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Laboratory adapted Escherichia coli K-12 becomes a pathogen of Caenorhabditis elegans upon restoration of O antigen biosynthesis

Browning, D.F.; Wells, T.J.; Franca, F.L.; Morris, F.C.; Sevastyanovich, Y.R.; Bryant, J.A.; Johnson, M.D.; Lund, P.A.; Cunningham, A.F.; Hobman, Jon L.; May, R.C.; Webber, M.A.; Henderson, I.R.

Authors

D.F. Browning

T.J. Wells

F.L. Franca

F.C. Morris

Y.R. Sevastyanovich

J.A. Bryant

M.D. Johnson

P.A. Lund

A.F. Cunningham

JON HOBMAN jon.hobman@nottingham.ac.uk
Associate Professor

R.C. May

M.A. Webber

I.R. Henderson



Abstract

Escherichia coli has been the leading model organism for many decades. It is a fundamental player in modern biology, facilitating the molecular biology revolution of the last century. The acceptance of E.?coli as model organism is predicated primarily on the study of one E. coli lineage; E. coli K-12. However, the antecedents of today's laboratory strains have undergone extensive mutagenesis to create genetically tractable offspring but which resulted in loss of several genetic traits such as O antigen expression. Here we have repaired the wbbL locus, restoring the ability of E. coli K-12 strain MG1655 to express the O antigen. We demonstrate that O antigen production results in drastic alterations of many phenotypes and the density of the O antigen is critical for the observed phenotypes. Importantly, O antigen production enables laboratory strains of E. coli to enter the gut of the Caenorhabditis elegans worm and to kill C. elegans at rates similar to pathogenic bacterial species. We demonstrate C. elegans killing is a feature of other commensal E.?coli. We show killing is associated with bacterial resistance to mechanical shear and persistence in the C. elegans gut. These results suggest C. elegans is not an effective model of human-pathogenic E. coli infectious disease.

Citation

Browning, D., Wells, T., Franca, F., Morris, F., Sevastyanovich, Y., Bryant, J., …Henderson, I. (2013). Laboratory adapted Escherichia coli K-12 becomes a pathogen of Caenorhabditis elegans upon restoration of O antigen biosynthesis. Molecular Microbiology, 87(5), https://doi.org/10.1111/mmi.12144

Journal Article Type Article
Publication Date Mar 1, 2013
Deposit Date Feb 11, 2016
Publicly Available Date Feb 11, 2016
Journal Molecular Microbiology
Print ISSN 0950-382X
Electronic ISSN 1365-2958
Publisher Wiley
Peer Reviewed Peer Reviewed
Volume 87
Issue 5
DOI https://doi.org/10.1111/mmi.12144
Public URL https://nottingham-repository.worktribe.com/output/1002561
Publisher URL http://onlinelibrary.wiley.com/doi/10.1111/mmi.12144/abstract
Additional Information This is the peer reviewed version of the following article: Browning, D. F., Wells, T. J., França, F. L. S., Morris, F. C., Sevastsyanovich, Y. R., Bryant, J. A., Johnson, M. D., Lund, P. A., Cunningham, A. F., Hobman, J. L., May, R. C., Webber, M. A. and Henderson, I. R. (2013), Laboratory adapted Escherichia coli K-12 becomes a pathogen of Caenorhabditis elegans upon restoration of O antigen biosynthesis. Molecular Microbiology, 87: 939–950, which has been published in final form at http://dx.doi.org/10.1111/mmi.12144. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.

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