A highly specific Serratia-infecting T7-like phage inhibits biofilm formation in two different genera of the Enterobacteriaceae family

Res Microbiol. 2021 Sep-Oct;172(6):103869. doi: 10.1016/j.resmic.2021.103869. Epub 2021 Jul 29.

Abstract

Due to the emergence of multidrug-resistant bacteria, bacteriophages have become a viable alternative in controlling bacterial growth or biofilm formation. Biofilm is formed by extracellular polymeric substances (EPS) and is one of the factors responsible for increasing bacterial resistance. Bacteriophages have been studied as a bacterial control agent by use of phage enzymes or due to their bactericidal activities. A specific phage against Serratia marcescens was isolated in this work and was evaluated its biological and genomic aspects. The object of this study was UFV01, a bacteriophage belonging to the Podoviridae family, genus Teseptimavirus (group of lytic viruses), specific to the species S. marcescens, which may be related to several amino acid substitutions in the virus tail fibers. Despite this high specificity, the phage reduced the biofilm formation of several Escherichia coli strains without infecting them. UFV01 presents a relationship with phages of the genus Teseptimavirus, although it does not infect any of the E. coli strains evaluated, as these others do. All the characteristics make the phage an interesting alternative in biofilm control in hospital environments since small breaks in the biofilm matrix can lead to a complete collapse.

Keywords: Bacteriophage; Biofilm; Serratia marcescens; Specificity; Tail fiber.

MeSH terms

  • Amino Acid Substitution
  • Biofilms / growth & development*
  • Escherichia coli / growth & development*
  • Genome, Viral
  • Host Specificity
  • Hydrogen-Ion Concentration
  • Microbial Interactions
  • Podoviridae / classification
  • Podoviridae / genetics
  • Podoviridae / isolation & purification
  • Podoviridae / physiology*
  • Protein Domains
  • Serratia liquefaciens / growth & development*
  • Serratia marcescens / growth & development*
  • Serratia marcescens / virology*
  • Temperature
  • Viral Tail Proteins / chemistry
  • Virus Latency

Substances

  • Viral Tail Proteins