A hamster-derived West Nile virus isolate induces persistent renal infection in mice

PLoS Negl Trop Dis. 2013 Jun 13;7(6):e2275. doi: 10.1371/journal.pntd.0002275. Print 2013.

Abstract

Background: West Nile virus (WNV) can persist long term in the brain and kidney tissues of humans, non-human primates, and hamsters. In this study, mice were infected with WNV strain H8912, previously cultured from the urine of a persistently infected hamster, to determine its pathogenesis in a murine host.

Methodology/principal findings: We found that WNV H8912 was highly attenuated for neuroinvasiveness in mice. Following a systemic infection, viral RNA could be detected quickly in blood and spleen and much later in kidneys. WNV H8912 induced constitutive IL-10 production, upregulation of IFN-β and IL-1β expression, and a specific IgM response on day 10 post-infection. WNV H8912 persisted preferentially in kidneys with mild renal inflammation, and less frequently in spleen for up to 2.5 months post infection. This was concurrent with detectable serum WNV-specific IgM and IgG production. There were also significantly fewer WNV- specific T cells and lower inflammatory responses in kidneys than in spleen. Previous studies have shown that systemic wild-type WNV NY99 infection induced virus persistence preferentially in spleen than in mouse kidneys. Here, we noted that splenocytes of WNV H8912-infected mice produced significantly less IL-10 than those of WNV NY99-infected mice. Finally, WNV H8912 was also attenuated in neurovirulence. Following intracranial inoculation, WNV persisted in the brain at a low frequency, concurrent with neither inflammatory responses nor neuronal damage in the brain.

Conclusions: WNV H8912 is highly attenuated in both neuroinvasiveness and neurovirulence in mice. It induces a low and delayed anti-viral response in mice and preferentially persists in the kidneys.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animal Structures / virology
  • Animals
  • Antibodies, Viral / blood
  • Chronic Disease
  • Cricetinae
  • Cytokines / metabolism
  • Disease Models, Animal
  • Female
  • Immunoglobulin G / blood
  • Immunoglobulin M / blood
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Nephritis / pathology
  • Nephritis / virology*
  • RNA, Viral / genetics
  • RNA, Viral / isolation & purification
  • West Nile Fever / pathology
  • West Nile Fever / virology*
  • West Nile virus / isolation & purification*
  • West Nile virus / pathogenicity

Substances

  • Antibodies, Viral
  • Cytokines
  • Immunoglobulin G
  • Immunoglobulin M
  • RNA, Viral