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University of Wisconsin-La Crosse
ABSTRACT
Uropathogenic Escherichia coli (UPEC) can grow in environments with significantly elevated osmolarities, such as the murine or human urinary tract. OmpR is the response regulator part of a two component OmpR-EnvZ regulatory system that responds to osmotic stresses. To determine the role of OmpR in UPEC survival, a
ompR mutant was created in the UPEC clinical isolate NU149. The
ompR mutant had a growth defect compared to the wild type strain under osmotic stress conditions, which was complemented by the full-length ompR gene on a plasmid but not with a mutant OmpR with an alanine substitution for aspartic acid at the phosphorylation site at position 55. Furthermore, the
ompR mutant displayed up to a two-log reduction in bacterial cell numbers in murine bladders and kidneys compared to wild type bacteria through five days of infection. The survivability of the bacteria was restored to wild type levels when the
ompR mutant strain was complemented with the wild type ompR but not the alanine substituted ompR gene. This study has fulfilled molecular Koch's postulates by showing the pivotal role OmpR plays in UPEC survival within the murine urinary tract.
1 E-mail: schwan.will{at}uwlax.edu
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