Abstract
A sequential and quantitative survey of brain and liver of suckling mice for infective virus and complement-fixing antigen, after infection with yellow fever virus, showed that while there was progressive increase of infective virus content in both organs, only the brain showed a corresponding rise in CF antigen. Histopathological examination revealed that the liver was not significantly involved. The target organ was the brain, where the progressive pathological changes culminated in an acute encephalitis by the 3rd day of experiment. Organ destruction began with the molecular layer of the grey matter. But by the 4th day after infection the entire cerebral cortex was involved. At the initial stages the hippocampus was particularly affected. Tissue damage did not appear to be entirely due to the differential quantitative localization of infective virus. It was hypothesized that the CF antigen acting singly or in conjunction with some hypothetical proteins may be principally involved in the pathological outcome of the disease.
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- Amako K., Dales S. Cytopathology of Mengovirus infection. I. Relationship between cellular disintegration and virulence. Virology. 1967 Jun;32(2):184–200. doi: 10.1016/0042-6822(67)90269-3. [DOI] [PubMed] [Google Scholar]
- BABLANIAN R., EGGERS H. J., TAMM I. STUDIES ON THE MECHANISM OF POLIOVIRUS-INDUCED CELL DAMAGE. II. THE RELATION BETWEEN POLIOVIRUS GROWTH AND VIRUS-INDUCED MORPHOLOGICAL CHANGES IN CELLS. Virology. 1965 May;26:114–121. doi: 10.1016/0042-6822(65)90031-0. [DOI] [PubMed] [Google Scholar]
- BALTIMORE D., EGGERS H. J., FRANKLIN R. M., TAMM I. Poliovirus-induced RNA polymerase and the effects of virus-specific inhibitors on its production. Proc Natl Acad Sci U S A. 1963 Jun;49:843–849. doi: 10.1073/pnas.49.6.843. [DOI] [PMC free article] [PubMed] [Google Scholar]
- BARUCH E., CARBONELL L., WEIBEL J. Fine structure of Councilman bodies in the liver of Aluatta seniculus seniculus L. infected with yellow fever virus. Exp Cell Res. 1963 Jan;29:50–53. doi: 10.1016/0014-4827(63)90356-2. [DOI] [PubMed] [Google Scholar]
- BERGOLD G. H., WEIBEL J. Demonstration of yellow fever virus with the electron microscope. Virology. 1962 Aug;17:554–562. doi: 10.1016/0042-6822(62)90155-1. [DOI] [PubMed] [Google Scholar]
- Bablanian R. Studies on the mechanism of vaccinia virus cytopathic effects: effect of inhibutors of RNA and protein synthesis on early virus-induced cell damage. J Gen Virol. 1970 Feb;6(2):221–230. doi: 10.1099/0022-1317-6-2-221. [DOI] [PubMed] [Google Scholar]
- DEFENDI V. Cytopathology of virus infection. Fed Proc. 1962 Nov-Dec;21:1113–1117. [PubMed] [Google Scholar]
- David-West T. S. Organ distribution of infectivity and complement-fixing antigen with two Nigerian arboviruses. Br J Exp Pathol. 1970 Jun;51(3):332–339. [PMC free article] [PubMed] [Google Scholar]
- GINSBERG H. S. Biological and biochemical basis for cell injury by animal viruses. Fed Proc. 1961 Jul;20:656–660. [PubMed] [Google Scholar]
- Guskey L. E., Smith P. C., Wolff D. A. Patterns of cytopathology and lysosomal enzyme release in poliovirus-infected HEp-2 cells treated with either 2-(alpha-hydroxybenzyl)-benzimidazole or guanidine HCl. J Gen Virol. 1970 Jan;6(1):151–161. doi: 10.1099/0022-1317-6-1-151. [DOI] [PubMed] [Google Scholar]
- MALLUCCI L., ALLISON A. C. LYSOSOMAL ENZYMES IN CELLS INFECTED WITH CYTOPATHIC AND NON-CYTOPATHIC VIRUSES. J Exp Med. 1965 Mar 1;121:477–485. doi: 10.1084/jem.121.3.477. [DOI] [PMC free article] [PubMed] [Google Scholar]
- PEREIRA H. G. The cytopathic effect of animal viruses. Adv Virus Res. 1961;8:245–285. doi: 10.1016/s0065-3527(08)60687-9. [DOI] [PubMed] [Google Scholar]
- Scholtissek C., Becht H., Drzeniek R. Biochemical studies on the cytopathic effect of influenza viruses. J Gen Virol. 1967 Apr;1(2):219–225. doi: 10.1099/0022-1317-1-2-219. [DOI] [PubMed] [Google Scholar]


