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Prophylaxis of Mycobacterium tuberculosis H37Rv Infection in a Preclinical Mouse Model via Inhalation of Nebulized Bacteriophage D29.
Carrigy, Nicholas B; Larsen, Sasha E; Reese, Valerie; Pecor, Tiffany; Harrison, Melissa; Kuehl, Philip J; Hatfull, Graham F; Sauvageau, Dominic; Baldwin, Susan L; Finlay, Warren H; Coler, Rhea N; Vehring, Reinhard.
Afiliación
  • Carrigy NB; Department of Mechanical Engineering, University of Alberta, Edmonton, Canada.
  • Larsen SE; Infectious Disease Research Institute, Seattle, USA.
  • Reese V; Infectious Disease Research Institute, Seattle, USA.
  • Pecor T; Infectious Disease Research Institute, Seattle, USA.
  • Harrison M; Department of Chemical and Materials Engineering, University of Alberta, Edmonton, Canada.
  • Kuehl PJ; Lovelace Biomedical, Albuquerque, USA.
  • Hatfull GF; Department of Biological Sciences, University of Pittsburgh, Pittsburgh, USA.
  • Sauvageau D; Department of Chemical and Materials Engineering, University of Alberta, Edmonton, Canada.
  • Baldwin SL; Infectious Disease Research Institute, Seattle, USA.
  • Finlay WH; Department of Mechanical Engineering, University of Alberta, Edmonton, Canada.
  • Coler RN; Infectious Disease Research Institute, Seattle, USA.
  • Vehring R; Department of Global Health, University of Washington, Seattle, USA.
Antimicrob Agents Chemother ; 63(12)2019 09 09.
Article en En | MEDLINE | ID: mdl-31527037
ABSTRACT
Globally, more people die annually from tuberculosis than from any other single infectious agent. Unfortunately, there is no commercially-available vaccine that is sufficiently effective at preventing acquisition of pulmonary tuberculosis in adults. In this study, pre-exposure prophylactic pulmonary delivery of active aerosolized anti-tuberculosis bacteriophage D29 was evaluated as an option for protection against Mycobacterium tuberculosis infection. An average bacteriophage concentration of approximately 1 PFU/alveolus was achieved in the lungs of mice using a nose-only inhalation device optimized with a dose simulation technique and adapted for use with a vibrating mesh nebulizer. Within 30 minutes of bacteriophage delivery, the mice received either a low dose (∼50-100 CFU), or an ultra-low dose (∼5-10 CFU), of M. tuberculosis H37Rv aerosol to the lungs. A prophylactic effect was observed with bacteriophage aerosol pre-treatment significantly decreasing M. tuberculosis burden in mouse lungs 24 hours and 3 weeks post-challenge (p < 0.05). These novel results indicate that a sufficient dose of nebulized mycobacteriophage aerosol to the lungs may be a valuable intervention to provide extra protection to health care professionals and other individuals at risk of exposure to M. tuberculosis.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Antimicrob Agents Chemother Año: 2019 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Antimicrob Agents Chemother Año: 2019 Tipo del documento: Article País de afiliación: Canadá