Flavivirus NS1 protein in infected host sera enhances viral acquisition by mosquitoes

Nat Microbiol. 2016 Jun 20;1(9):16087. doi: 10.1038/nmicrobiol.2016.87.

Abstract

The arbovirus life cycle involves viral transfer between a vertebrate host and an arthropod vector, and acquisition of virus from an infected mammalian host by a vector is an essential step in this process. Here, we report that flavivirus nonstructural protein-1 (NS1), which is abundantly secreted into the serum of an infected host, plays a critical role in flavivirus acquisition by mosquitoes. The presence of dengue virus (DENV) and Japanese encephalitis virus NS1s in the blood of infected interferon-α and γ receptor-deficient mice (AG6) facilitated virus acquisition by their native mosquito vectors because the protein enabled the virus to overcome the immune barrier of the mosquito midgut. Active immunization of AG6 mice with a modified DENV NS1 reduced DENV acquisition by mosquitoes and protected mice against a lethal DENV challenge, suggesting that immunization with NS1 could reduce the number of virus-carrying mosquitoes as well as the incidence of flaviviral diseases. Our study demonstrates that flaviviruses utilize NS1 proteins produced during their vertebrate phases to enhance their acquisition by vectors, which might be a result of flavivirus evolution to adapt to multiple host environments.

MeSH terms

  • Animals
  • Cell Line
  • Culicidae / immunology
  • Culicidae / virology*
  • Dengue Virus / genetics*
  • Drosophila
  • Encephalitis Virus, Japanese / genetics*
  • Female
  • Flavivirus / genetics
  • Flavivirus / immunology*
  • Flavivirus / metabolism
  • Flavivirus Infections / immunology
  • Flavivirus Infections / transmission*
  • Flavivirus Infections / virology
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Receptors, Interferon / genetics
  • Specific Pathogen-Free Organisms
  • Viral Nonstructural Proteins / blood
  • Viral Nonstructural Proteins / genetics
  • Viral Nonstructural Proteins / immunology*
  • Virion

Substances

  • NS1 protein, Flavivirus
  • Receptors, Interferon
  • Viral Nonstructural Proteins