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Updated: Aug 14, 2026

Arbovirus Infections As Screening Tools for the Identification of Viral Immunomodulators and Host Antiviral Factors
Published on: September 13, 2018
Mutational changes in the vesicular stomatitis virus glycoprotein affect the requirement of carbohydrate in
Abstract:
The role of carbohydrate in the morphogenesis of vesicular stomatitis virus was studied, using the antibiotic tunicamycin to inhibit glycosylation. It has been reported previously (Gibson et al., J. Biol. Chem. 254:3600-3607, 1979) that the San Juan strain of vesicular stomatitis virus requires carbohydrate for efficient migration of the glycoprotein (G) to the cell surface and for virion formation, whereas the prototype or Orsay strain of vesicular stomatitis virus is less stringent in its carbohydrate requirement at 30 degrees C. However, there are many differences between the two strains. We found that mutational changes within the G protein of the same strain of virus (prototype or Orsay) alters the requirement for carbohydrate at 30 degrees C. Group V or G protein mutants tsO45 and tsO44, like their prototype parent, did not require carbohydrate for efficient morphogenesis. In contrast, the G protein of another group V mutant, tsO110, was totally dependent upon carbohydrate addition for migration to the cell surface. Furthermore, no tsO110 particles were released in the absence of glycosylation. The wild-type prototype strain did require carbohydrate at 39.5 degrees C for insertion of the G protein into the plasma membrane and virion formation. However, a pseudorevertant of tsO44 (tsO44R), unlike the prototype parent, no longer exhibited this temperature-sensitive requirement for carbohydrate. At 39.5 degrees C in the presence of tunicamycin, tsO44R-infected cells released normal yields of particles and the unglycosylated G reached the cell surface very efficiently. In contrast to tsO110, which absolutely requires carbohydrate, mutational change in the tsO44R G protein has eliminated the requirement for carbohydrate. Thus, simple mutational changes, as opposed to many changes in the molecule, are sufficient to alter the carbohydrate requirement.
Insights
Simple mutations in vesicular stomatitis virus glycoprotein alter carbohydrate needs for virus formation. Some mutants, unlike wild-type virus, do not require glycosylation for efficient morphogenesis and particle release.
Area of Science:
- Virology
- Molecular Biology
- Biochemistry
Background:
- Vesicular stomatitis virus (VSV) morphogenesis is influenced by carbohydrate, with different strains exhibiting varying requirements.
- Previous studies indicated strain-specific differences in VSV glycoprotein (G) glycosylation needs for cell surface migration and virion formation.
Purpose of the Study:
- To investigate the role of carbohydrate in VSV morphogenesis.
- To determine how specific mutations in the G protein affect its requirement for glycosylation.
Main Methods:
- Utilized the antibiotic tunicamycin to inhibit glycosylation in VSV-infected cells.
- Compared the morphogenesis and G protein behavior of wild-type VSV strains and various G protein mutants (tsO45, tsO44, tsO110, tsO44R) under different temperature and tunicamycin conditions.
Main Results:
- Mutations within the G protein of the prototype VSV strain altered its carbohydrate requirement for morphogenesis at 30°C.
- Mutants tsO45 and tsO44 showed no carbohydrate requirement, while tsO110 was completely dependent on glycosylation for G protein cell surface migration and particle release.
- Wild-type VSV required carbohydrate at 39.5°C, but the tsO44R pseudorevertant eliminated this temperature-sensitive requirement, efficiently producing particles with unglycosylated G protein.
Conclusions:
- Specific mutations in the VSV G protein can significantly alter or even eliminate its requirement for glycosylation during morphogenesis.
- Simple mutational changes are sufficient to modify the carbohydrate dependency of viral glycoprotein processing and virion assembly.
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