Date of Award:

5-1-1981

Document Type:

Thesis

Degree Name:

Master of Science (MS)

Department:

Biology

Department name when degree awarded

Life Sciences:Biology

Committee Chair(s)

Rex S. Spendlove

Committee

Rex S. Spendlove

Abstract

Cell-culture adapted bovine rotavirus was inactivated by varying exposures to ultraviolet light. The purpose was twofold: (1) to ascertain if efficient recombination would be demonstrated with rotavirus and (2) to determine optimal radiation dosages required to induce lethal mutations while retaining a relatively high efficiency of recombination. When assayed by the immuno-fluorescent cell counting method, the irradiated virus exhibited the phenomenon of multiplicity reactivation, suggesting the existence of a mechanism of genetic recombination. Once it had been determined that the double-stranded genome was suitable for additional genetic studies, a modified plaque assay was employed to screen plaque-purified bovine rotavirus for chemically-induced temperature sensitivity.

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