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Studies on heterotypic interference between influenza A and B viruses: a differential inhibition of the synthesis of viral proteins and RNAs.

Abstract
Mixed infection of MDCK cells with influenza A and influenza B viruses leads to a reduction in the rate of synthesis of haemagglutinin (HA) and nucleoprotein (NP) as compared to their rate of synthesis in cells separately infected with these viruses. The reduction is much stronger for influenza A virus proteins. The synthesis of the nonstructural NS1 protein of both viruses is relatively resistant to the heterotypic interference. The synthesis of virus-specific mRNAs exhibits the same pattern: the formation of the transcripts of HA and NP genes is much more drastically reduced than the synthesis of NS gene transcripts. The effect is strongly dependent on the multiplicity of infection and on the ratio of influenza A and B viruses in the inoculum. Primary transcription in the presence of cycloheximide is almost unchanged in doubly infected cells as compared to single infection, and no indication of differential inhibition has been observed. The results are discussed in connection with the mechanism of heterotypic interference and the regulation of influenza virus protein synthesis.
AuthorsN V Kaverin, N L Varich, E I Sklyanskaya, T V Amvrosieva, J Petrik, T C Vovk
JournalThe Journal of general virology (J Gen Virol) Vol. 64 (Pt 10) Pg. 2139-46 (Oct 1983) ISSN: 0022-1317 [Print] England
PMID6619801 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Hemagglutinins, Viral
  • Nucleoproteins
  • RNA, Messenger
  • RNA, Viral
  • Viral Proteins
Topics
  • Animals
  • Chick Embryo
  • Chromatography, Agarose
  • Hemagglutinins, Viral
  • Influenza A virus (metabolism)
  • Nucleic Acid Hybridization
  • Nucleoproteins (antagonists & inhibitors)
  • Orthomyxoviridae (metabolism)
  • RNA, Messenger (antagonists & inhibitors)
  • RNA, Viral (analysis, antagonists & inhibitors)
  • Transcription, Genetic
  • Viral Interference
  • Viral Proteins (analysis, antagonists & inhibitors)

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