Affiliation:
1. Department of Molecular Genetics, Biochemistry and Microbiology, University of Cincinnati College of Medicine, Cincinnati, Ohio 45267-0524
2. Department of Pediatrics, Pathology and Laboratory Medicine, Children's Hospital, Cincinnati, Ohio 45229
3. TriHealth Laboratories, Bethesda and Good Samaritan Hospitals, Cincinnati, Ohio 45206
4. Aires Pharmaceuticals, Inc., San Diego, California 92121
Abstract
ABSTRACT
A hallmark of airways in patients with cystic fibrosis (CF) is highly refractory, chronic infections by several opportunistic bacterial pathogens. A recent study demonstrated that acidified sodium nitrite (A-NO
2
−
) killed the highly refractory mucoid form of
Pseudomonas aeruginosa
, a pathogen that significantly compromises lung function in CF patients (S. S. Yoon et al., J. Clin. Invest.
116:
436-446, 2006). Therefore, the microbicidal activity of A-NO
2
−
(pH 6.5) against the following three major CF pathogens was assessed:
P. aeruginosa
(a mucoid,
mucA22
mutant and a sequenced nonmucoid strain, PAO1),
Staphylococcus aureus
USA300 (methicillin resistant), and
Burkholderia cepacia
, a notoriously antibiotic-resistant organism. Under planktonic, anaerobic conditions, growth of all strains except for
P. aeruginosa
PAO1 was inhibited by 7.24 mM (512 μg ml
−1
NO
2
−
).
B. cepacia
was particularly sensitive to low concentrations of A-NO
2
−
(1.81 mM) under planktonic conditions. In antibiotic-resistant communities known as biofilms, which are reminiscent of end-stage CF airway disease, A-NO
2
−
killed mucoid
P. aeruginosa
,
S. aureus
, and
B. cepacia
; 1 to 2 logs of cells were killed after a 2-day incubation with a single dose of ∼15 mM A-NO
2
−
. Animal toxicology and phase I human trials indicate that these bactericidal levels of A-NO
2
−
can be easily attained by aerosolization. Thus, in summary, we demonstrate that A-NO
2
−
is very effective at killing these important CF pathogens and could be effective in other infectious settings, particularly under anaerobic conditions where bacterial defenses against the reduction product of A-NO
2
−
, nitric oxide (NO), are dramatically reduced.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
55 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献