Affiliation:
1. Department of Microbiology and Immunology
2. Department of Pediatrics, University of Rochester Medical Center, Rochester, New York 14642
Abstract
ABSTRACT
The nitrate dissimilation pathway is important for anaerobic growth in
Pseudomonas aeruginosa
. In addition, this pathway contributes to
P. aeruginosa
virulence by using the nematode
Caenorhabditis elegans
as a model host, as well as biofilm formation and motility. We used a set of nitrate dissimilation pathway mutants to evaluate the virulence of
P. aeruginosa
PA14 in a model of
P. aeruginosa
-phagocyte interaction by using the human monocytic cell line THP-1. Both membrane nitrate reductase and nitrite reductase enzyme complexes were important for cytotoxicity during the interaction of
P. aeruginosa
PA14 with THP-1 cells. Furthermore, deletion mutations in genes encoding membrane nitrate reductase (Δ
narGH
) and nitrite reductase (Δ
nirS
) produced defects in the expression of type III secretion system (T3SS) components, extracellular protease, and elastase. Interestingly, exotoxin A expression was unaffected in these mutants. Addition of exogenous nitric oxide (NO)-generating compounds to Δ
nirS
mutant cultures restored the production of T3SS phospholipase ExoU, whereas nitrite addition had no effect. These data suggest that NO generated via nitrite reductase NirS contributes to the regulation of expression of selected virulence factors in
P. aeruginosa
PA14.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Immunology,Microbiology,Parasitology
Cited by
46 articles.
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