Mumps Virus Is Released from the Apical Surface of Polarized Epithelial Cells, and the Release Is Facilitated by a

Hiroshi Katoh1, Yuichiro Nakatsu2, Toru Kubota2

  • 1Department of Virology III, National Institute of Infectious Diseases, Tokyo, Japan kato0704@nih.go.jp.

Journal of Virology
|September 18, 2015
PubMed
Abstract

Insights

Mumps virus enters and exits polarized epithelial cells through different surfaces, with Rab11 endosomes facilitating progeny virus release. This study clarifies mumps virus transmission and pathogenesis mechanisms.

Area of Science:

  • Virology
  • Cell Biology
  • Epithelial Biology

Background:

  • Mumps virus (MuV) causes systemic infection, but its epithelial barrier penetration mechanism is unclear.
  • Epithelial cells are a primary site for MuV replication in vivo.
  • Understanding MuV infection of epithelial cells is crucial for its transmission and pathogenesis.

Purpose of the Study:

  • To investigate the entry and release mechanisms of Mumps virus in polarized epithelial cells.
  • To determine the role of Rab11-positive endosomes and the microtubule network in MuV replication and release.
  • To elucidate the pathways of MuV transmission and pathogenesis.

Main Methods:

  • Utilized polarized epithelial cell models to study MuV infection.
  • Investigated MuV entry via apical and basolateral surfaces.
  • Analyzed intracellular transport of viral ribonucleoprotein (vRNP) complexes using Rab11-positive endosomes.
  • Assessed the impact of dominant-negative Rab11 (Rab11S25N) on virus release.

Main Results:

  • MuV entered polarized epithelial cells from both apical and basolateral surfaces.
  • Progeny MuV were predominantly released from the apical surface.
  • Intracellular transport of vRNP complexes to the apical membrane depended on Rab11-positive endosomes.
  • Rab11S25N expression reduced progeny virus release in polarized cells, but not nonpolarized cells.
  • Rab11 facilitated virus release but did not regulate the direction of apical release.

Conclusions:

  • MuV exhibits bipolar entry and predominantly apical release from polarized epithelial cells.
  • Rab11-positive endosomes and microtubules are essential for MuV release from polarized epithelial cells.
  • Selective apical release is a common strategy for paramyxoviruses, including MuV, facilitating transmission.

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