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Updated: May 23, 2026

Rapid, Seamless Generation of Recombinant Poxviruses using Host Range and Visual Selection
Published on: May 24, 2020
Poxvirus host cell entry
Florian Ingo Schmidt1, Christopher Karl Ernst Bleck, Jason Mercer
1Institute of Biochemistry, ETH Zurich, Schafmattstr. 18, 8093 Zurich, Switzerland.
Abstract:
Poxviruses are characterized by their large size, complex composition, and cytoplasmic life cycle. They produce two types of infectious particles: mature virions (MVs) and extracellular virions (EVs). Both MVs and EVs of vaccinia virus, the model poxvirus, take advantage of host cell endocytosis for internalization: they activate macropinocytosis-the most suitable form of endocytosis for large particles. Although largely dependent on the same cellular machinery, MV and EV entry differs with regard to the mechanisms used to trigger macropinocytosis and to undergo fusion. While EVs have to shed an additional membrane to expose the fusion complex, MV fusion requires the inactivation of fusion inhibitory proteins absent in EVs. This review highlights recent advances in the understanding of poxvirus MV and EV cell entry.
Insights
Poxviruses like vaccinia virus use macropinocytosis for cell entry. This review details differences in how mature virions (MVs) and extracellular virions (EVs) enter cells and fuse.
Area of Science:
- Virology
- Cell Biology
- Infectious Diseases
Background:
- Poxviruses are large, complex DNA viruses with a cytoplasmic life cycle.
- They generate two infectious forms: mature virions (MVs) and extracellular virions (EVs).
- Vaccinia virus serves as a model organism for studying poxvirus entry mechanisms.
Purpose of the Study:
- To review recent advances in understanding poxvirus cell entry.
- To compare and contrast the entry mechanisms of MVs and EVs.
- To highlight differences in macropinocytosis activation and membrane fusion.
Main Methods:
- Literature review of recent studies on poxvirus cell entry.
- Comparative analysis of MV and EV internalization pathways.
- Examination of molecular mechanisms governing viral fusion.
Main Results:
- Both MV and EV entry depend on host cell macropinocytosis.
- MV and EV entry differ in macropinocytosis triggering and fusion processes.
- EVs require shedding an extra membrane, while MVs must overcome fusion inhibitors.
Conclusions:
- Poxvirus entry is a complex process involving distinct mechanisms for MV and EV.
- Understanding these differences is crucial for developing antiviral strategies.
- Recent research provides new insights into poxvirus-host cell interactions.
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