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The serological and molecular epidemiology of GB virus C/hepatitis G virus infection in a hepatitis C and B endemic area

  • M. L. Yu
  • , W. L. Chuang
  • , C. Y. Dai
  • , S. N. Lu
  • , J. H. Wang
  • , J. F. Huang
  • , S. C. Chen
  • , Z. Y. Lin
  • , M. Y. Hsieh
  • , J. F. Tsai
  • , L. Y. Wang
  • , W. Y. Chang*
  • *Corresponding author for this work
  • Hepatobiliary Division
  • Chang Gung Memorial Hospital
  • Foo Yin Hospital

Research output: Contribution to journalJournal Article peer-review

16 Scopus citations

Abstract

Objectives: To investigate the serological and molecular characteristics of GB virus C/hepatitis G virus (GBV-C/HGV) infection in the hepatitis C virus (HCV)/hepatitis B virus (HBV)-endemic areas in Taiwan. Methods: Sera from 200 residents from Masago, an HCV/HBV-endemic community in Taiwan, and 400 blood donors were tested for GBV-C/HGV RNA by using nested reverse transcription-polymerase chain reaction and for antibodies to GBV-C/HGV E2-protein (anti-E2) by an enzyme-linked immunosorbent assay. Phylogenetic analysis of GBV-C/HGV was performed. Results: The prevalence of GBV-C/HGV viraemia, anti-E2 and GBV-C/HGV exposure among residents of Masago was significantly higher than that among donors (17.0%, 25.5% and 39.5% vs. 3.3%, 7.5% and 10.3%, respectively; all P<0.0001). In Masago, the prevalence of GBV-C/HGV exposure was significantly higher in residents exposed to HCV than in those without HCV exposure (45.8% vs. 24.1%; P=0.005). Based on multivariate analyses, HCV viraemia was the only significant factor associated with elevated levels of alanine aminotransferase in Masago. Phylogenetic analysis showed all 34 GBV-C/HGV isolates from Masago clustered within genotype 3. Conclusions: GBV-C/HGV was highly prevalent in Masago, an HCV/HBV-endemic community in Taiwan. HCV viraemia played the most important clinical hepatopathic role in the area. Infections with other hepatitis viruses did not influence the anti-E2 seroconversion from GBV-C/HGV infections.

Original languageEnglish
Pages (from-to)61-66
Number of pages6
JournalJournal of Infection
Volume42
Issue number1
DOIs
StatePublished - 2001
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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