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Oncogenic transformation of primary hamster embryo cells by equine herpesvirus type 3

  • Donna C. Sullivan
    ,
  • Sally S. Atherton
    ,
  • Gretchen B. Caughman
    ,
  • John Staczek
    ,
  • Dennis J. O'Callaghan(corresponding author)
*Corresponding author for this work
  • LSU Health Sciences Center - Shreveport
Scholary Output:
Contribution to journal
Article
Peer-review

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Infection of nonpermissive primary hamster embryo cells with equine herpesvirus type 3 (EHV-3; multiplicity of infection = 10 pfu/cell) resulted in an abortive infection and the development of several hundred foci of rapidly growing cells. Five of these foci were chosen at random for the establishment of transformed cell lines, designated EVD-1 (equine venereal disease) through 5. These transformed cell lines exhibited altered biological properties typical of transformed cells, including immortality, growth to high saturation density, colony formation in soft agar, reduced serum requirements, aneuploid karyotype, and oncogenicity in syngeneic animals. Subsequently, five corresponding tumor cell lines (EVD-1T through 5T) with similar biological properties were established. All EHV-3 transformed and tumor cell lines have been shown to express EHV-3-specific proteins by indirect immunofluorescence assays employing rabbit antisera to EHV-3 infected equine cells. None of the transformed cell lines were found to release infectious virus by infectious center or cocultivation assay or to contain viral particles by electron microscopy.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 201-212 (12 pages)

Journal (Volume, Issue Number)

Virus Research (Volume 5, Issue 2-3)

Publication milestones

  • Published - 08/1986

Publication status

Published - 08/1986

ISSN

0168-1702

Publication IDs

  • Scopus: 0022483698
  • PubMed: 3765823

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Scopus
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1
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4
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0.80
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1
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1

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Funding Details

We thank Cynthia Harrison and Angela Houston for typing the manuscript. We also thank Dr. John Jackson for the karyotype analyses. Support for this investigation was obtained from research grants AI 22001, A122894, and AI 21996 from the National Institutes of Health and a Grayson Foundation research grant.
FundersFunding number
NIH
-
NIAID
R01AI021996
GJCRF
-