The Crossroads between Host Copper Metabolism and Influenza Infection

Int J Mol Sci. 2021 May 23;22(11):5498. doi: 10.3390/ijms22115498.

Abstract

Three main approaches are used to combat severe viral respiratory infections. The first is preemptive vaccination that blocks infection. Weakened or dead viral particles, as well as genetic constructs carrying viral proteins or information about them, are used as an antigen. However, the viral genome is very evolutionary labile and changes continuously. Second, chemical agents are used during infection and inhibit the function of a number of viral proteins. However, these drugs lose their effectiveness because the virus can rapidly acquire resistance to them. The third is the search for points in the host metabolism the effect on which would suppress the replication of the virus but would not have a significant effect on the metabolism of the host. Here, we consider the possibility of using the copper metabolic system as a target to reduce the severity of influenza infection. This is facilitated by the fact that, in mammals, copper status can be rapidly reduced by silver nanoparticles and restored after their cancellation.

Keywords: ceruloplasmin; copper metabolism; influenza virus replicative cycle; silver nanoparticles.

Publication types

  • Review

MeSH terms

  • Animals
  • Antiviral Agents / pharmacology
  • Antiviral Agents / therapeutic use
  • Ceruloplasmin / physiology
  • Copper / metabolism*
  • Copper Transport Proteins / metabolism
  • Copper-Transporting ATPases / physiology
  • Drug Resistance, Viral
  • Host-Pathogen Interactions
  • Humans
  • Influenza A virus / physiology*
  • Influenza Vaccines
  • Influenza, Human / drug therapy
  • Influenza, Human / metabolism*
  • Influenza, Human / prevention & control
  • Influenza, Human / virology
  • Mammals / metabolism
  • Metal Nanoparticles / therapeutic use
  • Molecular Chaperones / metabolism
  • PrPC Proteins / physiology
  • RNA, Viral / physiology
  • Silver / therapeutic use
  • Superoxide Dismutase-1 / physiology
  • Viral Proteins / physiology
  • Virus Replication

Substances

  • Antiviral Agents
  • CCS protein, human
  • Copper Transport Proteins
  • Influenza Vaccines
  • Molecular Chaperones
  • PrPC Proteins
  • RNA, Viral
  • SOD1 protein, human
  • Viral Proteins
  • Silver
  • Copper
  • Superoxide Dismutase-1
  • Ceruloplasmin
  • ATP7A protein, human
  • Copper-Transporting ATPases