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High throughput platform technology for rapid target identification in personalized phage therapy.
Bayat, Fereshteh; Hilal, Arwa; Thirugnanasampanthar, Mathura; Tremblay, Denise; Filipe, Carlos D M; Moineau, Sylvain; Didar, Tohid F; Hosseinidoust, Zeinab.
Afiliación
  • Bayat F; School of Biomedical Engineering, McMaster University, Hamilton, Ontario, Canada.
  • Hilal A; School of Biomedical Engineering, McMaster University, Hamilton, Ontario, Canada.
  • Thirugnanasampanthar M; Department of Chemical Engineering, McMaster University, Hamilton, Ontario, Canada.
  • Tremblay D; Département de biochimie, de microbiologie et de bio-informatique, Faculté des sciences et de génie, Université Laval, Québec City, QC, Canada.
  • Filipe CDM; Groupe de recherche en écologie buccale, Faculté de médecine dentaire, Université Laval, Québec City, QC, Canada.
  • Moineau S; Félix d'Hérelle Reference Center for Bacterial Viruses, Université Laval, Québec City, QC, Canada.
  • Didar TF; Department of Chemical Engineering, McMaster University, Hamilton, Ontario, Canada.
  • Hosseinidoust Z; Département de biochimie, de microbiologie et de bio-informatique, Faculté des sciences et de génie, Université Laval, Québec City, QC, Canada.
Nat Commun ; 15(1): 5626, 2024 Jul 11.
Article en En | MEDLINE | ID: mdl-38992046
ABSTRACT
As bacteriophages continue to gain regulatory approval for personalized human therapy against antibiotic-resistant infections, there is a need for transformative technologies for rapid target identification through multiple, large, decentralized therapeutic phages biobanks. Here, we design a high throughput phage screening platform comprised of a portable library of individual shelf-stable, ready-to-use phages, in all-inclusive solid tablets. Each tablet encapsulates one phage along with luciferin and luciferase enzyme stabilized in a sugar matrix comprised of pullulan and trehalose capable of directly detecting phage-mediated adenosine triphosphate (ATP) release through ATP bioluminescence reaction upon bacterial cell burst. The tablet composition also enhances desiccation tolerance of all components, which should allow easier and cheaper international transportation of phages and as a result, increased accessibility to therapeutic phages. We demonstrate high throughput screening by identifying target phages for select multidrug-resistant clinical isolates of Pseudomonas aeruginosa, Salmonella enterica, Escherichia coli, and Staphylococcus aureus with targets identified within 30-120 min.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Staphylococcus aureus / Bacteriófagos / Escherichia coli / Medicina de Precisión / Ensayos Analíticos de Alto Rendimiento / Terapia de Fagos Límite: Humans Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2024 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Staphylococcus aureus / Bacteriófagos / Escherichia coli / Medicina de Precisión / Ensayos Analíticos de Alto Rendimiento / Terapia de Fagos Límite: Humans Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2024 Tipo del documento: Article País de afiliación: Canadá