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High-throughput fabrication of antimicrobial phage microgels and example applications in food decontamination.
Tian, Lei; Jackson, Kyle; He, Leon; Khan, Shadman; Thirugnanasampanthar, Mathura; Gomez, Mellissa; Bayat, Fereshteh; Didar, Tohid F; Hosseinidoust, Zeinab.
Afiliação
  • Tian L; Department of Chemical Engineering, McMaster University, Hamilton, Ontario, Canada.
  • Jackson K; Department of Chemical Engineering, McMaster University, Hamilton, Ontario, Canada.
  • He L; Farncombe Family Digestive Health Research Institute, McMaster University, Hamilton, Ontario, Canada.
  • Khan S; Department of Chemical Engineering, McMaster University, Hamilton, Ontario, Canada.
  • Thirugnanasampanthar M; School of Biomedical Engineering, McMaster University, Hamilton, Ontario, Canada.
  • Gomez M; Department of Chemical Engineering, McMaster University, Hamilton, Ontario, Canada.
  • Bayat F; Department of Chemical Engineering, McMaster University, Hamilton, Ontario, Canada.
  • Didar TF; School of Biomedical Engineering, McMaster University, Hamilton, Ontario, Canada.
  • Hosseinidoust Z; School of Biomedical Engineering, McMaster University, Hamilton, Ontario, Canada. didar@mcmaster.ca.
Nat Protoc ; 19(6): 1591-1622, 2024 Jun.
Article em En | MEDLINE | ID: mdl-38413781
ABSTRACT
Engineered by nature, biological entities are exceptional building blocks for biomaterials. These entities can impart enhanced functionalities on the final material that are otherwise unattainable. However, preserving the bioactive functionalities of these building blocks during the material fabrication process remains a challenge. We describe a high-throughput protocol for the bottom-up self-assembly of highly concentrated phages into microgels while preserving and amplifying their inherent antimicrobial activity and biofunctionality. Each microgel is comprised of half a million cross-linked phages as the sole structural component, self-organized in aligned bundles. We discuss common pitfalls in the preparation procedure and describe optimization processes to ensure the preservation of the biofunctionality of the phage building blocks. This protocol enables the production of an antimicrobial spray containing the manufactured phage microgels, loaded with potent virulent phages that effectively reduced high loads of multidrug-resistant Escherichia coli O157H7 on red meat and fresh produce. Compared with other microgel preparation methods, our protocol is particularly well suited to biological materials because it is free of organic solvents and heat. Bench-scale preparation of base materials, namely microporous films (the template for casting microgels) and pure concentrated phage suspension, requires 3.5 h and 5 d, respectively. A single production run, that yields over 1,750,000 microgels, ranges from 2 h to 2 d depending on the rate of cross-linking chemistry. We expect that this platform will address bottlenecks associated with shelf-stability, preservation and delivery of phage for antimicrobial applications, expanding the use of phage for prevention and control of bacterial infections and contaminants.
Assuntos

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 3_ND Base de dados: MEDLINE Assunto principal: Bacteriófagos / Microgéis Idioma: En Revista: Nat Protoc Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 3_ND Base de dados: MEDLINE Assunto principal: Bacteriófagos / Microgéis Idioma: En Revista: Nat Protoc Ano de publicação: 2024 Tipo de documento: Article