Abstract
The host range of the C particle produced by FLOPC-1 myeloma cells, FLOPC-1 murine myeloma-associated virus (FL-MuMAV), was assessed in terms of its ability to productively infect and/or induce new viral antigens in a variety of different cell lines. Production of C particle-like structures by cells exposed to FL-MuMAV) was determined by incorporation of [3H]uridine into particles with a density of 1.16 g/ml and/or measurement of RNA-dependent DNA polymerase activity in concentrated culture medium. to FL-MuMAV was capable of infecting NIH/3T3, normal rat kidney (NRK) cell, BALB/c 3T3, and the A31 clone of BALB/3T3 cells but not rabbit cell line, SIRC. Thus, it is an N, B-tropic murine virus as replication in NRK cells has been shown not to delineate a group of murine viruses with a separate host range (M. M. Lieber, C. J. Sherr, and G. J. Todero, 1974). Further neoantigens, reactive with anti-FL-MuMAV serum, were detected on infected cells. Production of the MuMAV-like particle and MuMAV-associated cell antigens in infected NIH/3T3 and NRK cells persisted for three subcultures. The limited production could not be explained by the lack of an RNA-dependent DNA polymerase or high-molecular-weight RNA as the particles possessed both of these properties. The particles produced by infected NIH/3T3 or NRK cells were antigenically and physicochemically similar to FL-MuMAV and not K-MuLV. The MuMAV-like particles produced by infected NIH/3T3 were capable of limited replication in NIH/3T3 and and BALB/3T3 cells, whereas NRK-MuMAV replicated for a limited period in NIH/3T3, NRK, and SIRC cells; i.e., they had a different host range than FL-MuMAV. The particles produced by infected BALB/3T3 and A31 cells had the same host range as FL-MuMAV. In certain situations, isotopically labeled particles with a density of 1.16 g/ml were produced which appeared to lack RNA-dependent DNA polymerase.
Full text
PDF








Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Aaronson S. A., Dunn C. Y. Endogenous C-type viruses of BALB-c cells: frequencies of spontaneous and chemical induction. J Virol. 1974 Jan;13(1):181–185. doi: 10.1128/jvi.13.1.181-185.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Aaronson S. A., Stephenson J. R. Independent segregation of loci for activation of biologically distinguishable RNA C-type viruses in mouse cells. Proc Natl Acad Sci U S A. 1973 Jul;70(7):2055–2058. doi: 10.1073/pnas.70.7.2055. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Aaronson S. A., Todaro G. J., Scolnick E. M. Induction of murine C-type viruses from clonal lines of virus-free BALB-3T3 cells. Science. 1971 Oct 8;174(4005):157–159. doi: 10.1126/science.174.4005.157. [DOI] [PubMed] [Google Scholar]
- Aoki T., Herberman R. B., Johnson P. A., Liu M., Sturm M. M. Wild-type gross leukemia virus: classification of soluble antigens (GSA). J Virol. 1972 Dec;10(6):1208–1219. doi: 10.1128/jvi.10.6.1208-1219.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Aoki T., Takahashi T. Viral and cellular surface antigens of murine leukemias and myelomas. Serological analysis by immunoelectron microscopy. J Exp Med. 1972 Mar 1;135(3):443–457. doi: 10.1084/jem.135.3.443. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Aoki T., Todaro G. J. Antigenic properties of endogenous type-C viruses from spontaneously transformed clones of BALB-3T3. Proc Natl Acad Sci U S A. 1973 May;70(5):1598–1602. doi: 10.1073/pnas.70.5.1598. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Benveniste R. E., Lieber M. M., Todaro G. J. A distinct class of inducible murine type-C viruses that replicates in the rabbit SIRC cell line. Proc Natl Acad Sci U S A. 1974 Mar;71(3):602–606. doi: 10.1073/pnas.71.3.602. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hartley J. W., Rowe W. P., Huebner R. J. Host-range restrictions of murine leukemia viruses in mouse embryo cell cultures. J Virol. 1970 Feb;5(2):221–225. doi: 10.1128/jvi.5.2.221-225.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Krueger R. G., Miller G. C. Relationship between the cellular and viral antigens of a BALB-c myeloma and murine leukemia virus. J Natl Cancer Inst. 1974 Oct;53(4):997–1004. doi: 10.1093/jnci/53.4.997. [DOI] [PubMed] [Google Scholar]
- Krueger R. G., Williams W. H., Miller G. C. Cellular and viral antigens of BALB-c myeloma. J Natl Cancer Inst. 1974 Apr;52(4):1203–1210. doi: 10.1093/jnci/52.4.1203. [DOI] [PubMed] [Google Scholar]
- Levy J. A. Xenotropic viruses: murine leukemia viruses associated with NIH Swiss, NZB, and other mouse strains. Science. 1973 Dec 14;182(4117):1151–1153. doi: 10.1126/science.182.4117.1151. [DOI] [PubMed] [Google Scholar]
- Lieber M. M., Sherr C. J., Todaro G. J. S-tropic murine type-C viruses: frequency of isolation from continuous cell lines, leukemia virus preparations and normal spleens. Int J Cancer. 1974 May 15;13(5):587–598. doi: 10.1002/ijc.2910130503. [DOI] [PubMed] [Google Scholar]
- Somers K. D., Kirsten W. H. Focus formation by murine sarcoma virus: enhancement by DEAE-dextran. Virology. 1968 Sep;36(1):155–157. doi: 10.1016/0042-6822(68)90129-3. [DOI] [PubMed] [Google Scholar]
- Stephenson J. R., Aaronson S. A., Arnstein P., Huebner R. J., Tronick S. R. Demonstration of two immunologically distinct xenotropic type C RNA viruses of mouse cells. Virology. 1974 Sep;61(1):56–63. doi: 10.1016/0042-6822(74)90241-4. [DOI] [PubMed] [Google Scholar]
- Volkman L. E., Krueger R. G. Characterization of C-type particles produced by a tissue culture-adapted murine myeloma. J Virol. 1973 Dec;12(6):1589–1597. doi: 10.1128/jvi.12.6.1589-1597.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Volkman L. E., Krueger R. G. XC cell cytopathogenicity as an assay for murine myeloma C-type virus. J Natl Cancer Inst. 1973 Oct;51(4):1205–1210. doi: 10.1093/jnci/51.4.1205. [DOI] [PubMed] [Google Scholar]
- Volkman L. E., Smuckler E. A., Krueger R. G. Mouse myeloma: differentiation of neoplastic cells accompanied by an increase in intracellular virus. J Natl Cancer Inst. 1971 May;46(5):953–962. [PubMed] [Google Scholar]