Circulation of hepatitis delta virus and occult hepatitis B virus infection amongst HIV/HBV co-infected patients in Korle-Bu, Ghana

PLoS One. 2021 Jan 7;16(1):e0244507. doi: 10.1371/journal.pone.0244507. eCollection 2021.

Abstract

Background: Within HIV/HBV infected patients, an increase in HDV infection has been observed; there is inadequate information on HDV prevalence as well as virologic profile in Ghana. This study sought to determine the presence of HDV in HIV/HBV co-infected patients in Ghana.

Methods: This was a longitudinal purposive study which enrolled 113 HIV/HBV co-infected patients attending clinic at Korle-Bu Teaching Hospital (KBTH) in Accra, Ghana. After consenting, 5 mL whole blood was collected at two-time points (baseline and 4-6 months afterwards). The sera obtained were tested to confirm the presence of HIV, HBV antibodies and/or antigens, and HBV DNA. Antibodies and viral RNA were also determined for HDV. Amplified HBV DNA and HDV RNA were sequenced and phylogenetic analysis carried out with reference sequences from the GenBank to establish the genotypes.

Results: Of the 113 samples tested 63 (55.7%) were females and 50 (44.25%) were males with a median age of 45 years. A total of 100 (88.5%) samples had detectable HBV surface antigen (HBsAg), and 32 out of the 113 had detectable HBV DNA. Nucleotide sequences were obtained for 15 and 2 samples of HBV and HDV, respectively. Phylogenetic analysis was predominantly genotype E for the HBVs and genotype 1 for the HDVs. Of the 13 samples that were HBsAg unreactive, 4 (30.8%) had detectable HBV DNA suggesting the incidence of occult HBV infections. The percentage occurrence of HDV in this study was observed to be 3.54.

Conclusion: Our data suggest the presence and circulation of HDV and incidence of occult HBV infection in HIV/HBV co-infected patients in Ghana. This informs health staff and makes it imperative to look out for the presence of HDV and occult HBV in HIV/HBV co-infected patients presenting with potential risk of liver cancers and HBV transmission through haemodialysis and blood transfusions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Alanine Transaminase / metabolism
  • Aspartate Aminotransferases / metabolism
  • Coinfection / enzymology
  • Coinfection / virology*
  • Female
  • Genotyping Techniques
  • Ghana
  • HIV Infections / enzymology
  • HIV Infections / virology*
  • Hepatitis B / enzymology
  • Hepatitis B / virology*
  • Hepatitis B virus / genetics
  • Hepatitis B virus / isolation & purification*
  • Hepatitis B virus / physiology*
  • Hepatitis Delta Virus / isolation & purification*
  • Hepatitis Delta Virus / physiology
  • Humans
  • Longitudinal Studies
  • Male
  • Middle Aged
  • Young Adult

Substances

  • Aspartate Aminotransferases
  • Alanine Transaminase

Grants and funding

KA received funding support through the West African Centre for Cell Biology of Infectious Pathogens (WACCBIP) under the World Bank’s African Centres of Excellence (ACE) Project (https://www.waccbip.org) and the WHO supported National Poliomyelitis Reference Laboratory, Ghana. The funders had no role in the study design, data collection and analysis, or preparation of manuscript.