Mitochondrial DNA mutations in ageing and disease: implications for HIV?

Antivir Ther. 2015;20(2):109-20. doi: 10.3851/IMP2824. Epub 2014 Jul 17.

Abstract

Mitochondrial DNA (mtDNA) mutations cause neurological and multisystem disease. Somatic (acquired) mtDNA mutations are also associated with degenerative diseases and with normal human ageing. It is well established that certain nucleoside reverse transcriptase inhibitor (NRTI) antiretroviral drugs cause inhibition of the mtDNA polymerase, pol γ, leading to a reduction in mtDNA content (depletion). Given this effect of NRTI therapy on mtDNA replication, it is plausible that NRTI treatment may also lead to increased mtDNA mutations. Here we review recent evidence for an effect of HIV infection or NRTI therapy on mtDNA mutations, as well as discussing the methodological challenges in addressing this question. Finally, we discuss the possible implications for HIV-infected persons, with particular reference to ageing.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Aging / drug effects
  • Aging / genetics*
  • Aging / metabolism
  • Aging / pathology
  • Anti-HIV Agents / administration & dosage
  • Anti-HIV Agents / adverse effects*
  • DNA Mutational Analysis / instrumentation
  • DNA Mutational Analysis / methods
  • DNA Polymerase gamma
  • DNA, Mitochondrial / chemistry
  • DNA, Mitochondrial / genetics*
  • DNA, Mitochondrial / metabolism
  • DNA-Directed DNA Polymerase / genetics*
  • DNA-Directed DNA Polymerase / metabolism
  • HIV / drug effects
  • HIV / enzymology
  • HIV / growth & development
  • HIV Infections / drug therapy
  • HIV Infections / enzymology
  • HIV Infections / genetics
  • HIV Infections / pathology
  • Humans
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Mitochondria / pathology
  • Mitochondrial Proteins / genetics*
  • Mitochondrial Proteins / metabolism
  • Mutation
  • Reverse Transcriptase Inhibitors / administration & dosage
  • Reverse Transcriptase Inhibitors / adverse effects*

Substances

  • Anti-HIV Agents
  • DNA, Mitochondrial
  • Mitochondrial Proteins
  • Reverse Transcriptase Inhibitors
  • DNA Polymerase gamma
  • DNA-Directed DNA Polymerase
  • POLG protein, human