4.7 Article

Structural and functional characterization of the receptor binding proteins of Escherichia coli O157 phages EP75 and EP335

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ELSEVIER
DOI: 10.1016/j.csbj.2021.06.001

关键词

Bacteriophage; STEC; Escherichia coli O157; Salmonella; Tail fiber; Tailspike; Receptor binding protein; Lipopolysaccharide; O-antigen

资金

  1. program for stimulating innovation (WBSO) of the Dutch ministry of Economic Affairs and Climate policy
  2. EFRO

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Bacteriophages are widely used as biocontrol agents in food production and surface treatment. Their infectivity is determined by the receptor binding proteins on the tail fibers, which also dictate their suitability as antibacterial agents. Phages EP75 and EP335 exhibit broad infectivity towards certain strains of bacteria.
Bacteriophages (phages) are widely used as biocontrol agents in food and as antibacterial agents for treatment of food production plant surfaces. An important feature of such phages is broad infectivity towards a given pathogenic species. Phages attach to the surfaces of bacterial cells using receptor binding proteins (RBPs), namely tail fibers or tailspikes (TSPs). The binding range of RBPs is the primary determinant of phage host range and infectivity, and therefore dictates a phage's suitability as an antibacterial agent. Phages EP75 and EP335 broadly infect strains of E. coli serotype O157. To better understand host recognition by both phages, here we focused on characterizing the structures and functions of their RBPs. We identified two distinct tail fibers in the genome of the podovirus EP335: gp12 and gp13. Using fluo-rescence microscopy, we reveal how gp13 recognizes strains of E. coli serotypes O157 and O26. Phage EP75 belongs to the Kuttervirus genus within the Ackermannviridae family and features a four TSP complex (TSPs 1-4) that is universal among such phages. We demonstrate enzymatic activity of TSP1 (gp167) and TSP2 (gp168) toward the O18A and O157 O-antigens of E. coli, respectively, as well as TSP3 activity (gp169.1) against O4, O7, and O9 Salmonella O-antigens. TSPs of EP75 present high similarity to TSPs from E. coli phages CBA120 (TSP2) and HK620 (TSP1) and Salmonella myovirus Det7 (TSP3), which helps explain the cross-genus infectivity observed for EP75. (C) 2021 The Author(s). Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology.

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