Skip to main content
PMC home page
Bacteriological Reviews logoLink to Bacteriological Reviews
. 1964 Mar;28(1):2–13. doi: 10.1128/br.28.1.2-13.1964

ENTEROVIRUS ENTRANCE INTO SPECIFIC HOST CELLS, AND SUBSEQUENT ALTERATIONS OF CELL PROTEIN AND NUCLEIC ACID SYNTHESIS

John J Holland 1
PMCID: PMC441207  PMID: 14127971

Full text

PDF
6

Images in this article

2Image
on p.2

Selected References

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

  1. ACKERMANN W. W., LOH P. C., PAYNE F. E. Studies of the biosynthesis of protein and ribonucleic acid in HeLa cells infected with poliovirus. Virology. 1959 Feb;7(2):170–183. doi: 10.1016/0042-6822(59)90185-0. [DOI] [PubMed] [Google Scholar]
  2. ATTARDI G., SMITH J. Virus specific protein and a ribo-nucleic acid associated with ribosomes in poliovirus infected HeLa cells. Cold Spring Harb Symp Quant Biol. 1962;27:271–292. doi: 10.1101/sqb.1962.027.001.026. [DOI] [PubMed] [Google Scholar]
  3. BALTIMORE D., EGGERS H. J., FRANKLIN R. M., TAMM I. Poliovirus-induced RNA polymerase and the effects of virus-specific inhibitors on its production. Proc Natl Acad Sci U S A. 1963 Jun;49:843–849. doi: 10.1073/pnas.49.6.843. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. BALTIMORE D., FRANKLIN R. M. A NEW RIBONUCLEIC ACID POLYMERASE APPEARING AFTER MENGOVIRUS INFECTION OF L-CELLS. J Biol Chem. 1963 Oct;238:3395–3400. [PubMed] [Google Scholar]
  5. BALTIMORE D., FRANKLIN R. M. Preliminary data on a virus-specific enzyme system responsible for the synthesis of viral RNA. Biochem Biophys Res Commun. 1962 Nov 27;9:388–392. doi: 10.1016/0006-291x(62)90021-9. [DOI] [PubMed] [Google Scholar]
  6. BALTIMORE D., FRANKLIN R. M. The effect of Mengovirus infection on the activity of the DNA-dependent RNA polymerase of L-cells. Proc Natl Acad Sci U S A. 1962 Aug;48:1383–1390. doi: 10.1073/pnas.48.8.1383. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. BARSKI G., KOURILSKY R., CORNEFERT F. Resistance of respiratory ciliated epithelium to action of polio and adeno viruses in vitro. Proc Soc Exp Biol Med. 1957 Nov;96(2):386–391. doi: 10.3181/00379727-96-23485. [DOI] [PubMed] [Google Scholar]
  8. BODIAN D. Viremia in experimental poliomyelitis. I. General aspects of infection after intravascular inoculation with strains of high and of low invasiveness. Am J Hyg. 1954 Nov;60(3):339–357. [PubMed] [Google Scholar]
  9. CROWTHER D., MELNICK J. L. Studies of the inhibitory action of guanidine on poliovirus multiplication in cell cultures. Virology. 1961 Sep;15:65–74. doi: 10.1016/0042-6822(61)90078-2. [DOI] [PubMed] [Google Scholar]
  10. DARNELL J. E., Jr, SAWYER T. K. The basis for variation in susceptibility to poliovirus in HeLa cells. Virology. 1960 Aug;11:665–675. doi: 10.1016/0042-6822(60)90113-6. [DOI] [PubMed] [Google Scholar]
  11. DE SOMER P., PRINZIE A., SCHONNE E. Infectivity of polio virus ribonucleic acid for embryonated eggs and unsusceptible cell lines. Nature. 1959 Aug 22;184(Suppl 9):652–653. doi: 10.1038/184652a0. [DOI] [PubMed] [Google Scholar]
  12. DOI R. H., SPIEGELMAN S. Homology test between the nucleic acid of an RNA virus and the DNA in the host cell. Science. 1962 Dec 14;138(3546):1270–1272. doi: 10.1126/science.138.3546.1270. [DOI] [PubMed] [Google Scholar]
  13. EVANS C. A., HOSHIWARA I. Local increase of poliomyelitis virus in healing wound tissue of cynomolgus monkeys. Proc Soc Exp Biol Med. 1955 May;89(1):86–89. doi: 10.3181/00379727-89-21723. [DOI] [PubMed] [Google Scholar]
  14. Enders J. F., Weller T. H., Robbins F. C. Cultivation of the Lansing Strain of Poliomyelitis Virus in Cultures of Various Human Embryonic Tissues. Science. 1949 Jan 28;109(2822):85–87. doi: 10.1126/science.109.2822.85. [DOI] [PubMed] [Google Scholar]
  15. FASTIER L. B. Infectivity titrations of the viruses of Western equine encephalomyelitis and Newcastle disease by tissue culture methods. J Immunol. 1954 May;72(5):341–347. [PubMed] [Google Scholar]
  16. FENWICK M. L. The influence of poliovirus infection of RNA synthesis in mammalian cells. Virology. 1963 Mar;19:241–249. doi: 10.1016/0042-6822(63)90061-8. [DOI] [PubMed] [Google Scholar]
  17. FRANKLIN R. M., BALTIMORE D. Patterns of macromolecular synthesis in normal and virus-infected mammalian cells. Cold Spring Harb Symp Quant Biol. 1962;27:175–198. doi: 10.1101/sqb.1962.027.001.019. [DOI] [PubMed] [Google Scholar]
  18. GOLDBERG I. H. Ribonucleic acid synthesis in nuclear extracts of mammalian cells grown in suspension culture; effect of ionic strength and surface-active agents. Biochim Biophys Acta. 1961 Jul 22;51:201–204. doi: 10.1016/0006-3002(61)91042-3. [DOI] [PubMed] [Google Scholar]
  19. GOMATOS P. J., TAMM I. MACROMOLECULAR SYNTHESIS IN REOVIRUS-INFECTED L CELLS. Biochim Biophys Acta. 1963 Aug 20;72:651–653. [PubMed] [Google Scholar]
  20. HERMODSSON S., WESSLEN T. Multiplication of poliomyelitis virus in hetero-transplanted human embryonic tissue. Acta Pathol Microbiol Scand. 1958;42(4):371–379. doi: 10.1111/j.1699-0463.1958.tb01750.x. [DOI] [PubMed] [Google Scholar]
  21. HOLLAND J. J. Altered base ratios in HeLa cell RNA during poliovirus infection. Biochem Biophys Res Commun. 1961 Nov 20;6:196–200. doi: 10.1016/0006-291x(61)90128-0. [DOI] [PubMed] [Google Scholar]
  22. HOLLAND J. J. Altered base ratios in RNA synthesized during enterovirus infection of human cells. Proc Natl Acad Sci U S A. 1962 Dec 15;48:2044–2051. doi: 10.1073/pnas.48.12.2044. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. HOLLAND J. J. Depression of host-controlled RNA synthesis in human cells during poliovirus infection. Proc Natl Acad Sci U S A. 1963 Jan 15;49:23–28. doi: 10.1073/pnas.49.1.23. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. HOLLAND J. J. EFFECTS OF PUROMYCIN ON RNA SYNTHESIS IN MAMMALIAN CELLS. Proc Natl Acad Sci U S A. 1963 Sep;50:436–446. doi: 10.1073/pnas.50.3.436. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. HOLLAND J. J. Inhibition of DNA-primed RNA synthesis during poliovirus infection of human cells. Biochem Biophys Res Commun. 1962 Dec 19;9:556–562. doi: 10.1016/0006-291x(62)90125-0. [DOI] [PubMed] [Google Scholar]
  26. HOLLAND J. J. Irreversible eclipse of poliovirus by HeLa cells. Virology. 1962 Feb;16:163–176. doi: 10.1016/0042-6822(62)90292-1. [DOI] [PubMed] [Google Scholar]
  27. HOLLAND J. J., McLAREN L. C., HOYER B. H., SYVERTON J. T. Enteroviral ribonucleic acid. II. Biological, physical, and chemical studies. J Exp Med. 1960 Nov 1;112:841–864. doi: 10.1084/jem.112.5.841. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. HOLLAND J. J., McLAREN L. C., SYVERTON J. T. The mammalian cell-virus relationship. IV. Infection of naturally insusceptible cells with enterovirus ribonucleic acid. J Exp Med. 1959 Jul 1;110(1):65–80. doi: 10.1084/jem.110.1.65. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. HOLLAND J. J., McLAREN L. C. The location and nature of enterovirus receptors in susceptible cells. J Exp Med. 1961 Aug 1;114:161–171. doi: 10.1084/jem.114.2.161. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. HOLLAND J. J., McLAREN L. C. The mammalian cell-virus relationship. II. Adsorption, reception, and eclipse of poliovirus by HeLa cells. J Exp Med. 1959 May 1;109(5):487–504. doi: 10.1084/jem.109.5.487. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. HOLLAND J. J. Receptor affinities as major determinants of enterovirus tissue tropisms in humans. Virology. 1961 Nov;15:312–326. doi: 10.1016/0042-6822(61)90363-4. [DOI] [PubMed] [Google Scholar]
  32. KAPLAN A. S. Comparison of susceptible and resistant cells to infection with poliomyelitis virus. Ann N Y Acad Sci. 1955 Sep 27;61(4):830-8; discussion, 838-9. doi: 10.1111/j.1749-6632.1955.tb42539.x. [DOI] [PubMed] [Google Scholar]
  33. KERR I. M., MARTIN E. M., HAMILTON M. G., WORK T. S. The initiation of virus protein synthesis in Krebs ascites tumor cells infected with EMC virus. Cold Spring Harb Symp Quant Biol. 1962;27:259–269. doi: 10.1101/sqb.1962.027.001.025. [DOI] [PubMed] [Google Scholar]
  34. KUNIN C. M., JORDAN W. S., Jr In vitro absorption of poliovirus by noncultured tissues. Effect of species, age and malignancy. Am J Hyg. 1961 May;73:245–257. doi: 10.1093/oxfordjournals.aje.a120183. [DOI] [PubMed] [Google Scholar]
  35. KUNIN C. M. Virus-tissue union and the pathogenesis of enterovirus infections. J Immunol. 1962 May;88:556–569. [PubMed] [Google Scholar]
  36. LEDINKO N. Production of noninfectious complement-fixing poliovirus particles in HeLa cells treated with proflavine. Virology. 1958 Oct;6(2):512–524. doi: 10.1016/0042-6822(58)90098-9. [DOI] [PubMed] [Google Scholar]
  37. LI C. P., SCHAEFFER M., NELSON D. B. Experimentally produced variants of poliomyelitis virus combining in vivo and in vitro techniques. Ann N Y Acad Sci. 1955 Sep 27;61(4):902–910. doi: 10.1111/j.1749-6632.1955.tb42549.x. [DOI] [PubMed] [Google Scholar]
  38. LODDO B. [Inhibition of the in vitro multiplication of poliomyelitis viruses using guanidine]. Boll Soc Ital Biol Sper. 1961 May 15;37:395–397. [PubMed] [Google Scholar]
  39. McLAREN L. C., HOLLAND J. J., SYVERTON J. T. The mammalian cell-virus relationship. I. Attachment of poliovirus to cultivated cells of primate and non-primate origin. J Exp Med. 1959 May 1;109(5):475–485. doi: 10.1084/jem.109.5.475. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. NEVILLE D. M., Jr The isolation of a cell membrane fraction from rat liver. J Biophys Biochem Cytol. 1960 Oct;8:413–422. doi: 10.1083/jcb.8.2.413. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. NOMURA M., OKAMOTO K., ASANO K. RNA metabolism in Escherichia coli infected with bacteriophage T4. Inhibition of host ribosomal and soluble RNA synthesis by phage and effect of chloromycetin. J Mol Biol. 1962 May;4:376–387. doi: 10.1016/s0022-2836(62)80018-7. [DOI] [PubMed] [Google Scholar]
  42. Penman S., Scherrer K., Becker Y., Darnell J. E. POLYRIBOSOMES IN NORMAL AND POLIOVIRUS-INFECTED HELA CELLS AND THEIR RELATIONSHIP TO MESSENGER-RNA. Proc Natl Acad Sci U S A. 1963 May;49(5):654–662. doi: 10.1073/pnas.49.5.654. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. REICH E., FRANKLIN R. M. Effect of mitomycin C on the growth of some animal viruses. Proc Natl Acad Sci U S A. 1961 Aug;47:1212–1217. doi: 10.1073/pnas.47.8.1212. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. REICH E., FRANKLIN R. M., SHATKIN A. J., TATUM E. L. Effect of actinomycin D on cellular nucleic acid synthesis and virus production. Science. 1961 Aug 25;134(3478):556–557. doi: 10.1126/science.134.3478.556. [DOI] [PubMed] [Google Scholar]
  45. RIGHTSEL W. A., DICE J. R., McALPINE R. J., TIMM E. A., McLEAN I. W., Jr, DIXON G. J., SCHABEL F. M., Jr Antiviral effect of guanidine. Science. 1961 Aug 25;134(3478):558–559. doi: 10.1126/science.134.3478.558. [DOI] [PubMed] [Google Scholar]
  46. SALZMAN N. P., LOCKART R. Z., Jr, SEBRING E. D. Alterations in HeLa cell metabolism resulting from poliovirus infection. Virology. 1959 Oct;9:244–259. doi: 10.1016/0042-6822(59)90118-7. [DOI] [PubMed] [Google Scholar]
  47. SCHAFFER F. L. Binding of proflavine by and photoinactivation of poliovirus propagated in the presence of the dye. Virology. 1962 Nov;18:412–425. doi: 10.1016/0042-6822(62)90032-6. [DOI] [PubMed] [Google Scholar]
  48. SCHAFFER F. L., MOORE H. F., SCHWERDT C. E. Base composition of the ribonucleic acids of the three types of poliovirus. Virology. 1960 Apr;10:530–537. doi: 10.1016/0042-6822(60)90134-3. [DOI] [PubMed] [Google Scholar]
  49. SCHARFF M. D., SHATKIN A. J., LEVINTOW L. ASSOCIATION OF NEWLY FORMED VIRAL PROTEIN WITH SPECIFIC POLYRIBOSOMES. Proc Natl Acad Sci U S A. 1963 Oct;50:686–694. doi: 10.1073/pnas.50.4.686. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. SCHOLTISSEK C., ROTT R., HAUSEN P., HAUSEN H., SCHAEFER W. Conparative studies of RNA and protein synthesis with a myxovirus and a small polyhedral virus. Cold Spring Harb Symp Quant Biol. 1962;27:245–257. doi: 10.1101/sqb.1962.027.001.024. [DOI] [PubMed] [Google Scholar]
  51. SINSHEIMER R. L., STARMAN B., NAGLER C., GUTHRIE S. The process of infection with bacteriophage phi-XI74. I. Evidence for a "replicative form". J Mol Biol. 1962 Mar;4:142–160. doi: 10.1016/s0022-2836(62)80047-3. [DOI] [PubMed] [Google Scholar]
  52. TISSIERES A., BOURGEOIS S., GROS F. Inhibition of RNA polymerase by RNA. J Mol Biol. 1963 Jul;7:100–103. doi: 10.1016/s0022-2836(63)80024-8. [DOI] [PubMed] [Google Scholar]
  53. VOGT M., DULBECCO R. Properties of a HeLa cell culture with increased resistance to poliomyelitis virus. Virology. 1958 Jun;5(3):425–434. doi: 10.1016/0042-6822(58)90037-0. [DOI] [PubMed] [Google Scholar]
  54. WARNER J., MADDEN M. J., DARNELL J. E. The interaction of poliovirus RNA with Escherichia coli ribosomes. Virology. 1963 Mar;19:393–399. doi: 10.1016/0042-6822(63)90079-5. [DOI] [PubMed] [Google Scholar]
  55. WECKER E., RICHTER A. Conditions for the replication of infectious viral RNA. Cold Spring Harb Symp Quant Biol. 1962;27:137–148. doi: 10.1101/sqb.1962.027.001.016. [DOI] [PubMed] [Google Scholar]
  56. WENNER H. A. Some comparative observations on the behavior of poliomyelitis viruses in animals and in tissue culture. Ann N Y Acad Sci. 1955 Sep 27;61(4):840–847. doi: 10.1111/j.1749-6632.1955.tb42540.x. [DOI] [PubMed] [Google Scholar]
  57. Weiss S. B. ENZYMATIC INCORPORATION OF RIBONUCLEOSIDE TRIPHOSPHATES INTO THE INTERPOLYNUCLEOTIDE LINKAGES OF RIBONUCLEIC ACID. Proc Natl Acad Sci U S A. 1960 Aug;46(8):1020–1030. doi: 10.1073/pnas.46.8.1020. [DOI] [PMC free article] [PubMed] [Google Scholar]
  58. ZIMMERMAN E. F., HEETER M., DARNELL J. E. RNA synthesis in poliovirus-infected cells. Virology. 1963 Mar;19:400–408. doi: 10.1016/0042-6822(63)90080-1. [DOI] [PubMed] [Google Scholar]

Articles from Bacteriological Reviews are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES