Key result
Cell lines expressing minor glycoproteins successfully rescued disabled Equine arteritis virus mutants, initiating a self-limiting single cycle of replication in non-complementing cells.
Answers are grounded in this paper and cite their sources.
Disabled infectious single-cycle (DISC) arteriviruses can be generated using complementing cell lines, offering potential for fundamental research and vaccine development.
Equine arteritis virus (EAV) contains seven structural proteins that are all required to produce infectious progeny. Alphavirus-based expression vectors have been generated for each of these proteins to explore the possibilities for their constitutive expression in cell lines. This approach was successful for minor glycoproteins GP(2b), GP(3) and GP(4) and for the E protein. Subsequently, it was demonstrated that cell lines expressing these proteins could rescue EAV mutants that were disabled in the expression of the corresponding gene, resulting in the production of virus particles carrying the mutant genome. This system was particularly efficient for GP(2b)- and GP(4)-knockout mutants. Upon infection of non-complementing cells with these mutants, a self-limiting single cycle of replication was initiated, resulting in the expression of all but one of the viral proteins. These disabled infectious single-cycle (DISC) arteriviruses can also be used to express foreign sequences and are potentially useful in both fundamental research and vaccine development.
No takes yet. Share an insight, caveat, or question.
Zevenhoven-Dobbe et al. (2004) studied Equine arteritis virus (EAV). Complementing cell lines expressing minor structural glycoproteins vs. Non-complementing cells was evaluated on Rescue of EAV mutants and production of virus particles. Cell lines expressing minor glycoproteins successfully rescued disabled Equine arteritis virus mutants, initiating a self-limiting single cycle of replication in non-complementing cells.
Synapse has enriched 10 related papers. Consider them for comparative context: