Abstract
Conclusion
Evidence has been brought forward to indicate that Columbia SK, Columbia MM, Mengo encephalomyelitis and encephalomyocarditis viruses agglutinate sheep red cells. It is therefore possible to identify these viruses by means of hemagglutination and to measure the antibody content of antisera. Since the viruses show characteristic spontaneous elution or dispersion from the erythrocytes, the method can be used for purposes of selective adsorption of the viruses without loss of their hemagglutinative activity. Moreover, the uniformity of the hemagglutination reaction shown by the 4 viruses and the cross-inhibition that exists among them supports the findings of Warren and Smadel 6 and of Dick 7 that these viruses are similar in many repects and are of the same group.
Seventeen other neurotropic viruses were tested for their capacity to agglutinate characteristically erythrvcytes deriving from sheep, man (group O), chicken, horse, hamster, dog, cat and guinea pig; these tests failed.
Another phenomenon that was observed is the nonspecific agglutination of dog, cat and guinea pig erythrocytes by normal or virusinfected mouse brains. With respect to agglutination of hamster cells, an inhibitor of agglutination is present not only in suspensions of normal mouse brain but also in normal serum and antiserum against the neurotropic viruses.
The fact that neurotropic viruses are often used in the form of mouse brain suspensions renders it important therefore for investigators to use proper controls for the variable of the test and, in addition, to identify positive reactions by specific means.
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