Intracellular iron positively modulates the replicative cycle of mimiviruses, increasing virus production

Juliana Dos Santos Oliveira1, Claudia F Dick2, Gabriel Henrique Pereira Nunes1

  • 1Laboratório de Virologia e Espectrometria de Massas, Instituto de Microbiologia Paulo de Góes, Departamento de Virologia, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.

Journal of Virology
|October 1, 2025
PubMed

Insights

Giant viruses, including mimiviruses, exploit host cell iron uptake for replication. Increased intracellular iron enhances viral production, revealing a novel virus-host interaction where a defense mechanism becomes a viral advantage.

Area of Science:

  • Virology
  • Microbiology
  • Cellular Biology

Background:

  • Mimiviruses (Nucleocytoviricota) infect phagocytic amoebae, delivering their core via a unique 'stargate'.
  • Amoebae normally eliminate pathogens using antimicrobial mechanisms, including metal ion concentration changes within phagolysosomes.
  • Giant viruses exhibit adaptations to survive and replicate within these hostile host environments.

Purpose of the Study:

  • To investigate the role of metal ions, specifically iron, in the replication of three giant viruses: Acanthamoeba polyphaga mimivirus (APMV), Antarctica virus, and Tupanvirus (TPV).
  • To elucidate the interaction between viral replication and host cell iron metabolism.

Main Methods:

  • Comparative analysis of viral replication in the presence of varying iron concentrations.
  • Measurement of cellular iron uptake during giant virus infection.

Main Results:

  • Infection by APMV, Antarctica virus, and Tupanvirus increases host cell iron uptake.
  • Elevated intracellular iron levels significantly enhance the replication of these giant viruses.
  • Iron availability acts as a positive modulator for the viral replicative cycle.

Conclusions:

  • Giant viruses have evolved to leverage host iron availability for successful replication.
  • This study reveals a sophisticated viral strategy of exploiting host defense mechanisms, specifically iron sequestration, for their benefit.
  • Understanding the role of iron opens new avenues for studying giant virus-host interactions and viral adaptation.

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