Direct entry of rabies virus into the central nervous system without prior local replication

J Virol. 1991 May;65(5):2736-8. doi: 10.1128/JVI.65.5.2736-2738.1991.

Abstract

Rabies virus pathogenesis was studied in a mouse model by inoculation of the masseter muscle. At different intervals, the masseter muscle, trigeminal ganglia, and brain were analyzed for virus-specific RNA with a polymerase chain reaction assay, which revealed that as early as 18 h postinfection (p.i.), virus-specific RNA was present in the trigeminal ganglia, and at 24 h p.i., viral RNA was identified in the brain stem. Analysis of the masseter muscle demonstrated virus at 1 h p.i. but no virus-specific RNA between 6 and 30 h p.i., indicating that virus invaded the nerve ending directly, without prior replication in the muscle. At 36 h p.i., viral RNA was detected again in the masseter muscle. Selective amplification of plus- and minus-strand RNA isolated from the masseter muscle at 96 h p.i. revealed that the majority of the rabies virus-specific RNA was in the positive sense, suggesting virus replication in muscle tissue during late stages of infection.

Publication types

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

MeSH terms

  • Animals
  • Antibodies, Monoclonal / immunology
  • Base Sequence
  • Central Nervous System / microbiology*
  • Female
  • Mice
  • Mice, Inbred ICR
  • Molecular Sequence Data
  • Muscles / microbiology
  • Neutralization Tests
  • Oligonucleotide Probes
  • Polymerase Chain Reaction
  • RNA, Viral / analysis
  • Rabies / microbiology*
  • Rabies virus / genetics
  • Rabies virus / immunology
  • Rabies virus / pathogenicity*
  • Virus Replication

Substances

  • Antibodies, Monoclonal
  • Oligonucleotide Probes
  • RNA, Viral