Buoyant Density of Bovine Viral Diarrhea Virus
@article{Parks1972BuoyantDO, title={Buoyant Density of Bovine Viral Diarrhea Virus}, author={J B Parks and Randall F. Pritchett and Yuan Chung Zee}, journal={Proceedings of the Society for Experimental Biology and Medicine}, year={1972}, volume={140}, pages={595 - 598} }
Summary Bovine viral diarrhea virus (BV DV), strain NADL, was purified by removing extracellular fluid from infected cultures at 96 hr postinoculation and clarifying by low speed centrifugation. Clarified fluid was concentrated by centrifugation onto a two-step 20-50% sucrose discontinuous gradient. Most of the infectivity was associated with a light scattering band in the region of 20% sucrose. 3H-Uridine labeled and unlabeled viral band material was then pooled, diluted, and isopycnically…
10 Citations
Comparison of methods for concentration and purification of bovine viral diarrhea virus.
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Characterization of bovine viral diarrhea virus RNA
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RNA extracted from isopycnically banded [3-H]uridine-labeled bovine viral diarrhea virus with sodium dodecyl sulfate was resolved into one major and two minor components by both sedimentation…
Inhibition of host ER glucosidase activity prevents Golgi processing of virion-associated bovine viral diarrhea virus E2 glycoproteins and reduces infectivity of secreted virions.
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Results suggest that BVDV is secreted through a Golgi-mediated pathway and that host ER glucosidase activity is required for production of infectious virions and Golgi processing of envelope E2 protein during virus egress.
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SummaryThe sedimentation coefficient and buoyant density of hog cholera, bovine viral diarrhea and Border disease viruses, have been compared with those of representative members of the family…
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The cytopathogenicity proved to be stable and growth parameters did not differ from those other cell cultures of bovine origin, and a significantly slower multiplication rate was observed with non-cytopathogenic strains.