Hepatitis B virus surface protein induces oxidative stress by increasing peroxides and inhibiting antioxidant defences in human spermatozoa

Reprod Fertil Dev. 2020 Oct;32(14):1180-1189. doi: 10.1071/RD20130.

Abstract

Hepatitis B virus (HBV) infection may affect sperm motility in patients with HBV. HBV surface protein (HBs) decreases mitochondrial membrane potential, impairs motility and induces apoptotic-like changes in human spermatozoa. However, little is known about how human spermatozoa respond to reactive oxygen species (ROS; mainly peroxides) induced by HBs. In this study, HBs induced supraphysiological ROS levels in human spermatozoa and reduced the formation of 2-cell embryos (obtained from hamster oocytes and human spermatozoa). HBs induced a pre-apoptotic status in human spermatozoa, as well as antioxidant defences by increasing glutathione peroxidase 4 (GPX4) and peroxiredoxin 5 (PRDX5) levels. These results highlight the molecular mechanism responsible for the oxidative stress in human spermatozoa exposed to HBV and the antioxidant defence response involving GPX4 and PRDX5.

MeSH terms

  • Antioxidants / metabolism
  • DNA Damage / physiology
  • Hepatitis B virus / metabolism*
  • Humans
  • Male
  • Mitochondria / metabolism
  • Oxidative Stress / physiology*
  • Peroxides / metabolism*
  • Peroxiredoxins / metabolism
  • Phospholipid Hydroperoxide Glutathione Peroxidase / metabolism
  • Reactive Oxygen Species / metabolism
  • Sperm Motility / physiology
  • Spermatozoa / metabolism*
  • Spermatozoa / virology

Substances

  • Antioxidants
  • Peroxides
  • Reactive Oxygen Species
  • Phospholipid Hydroperoxide Glutathione Peroxidase
  • Peroxiredoxins