Affiliation:
1. Department of Surgery, School of Medicine, Western Sydney University, Campbelltown, New South Wales, Australia
Abstract
ABSTRACT
Silver has emerged as an important therapeutic option for wound infections in recent years due to its broad-spectrum antimicrobial activity. The silver cation (Ag
+
), but not the bulk metal (Ag
0
), is highly toxic for most microorganisms, although resistance due to genetic modification or horizontal gene transfer does occur.
Pseudomonas aeruginosa
, however, achieves silver resistance by producing the redox-active metabolite pyocyanin that reduces Ag
+
to nontoxic Ag
0
. Pyocyanin also possesses broad-spectrum antimicrobial activity. Many microbial species reduce pyocyanin, which reduces molecular oxygen to antimicrobial hydrogen peroxide. In this study, it was hypothesized that both Ag
+
and oxygen would act as competing terminal electron acceptors for pyocyanin, thus acting as a universal microbial protectant from Ag
+
while avoiding hydrogen peroxide formation.
Escherichia coli
and
Staphylococcus aureus
efficiently reduced pyocyanin and generated hydrogen peroxide, while Ag
+
markedly reduced the amount of hydrogen peroxide produced. Although unable to reduce directly Ag
+
to Ag
0
on their own,
E. coli
and
S. aureus
did so when pyocyanin was present, resulting in increased survival when exposed to Ag
+
. Coincubation experiments with either
E. coli
or
S. aureus
with
P. aeruginosa
demonstrated increased survival for those species to Ag
+
, but only if pyocyanin was present. These data demonstrate that microorganisms that display no intrinsic silver resistance may survive and proliferate under potentially toxic conditions, provided their environment contains a suitable redox-active metabolite-producing bacterium. Chronic wounds are often polymicrobial in nature, with pyocyanin-producing
P. aeruginosa
bacteria frequently being present; therefore, redox-based silver resistance may compromise treatment efforts.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
33 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