Affiliation:
1. Institut für Molekulare Infektionsbiologie, Universität Würzburg, D-97070 Würzburg, Germany
2. Institute of Medical Microbiology and Immunology, University of Pécs Medical School, H-7624 Pécs, Hungary
3. Department of Molecular Biology, Umeå University, S-90187 Umeå, Sweden
Abstract
ABSTRACT
The histone-like protein H-NS is a global regulator in
Escherichia coli
that has been intensively studied in nonpathogenic strains. However, no comprehensive study on the role of H-NS and its paralogue, StpA, in gene expression in pathogenic
E. coli
has been carried out so far. Here, we monitored the global effects of H-NS and StpA in a uropathogenic
E. coli
isolate by using DNA arrays. Expression profiling revealed that more than 500 genes were affected by an
hns
mutation, whereas no effect of StpA alone was observed. An
hns stpA
double mutant showed a distinct gene expression pattern that differed in large part from that of the
hns
single mutant. This suggests a direct interaction between the two paralogues and the existence of distinct regulons of H-NS and an H-NS/StpA heteromeric complex.
hns
mutation resulted in increased expression of alpha-hemolysin, fimbriae, and iron uptake systems as well as genes involved in stress adaptation. Furthermore, several other putative virulence genes were found to be part of the H-NS regulon. Although the lack of H-NS, either alone or in combination with StpA, has a huge impact on gene expression in pathogenic
E. coli
strains, its effect on virulence is ambiguous. At a high infection dose,
hns
mutants trigger more sudden lethality due to their increased acute toxicity in murine urinary tract infection and sepsis models. At a lower infectious dose, however, mutants lacking H-NS are attenuated through their impaired growth rate, which can only partially be compensated for by the higher expression of numerous virulence factors.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
93 articles.
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