AJTMH Transactions of the Royal Society of Tropical Medicine and Hygiene
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Am. J. Trop. Med. Hyg., 12(4), 1963, pp. 647-652
Copyright © 1963 by The American Society of Tropical Medicine and Hygiene

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Study of the Antigenic Relationships between Junín Virus, the Etiological Agent of Argentinian Hemorrhagic Fever, and Other Arthropod-Borne Viruses

Norma E. Mettler*, Jordi Casals AND Robert E. Shope
The Rockefeller Foundation Virus Laboratories, New York, New York

Strains XJ, R and F of Junín virus, which were isolated by two different groups of investigators, have been compared for the first time and been found to be indistinguishable by complement-fixation test. Neutralization test comparisons are pending.

Junín and Tacaribe virus from Trinidad have been shown to be closely related by complement-fixation test, although distinguishable on the basis of serum titers. In limited studies by neutralization test they were easily separable. It is of interest that sera from persons convalescing from Argentinian hemorrhagic fever fixed complement in the presence of Tacaribe antigen.

No cross-reactions were observed between Junín complement-fixing antigens and immune sera for 139 other arthropod-borne viruses, or between Junín antisera and hemagglutinating antigens from 41 arboviruses. Junín antigens likewise failed to react by complement-fixation test with various non-arboviruses including encephalomyocarditis, mouse encephalomyelitis and several rickettsiae.

From descriptions in the literature there appears to be a degree of clinical resemblance between Korean and Argentinian hemorrhagic fevers; sera from six human patients convalescing from the former failed to react with a Junín complement-fixing antigen.

Junín antigens with consistently good complement-fixing titers between 1:32 and 1:128 were obtained by harvesting infected mouse brain tissue 7 or 8 days after inoculation. A growth curve study showed maximal virus titer at that time in the absence or near absence of signs of illness.

Junín strain XJ, which originally was highly pathogenic for guinea pigs by the intraperitoneal route of inoculation, appeared to have lost its pathogenicity for guinea pigs by that route after about 40 passages in newborn mice.


* Permanent address: Department of Microbiology and Parasitology, Medical School, University of Buenos Aires; holder of a fellowship from Consejo Nacional de Investigaciones Cientificas y Técnicas, Argentine Republic.




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K. M. Johnson, R. B. Mackenzie, P. A. Webb, and M. L. Kuns
Chronic Infection of Rodents by Machupo Virus
Science, December 17, 1965; 150(3703): 1618 - 1619.
[Abstract] [PDF]




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Copyright © 1963 by the American Society of Tropical Medicine and Hygiene.