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Nuclear F-actin is required for AcMNPV nucleocapsid morphogenesis
1Department of Plant and Microbial Biology, University of California, Berkeley, California 94720-3102, USA.
Virology
|November 2, 1999
Summary
Filamentous actin (F-actin) is crucial for Autographa californica M nucleopolyhedrovirus (AcMNPV) assembly in host cells. Disrupting F-actin with Cytochalasin D (CD) halts virus production, highlighting F-actin
Area of Science:
- Molecular Virology
- Cell Biology
- Insect Pathology
Background:
- Filamentous actin (F-actin) colocalizes with the major capsid protein of Autographa californica M nucleopolyhedrovirus (AcMNPV) during nucleocapsid assembly in infected lepidopteran host cells.
- Cytochalasin D (CD), an actin polymerization inhibitor, prevents the assembly of progeny AcMNPV, indicating a potential role for nuclear F-actin in viral morphogenesis.
Purpose of the Study:
- To investigate the essential role of nuclear F-actin in the morphogenesis of Autographa californica M nucleopolyhedrovirus (AcMNPV).
- To provide direct evidence for the necessity of F-actin in AcMNPV nucleocapsid assembly.
Main Methods:
- Utilized Cytochalasin D (CD) to disrupt actin filaments in infected lepidopteran host cells.
- Engineered two AcMNPV recombinants expressing either wild-type or CD-resistant actin at equivalent rates.
- Assessed the differential sensitivity of these recombinants to CD treatment.
Main Results:
- AcMNPV nucleocapsid assembly was observed to colocalize with F-actin within the nuclei of infected host cells.
- CD treatment significantly inhibited progeny AcMNPV assembly, confirming the importance of F-actin.
- AcMNPV recombinants expressing CD-resistant actin exhibited reduced sensitivity to CD compared to those with wild-type actin.
Conclusions:
- Nuclear F-actin is essential for the morphogenesis of Autographa californica M nucleopolyhedrovirus (AcMNPV) nucleocapsids.
- The dependence of AcMNPV on nuclear F-actin is a unique characteristic among intracellular pathogens.
- This F-actin requirement may function as a significant host range factor for AcMNPV.