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Studies of GB hepatitis agent in tamarins

✍ Scribed by Peter Karayiannis; Lidija M. Petrovic; Mark Fry; Duncan Moore; Mike Enticott; Michael J. McGarvey; Peter J. Scheuer; Howard C. Thomas


Book ID
102850728
Publisher
John Wiley and Sons
Year
1989
Tongue
English
Weight
932 KB
Volume
9
Category
Article
ISSN
0270-9139

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✦ Synopsis


Three tamarins (Saguinus labiatus), two of which had previously been infected with hepatitis A virus and parenteral non-A, non-B hepatitis, were inoculated intravenously with the agent of GB hepatitis. All three animals developed alanine aminotransferase abnormalities 2, weeks after inoculation. Peak alanine aminotransferase levels were recorded 4 weeks postinoculation. These declined thereafter but continued to fluctuate at abnormal levels for 32 weeks. Liver biopsies showed liver cell swelling and inflammation with focal necrosis. Portal tracts and areas around central veins were heavily infiltrated with mononuclear cells. A fourth animal (no previous exposure to hepatitis viruses) inoculated with GB was killed on Day 15 postinoculation. Serum and extracts of liver and feces from this day were used as inocula for three other animals. Only the serum and liver extract transmitted GB hepatitis. The fecal specimen did not transmit and a fecal extract taken at a later date from another animal was also noninfectious.

GB hepatitis virus is distinct from the viruses causing Type A and blood-borne non-A, non-B-hepatitis. Although the virus is present in serum and has previously been transmitted per os, it is not shed in feces.

The agent of GB hepatitis was transmitted initially to tamarins following inoculation with serum obtained on the third day of jaundice from a surgeon in Chicago with acute hepatitis (1). Following the isolation and characterization of hepatitis A virus (HAV) (2-4) and from cross-challenge experiments in tamarins (5,6), it became apparent that the GB agent was unrelated to any human hepatitis virus known at the time, although some antigenic cross-reactivity with HAV could not be discounted (6). Further work with this agent has been plagued by controversy concerning its nature and origin. Parks and coworkers (7, 8) have questioned the human origin of GB, particularly since the virus appeared less ether and heat stable than HAY they claimed instead that it probably was a latent tamarin virus.

Attempts to isolate the virus from tamarin serum and liver extracts have produced equivocal results. Almeida et al. ( 9) detected aggregates of small spherical particles


πŸ“œ SIMILAR VOLUMES


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