TY - JOUR
T1 - Expression of avian reticuloendotheliosis virus envelope confers host resistance
AU - Federspiel, Mark J.
AU - Crittenden, Lyman B.
AU - Hughes, Stephen H.
N1 - Funding Information:
We are most grateful to Dr. Howard Temin for the gifts of REV-A-and SNV-cloned DNA and the hygromycin vector/helper cell line. We are also grateful to Dr. Lucy Lee for the gifts of REV-recognizing monoclonal antibodies. We acknowledge the excellent technical assistance of C. Cantwell and B. Riegle, and thank H. Marusiodis for preparing the manuscript. This research was supported in part by Grant US-8 1 l-84 from BARD, the United States-Israel Binational Agricultural Research and Development Fund, Grant 88-37266-4141 from the U.S. Department of Agriculture, and the National Cancer Institute, DHHS, undercontract No. NOl-CO-74101 with BRI.
PY - 1989/11
Y1 - 1989/11
N2 - We constructed two reticuloendotheliosis virus (REV) envelope gene expression plasmids, one containing the REV-A envelope gene, the other the spleen necrosis virus (SNV) envelope gene. Cell lines were generated by transfecting each of the REV envelope plasmids into D17 cells, a canine cell line. The levels of REV envelope glycoprotein in the cell lines were assayed by immunoprecipitating the envelope glycoproteins from lysates of cells that were labeled with [35S]methionine. Virological challenge assays determined the degree of resistance of each of the cell lines to REV-A or SNV infection. The expression of either envelope gene protected the cells from infection by either REV-A or SNV virus. Several cell lines were significantly more resistant to REV infection than the parental D17 cells, and two lines were 25,000-fold more resistant, approaching the resistance of REV-infected D17 cells to reinfection. The resistant cell lines were not able to confer resistance to susceptible cells by cocultivation. The level of resistance was correlated with the uniformity of expression of the REV envelope glycoproteins by the individual cells in a cell line and not with the absolute level of expression by the population of cells.
AB - We constructed two reticuloendotheliosis virus (REV) envelope gene expression plasmids, one containing the REV-A envelope gene, the other the spleen necrosis virus (SNV) envelope gene. Cell lines were generated by transfecting each of the REV envelope plasmids into D17 cells, a canine cell line. The levels of REV envelope glycoprotein in the cell lines were assayed by immunoprecipitating the envelope glycoproteins from lysates of cells that were labeled with [35S]methionine. Virological challenge assays determined the degree of resistance of each of the cell lines to REV-A or SNV infection. The expression of either envelope gene protected the cells from infection by either REV-A or SNV virus. Several cell lines were significantly more resistant to REV infection than the parental D17 cells, and two lines were 25,000-fold more resistant, approaching the resistance of REV-infected D17 cells to reinfection. The resistant cell lines were not able to confer resistance to susceptible cells by cocultivation. The level of resistance was correlated with the uniformity of expression of the REV envelope glycoproteins by the individual cells in a cell line and not with the absolute level of expression by the population of cells.
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U2 - 10.1016/0042-6822(89)90232-8
DO - 10.1016/0042-6822(89)90232-8
M3 - Article
C2 - 2554569
AN - SCOPUS:0024443819
SN - 0042-6822
VL - 173
SP - 167
EP - 177
JO - Virology
JF - Virology
IS - 1
ER -