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[Protective action of remantadine in experimental influenzal-staphylococcal infection]

Voprosy Virusologii
|September 1, 1987
PubMed

Insights

Remantadine effectively treated influenza A virus and Staphylococcus infections in mice, reducing mortality and pneumonia. However, it showed no significant benefit against remantadine-resistant influenza strains.

Area of Science:

  • Microbiology
  • Virology
  • Pharmacology

Background:

  • Coinfections with influenza viruses and Staphylococcus are a significant cause of respiratory illness.
  • Antiviral drugs are crucial for managing influenza, but resistance can emerge.

Purpose of the Study:

  • To investigate the efficacy of remantadine against a combined influenzal-staphylococcal infection in a murine model.
  • To assess the impact of remantadine on mortality, disease progression, and viral load in influenza A virus and Staphylococcus aureus coinfection.

Main Methods:

  • White mice were infected with either a remantadine-sensitive or remantadine-resistant strain of influenza A virus along with Staphylococcus.
  • Remantadine treatment was administered, and outcomes including lethality, survival time, pneumonia incidence and intensity, and lung virus titers were measured.

Main Results:

  • Remantadine significantly reduced lethality (93.3% to 26.7%), increased survival time (3.8 to 10.1 days), and decreased pneumonia incidence and intensity in mice infected with the remantadine-sensitive strain.
  • In contrast, remantadine showed minimal effect on these parameters when mice were infected with the remantadine-resistant influenza strain, with only a slight decrease in lethality and survival time.
  • Lung virus titers were significantly reduced (3.5-4.0 lg EID50) in the sensitive strain group, but not in the resistant strain group.

Conclusions:

  • Remantadine demonstrates significant therapeutic potential against remantadine-sensitive influenza A virus and Staphylococcus coinfections in mice.
  • The emergence of remantadine resistance in influenza A virus compromises the drug's efficacy, highlighting the importance of monitoring resistance patterns.

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