Absence of superinfection exclusion during asynchronous reovirus infections of mouse, monkey, and human cell lines

Virus Research

Volumn 54, Issue 2, 1998, Pages 225-235

  Keirstead, Natalie D ^a   Coombs, Kevin M ^a  

^a UNIVERSITY OF MANITOBA   (Canada)

Author keywords

Double stranded RNA; Human; Monkey; Mouse; Reovirus; Temperature sensitive

Indexed keywords

DOUBLE STRANDED RNA;

ANIMAL CELL; ARTICLE; CONTROLLED STUDY; HUMAN; HUMAN CELL; MIXED INFECTION; MONKEY; NONHUMAN; PRIORITY JOURNAL; REOVIRUS; SUPERINFECTION; VIRUS GENOME; VIRUS INFECTION; VIRUS MUTANT;

ANIMALS; CELL LINE; HAPLORHINI; HT29 CELLS; HUMANS; MICE; REOVIRIDAE; TIME FACTORS; VIRAL INTERFERENCE;

MAMMALIA; ORTHOREOVIRUS; REOVIRUS SP.;

EID: 0032052218     PISSN: 01681702     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0168-1702(98)00023-9     Document Type: Article

References (47)

1. Ahmed R., Fields B.N. Reassortment of genome segments between reovirus defective interfering particles and infectious virus: construction of temperature-sensitive and attenuated viruses by rescue of mutations from DI particles. Virology. 111:1981;351-363.
2. Antczak J.B., Joklik W.K. Reovirus genome segment assortment into progeny genomes studied by the use of monoclonal antibodies directed against reovirus proteins. Virology. 187:1992;760-776.
3. Bass D.M., Trier J.S., Dambrauskas R., Wolf J.L. Reovirus type I infection of small intestinal epithelium in suckling mice and its effect on M cells. Lab. Invest. 58:1988;226-235.
4. Chakraborty P.R., Ahmed R., Fields B.N. Genetics of reovirus: the relationship of interference to complementation and reassortment of temperature-sensitive mutants at non-permissive temperatures. Virology. 94:1979;119-127.
5. Christen L., Seto J., Niles E.G. Superinfection exclusion of vaccinia virus in virus-infected cell cultures. Virology. 174:1990;35-42.
6. Cohen J.A., Williams W.V., Weiner D.B., Geller H.M., Greene M.I. Ligand binding to the cell surface receptor for reovirus type 3 stimulates galactocerebroside expression by developing oligodendrocytes. Proc. Natl. Acad. Sci. (USA). 87:1990;4922-4926.
7. Coombs K.M. Identification and characterization of a double-stranded RNA-reovirus temperature-sensitive mutant defective in minor core protein μ2. J. Virol. 70:1996;4237-4245.
8. Coombs K.M. Temperature-sensitive mutants of reovirus. Curr. Top. Microbiol. Immunol. 233:1998;69-107.
9. Coombs K.M., Mak S.C., Petrycky-Cox L.D. Studies of the major reovirus core protein sigma 2: reversion of the assembly-defective mutant tsC447 is an intragenic process and involves back mutation of Asp-383 to Asn. J. Virol. 68:1994;177-186.
10. Dean H.J., Warner M.S., Terhune S.S., Johnson R.M., Spear P.G. Viral determinants of the variable sensitivity of herpes simplex virus strains to gD-mediated interference. J. Virol. 69:1995;5171-5176.
11. Dichter M.A., Weiner H.L. Infection of neuronal cell cultures with reovirus mimics in vitro patterns of neurotropism. Ann. Neurol. 16:1984;603-610.
12. Dulbecco R. Mutual exclusion between related phages. J. Bacteriol. 63:1952;209-217.
13. el-Hussein A., Ramig R.F., Holbrook F.R., Beaty B.J. Asynchronous mixed infection of Culicoides variipennis with bluetongue virus serotypes 10 and 17. J. Gen. Virol. 70:1989;3355-3362.
14. Farone A.L., O'Brien P.C., Cox D.C. Tumor necrosis factor-alpha induction by reovirus serotype 3. J. Leuk. Biol. 53:1993;133-137.
15. Fields B.N. Temperature-sensitive mutants of reovirus type 3: Features of genetic recombination. Virology. 46:1971;142-148.
16. Fields B.N., Greene M.I. Genetic and molecular mechanisms of viral pathogenesis: implications for prevention and treatment. Nature. 300:1982;19-23.
17. Fields B.N., Joklik W.K. Isolation and preliminary genetic and biochemical characterization of temperature-sensitive mutants of reovirus. Virology. 37:1969;335-342.
18. Flamand A., Gagner J.P., Morrison L.A., Fields B.N. Penetration of the nervous systems of suckling mice by mammalian reoviruses. J. Virol. 65:1991;123-131.
19. Frey T.K., Hemphill M.L. Generation of defective-interfering particles by rubella virus in Vero cells. Virology. 164:1988;22-29.
20. Gombold J.L., Ramig R.F. Genetics of the rotaviruses. Curr. Top. Microbiol. Immunol. 185:1994;129-177.
21. Hrdy D.B., Rubin D.H., Fields B.N. Molecular basis of reovirus neurovirulence: role of the M2 gene in avirulence. Proc. Natl. Acad. Sci. (USA). 79:1982;1298-1302.
22. Johansson P.J., Sveger T., Ahlfors K., Ekstrand J., Svensson L. Reovirus type 1 associated with meningitis. Scan. J. Inf. Dis. 28:1996;117-120.
23. Joklik W.K., Roner M.R. Molecular recognition in the assembly of the segmented reovirus genome. Prog. Nucleic Acid Res. Mol. Biol. 53:1996;249-281.
24. Karpf A.R., Lenches E., Strauss E.G., Strauss J.H., Brown D.T. Superinfection exclusion of alphaviruses in three mosquito cell lines persistently infected with Sindbis virus. J. Virol. 71:1997;7119-7123.
25. Krug R.M., Morgan M.A., Shatkin A.J. Influenza viral mRNA contains internal N6-methyladenosine and 5′-terminal 7-methylguanosine in cap structures. J. Virol. 20:1976;45-53.
26. Kuge S., Saito I., Nomoto A. Primary structure of poliovirus defective-interfering particle genomes and possible generation mechanisms of the particles. J. Mol. Biol. 192:1986;473-487.
27. Lazzarini R.A., Keene J.D., Schubert M. The origins of defective interfering particles of the negative-strand RNA viruses. Cell. 26:1981;145-154.
28. Margolis G., Kilham L., Gomatos N. Reovirus type III encephalitis: Observations of virus-cell interactions in neural tissues. I. Light microscopy studies. Lab. Invest. 24:1971;91-109.
29. McNulty M.S., Curran W.L., Allan G.M., McFerran J.B. Synthesis of coreless, probably defective virus particles in cell cultures infected with rotaviruses. Arch. Virol. 58:1978;193-202.
30. Ni Y., Kemp M.C. Selection of genome segments following coinfection of chicken fibroblasts with avian reoviruses. Virology. 177:1990;625-633.
31. Odagiri T., Tominaga K., Tobita K., Ohta S. An amino acid change in the nonstructural 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. 75:1994;43-53.
32. Palese P., Young J.F. Variation of influenza A. B, and C viruses. Science. 215:1982;1468-1474.
33. Palese P., Tobita K., Ueda M., Compans R.W. Characterization of temperature sensitive influenza virus mutants defective in neuraminidase. Virology. 61:1974;397-410.
34. Perrault J. Origin and replication of defective interfering particles. Curr. Top. Microbiol. Immunol. 93:1981;151-207.
35. Plotch S.J., Bouloy M., Krug R.M. Transfer of 5′-terminal cap of globin mRNA to influenza viral complementary RNA during transcription in vitro. Proc. Natl. Acad. Sci. (USA). 76:1979;1618-1622.
36. Plotch S.J., Bouloy M., Ulmanen I., Krug R.M. A unique cap(m7GpppXm)-dependent influenza virion endonuclease cleaves capped mRNAs to generate primers that initiate viral RNA transcription. Cell. 23:1981;847-858.
37. Ramig R.F. Factors that affect genetic interactions during mixed infection with temperature- sensitive mutants of simian rotavirus SA11. Virology. 127:1983;91-99.
38. Ramig R.F. Superinfecting rotaviruses are not excluded from genetic interactions during asynchronous mixed infections in vitro. Virology. 176:1990;308-310.
39. Ramig R.F., Fields B.N. Revertants of temperature-sensitive mutants of reovirus: evidence for frequent extragenic suppression. Virology. 92:1979;155-167.
40. Ramig, R., Fields, B.N., 1983. Genetics of Reovirus. In: Joklik, W. (Ed.), The Reoviridae. Plenum Press, New York, pp. 197-228.
41. Ramig R.F., Ward R.L. Genomic segment reassortment in rotaviruses and other Reoviridae. Adv. Virus Res. 39:1991;163-207.
42. Ramig R.F., Garrison C., Chen D., Bell-Robinson D. Analysis of reassortment and superinfection during mixed infection of Vero cells with bluetongue virus serotypes 10 and 17. J. Gen. Virol. 70:1989;2595-2603.
43. Shing M., Coombs K.M. Assembly of the reovirus outer capsid requires mu1/sigma3 interactions which are prevented by misfolded sigma3 protein in reovirus temperature-sensitive mutant tsG453. Virus Res. 46:1996;19-29.
44. Visconti D. Resistance to lysis from without in bacteria infected with T2 bacteriophage. J. Bacteriol. 66:1953;247-253.
45. Vlasak R., Luytjes W., Leider J., Spaan W., Palese P. The E3 protein of bovine coronavirus is a receptor-destroying enzyme with acetylesterase activity. J. Virol. 62:1988;4686-4690.
46. Whitaker-Dowling P., Youngner J.S., Widnell C.C., Wilcox D.K. Superinfection exclusion by vesicular stomatitis virus. Virology. 131:1983;137-143.
47. Young J.F., Palese P. Evolution of human influenza A viruses in nature: recombination contributes to genetic variation of H1N1 strains. Proc. Natl. Acad. Sci. (USA). 76(12):1979;6547-6551.