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RB49-like Bacteriophages Recognize O Antigens as One of the Alternative Primary Receptors.

Alexandr D EfimovAlla K GolomidovaEugene E KulikovIlya S BelalovPavel A IvanovAndrey V Letarov
Published in: International journal of molecular sciences (2022)
The power of most of the enterobacterial O antigen types to provide robust protection against direct recognition of the cell surface by bacteriophage receptor-recognition proteins (RBP) has been recently recognized. The bacteriophages infecting O antigen producing strains of E. coli employ various strategies to tackle this nonspecific protection. T-even related phages, including RB49-like viruses, often have wide host ranges, being considered good candidates for use in phage therapy. However, the mechanisms by which these phages overcome the O antigen barrier remain unknown. We demonstrate here that RB49 and related phages Cognac49 and Whisky49 directly use certain types of O antigen as their primary receptors recognized by the virus long tail fibers (LTF) RBP gp38, so the O antigen becomes an attractant instead of an obstacle. Simultaneously to recognize multiple O antigen types, LTFs of each of these phages can bind to additional receptors, such as OmpA protein, enabling them to infect some rough strains of E. coli . We speculate that the mechanical force of the deployment of the short tail fibers (STF) triggered by the LTF binding to the O antigen or underneath of it, allows the receptor binding domains of STF to break through the O polysaccharide layer.
Keyphrases
  • escherichia coli
  • cell surface
  • binding protein
  • pseudomonas aeruginosa
  • transcription factor
  • single molecule
  • cell therapy
  • drug induced