Evidence that the GBV-C/hepatitis G virus is primarily a lymphotropic virus
Corresponding Author
Timothy J. Tucker
Department of Medical Microbiology/SAIMR, University of Cape Town, Observatory, Cape Town, South Africa
MRC/UCT Liver Research Centre, University of Cape Town, Observatory, Cape Town, South Africa
Department of Medical Microbiology, Medical School, University of Cape Town, Observatory, 7925, South Africa===Search for more papers by this authorHeidi E.M. Smuts
Department of Medical Microbiology/SAIMR, University of Cape Town, Observatory, Cape Town, South Africa
Search for more papers by this authorChristopher Eedes
Department of Forensic Medicine and Toxicology, University of Cape Town, Observatory, Cape Town, South Africa
Search for more papers by this authorGideon D. Knobel
Department of Forensic Medicine and Toxicology, University of Cape Town, Observatory, Cape Town, South Africa
Search for more papers by this authorPeter Eickhaus
Department of Medical Microbiology/SAIMR, University of Cape Town, Observatory, Cape Town, South Africa
MRC/UCT Liver Research Centre, University of Cape Town, Observatory, Cape Town, South Africa
Search for more papers by this authorSimon C. Robson
MRC/UCT Liver Research Centre, University of Cape Town, Observatory, Cape Town, South Africa
Search for more papers by this authorRalph E. Kirsch
MRC/UCT Liver Research Centre, University of Cape Town, Observatory, Cape Town, South Africa
Search for more papers by this authorCorresponding Author
Timothy J. Tucker
Department of Medical Microbiology/SAIMR, University of Cape Town, Observatory, Cape Town, South Africa
MRC/UCT Liver Research Centre, University of Cape Town, Observatory, Cape Town, South Africa
Department of Medical Microbiology, Medical School, University of Cape Town, Observatory, 7925, South Africa===Search for more papers by this authorHeidi E.M. Smuts
Department of Medical Microbiology/SAIMR, University of Cape Town, Observatory, Cape Town, South Africa
Search for more papers by this authorChristopher Eedes
Department of Forensic Medicine and Toxicology, University of Cape Town, Observatory, Cape Town, South Africa
Search for more papers by this authorGideon D. Knobel
Department of Forensic Medicine and Toxicology, University of Cape Town, Observatory, Cape Town, South Africa
Search for more papers by this authorPeter Eickhaus
Department of Medical Microbiology/SAIMR, University of Cape Town, Observatory, Cape Town, South Africa
MRC/UCT Liver Research Centre, University of Cape Town, Observatory, Cape Town, South Africa
Search for more papers by this authorSimon C. Robson
MRC/UCT Liver Research Centre, University of Cape Town, Observatory, Cape Town, South Africa
Search for more papers by this authorRalph E. Kirsch
MRC/UCT Liver Research Centre, University of Cape Town, Observatory, Cape Town, South Africa
Search for more papers by this authorAbstract
GB virus-C and the hepatitis G virus (GBV-C/HGV) are variants of the same positive sense RNA flavivirus, initially thought to be associated with hepatitis. The tissue tropism of GBV-C/HGV in normal subjects has not been evaluated to date using an extended tissue spectrum. Therefore, the sites of GBV-C/HGV replication were investigated in serum and twenty-three tissues collected during post-mortem examination of four apparently healthy individuals who died accidental deaths, who were infected with GBV-C/HGV. All were anti-HIV and anti-HCV negative and three out of four were HBsAg negative. Tissues were collected carefully to prevent cross contamination. A highly strand-specific RT-PCR assay was employed for the detection of either GBV-C/HGV positive strand RNA (virion) or negative strand RNA (replicative intermediary). Strand specificity of the RT-PCR assay was assessed with synthetic positive-and negative strand GBV-C/HGV RNA generated from a plasmid, using T7 and T3 RNA polymerases. The spleen and bone marrow biopsies were found to be uniformly positive for both negative-and positive strand GBV-C/HGV RNA. In addition, one cadaver was positive for both RNA strands in the kidney, and another positive for both in the liver. No negative strand RNA was detected in the following: brain, muscle, heart, thyroid, salivary gland, tonsil, lung, lymph nodes, gall bladder, pancreas, oesophagus, stomach, small bowel, large bowel, adrenal gland, gonad, aorta, skin and cartilage. This preliminary study concludes that GBV-C/HGV is a lymphotropic virus that replicates primarily in the spleen and bone marrow. J. Med. Virol. 61:52–58, 2000. © 2000 Wiley-Liss, Inc.
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