Adaptation of reovirus to growth in the presence of protease inhibitor E64 segregates with a mutation in the carboxy terminus of viral outer-capsid protein sigma3

J Virol. 2001 Apr;75(7):3197-206. doi: 10.1128/JVI.75.7.3197-3206.2001.

Abstract

Reovirus virions are internalized into cells by receptor-mediated endocytosis. Within the endocytic compartment, the viral outer capsid undergoes acid-dependent proteolysis leading to degradation of sigma3 protein and proteolytic cleavage of micro1/micro1C protein. E64 is a specific inhibitor of cysteine-containing proteases that blocks disassembly of reovirus virions. To identify domains in reovirus proteins that influence susceptibility to E64-mediated inhibition of disassembly, we selected variant viruses by serial passage of strain type 3 Dearing (T3D) in murine L929 cells treated with E64. E64-adapted variant viruses (D-EA viruses) produced 7- to 17-fold-greater yields than T3D did after infection of cells treated with 100 microM E64. Viral genes that segregate with growth of D-EA viruses in the presence of E64 were identified by using reassortant viruses isolated from independent crosses of E64-sensitive strain type 1 Lang and two prototype D-EA viruses. Growth of reassortant viruses in the presence of E64 segregated with the S4 gene, which encodes outer-capsid protein sigma3. Sequence analysis of S4 genes of three D-EA viruses isolated from independent passage series revealed a common tyrosine-to-histidine mutation at amino acid 354 in the deduced amino acid sequence of sigma3. Proteolysis of D-EA virions by endocytic protease cathepsin L occurred with faster kinetics than proteolysis of wild-type T3D virions. Treatment of D-EA virions, but not T3D virions, with cathepsin D resulted in proteolysis of sigma3, a property that also was found to segregate with the D-EA S4 gene. These results indicate that a region in sigma3 protein containing amino acid 354 influences susceptibility of sigma3 to proteolysis during reovirus disassembly.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adaptation, Physiological
  • Animals
  • Capsid / chemistry
  • Capsid / physiology*
  • Capsid Proteins*
  • Cathepsin D / pharmacology
  • Cathepsin L
  • Cathepsins / pharmacology
  • Cysteine Endopeptidases
  • Cysteine Proteinase Inhibitors / pharmacology*
  • Endopeptidases*
  • L Cells
  • Leucine / analogs & derivatives*
  • Leucine / pharmacology*
  • Mice
  • Mutation
  • RNA-Binding Proteins*
  • Reoviridae / drug effects
  • Reoviridae / genetics
  • Reoviridae / physiology*
  • Structure-Activity Relationship
  • Virus Assembly

Substances

  • Capsid Proteins
  • Cysteine Proteinase Inhibitors
  • RNA-Binding Proteins
  • sigma protein 3, Reovirus
  • Cathepsins
  • Endopeptidases
  • Cysteine Endopeptidases
  • Cathepsin L
  • Ctsl protein, mouse
  • Cathepsin D
  • Leucine
  • E 64