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Updated: Apr 25, 2026

Dissecting Host-virus Interaction in Lytic Replication of a Model Herpesvirus
Published on: October 7, 2011
Cell migration is another player of the minute virus of mice infection
Pierre O Garcin1, Nelly Panté1
1Department of Zoology, University of British Columbia, 6270 University Boulevard, Vancouver, British Columbia, Canada V6T 1Z4.
Abstract:
The parvovirus minute virus of mice, prototype strain (MVMp), preferentially infects and kills cancer cells. This intrinsic MVMp oncotropism may depend in part on the early stages of MVMp infection. To test this hypothesis, we investigated the early events of MVMp infection in mouse LA9 fibroblasts and a highly invasive mouse mammary tumor cell line derived from polyomavirus middle T antigen-mediated transformation. Using a combination of fluorescence and electron microscopy, we found that various parameters of the cell migration process affect MVMp infection. We show that, after binding to the plasma membrane, MVMp particles rapidly cluster at the leading edge of migrating cells, which exhibit higher levels of MVMp uptake than non-motile cells. Moreover, promoting cell migration on a fibronectin matrix increased MVMp infection, and induction of epithelial-mesenchymal transition allowed MVMp replication in non-permissive epithelial cells. Hence, we propose that cell migration influences the early stages of MVMp infection.
Insights
Minute virus of mice (MVMp) preferentially infects cancer cells. Cell migration enhances MVMp uptake and replication, suggesting migration influences early viral infection stages.
Area of Science:
- Virology
- Cell Biology
- Cancer Research
Background:
- Minute virus of mice (MVMp) exhibits oncotropism, preferentially infecting and killing cancer cells.
- The early stages of MVMp infection are hypothesized to contribute to its cancer-targeting ability.
Purpose of the Study:
- To investigate the influence of cell migration on the early events of MVMp infection.
- To determine if MVMp infection is affected by cellular motility and the epithelial-mesenchymal transition (EMT).
Main Methods:
- Utilized fluorescence and electron microscopy to observe MVMp infection dynamics.
- Examined MVMp infection in motile and non-motile mouse fibroblasts and a mammary tumor cell line.
- Investigated the effect of fibronectin matrix and EMT induction on MVMp infection and replication.
Main Results:
- MVMp particles rapidly cluster at the leading edge of migrating cells after binding.
- Migrating cells demonstrated higher MVMp uptake compared to non-motile cells.
- Enhanced cell migration on fibronectin and EMT induction increased MVMp infection and allowed replication in non-permissive cells.
Conclusions:
- Cell migration significantly influences the early stages of MVMp infection.
- Cellular motility and EMT are critical factors affecting MVMp's ability to infect and replicate.
- These findings provide insights into the mechanisms underlying MVMp oncotropism.
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