1997 Volume 183 Issue 2 Pages 101-112
A recently discovered non-A non-B hepatitis virus has been designated hepatitis G virus (HGV). Blood contamination has been proposed as its mode of transmission. We studied the genoprevalence of HGV in Japanese people at high risk. HGV was identified in serum by a reverse-transcription polymerase chain reaction. HGV was detected in 16.0% of intravenous drug users (IDUs) (n=25), 16.2% of those with tattoos (n=37), 10.9% of IDUs with tattoos (n=55), 5.7% of chronic hepatitis (CH)-C patients (n=87), and in none of the CH-B (n=50) or CH non-B non-C (n=46) patients. Serum alanine aminotransferase (ALT) levels of those infected with HGV alone (n=3) were all within normal range. In the patients with CH-C, serum ALT levels of those coinfected with HGV were similar to serum ALT levels of those without HGV infection. A phylogenetic tree of isolated HGV clones showed that the HGVs of these subjects bore only a distant-resemblance to clones reported from Africa and North America, and that variation in the phylogenetic index of HGV clones was small. These results suggest that HGV clones from different areas have genetic heterogeneity and that HGV causes no or mild hepatitis.
