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The Large Marseillevirus Explores Different Entry Pathways by Forming Giant Infectious Vesicles
Thalita Souza Arantes1, Rodrigo Araújo Lima Rodrigues1, Ludmila Karen Dos Santos Silva1
1Department of Microbiology, Institute of Biological Sciences, Unviversidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Marseillevirus marseillevirus (MsV), a giant virus, replicates in amoebas by forming large vesicles that trigger phagocytosis. This unusual mechanism bypasses the typical >500 nm size requirement for giant virus entry.
Area of Science:
- Virology
- Cell Biology
- Microbiology
Background:
- Giant viruses typically require amoebal phagocytosis for replication, a process usually triggered by particles >500 nm.
- Marseillevirus marseillevirus (MsV) is an unusual giant virus that replicates in Acanthamoeba despite having a smaller capsid size (~250 nm).
Purpose of the Study:
- To investigate the replication cycle of Marseillevirus marseillevirus (MsV) in Acanthamoeba.
- To elucidate the mechanism by which MsV initiates its replication despite not meeting the typical size requirement for phagocytosis.
Main Methods:
- Virological assays
- Molecular assays
- Microscopic analyses (immunofluorescence, scanning electron microscopy, transmission electron microscopy)
Main Results:
- MsV forms giant vesicles containing numerous viral particles, enclosed by membranes from the amoebal endoplasmic reticulum.
- These giant vesicles stimulate amoebal phagocytosis via an acidification-independent process.
- MsV entry can occur through phagocytosis of grouped particles or an endosome-stimulated pathway triggered by single particles.
Conclusions:
- MsV utilizes a novel replication strategy involving the formation of infective giant vesicles.
- This mechanism allows MsV to infect Acanthamoeba without fulfilling the conventional >500 nm size prerequisite for giant virus phagocytosis.
- This study reports, for the first time, the formation of giant infective vesicles associated with a large DNA virus.
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