Establishing a small animal model for evaluating protective immunity against mumps virus

PLoS One. 2017 Mar 31;12(3):e0174444. doi: 10.1371/journal.pone.0174444. eCollection 2017.

Abstract

Although mumps vaccines have been used for several decades, protective immune correlates have not been defined. Recently, mumps outbreaks have occurred in vaccinated populations. To better understand the causes of the outbreaks and to develop means to control outbreaks in mumps vaccine immunized populations, defining protective immune correlates will be critical. Unfortunately, no small animal model for assessing mumps immunity exists. In this study, we evaluated use of type I interferon (IFN) alpha/beta receptor knockout mice (IFN-α/βR-/-) for such a model. We found these mice to be susceptible to mumps virus administered intranasally and intracranially. Passive transfer of purified IgG from immunized mice protected naïve mice from mumps virus infection, confirming the role of antibody in protection and demonstrating the potential for this model to evaluate mumps immunity.

MeSH terms

  • Animals
  • Antibodies, Viral / immunology
  • Antibodies, Viral / metabolism
  • Chlorocebus aethiops
  • Disease Models, Animal*
  • Enzyme-Linked Immunosorbent Assay
  • Immunoglobulin G / metabolism
  • Kinetics
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Models, Animal
  • Mumps / immunology
  • Mumps / metabolism
  • Mumps / prevention & control*
  • Mumps / virology*
  • Mumps virus / immunology*
  • Mumps virus / pathogenicity*
  • Receptor, Interferon alpha-beta / genetics
  • Receptor, Interferon alpha-beta / metabolism
  • Vero Cells

Substances

  • Antibodies, Viral
  • Immunoglobulin G
  • Receptor, Interferon alpha-beta