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Inhibition of Sindbis virus release by media of low ionic strength: an electron microscope study
Abstract:
Release of Sindbis virus from infected cells is inhibited by lowering the ionic strength of the medium. To determine the nature of the inhibited step, we examined, by electron microscopy, both freeze-etched and thin-sectioned preparations which had been fixed with either glutaraldehyde or formaldehyde. Inhibitory medium had two different effects on Sindbis virus release: virus budding was partially inhibited, and those virions which did mature were precipitated on the surface of the cell. Freeze-etched, inhibited cells showed very few viral buds. After shift to normal medium, the number of budding virions increased dramatically, far exceeding the quantity found in normal controls. Thus, low ionic strength medium clearly inhibited an early stage of virus maturation. The results were the same regardless of the fixative. Thin sections of glutaraldehyde-fixed, inhibited cells contained large extracellular aggregates of mature virus which were not present in similar, formaldehyde-fixed preparations. Fixation of radioactively-labeled, inhibited cultures revealed that approximately half of the virus that could be released from inhibited cells by raising the ionic strength of the medium could also be released by formaldehyde, but not by glutaraldehyde. This fraction probably represents mature virus attached to the cell surface by the ionic conditions.
Insights
Lowering medium ionic strength inhibits Sindbis virus release by blocking early maturation. Virus budding is reduced, and mature virions aggregate on the cell surface.
Area of Science:
- Virology
- Cell Biology
- Biochemistry
Background:
- Sindbis virus (SINV) is an enveloped alphavirus.
- Virus release from infected cells is a critical step in the viral life cycle.
Purpose of the Study:
- To investigate the specific stage of Sindbis virus release inhibited by low ionic strength medium.
- To characterize the effects of ionic strength on virus maturation and cell surface association.
Main Methods:
- Electron microscopy (freeze-etching and thin-sectioning) of infected cells.
- Fixation with glutaraldehyde and formaldehyde.
- Analysis of virus budding and extracellular virion aggregation.
Main Results:
- Low ionic strength partially inhibited virus budding and caused mature virions to aggregate on the cell surface.
- Freeze-etching revealed significantly fewer viral buds in inhibited cells.
- Formaldehyde fixation, unlike glutaraldehyde, released cell-surface-associated virus, indicating ionic-dependent attachment.
Conclusions:
- Low ionic strength medium inhibits an early stage of Sindbis virus maturation.
- Ionic conditions play a crucial role in the release and/or egress of mature Sindbis virus particles from infected cells.