There currently is little known about the genetic and biological functions
of avian reovirus (ARV), an atypical member of the family Reoviridae and th
e prototype of all nonenveloped viruses that induce syncytia formation. In
this study, we created ARV temperature-sensitive (ts) mutants by chemical m
utagenesis of ARV strain 138. We developed a novel efficiency of lysis (EOL
) screening technique and used it and the classical efficiency of plating (
EOP) assay to identify 17 ARV ts mutants. Pairwise mixed infections of thes
e mutants and evaluation of recombinant progeny ts status led to their orga
nization into seven recombination groups. This indicates that these new gro
ups of mutants represent the majority of the ARV genome. To phenotypically
characterize the ts mutants, progeny double-stranded RNA (dsRNA) produced a
t permissive and nonpermissive temperature was measured. Some mutants were
capable of dsRNA synthesis at the restrictive temperature (RNA(+)), which i
ndicates the effects of their ts lesions occur after RNA replication. Most
mutants were RNA(-), which suggests their mutations affect stages in Viral
replication that precede progeny genome synthesis. (C) 2001 Academic Press.