TY - JOUR
T1 - Defective-interfering particles of Sindbis virus. I. Isolation and some chemical and biological properties
AU - Shenk, Thomas E.
AU - Stollar, Victor
N1 - Funding Information:
1 This investigation was supported by the United States-Japan Cooperative Medical Science Program administered by the National Institute of Allergy and Infectious Diseases of the National Institutes of Health (Grant A105920). 2 Supported by a National Institutes of Health Predoctoral Fellowship (GM48773). The work reported in this paper will be included in the dissertation to be submitted by T. E. S. in partial fulfillment of the requirements for the Ph.D. degree in Microbiology awarded by the Graduate School of Rutgers University.
PY - 1973/5
Y1 - 1973/5
N2 - Three different virus-specific particles were identified in stocks of SV which had been serially passaged without dilution through BHK21 cells. These particles had densities of 1.16, 1.20, and 1.22 g/cc in sucrose gradients prepared in D2O. The 1.20 g/cc particle was infective, contained 42 S RNA, and was the only species present in stocks prepared by infecting BHK21 cells with plaque-purified virus. The 1.16 g/cc particle was not infective and contained heterogeneous RNA species. No additional intracellular viral RNA species were produced in BHK21 cells coinfected with the 1.16 g/cc particle and unpassaged virus compared to cells infected with unpassaged virus alone. The 1.22 g/cc particle was not infective although it contained an RNA molecule which migrated identically with the RNA of infective virions in polyacrylamide-agarose gels. Cells coinfected with the 1.22 g/cc particle and unpassaged SV synthesized 12 S double-stranded RNA and small, single-stranded RNA species not present when cells were infected with only unpassaged SV. RNA synthesis by the 1.22 g/cc particles, however, appeared to require the presence of infective virions. The 1.22 g/cc particle also interfered with RNA synthesis by unpassaged SV, and, therefore, can be designated a defective-interfering particle.
AB - Three different virus-specific particles were identified in stocks of SV which had been serially passaged without dilution through BHK21 cells. These particles had densities of 1.16, 1.20, and 1.22 g/cc in sucrose gradients prepared in D2O. The 1.20 g/cc particle was infective, contained 42 S RNA, and was the only species present in stocks prepared by infecting BHK21 cells with plaque-purified virus. The 1.16 g/cc particle was not infective and contained heterogeneous RNA species. No additional intracellular viral RNA species were produced in BHK21 cells coinfected with the 1.16 g/cc particle and unpassaged virus compared to cells infected with unpassaged virus alone. The 1.22 g/cc particle was not infective although it contained an RNA molecule which migrated identically with the RNA of infective virions in polyacrylamide-agarose gels. Cells coinfected with the 1.22 g/cc particle and unpassaged SV synthesized 12 S double-stranded RNA and small, single-stranded RNA species not present when cells were infected with only unpassaged SV. RNA synthesis by the 1.22 g/cc particles, however, appeared to require the presence of infective virions. The 1.22 g/cc particle also interfered with RNA synthesis by unpassaged SV, and, therefore, can be designated a defective-interfering particle.
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U2 - 10.1016/0042-6822(73)90475-3
DO - 10.1016/0042-6822(73)90475-3
M3 - Article
C2 - 4735935
AN - SCOPUS:0015863728
SN - 0042-6822
VL - 53
SP - 162
EP - 173
JO - Virology
JF - Virology
IS - 1
ER -