Spontaneous and transient defence against bacteriophage by phase-variable glucosylation of O-antigen in Salmonella enterica serovar Typhimurium

Minsik Kim, Sangryeol Ryu

Research output: Contribution to journalArticle

43 Citations (Scopus)

Abstract

As natural killers of bacteria, bacteriophages have forced bacteria to develop a variety of defence mechanisms. The alteration of host receptors is one of the most common bacterial defence strategies against phage infection, which completely blocks phage attachment but comes at a potential fitness cost to the bacteria. Here, we report the cost-free, transient emergence of phage resistance in Salmonella enterica subspecies enterica serovar Typhimurium through a phase-variable modification of the O-antigen. Phage SPC35 typically requires BtuB as a host receptor but also uses the Salmonella O12-antigen as an adsorption-assisting apparatus for the successful infection of S.Typhimurium. The α-1,4-glucosylation of galactose residues in the O12-antigen by phase variably expressed O-antigen glucosylating genes, designated the LT 2 gtrABC1 cluster, blocks the adsorption-assisting function of the O12-antigen. Consequently, it confers transient SPC35 resistance to Salmonella without any mutations to the btuB gene. This temporal switch-off of phage adsorption through phase-variable antigenic modification may be widespread among Gram-negative bacteria-phage systems.

Original languageEnglish
Pages (from-to)411-425
Number of pages15
JournalMolecular Microbiology
Volume86
Issue number2
DOIs
Publication statusPublished - 2012 Oct 1

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O Antigens
Salmonella enterica
Bacteriophages
Adsorption
Bacteria
Antigens
Salmonella
Costs and Cost Analysis
Infection
Serogroup
Gram-Negative Bacteria
Galactose
Genes
Mutation

All Science Journal Classification (ASJC) codes

  • Microbiology
  • Molecular Biology

Cite this

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Spontaneous and transient defence against bacteriophage by phase-variable glucosylation of O-antigen in Salmonella enterica serovar Typhimurium. / Kim, Minsik; Ryu, Sangryeol.

In: Molecular Microbiology, Vol. 86, No. 2, 01.10.2012, p. 411-425.

Research output: Contribution to journalArticle

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