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. 1964 Jul;88(1):187–199. doi: 10.1128/jb.88.1.187-199.1964

VIRUS BIOGRAPHIES I.

Growth of West Nile and Guaroa Viruses in Tissue Culture1

Chester M Southam 1,2, Frederick H Shipkey 1,2, Virginia I Babcock 1,2, Roller Bailey 1,2, Robert A Erlandson 1,2
PMCID: PMC277276  PMID: 14197886

Abstract

Southam, Chester M. (Sloan-Kettering Institute for Cancer Research, New York, N.Y.), Frederick H. Shipkey, Virginia I. Babcock Roller Bailey, and Robert A. Erlandson. Virus biographies. I. Growth of West Nile and Guaroa viruses in tissue culture. J. Bacteriol. 88:187–199. 1964.—Monolayer tissue cultures of HEp 2 cells (human epidermoid carcinoma) were inoculated with Guaroa or West Nile viruses. At daily intervals for 4 days thereafter, these cultures were studied by (i) light microscopy of living cultures and stained cultures, (ii) intracerebral inoculation of mice to titrate infectivity, (iii) acridine orange stain to observe nucleic acid changes, (iv) fluorescein-labeled antibody technique to observe specific viral antigen, and (v) electron microscopy to observe virus particles. Guaroa virus infectivity increased progressively over the 4-day period, and caused definite cytolysis by day 3. Cytoplasmic ribonucleic acid (RNA) staining was increased by 24 hr, and by 48 hr the RNA formed globular masses, particularly in degenerating cells. Viral antigen was occasionally seen on day 1, and increased progressively thereafter, forming numerous sharply outlined particles in cytoplasm concentrated at the cell membrane. Virus particles were ellipsoids with a dense nucleoid and a single membrane approximately 70 by 90 mμ, which appeared to form at the cell membrane just before being discharged. West Nile virus infectivity increased sharply between 1 and 2 days, but caused little cytolysis even by 4 days. Cytoplasmic RNA staining increased progressively for the 4 days, usually forming a large juxtanuclear mass in each affected cell. Viral antigen was not detected on day 1, but increased progressively thereafter, forming a crescent or a single diffuse mass adjacent to the nucleus. Virus particles were spheres approximately 30 mμ in diameter, with a dense nucleoid and a single membrane. They appeared to form in granular foci in the cytoplasm and then to fill the channels of the endoplasmic reticulum. No significant nuclear changes were observed with either virus by any of these techniques.

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Selected References

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  1. BARUCH E. ELECTRON MICROSCOPIC STUDY OF SPINAL CORD OF MICE INFECTED WITH YELLOW FEVER VIRUS. J Ultrastruct Res. 1963 Oct;59:209–224. doi: 10.1016/s0022-5320(63)80003-9. [DOI] [PubMed] [Google Scholar]
  2. BERGOLD G. H., WEIBEL J. Demonstration of yellow fever virus with the electron microscope. Virology. 1962 Aug;17:554–562. doi: 10.1016/0042-6822(62)90155-1. [DOI] [PubMed] [Google Scholar]
  3. CASALS J. Procedures for identification of arthropod-borne viruses. Bull World Health Organ. 1961;24:723–734. [PMC free article] [PubMed] [Google Scholar]
  4. COLTER J. S., BIRD H. H., MOYER A. W., BROWN R. A. Infectivity of ribonucleic acid isolated from virus-infected tissues. Virology. 1957 Dec;4(3):522–532. doi: 10.1016/0042-6822(57)90084-3. [DOI] [PubMed] [Google Scholar]
  5. COONS A. H. Fluorescent antibody methods. Gen Cytochem Methods. 1958;1:399–422. [PubMed] [Google Scholar]
  6. EAGLE H. The minimum vitamin requirements of the L and HeLa cells in tissue culture, the production of specific vitamin deficiencies, and their cure. J Exp Med. 1955 Nov 1;102(5):595–600. doi: 10.1084/jem.102.5.595. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. GROOT H., OYA A., BERNAL C., BARRETO-REYES P. Guaroa virus, a new agent isolated in Colombia, South America. Am J Trop Med Hyg. 1959 Sep;8:604–609. doi: 10.4269/ajtmh.1959.8.604. [DOI] [PubMed] [Google Scholar]
  8. KARNOVSKY M. J. Simple methods for "staining with lead" at high pH in electron microscopy. J Biophys Biochem Cytol. 1961 Dec;11:729–732. doi: 10.1083/jcb.11.3.729. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. KOPROWSKI H. Ascites tumors as culture media in quantitative growth studies of viral agents. Ann N Y Acad Sci. 1956 Mar 14;63(5):895–914. doi: 10.1111/j.1749-6632.1956.tb50899.x. [DOI] [PubMed] [Google Scholar]
  10. LUFT J. H. Improvements in epoxy resin embedding methods. J Biophys Biochem Cytol. 1961 Feb;9:409–414. doi: 10.1083/jcb.9.2.409. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. MELNICK J. L., PAUL J. R., RIORDAN J. T., BARNETT V. H., GOLDBLUM N., ZABIN E. Isolation from human sera in Egypt of a virus apparently identical to West Nile virus. Proc Soc Exp Biol Med. 1951 Aug;77(4):661–665. doi: 10.3181/00379727-77-18884. [DOI] [PubMed] [Google Scholar]
  12. MOORE A. E., SABACHEWSKY L., TOOLAN H. W. Culture characteristics of four permanent lines of human cancer cells. Cancer Res. 1955 Oct;15(9):598–602. [PubMed] [Google Scholar]
  13. NIVEN J. S., ARMSTRONG J. A., BALFOUR B. M., KLEMPERER H. G., TYRRELL D. A. Cellular changes accompanying the growth of influenza virus in bovine cell cultures. J Pathol Bacteriol. 1962 Jul;84:1–18. [PubMed] [Google Scholar]
  14. SMITHBURN K. C., BUGHER J. C. Ultrafiltration of recently isolated neurotropic viruses. J Bacteriol. 1953 Aug;66(2):173–177. doi: 10.1128/jb.66.2.173-177.1953. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. WATSON M. L. Staining of tissue sections for electron microscopy with heavy metals. J Biophys Biochem Cytol. 1958 Jul 25;4(4):475–478. doi: 10.1083/jcb.4.4.475. [DOI] [PMC free article] [PubMed] [Google Scholar]

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