Abstract
Summary Foot-and-mouth disease virus RNA infectivity for calf-kidney cultures was 102- to 107-fold higher in the presence of DEAE-dextran than in its absence. By comparison, this polycation had no effect on the sensitivity of the plaque assay of the intact virus. At an optimum concentration of DEAE-dextran of about 1000 μg/ml, the infectivity of different lots of RNA ranged from 10-2 to 102 times that of the virus. A linear relationship between plaque numbers and dilution was observed, and the assay was highly reproducible. DEAE-dextran did not raise the temperature of half-melting of the RNA.

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