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Harnessing the diversity of Burkholderia spp. prophages for therapeutic potential.
Nordstrom, Hayley R; Griffith, Marissa P; Srinivasa, Vatsala Rangachar; Wallace, Nathan R; Li, Anna; Cooper, Vaughn S; Shields, Ryan K; Van Tyne, Daria.
Afiliación
  • Nordstrom HR; Division of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
  • Griffith MP; Division of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
  • Srinivasa VR; Division of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
  • Wallace NR; Division of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
  • Li A; Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
  • Cooper VS; Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
  • Shields RK; Center for Evolutionary Biology and Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
  • Van Tyne D; Division of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
bioRxiv ; 2024 Jan 25.
Article en En | MEDLINE | ID: mdl-38328162
ABSTRACT
Burkholderia spp. are often resistant to antibiotics, and infections with these organisms are difficult to treat. A potential alternative treatment for Burkholderia spp. infections is bacteriophage (phage) therapy; however, it can be difficult to locate phages that target these bacteria. Prophages incorporated into the bacterial genome have been identified within Burkholderia spp. and may represent a source of useful phages for therapy. Here we investigate whether prophages within Burkholderia spp. clinical isolates can kill conspecific and heterospecific isolates. Thirty-two Burkholderia spp. isolates were induced for prophage release, and harvested prophages were tested for lytic activity against the same 32 isolates. Lytic phages were passaged and their host ranges were determined, resulting in four unique phages of prophage origin that showed different ranges of lytic activity. We also analyzed the prophage content of 35 Burkholderia spp. clinical isolate genomes, and identified several prophages present in the genomes of multiple isolates of the same species. Finally, we observed that B. cenocepacia isolates were more phage-susceptible than Burkholderia multivorans isolates. Overall, our findings suggest that prophages present within Burkholderia spp. genomes are a potentially useful starting point for the isolation and development of novel phages for use in phage therapy.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: BioRxiv Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: BioRxiv Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos