Mucosal Taï Forest virus infection causes disease in ferrets

Paige Fletcher1, Kyle L O'Donnell1, Joseph F Rhoderick1

  • 1Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana, United States of America.

Plos Pathogens
|October 13, 2025
PubMed

Insights

Ferrets infected with Taï Forest virus (TAFV) via mucosal routes developed severe disease, unlike intramuscular exposure. Mucosal TAFV infection in ferrets may offer cross-protection against Ebola virus (EBOV).

Area of Science:

  • Virology
  • Infectious Diseases
  • Animal Models

Background:

  • Taï Forest virus (TAFV) is a filovirus that has caused human infections.
  • Natural filovirus exposure likely occurs via mucosal routes, but animal models typically use intramuscular (IM) inoculation.
  • Developing a TAFV ferret model using mucosal exposure is crucial for understanding pathogenicity.

Purpose of the Study:

  • To develop and characterize a ferret disease model for TAFV infection via intramuscular (IM), intranasal (IN), and aerosol routes.
  • To assess the potential cross-protection between TAFV and Ebola virus (EBOV) in ferrets.

Main Methods:

  • Ferrets were inoculated with TAFV via IM, IN, or aerosol routes.
  • Survivors of TAFV infection were rechallenged with EBOV via IM or IN routes.
  • Disease severity, lethality, and protective effects were monitored.

Main Results:

  • Intranasal and aerosol TAFV inoculation caused moderate to severe disease and partial lethality in ferrets, while IM inoculation resulted in minimal signs.
  • Only ferrets that were intranasally inoculated with TAFV and subsequently intranasally inoculated with EBOV were protected from disease.
  • Other ferrets succumbed to EBOV infection after rechallenge, indicating limited cross-protection.

Conclusions:

  • Ferrets are a suitable animal model for assessing TAFV pathogenicity, particularly via mucosal exposure routes.
  • Mucosal exposure to TAFV may induce cross-protection against EBOV, but this effect appears route-dependent.

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