile virus (WNV) is an important re-emerging neurotropic arbovirus, that continues to cause severe outbreaks world-wide

  • A total of 63 rabbits were experimentally infected with outbreak strains of flavivirus originally isolated from Australia (WNVNSW2011 and MVE1-51 [16,18]) and North America (WNV TX8667)

  • Inocula were administered intradermally in the left hind footpad at the dose of 105 TCID50 for New Zealand White rabbits (NZWR) infected with WNVNSW2011 and MVE1-51, or 105 PFU for cottontail rabbits (CTR) infected with WNVNSW2011 and WNVTX8667

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Summary

Introduction

West Nile virus (WNV) is an important re-emerging neurotropic arbovirus, that continues to cause severe outbreaks world-wide. The majority of WNV infections in humans and horses, the incidental hosts of the transmission cycle, is non-lethal and subclinical [1,2,3,4,5]. The reported mortality rate in humans and horses from neuroinvasive WNV disease is

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