Multiplicity Reactivation of Reovirus Particles After Exposure to Ultraviolet Light

McClain, Mary E. (California State Department of Public Health, Berkeley), and Rex S. Spendlove. Multiplicity reactivation of reovirus particles after exposure to ultraviolet light. J. Bacteriol. 92:1422–1429. 1966.—Exposure of reovirus suspensions to moderate doses of ultraviolet light results in essentially exponential inactivation of infectivity to survivals of 10−2 to 10−3. With suspensions of sufficiently high particle concentration, larger doses of ultraviolet light (6 to 12 min) are associated with multiplicity reactivation (MR) which is demonstrable both by immunofluorescent-cell count and by plaque assay in FL human amnion cells. Similar effects are produced by photodynamic inactivation in the presence of proflavine, but not by thermal inactivation at 50 C. All three reovirus types exhibit MR under appropriate conditions, and all three interact in mixed ultraviolet suspensions with high efficiency. Progeny from FL cells infected under conditions of MR were as infectious as those of unirradiated inocula, with yields per cell ranging from 104 to 4 × 104 infective units.

[1]  S. Luria Reactivation of Irradiated Bacteriophage by Transfer of Self-Reproducing Units. , 1947, Proceedings of the National Academy of Sciences of the United States of America.

[2]  R. Dulbecco,et al.  Genetic Recombinations Leading to Production of Active Bacteriophage from Ultraviolet Inactivated Bacteriophage Particles. , 1949, Genetics.

[3]  J. Drake,et al.  Interference and multiplicity reactivation in polioviruses. , 1958, Virology.

[4]  S. A. Ellison,et al.  A host effect on bacteriophage survival after ultraviolet irradiation. , 1960, Virology.

[5]  R. D. Barry The multiplication of influenza virus. II. Multiplicity reactivation of ultraviolet irradiated virus. , 1961, Virology.

[6]  C. S. Rupert Photoenzymatic Repair of Ultraviolet Damage in DNA : I. Kinetics of the reaction , 1962 .

[7]  R. Setlow,et al.  Evidence that ultraviolet-induced thymine dimers in DNA cause biological damage. , 1962, Proceedings of the National Academy of Sciences of the United States of America.

[8]  P. Abel Multiplicity reactivation and marker rescue with vaccinia virus. , 1962, Virology.

[9]  J. Drake MULTIPLICITY REACTIVATION OF NEWCASTLE DISEASE VIRUS , 1962, Journal of bacteriology.

[10]  C. S. Rupert Photoenzymatic repair of ultraviolet damage in DNA. II. Formation of an enzyme-substrate complex. , 1962 .

[11]  R. Setlow,et al.  Ultraviolet inactivation of DNA primer activity. I. Effects of different wavelengths and doses. , 1963, Biochimica et biophysica acta.

[12]  P. Howard-Flanders,et al.  RELEASE OF ULTRAVIOLET LIGHT-INDUCED THYMINE DIMERS FROM DNA IN E. COLI K-12. , 1964, Proceedings of the National Academy of Sciences of the United States of America.

[13]  R. Setlow,et al.  THE DISAPPEARANCE OF THYMINE DIMERS FROM DNA: AN ERROR-CORRECTING MECHANISM. , 1964, Proceedings of the National Academy of Sciences of the United States of America.

[14]  R. Spendlove,et al.  EFFECT OF ANTIMITOTIC AGENTS ON INTRACELLULAR REOVIRUS ANTIGEN. , 1964, Cancer research.

[15]  C. Wallis,et al.  REOVIRUS ACTIVATION BY HEATING AND INACTIVATION BY COOLING IN MGC12 SOLUTIONS. , 1964, Virology.

[16]  R. Spendlove,et al.  Enzymatic Enhancement of Infectivity of Reovirus , 1965, Journal of bacteriology.

[17]  E. H. Simon,et al.  A radiobiological study of the development of Newcastle disease virus. , 1965, Virology.

[18]  A. Rauth The Physical State of Viral Nucleic Acid and the Sensitivity of Viruses to Ultraviolet Light. , 1965, Biophysical journal.

[19]  R. Lorenz,et al.  An estimation of the overlap bias in plaque assay. , 1966, Virology.