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. 1974 Jul;14(1):162–169. doi: 10.1128/jvi.14.1.162-169.1974

Newcastle Disease Virus Infection of L Cells

Toby T Hecht a,1, Donald F Summers a
PMCID: PMC355490  PMID: 4836600

Abstract

Newcastle disease virus (NDV) California strain reportedly grows poorly in L cells but replicates very well in chicken embryo cells. NDV-infected L cell cultures show a characteristic virus growth curve with respect to uridine incorporation, but plaque assays of the virus produced 24 h postinfection (PI) show no infectious particles when assayed on L cell monolayers and only a very low titer on chick cell monolayers. Plasma membranes isolated and purified from infected L cells 8 h PI contain all of the major virion proteins. In addition, NDV-infected L cells show a 50% loss of H-2 antigenic activity, a phenomenon previously observed in cells productively infected with vesicular stomatitis virus. These results suggest that at least part of the normal process of NDV maturation occurs in NDV-infected L cells. Sodium dodecyl sulfate-polyacrylamide gel patterns of supernatant virus purified from cells radiolabeled with amino acids from 3 to 24 h PI in the presence of actinomycin D show that all the major NDV structural proteins are present. Electron micrographs of NDV-infected L cells show extensive virus maturation at cell membranes. It can be concluded that infection of L cells with NDV results in a normal production of virus-specific RNA, synthesis of all the major structural proteins, association of the viral envelope proteins with the L cell plasma membrane, and the loss of cell surface H-2 antigenic activity. However, most of the virus particles produced are noninfectious.

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Selected References

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

  1. 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]
  2. Atkinson P. H., Summers D. F. Purification and properties of HeLa cell plasma membranes. J Biol Chem. 1971 Aug 25;246(16):5162–5175. [PubMed] [Google Scholar]
  3. Feller U., Dougherty R. M., Di Stefano H. S. Morphogenesis of Newcastle disease virus in chorioallantoic membrane. J Virol. 1969 Nov;4(5):753–762. doi: 10.1128/jvi.4.5.753-762.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Haslam E. A., Cheyne I. M., White D. O. The structural proteins of Newcastle disease virus. Virology. 1969 Sep;39(1):118–129. doi: 10.1016/0042-6822(69)90353-5. [DOI] [PubMed] [Google Scholar]
  5. Hecht T. T., Summers D. F. Effect of vesicular stomatitis virus infection on the histocompatibility antigen of L cells. J Virol. 1972 Oct;10(4):578–585. doi: 10.1128/jvi.10.4.578-585.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hecht T. T., Summers D. F. The effect of phleomycin on poliovirus RNA replication. Virology. 1970 Mar;40(3):441–447. doi: 10.1016/0042-6822(70)90187-x. [DOI] [PubMed] [Google Scholar]
  7. Homma M., Ouchi M. Trypsin action on the growth of Sendai virus in tissue culture cells. 3. Structural difference of Sendai viruses grown in eggs and tissue culture cells. J Virol. 1973 Dec;12(6):1457–1465. doi: 10.1128/jvi.12.6.1457-1465.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Iinuma M., Yoshida T., Nagai Y., Maeno K., Matsumoto T. Subunits of NDV. Hemagglutinin and neuraminidase subunits of Newcastle disease virus. Virology. 1971 Dec;46(3):663–677. doi: 10.1016/0042-6822(71)90069-9. [DOI] [PubMed] [Google Scholar]
  9. Jimenez L., Bloom B. R., Blume M. R., Oettgen H. F. On the number and nature of antigen-sensitive lymphocytes in the blood of delayed-hypersensitive human donors. J Exp Med. 1971 Apr 1;133(4):740–751. doi: 10.1084/jem.133.4.740. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Klenk H. D., Choppin P. W. Glycosphingolipids of plasma membranes of cultured cells and an enveloped virus (SV5) grown in these cells. Proc Natl Acad Sci U S A. 1970 May;66(1):57–64. doi: 10.1073/pnas.66.1.57. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Klenk H. D., Choppin P. W. Lipids of plasma membranes of monkey and hamster kidney cells and of parainfluenza virions grown in these cells. Virology. 1969 Jun;38(2):255–268. doi: 10.1016/0042-6822(69)90367-5. [DOI] [PubMed] [Google Scholar]
  12. Levinson W., Rubin H. Radiation studies of avian tumor viruses and of Newcastle disease virus. Virology. 1966 Apr;28(4):533–542. doi: 10.1016/0042-6822(66)90238-8. [DOI] [PubMed] [Google Scholar]
  13. MARCUS P. I. Dynamics of surface modification in myxovirus-infected cells. Cold Spring Harb Symp Quant Biol. 1962;27:351–365. doi: 10.1101/sqb.1962.027.001.033. [DOI] [PubMed] [Google Scholar]
  14. Meager A., Burke D. C. Studies on the structural basis of the RNA polymerase activity of newcastle disease virus particles. J Gen Virol. 1973 Mar;18(3):305–317. doi: 10.1099/0022-1317-18-3-305. [DOI] [PubMed] [Google Scholar]
  15. Mountcastle W. E., Compans R. W., Choppin P. W. Proteins and glycoproteins of paramyxoviruses: a comparison of simian virus 5, Newcastle disease virus, and Sendai virus. J Virol. 1971 Jan;7(1):47–52. doi: 10.1128/jvi.7.1.47-52.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Nathenson S. G., Davies D. A. Solubilization and partial purification of mouse histocompatibility antigens from a membranous lipoprotein fraction. Proc Natl Acad Sci U S A. 1966 Aug;56(2):476–483. doi: 10.1073/pnas.56.2.476. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Preble O. T., Youngner J. S. Selection of temperature-sensitive mutants during persistent infection: role in maintenance of persistent Newcastle disease virus infections of L cells. J Virol. 1973 Sep;12(3):481–491. doi: 10.1128/jvi.12.3.481-491.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Preble O. T., Youngner J. S. Temperature-sensitive defect of mutants isolated from L cells persistently infected with Newcastle disease virus. J Virol. 1973 Sep;12(3):472–480. doi: 10.1128/jvi.12.3.472-480.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. REDA I. M., ROTT R., SCHAEFER W. FLUORESCENT ANTIBODY STUDIES WITH NDV-INFECTED CELL SYSTEMS. Virology. 1964 Mar;22:422–425. doi: 10.1016/0042-6822(64)90033-9. [DOI] [PubMed] [Google Scholar]
  20. Renkonen O., Käräinen L., Simons K., Gahmberg C. G. The lipid class composition of Semliki forest virus and plasma membranes of the host cells. Virology. 1971 Nov;46(2):318–326. doi: 10.1016/0042-6822(71)90033-x. [DOI] [PubMed] [Google Scholar]
  21. Samson A. C., Fox C. F. Precursor protein for Newcastle disease virus. J Virol. 1973 Sep;12(3):579–587. doi: 10.1128/jvi.12.3.579-587.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Scheid A., Choppin P. W. Isolation and purification of the envelope proteins of Newcastle disease virus. J Virol. 1973 Feb;11(2):263–271. doi: 10.1128/jvi.11.2.263-271.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Schlesinger S., Schlesinger M. J. Formation of Sindbis virus proteins: identification of a precursor for one of the envelope proteins. J Virol. 1972 Nov;10(5):925–932. doi: 10.1128/jvi.10.5.925-932.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Shapiro A. L., Viñuela E., Maizel J. V., Jr Molecular weight estimation of polypeptide chains by electrophoresis in SDS-polyacrylamide gels. Biochem Biophys Res Commun. 1967 Sep 7;28(5):815–820. doi: 10.1016/0006-291x(67)90391-9. [DOI] [PubMed] [Google Scholar]
  25. Strauss J. H., Jr, Burge B. W., Darnell J. E. Carbohydrate content of the membrane protein of Sindbis virus. J Mol Biol. 1970 Feb 14;47(3):437–448. doi: 10.1016/0022-2836(70)90313-x. [DOI] [PubMed] [Google Scholar]
  26. Thacore H., Youngner J. S. Cells persistently infected with Newcastle disease virus. II. Ribonucleic acid and protein synthesis in cells infected with mutants isolated from persistently infected L cells. J Virol. 1970 Jul;6(1):42–48. doi: 10.1128/jvi.6.1.42-48.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Thacore H., Youngner J. S. Cells persistently infected with newcastle disease virus: I. Properties of mutants isolated from persistently infected L cells. J Virol. 1969 Sep;4(3):244–251. doi: 10.1128/jvi.4.3.244-251.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. WHEELOCK E. F., TAMM I. Effect of multiplicity of infection on Newcastle disease virus-HeLa cell interaction. J Exp Med. 1961 Feb 1;113:317–338. doi: 10.1084/jem.113.2.317. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Wainberg M. A., Howe C. Factors affecting cell fusion induced by Sendai virus. J Virol. 1973 Oct;12(4):937–939. doi: 10.1128/jvi.12.4.937-939.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Youngner J. S., Scott A. W. Relation of interferon synthesis to abortive replication of Newcastle disease virus in L cells. J Virol. 1968 Jan;2(1):81–82. doi: 10.1128/jvi.2.1.81-82.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]

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