Nitric Oxide, an Old Molecule With Noble Functions in Pseudomonas aeruginosa Biology.

2区 生物学 Q1 Biochemistry, Genetics and Molecular Biology Advances in Microbial Physiology Pub Date : 2018-01-01 Epub Date: 2018-02-19 DOI:10.1016/bs.ampbs.2018.01.005
Masanori Toyofuku, Sang-Sun Yoon
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引用次数: 14

Abstract

Pseudomonas aeruginosa, a Gram-negative bacterium, is characterized by its versatility that enables persistent survival under adverse conditions. It can grow on diverse energy sources and readily acquire resistance to antimicrobial agents. As an opportunistic human pathogen, it also causes chronic infections inside the anaerobic mucus airways of cystic fibrosis patients. As a strict respirer, P. aeruginosa can grow by anaerobic nitrate ( [Formula: see text] ) respiration. Nitric oxide (NO) produced as an intermediate during anaerobic respiration exerts many important effects on the biological characteristics of P. aeruginosa. This review provides information regarding (i) how P. aeruginosa grows by anaerobic respiration, (ii) mechanisms by which NO is produced under such growth, and (iii) bacterial adaptation to NO. We also review the clinical relevance of NO in the fitness of P. aeruginosa and the use of NO as a potential therapeutic for treating P. aeruginosa infection.

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一氧化氮:铜绿假单胞菌生物学中一种具有重要功能的古老分子。
铜绿假单胞菌是一种革兰氏阴性菌,其特点是具有多功能性,能够在不利条件下持续生存。它可以在各种能源上生长,并且很容易对抗菌剂产生耐药性。作为一种机会性人类病原体,它也会在囊性纤维化患者的厌氧粘液气道内引起慢性感染。作为一个严格的呼吸者,铜绿假单胞菌可以通过厌氧硝酸盐(公式:见文本)呼吸生长。在厌氧呼吸过程中产生的一氧化氮(NO)对铜绿假单胞菌的生物学特性有许多重要影响。这篇综述提供了以下方面的信息:(i) P. aeruginosa如何通过厌氧呼吸生长,(ii)在这种生长下产生NO的机制,以及(iii)细菌对NO的适应。我们还回顾了NO在P. aeruginosa的适应度中的临床相关性以及NO作为治疗P. aeruginosa感染的潜在治疗方法的使用。
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来源期刊
Advances in Microbial Physiology
Advances in Microbial Physiology 生物-生化与分子生物学
CiteScore
6.20
自引率
0.00%
发文量
16
期刊介绍: Advances in Microbial Physiology publishes topical and important reviews, interpreting physiology to include all material that contributes to our understanding of how microorganisms and their component parts work. First published in 1967, the editors have always striven to interpret microbial physiology in the broadest context and have never restricted the contents to traditional views of whole cell physiology.
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Preface. Biological functions of bacterial lysophospholipids. Redefining the bacterial Type I protein secretion system. Purine catabolism by enterobacteria. Fumarate, a central electron acceptor for Enterobacteriaceae beyond fumarate respiration and energy conservation.
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