Pseudorabies virus, Iowa strain ("mad itch"), after passage through guinea pig brain, fails to produce infection in guinea pigs when injected subcutaneously unless enormous doses are employed. Such virus is still pathogenic for rabbits when given subcutaneously and for rabbits and guinea pigs intracerebrally. Comparison of the amounts of virus present in the brains of rabbits and guinea pigs following fatal cerebral infection shows that the latter contain, per gram, only approximately one-tenth the amount of virus in the former. Comparing the resistance of the two species to subcutaneously administered pseudorabies virus it has been found that rabbits are approximately 100 times more susceptible than guinea pigs. Over and above the working of these two factors, guinea pig passage appears to achieve some actual attenuation of virus when tested by subcutaneous inoculation into guinea pigs.
Skip Nav Destination
Article navigation
1 June 1933
Article|
June 01 1933
MODIFICATION OF THE PATHOGENICITY OF PSEUDORABIES VIRUS BY ANIMAL PASSAGE
Richard E. Shope
Richard E. Shope
From the Department of Animal and Plant Pathology of The Rockefeller Institute for Medical Research, Princeton, N. J.
Search for other works by this author on:
Richard E. Shope
From the Department of Animal and Plant Pathology of The Rockefeller Institute for Medical Research, Princeton, N. J.
Received:
March 16 1933
Online ISSN: 1540-9538
Print ISSN: 0022-1007
Copyright, 1933, by The Rockefeller Institute for Medical Research New York
1933
J Exp Med (1933) 57 (6): 925–931.
Article history
Received:
March 16 1933
Citation
Richard E. Shope; MODIFICATION OF THE PATHOGENICITY OF PSEUDORABIES VIRUS BY ANIMAL PASSAGE . J Exp Med 1 June 1933; 57 (6): 925–931. doi: https://doi.org/10.1084/jem.57.6.925
Download citation file:
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Sign in via your Institution
Sign in via your InstitutionSuggested Content
Email alerts
Advertisement