4.7 Article

Isolation and Characterization of a Novel Temperate Escherichia coli Bacteriophage, Kapi1, Which Modifies the O-Antigen and Contributes to the Competitiveness of Its Host during Colonization of the Murine Gastrointestinal Tract

Journal

MBIO
Volume 13, Issue 1, Pages -

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/mbio.02085-21

Keywords

gastrointestinal colonization; lysogen; temperate

Categories

Funding

  1. National Sciences and Engineering Research Council (NSERC)
  2. Canadian Institutes of Health Research (CIHR)
  3. AMR-One Health Consortium - Major Innovation Fund program of the Ministry of Jobs, Economy and Innovation, Government of Alberta
  4. Canada Research Chairs program
  5. NSERC Alexander Graham Bell Canada Graduate Scholarship-Master's, Walter H Johns Graduate Fellowship, University of Alberta Science Graduate Scholarship
  6. Susan Eberlein Graduate Scholarship in Genetics

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In this study, a novel temperate bacteriophage, Kapi1, was isolated and characterized from the gastrointestinal tract of healthy mice. Kapi1 shows limited homology to other prophages and alters the O-antigen structure of its host, enhancing its competitive advantage and potentially playing a role in gut colonization.
In this study, we describe the isolation and characterization of novel bacteriophage vB_EcoP_Kapi1 (Kapi1) isolated from a strain of commensal Escherichia coli inhabiting the gastrointestinal tract of healthy mice. We show that Kapi1 is a temperate phage integrated into tRNA argW of strain MP1 and describe its genome annotation and structure. Kapi1 shows limited homology to other characterized prophages but is most similar to the seroconverting phages of Shigella flexneri and clusters taxonomically with P22-like phages. The receptor for Kapi1 is the lipopolysaccharide O-antigen, and we further show that Kapi1 alters the structure of its host's O-antigen in multiple ways. Kapi1 displays unstable lysogeny, and we find that the lysogenic state is more stable during growth in simulated intestinal fluid. Furthermore, Kapi1 lysogens have a competitive advantage over their nonlysogenic counterparts both in vitro and in vivo, suggesting a role for Kapi1 during colonization. We thus report the use of MP1 and Kapi1 as a model system to explore the molecular mechanisms of mammalian colonization by E. coli to ask what the role(s) of prophages in this context might be. IMPORTANCE Although research exploring the microbiome has exploded in recent years, our understanding of the viral component of the microbiome is lagging far behind our understanding of the bacterial component. The vast majority of intestinal bacteria carry prophages integrated into their chromosomes, but most of these bacteriophages remain uncharacterized and unexplored. Here, we isolate and characterize a novel temperate bacteriophage infecting a commensal strain of Escherichia coli. We aim to explore the interactions between bacteriophages and their hosts in the context of the gastrointestinal tract, asking what role(s) temperate bacteriophages may play in growth and survival of bacteria in the gut. Understanding the fundamental biology of gut commensal bacteria can inform the development of novel antimicrobial or probiotic strategies for intestinal infections.

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