Skip to main content
Journal of Virology logoLink to Journal of Virology
. 1997 Mar;71(3):2138–2145. doi: 10.1128/jvi.71.3.2138-2145.1997

Segment-specific noncoding sequences of the influenza virus genome RNA are involved in the specific competition between defective interfering RNA and its progenitor RNA segment at the virion assembly step.

T Odagiri 1, M Tashiro 1
PMCID: PMC191316  PMID: 9032347

Abstract

The generation of influenza A virus defective interfering (DI) particles was studied by using an NS2 mutant which produces, in a single cycle of virus replication, a large amount of DI particles lacking the PA polymerase gene. The decrease in PA gene replication has been shown to occur primarily at the cRNA synthesis step, with preferential amplification of PA DI RNA species present in a marginal amount in the virus stock. In addition, at the assembly step the PA DI RNAs were preferentially incorporated into virions, resulting in selective reduction in the packaging of the PA gene into virions. Similarly, in cells dually infected with the NS2 mutant and wild-type viruses, packaging of the wild-type PA gene was also greatly suppressed. In contrast, incorporation of other RNA segments, i.e., the PB2 and NS genes, was not affected, suggesting that the PA DI RNAs competed only with the PA gene in a segment-specific manner. Experiments involving rescue of recombinant chloramphenicol acetyltransferase (CAT) RNA flanked by the noncoding regions of the PA (PA/CAT RNA) and PB2 (PB2/CAT RNA) genes into viral particles showed that only PA/CAT RNA was not rescued by infection with the NS2 mutant virus containing the PA DI RNAs. However, recombinant PA/CAT RNA in which either the 3' or 5' noncoding region was replaced with that of the PB2 gene was rescued by the NS2 mutant. These results suggest that the noncoding regions of the PA gene are responsible for the competition with PA DI RNA species at the virus assembly step and that coexistence of the both noncoding regions would be a prerequisite for this phenomenon. Decreased packaging of the progenitor RNA by the DI RNA, in addition to the suppression of cRNA synthesis, is likely involved in the production of DI particles.

Full Text

The Full Text of this article is available as a PDF (589.4 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Barclay W. S., Palese P. Influenza B viruses with site-specific mutations introduced into the HA gene. J Virol. 1995 Feb;69(2):1275–1279. doi: 10.1128/jvi.69.2.1275-1279.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bergmann M., Muster T. The relative amount of an influenza A virus segment present in the viral particle is not affected by a reduction in replication of that segment. J Gen Virol. 1995 Dec;76(Pt 12):3211–3215. doi: 10.1099/0022-1317-76-12-3211. [DOI] [PubMed] [Google Scholar]
  3. Chomczynski P., Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem. 1987 Apr;162(1):156–159. doi: 10.1006/abio.1987.9999. [DOI] [PubMed] [Google Scholar]
  4. Desselberger U., Racaniello V. R., Zazra J. J., Palese P. The 3' and 5'-terminal sequences of influenza A, B and C virus RNA segments are highly conserved and show partial inverted complementarity. Gene. 1980 Feb;8(3):315–328. doi: 10.1016/0378-1119(80)90007-4. [DOI] [PubMed] [Google Scholar]
  5. Duhaut S. D., McCauley J. W. Defective RNAs inhibit the assembly of influenza virus genome segments in a segment-specific manner. Virology. 1996 Feb 15;216(2):326–337. doi: 10.1006/viro.1996.0068. [DOI] [PubMed] [Google Scholar]
  6. Enami K., Sato T. A., Nakada S., Enami M. Influenza virus NS1 protein stimulates translation of the M1 protein. J Virol. 1994 Mar;68(3):1432–1437. doi: 10.1128/jvi.68.3.1432-1437.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Enami M., Palese P. High-efficiency formation of influenza virus transfectants. J Virol. 1991 May;65(5):2711–2713. doi: 10.1128/jvi.65.5.2711-2713.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Enami M., Sharma G., Benham C., Palese P. An influenza virus containing nine different RNA segments. Virology. 1991 Nov;185(1):291–298. doi: 10.1016/0042-6822(91)90776-8. [DOI] [PubMed] [Google Scholar]
  9. Fodor E., Pritlove D. C., Brownlee G. G. Characterization of the RNA-fork model of virion RNA in the initiation of transcription in influenza A virus. J Virol. 1995 Jul;69(7):4012–4019. doi: 10.1128/jvi.69.7.4012-4019.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Fodor E., Pritlove D. C., Brownlee G. G. The influenza virus panhandle is involved in the initiation of transcription. J Virol. 1994 Jun;68(6):4092–4096. doi: 10.1128/jvi.68.6.4092-4096.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Fodor E., Seong B. L., Brownlee G. G. Photochemical cross-linking of influenza A polymerase to its virion RNA promoter defines a polymerase binding site at residues 9 to 12 of the promoter. J Gen Virol. 1993 Jul;74(Pt 7):1327–1333. doi: 10.1099/0022-1317-74-7-1327. [DOI] [PubMed] [Google Scholar]
  12. Hirst G. K., Pons M. W. Mechanism of influenza recombination. II. Virus aggregation and its effect on plaque formation by so-called noninfective virus. Virology. 1973 Dec;56(2):620–631. doi: 10.1016/0042-6822(73)90063-9. [DOI] [PubMed] [Google Scholar]
  13. Honda A., Uéda K., Nagata K., Ishihama A. Identification of the RNA polymerase-binding site on genome RNA of influenza virus. J Biochem. 1987 Nov;102(5):1241–1249. doi: 10.1093/oxfordjournals.jbchem.a122163. [DOI] [PubMed] [Google Scholar]
  14. Hsu M. T., Parvin J. D., Gupta S., Krystal M., Palese P. Genomic RNAs of influenza viruses are held in a circular conformation in virions and in infected cells by a terminal panhandle. Proc Natl Acad Sci U S A. 1987 Nov;84(22):8140–8144. doi: 10.1073/pnas.84.22.8140. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Inglis S. C., Carroll A. R., Lamb R. A., Mahy B. W. Polypeptides specified by the influenza virus genome I. Evidence for eight distinct gene products specified by fowl plague virus. Virology. 1976 Oct 15;74(2):489–503. doi: 10.1016/0042-6822(76)90355-x. [DOI] [PubMed] [Google Scholar]
  16. Kaptein J. S., Nayak D. P. Complete nucleotide sequence of the polymerase 3 gene of human influenza virus A/WSN/33. J Virol. 1982 Apr;42(1):55–63. doi: 10.1128/jvi.42.1.55-63.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Lamb R. A., Choppin P. W. The gene structure and replication of influenza virus. Annu Rev Biochem. 1983;52:467–506. doi: 10.1146/annurev.bi.52.070183.002343. [DOI] [PubMed] [Google Scholar]
  18. Li X., Palese P. Mutational analysis of the promoter required for influenza virus virion RNA synthesis. J Virol. 1992 Jul;66(7):4331–4338. doi: 10.1128/jvi.66.7.4331-4338.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Luytjes W., Krystal M., Enami M., Parvin J. D., Palese P. Amplification, expression, and packaging of foreign gene by influenza virus. Cell. 1989 Dec 22;59(6):1107–1113. doi: 10.1016/0092-8674(89)90766-6. [DOI] [PubMed] [Google Scholar]
  20. McGeoch D., Fellner P., Newton C. Influenza virus genome consists of eight distinct RNA species. Proc Natl Acad Sci U S A. 1976 Sep;73(9):3045–3049. doi: 10.1073/pnas.73.9.3045. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Mena I., Vivo A., Pérez E., Portela A. Rescue of a synthetic chloramphenicol acetyltransferase RNA into influenza virus-like particles obtained from recombinant plasmids. J Virol. 1996 Aug;70(8):5016–5024. doi: 10.1128/jvi.70.8.5016-5024.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Muster T., Subbarao E. K., Enami M., Murphy B. R., Palese P. An influenza A virus containing influenza B virus 5' and 3' noncoding regions on the neuraminidase gene is attenuated in mice. Proc Natl Acad Sci U S A. 1991 Jun 15;88(12):5177–5181. doi: 10.1073/pnas.88.12.5177. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Nakajima K., Ueda M., Sugiura A. Origin of small RNA in von Magnus particles of influenza virus. J Virol. 1979 Mar;29(3):1142–1148. doi: 10.1128/jvi.29.3.1142-1148.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Nayak D. P., Sivasubramanian N., Davis A. R., Cortini R., Sung J. Complete sequence analyses show that two defective interfering influenza viral RNAs contain a single internal deletion of a polymerase gene. Proc Natl Acad Sci U S A. 1982 Apr;79(7):2216–2220. doi: 10.1073/pnas.79.7.2216. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Odagiri T., Tobita K. Mutation in NS2, a nonstructural protein of influenza A virus, extragenically causes aberrant replication and expression of the PA gene and leads to generation of defective interfering particles. Proc Natl Acad Sci U S A. 1990 Aug;87(15):5988–5992. doi: 10.1073/pnas.87.15.5988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Odagiri T., Tobita K. Nucleotide sequence of the PA gene of influenza A/WSN/33(H1N1). Nucleic Acids Res. 1990 Feb 11;18(3):654–654. doi: 10.1093/nar/18.3.654. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Odagiri T., Tominaga K., Tobita K., Ohta S. An amino acid change in the non-structural NS2 protein of an influenza A virus mutant is responsible for the generation of defective interfering (DI) particles by amplifying DI RNAs and suppressing complementary RNA synthesis. J Gen Virol. 1994 Jan;75(Pt 1):43–53. doi: 10.1099/0022-1317-75-1-43. [DOI] [PubMed] [Google Scholar]
  28. Palese P., Schulman J. L. Differences in RNA patterns of influenza A viruses. J Virol. 1976 Mar;17(3):876–884. doi: 10.1128/jvi.17.3.876-884.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Parvin J. D., Palese P., Honda A., Ishihama A., Krystal M. Promoter analysis of influenza virus RNA polymerase. J Virol. 1989 Dec;63(12):5142–5152. doi: 10.1128/jvi.63.12.5142-5152.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Robertson J. S. 5' and 3' terminal nucleotide sequences of the RNA genome segments of influenza virus. Nucleic Acids Res. 1979 Aug 24;6(12):3745–3757. doi: 10.1093/nar/6.12.3745. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Saiki R. K., Gelfand D. H., Stoffel S., Scharf S. J., Higuchi R., Horn G. T., Mullis K. B., Erlich H. A. Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. Science. 1988 Jan 29;239(4839):487–491. doi: 10.1126/science.2448875. [DOI] [PubMed] [Google Scholar]
  32. Scholtissek C., Rohde W., Harms E., Rott R., Orlich M., Boschek C. B. A possible partial heterozygote of an influenza A virus. Virology. 1978 Sep;89(2):506–516. doi: 10.1016/0042-6822(78)90192-7. [DOI] [PubMed] [Google Scholar]
  33. Seong B. L., Brownlee G. G. Nucleotides 9 to 11 of the influenza A virion RNA promoter are crucial for activity in vitro. J Gen Virol. 1992 Dec;73(Pt 12):3115–3124. doi: 10.1099/0022-1317-73-12-3115. [DOI] [PubMed] [Google Scholar]
  34. Shapiro G. I., Gurney T., Jr, Krug R. M. Influenza virus gene expression: control mechanisms at early and late times of infection and nuclear-cytoplasmic transport of virus-specific RNAs. J Virol. 1987 Mar;61(3):764–773. doi: 10.1128/jvi.61.3.764-773.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Smith G. L., Hay A. J. Replication of the influenza virus genome. Virology. 1982 Apr 15;118(1):96–108. doi: 10.1016/0042-6822(82)90323-3. [DOI] [PubMed] [Google Scholar]
  36. Stoeckle M. Y., Shaw M. W., Choppin P. W. Segment-specific and common nucleotide sequences in the noncoding regions of influenza B virus genome RNAs. Proc Natl Acad Sci U S A. 1987 May;84(9):2703–2707. doi: 10.1073/pnas.84.9.2703. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Ueda M., Nakajima K., Sugiura A. Extra RNAs of von Magnus particles of influenza virus cause reduction of particular polymerase genes. J Virol. 1980 Apr;34(1):1–8. doi: 10.1128/jvi.34.1.1-8.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Zheng H., Palese P., García-Sastre A. Nonconserved nucleotides at the 3' and 5' ends of an influenza A virus RNA play an important role in viral RNA replication. Virology. 1996 Mar 1;217(1):242–251. doi: 10.1006/viro.1996.0111. [DOI] [PubMed] [Google Scholar]
  39. de la Luna S., Fortes P., Beloso A., Ortín J. Influenza virus NS1 protein enhances the rate of translation initiation of viral mRNAs. J Virol. 1995 Apr;69(4):2427–2433. doi: 10.1128/jvi.69.4.2427-2433.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Virology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES