Determination of the Infection Dynamics of Escherichia coli O157:H7 by Bacteriophage ΦV10

ΦV10 is an <i>Escherichia coli</i> O157:H7-specific bacteriophage that has been used to develop luminescent reporter assays for the detection of this important foodborne pathogen. Previous work demonstrated the specificity of ΦV10 for infection of <i>E.coli</i> O157:H7 through interaction with the O157 antigen. In addition, modification of the lipopolysaccharide (LPS) via O-acetylation prevents ΦV10 infection in an <i>E. coli</i> O157:H7 expressing a phage-encoded O-acetylase gene. Through assays for phage binding, plaque formation, and lysogeny using non-O157:H7 and O157: non-H7 strains, as well as complementation of an O157:H<sup>-</sup> strain, it is demonstrated in this study that both the somatic O157 antigen and flagellar H7 antigen are required for productive infection of <i>E. coli</i> O157:H7 by ΦV10. Together, the results indicate that the O157 antigen is required for phage binding and that the H7 antigen is necessary to complete the infection process.

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Publication Details

Journal
Foods
Published
2025-02-13
DOI
https://doi.org/10.3390/foods14040617
Citations
1
Primary Topic
Escherichia coli research studies
Type
article
Field-Weighted Citation Impact
1.80

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article

Determination of the Infection Dynamics of Escherichia coli O157:H7 by Bacteriophage ΦV10

Bruce Applegate, Claudia P. Coronel-Aguilera, George C. Paoli, Arun K. Bhunia et al.
1 citations
Foods
Escherichia coli research studies
1.80
article

Determination of the Infection Dynamics of Escherichia coli O157:H7 by Bacteriophage ΦV10

Bruce Applegate, Claudia P. Coronel-Aguilera, George C. Paoli, Arun K. Bhunia, Andrew Gehring, László N. Csonka, Michael F. Oats
article en
1 citations

Abstract

ΦV10 is an <i>Escherichia coli</i> O157:H7-specific bacteriophage that has been used to develop luminescent reporter assays for the detection of this important foodborne pathogen. Previous work demonstrated the specificity of ΦV10 for infection of <i>E.coli</i> O157:H7 through interaction with the O157 antigen. In addition, modification of the lipopolysaccharide (LPS) via O-acetylation prevents ΦV10 infection in an <i>E. coli</i> O157:H7 expressing a phage-encoded O-acetylase gene. Through assays for phage binding, plaque formation, and lysogeny using non-O157:H7 and O157: non-H7 strains, as well as complementation of an O157:H<sup>-</sup> strain, it is demonstrated in this study that both the somatic O157 antigen and flagellar H7 antigen are required for productive infection of <i>E. coli</i> O157:H7 by ΦV10. Together, the results indicate that the O157 antigen is required for phage binding and that the H7 antigen is necessary to complete the infection process.

FoodsVol. 14(4)
Agricultural Research Service (US), Purdue University West Lafayette (US), Eastern Regional Research Center (US)
U.S. Department of Agriculture, Purdue University, National Institute of Food and Agriculture, Agricultural Research Service
Openalex Percentile: Top 21%
Escherichia coli research studies
1.80
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