Mumps Virus Is Released from the Apical Surface of Polarized Epithelial Cells, and the Release Is Facilitated by a Rab11-Mediated Transport System
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Updated: Apr 3, 2026

Analyzing the Function of Small GTPases by Microinjection of Plasmids into Polarized Epithelial Cells
Published on: May 31, 2011
Hiroshi Katoh1, Yuichiro Nakatsu2, Toru Kubota2
1Department of Virology III, National Institute of Infectious Diseases, Tokyo, Japan kato0704@nih.go.jp.
Unlabelled:
Mumps virus (MuV) is an airborne virus that causes a systemic infection in patients. In vivo, the epithelium is a major replication site of MuV, and thus, the mode of MuV infection of epithelial cells is a subject of interest. Our data in the present study showed that MuV entered polarized epithelial cells via both the apical and basolateral surfaces, while progeny viruses were predominantly released from the apical surface. In polarized cells, intracellular transport of viral ribonucleoprotein (vRNP) complexes was dependent on Rab11-positive endosomes, and vRNP complexes were transported to the apical membrane. Expression of a dominant negative form of Rab11 (Rab11S25N) reduced the progeny virus release in polarized cells but not in nonpolarized cells. Although in this way these effects were correlated with cell polarity, Rab11S25N did not modulate the direction of virus release from the apical surface. Therefore, our data suggested that Rab11 is not a regulator of selective apical release of MuV, although it acts as an activator of virus release from polarized epithelial cells. In addition, our data and previous studies on Sendai virus, respiratory syncytial virus, and measles virus suggested that selective apical release from epithelial cells is used by many paramyxoviruses, even though they cause either a systemic infection or a local respiratory infection.
Importance:
Mumps virus (MuV) is the etiological agent of mumps and causes a systemic infection. However, the precise mechanism by which MuV breaks through the epithelial barriers and achieves a systemic infection remains unclear. In the present study, we show that the entry of MuV is bipolar, while the release is predominantly from the apical surface in polarized epithelial cells. In addition, the release of progeny virus was facilitated by a Rab11-positive recycling endosome and microtubule network. Our data provide important insights into the mechanism of transmission and pathogenesis of MuV.
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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