Summary
A 0.75% agarose overlay procedure is described which has the advantages of being easy to prepare and perform, and is applicable to several commonly used insect cell lines and viruses. In addition, plaque variants which do not produce polyhedra can be easily detected.
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Brown, M.; Faulkner, P. Plaque assay of nuclear polyhedrosis viruses in cell culture. Appl. Environ. Microbiol. 36: 31–35; 1978.
Carstens, E. B.; Tija, S. T.; Doerfler, W. Infectious DNA fromAutographa californica nuclear polyhedrosis virus. Virology 101: 311–314; 1980.
Fraser, M. J.; Hink, W. F. Comparative sensitivity of several plaque assay techniques employing TN-368 and IPLB-SF 21AE insect cell lines for plaque variants ofGalleria mellonella nuclear polyhedrosis virus. J. Invertebr. Pathol. In press.
Knudson, D. L. Plaque assay of Baculoviruses employing an agarose-nutrient overlay. Intervirology 11: 40–46; 1979.
Lee, H. H.; Miller, L. K. Isolation of genotypic variants ofAutographa californica nuclear polyhedrosis virus. J. Virol. 27: 754–767; 1978.
Smith, G. E.; Summers, M. D. Analysis of baculovirus genomes with restriction endonucleases. Virology 89: 517–527; 1978.
Wood, H. A. An agarose overlay plaque assay method forAutographa californica nuclear polyhedrosis virus. J. Invertebr. Pathol. 29: 304–344; 1977.
Lynn, D. E.; Hink, W. F. Infection of synchronized TN-368 cell cultures with alfalfa looper nuclear polyhedrosis virus. J. Invertebr. Pathol. 32: 1–5; 1978.
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Fraser, M.J. Simplified agarose overlay plaque assay for insect cell lines and insect nuclear polyhedrosis viruses. Journal of Tissue Culture Methods 7, 43–46 (1982). https://doi.org/10.1007/BF01666880
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DOI: https://doi.org/10.1007/BF01666880