Abstract

We describe an assay procedure to quantitate relative DI resistance of a variety of DI particle resistant (Sdi −) mutants of vesicular stomatitis virus (VSV). We show that numerous diverse Sdi − mutants of VSV are selected continuously in a stepwise manner during persistent infections, and also during serial undiluted lytic passages initiated with cloned virus. Concurrently with the successive appearance and disappearance of different Sdi − mutants of infectious VSV, new DI particle types with altered interference properites also appear and disappear, resulting in rapid “coevolution” of virus and DI particle populations. Complementation tests with Sdi − mutants indicate that mutations in at least two different virus factors (presumably associated with replication-encapsidation) can give rise to Sdi − mutants. Interference studies with chimeric DI particles indicate that DI particle template RNA rather than DI particle protein determines the interference properties of DI particles interacting with Sdi − and Sdi + mutants of helper virus.

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