Tailoring the Host Range of Ackermannviridae Bacteriophages through Chimeric Tailspike Proteins

Viruses. 2023 Jan 19;15(2):286. doi: 10.3390/v15020286.

Abstract

Host range is a major determinant in the industrial utility of a bacteriophage. A model host range permits broad recognition across serovars of a target bacterium while avoiding cross-reactivity with commensal microbiota. Searching for a naturally occurring bacteriophage with ideal host ranges is challenging, time-consuming, and restrictive. To address this, SPTD1.NL, a previously published luciferase reporter bacteriophage for Salmonella, was used to investigate manipulation of host range through receptor-binding protein engineering. Similar to related members of the Ackermannviridae bacteriophage family, SPTD1.NL possessed a receptor-binding protein gene cluster encoding four tailspike proteins, TSP1-4. Investigation of the native gene cluster through chimeric proteins identified TSP3 as the tailspike protein responsible for Salmonella detection. Further analysis of chimeric phages revealed that TSP2 contributed off-target Citrobacter recognition, whereas TSP1 and TSP4 were not essential for activity against any known host. To improve the host range of SPTD1.NL, TSP1 and TSP2 were sequentially replaced with chimeric receptor-binding proteins targeting Salmonella. This engineered construct, called RBP-SPTD1-3, was a superior diagnostic reporter, sensitively detecting additional Salmonella serovars while also demonstrating improved specificity. For industrial applications, bacteriophages of the Ackermannviridae family are thus uniquely versatile and may be engineered with multiple chimeric receptor-binding proteins to achieve a custom-tailored host range.

Keywords: Ackermannviridae; Salmonella enterica; bacteriophage; luciferase reporter phage; phage-based detection; receptor-binding protein; tailspike protein.

MeSH terms

  • Bacteriophages* / genetics
  • Caudovirales*
  • Cross Reactions
  • Host Specificity
  • Protein Engineering
  • Recombinant Fusion Proteins / metabolism

Substances

  • Recombinant Fusion Proteins

Grants and funding

This research received no external funding.