Affiliation:
1. Department of Genetics1 and
2. Department of Molecular Biology2 and
3. Department of Surgery,3 Harvard Medical School, and
4. Shriner's Burns Institute,4Massachusetts General Hospital, Boston, Massachusetts 02114
Abstract
ABSTRACT
We cloned the
rpoN (ntrA
,
glnF)
gene encoding the alternate sigma factor ς
54
from the opportunistic multihost pathogen
Pseudomonas aeruginosa
strain PA14. A marker exchange protocol was used to construct the PA14
rpoN
insertional mutation
rpoN
::Gen
r
. PA14
rpoN
::Gen
r
synthesized reduced levels of pyocyanin and displayed a variety of phenotypes typical of
rpoN
mutants, including a lack of motility and the failure to grow on nitrate, glutamate, or histidine as the sole nitrogen source. Compared to wild-type PA14,
rpoN
::Gen
r
was ca. 100-fold less virulent in a mouse thermal injury model and was significantly impaired in its ability to kill the nematode
Caenorhabditis elegans
. In an
Arabidopsis thaliana
leaf infectivity assay, although
rpoN
::Gen
r
exhibited significantly reduced attachment to trichomes, stomata, and the epidermal cell surface, did not attach perpendicularly to or perforate mesophyll cell walls, and proliferated less rapidly in
Arabidopsis
leaves, it nevertheless elicited similar disease symptoms to wild-type
P. aeruginosa
PA14 at later stages of infection.
rpoN
::Gen
r
was not impaired in virulence in a
Galleria mellonella
(greater wax moth) pathogenicity model. These data indicate that
rpoN
does not regulate the expression of any genes that encode virulence factors universally required for
P. aeruginosa
pathogenicity in diverse hosts.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
105 articles.
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