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A bacteriocin expression platform for targeting pathogenic bacterial species.
Rutter, Jack W; Dekker, Linda; Clare, Chania; Slendebroek, Zoe F; Owen, Kimberley A; McDonald, Julie A K; Nair, Sean P; Fedorec, Alex J H; Barnes, Chris P.
Affiliation
  • Rutter JW; Department of Cell and Developmental Biology, University College London, London, UK.
  • Dekker L; Department of Cell and Developmental Biology, University College London, London, UK.
  • Clare C; Department of Cell and Developmental Biology, University College London, London, UK.
  • Slendebroek ZF; Department of Cell and Developmental Biology, University College London, London, UK.
  • Owen KA; Department of Cell and Developmental Biology, University College London, London, UK.
  • McDonald JAK; Centre for Bacterial Resistance Biology, Department of Life Sciences, Imperial College London, London, UK.
  • Nair SP; Department of Microbial Diseases, UCL Eastman Dental Institute, University College London, London, UK.
  • Fedorec AJH; Department of Cell and Developmental Biology, University College London, London, UK.
  • Barnes CP; Department of Cell and Developmental Biology, University College London, London, UK. christopher.barnes@ucl.ac.uk.
Nat Commun ; 15(1): 6332, 2024 Jul 27.
Article in En | MEDLINE | ID: mdl-39068147
ABSTRACT
Bacteriocins are antimicrobial peptides that are naturally produced by many bacteria. They hold great potential in the fight against antibiotic resistant bacteria, including ESKAPE pathogens. Engineered live biotherapeutic products (eLBPs) that secrete bacteriocins can be created to deliver targeted bacteriocin production. Here we develop a modular bacteriocin secretion platform that can be used to express and secrete multiple bacteriocins from non-pathogenic Escherichia coli host strains. As a proof of concept we create Enterocin A (EntA) and Enterocin B (EntB) secreting strains that show strong antimicrobial activity against Enterococcus faecalis and Enterococcus faecium in vitro, and characterise this activity in both solid culture and liquid co-culture. We then develop a Lotka-Volterra model that can be used to capture the interactions of these competitor strains. We show that simultaneous exposure to EntA and EntB can delay Enterococcus growth. Our system has the potential to be used as an eLBP to secrete additional bacteriocins for the targeted killing of pathogenic bacteria.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bacteriocins / Enterococcus faecium / Enterococcus faecalis / Escherichia coli / Anti-Bacterial Agents Language: En Journal: Nat Commun Journal subject: BIOLOGIA / CIENCIA Year: 2024 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bacteriocins / Enterococcus faecium / Enterococcus faecalis / Escherichia coli / Anti-Bacterial Agents Language: En Journal: Nat Commun Journal subject: BIOLOGIA / CIENCIA Year: 2024 Document type: Article Country of publication: