| Literature DB >> 3942507 |
G Carloni, C Delfini, S Colloca, E Alfani, G Taliani, C De Bac.
Abstract
The presence of Hepatitis B virus (HBV) DNA in sera of patients with HBV related diseases is considered a reliable marker of virus active replication. In this paper HBV DNA was assayed by the molecular hybridization method with a 32P labeled nick translated HBV probe. The assay was positive in sera of 21 out of 22 HBeAg-positive and 4 out of 8 HBeAg-negative asymptomatic HBsAg carriers. 15 HBsAg-negative sera obtained from healthy donors showed no HBV DNA. Almost 80 per cent of HBeAg and HBV DNA positive sera revealed a DNA-polymerase activity. In order to determine the infectivity of HBsAg carriers, it appears that, whenever possible, the HBV DNA spot hybridization should be performed in conjunction with the DNA-polymerase, HBsAg and HBeAg tests.Entities:
Mesh:
Substances:
Year: 1986 PMID: 3942507 DOI: 10.1007/bf01310546
Source DB: PubMed Journal: Arch Virol ISSN: 0304-8608 Impact factor: 2.574