The histidine kinase NahK regulates denitrification and nitric oxide accumulation through RsmA in Pseudomonas aeruginosa.

IF 2.7 3区 生物学 Q3 MICROBIOLOGY
Journal of Bacteriology Pub Date : 2025-01-31 Epub Date: 2024-12-11 DOI:10.1128/jb.00408-24
Danielle Guercio, Elizabeth Boon
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引用次数: 0

Abstract

Pseudomonas aeruginosa have a versatile metabolism; they can adapt to many stressors, including limited oxygen and nutrient availability. This versatility is especially important within a biofilm where multiple microenvironments are present. As a facultative anaerobe, P. aeruginosa can survive under anaerobic conditions utilizing denitrification. This process produces nitric oxide (NO) which has been shown to result in cell elongation. However, the molecular mechanism underlying this phenotype is poorly understood. Our laboratory has previously shown that NosP is a NO-sensitive hemoprotein that works with the histidine kinase NahK to regulate biofilm formation in P. aeruginosa. In this study, we identify NahK as a novel regulator of denitrification under anaerobic conditions. Under anaerobic conditions, deletion of nahK leads to a reduction of growth coupled with reduced transcriptional expression and activity of the denitrification reductases. Furthermore, during stationary phase under anaerobic conditions, ΔnahK does not exhibit cell elongation, which is characteristic of P. aeruginosa. We determine the loss of cell elongation is due to changes in NO accumulation in ΔnahK. We further provide evidence that NahK may regulate denitrification through modification of RsmA levels.

Importance: Pseudomonas aeruginosa is an opportunistic multi-drug resistance pathogen that is associated with hospital-acquired infections. P. aeruginosa is highly virulent, in part due to its versatile metabolism and ability to form biofilms. Therefore, better understanding of the molecular mechanisms that regulate these processes should lead to new therapeutics to treat P. aeruginosa infections. The histidine kinase NahK has been previously shown to be involved in both nitric oxide (NO) signaling and quorum sensing through RsmA. The data presented here demonstrate that NahK is responsive to NO produced during denitrification to regulate cell morphology. Understanding the role of NahK in metabolism under anaerobic conditions has larger implications in determining its role in a heterogeneous metabolic environment such as a biofilm.

组氨酸激酶NahK通过RsmA调节铜绿假单胞菌的反硝化和一氧化氮积累。
铜绿假单胞菌有多种代谢;它们可以适应许多压力源,包括有限的氧气和营养供应。这种多功能性在存在多个微环境的生物膜中尤为重要。作为兼性厌氧菌,铜绿假单胞菌可以利用反硝化作用在厌氧条件下生存。这个过程产生一氧化氮(NO),这已被证明导致细胞伸长。然而,这种表型的分子机制尚不清楚。我们的实验室先前已经表明,NosP是一种no敏感的血红蛋白,与组氨酸激酶NahK一起调节铜绿假单胞菌的生物膜形成。在这项研究中,我们发现NahK是厌氧条件下反硝化的一种新型调节剂。在厌氧条件下,nahK的缺失导致生长减少,同时反硝化还原酶的转录表达和活性降低。此外,在厌氧条件下的固定阶段,ΔnahK不表现出细胞伸长,这是铜绿假单胞菌的特征。我们确定细胞伸长的损失是由于ΔnahK中NO积累的变化。我们进一步提供证据表明,NahK可能通过改变RsmA水平来调节反硝化。重要性:铜绿假单胞菌是一种与医院获得性感染相关的机会性多重耐药病原体。铜绿假单胞菌是高毒力的,部分原因是由于它的多种代谢和形成生物膜的能力。因此,更好地了解调节这些过程的分子机制应该会导致新的治疗方法来治疗铜绿假单胞菌感染。组氨酸激酶NahK先前已被证明通过RsmA参与一氧化氮(NO)信号传导和群体感应。这里的数据表明,NahK对反硝化过程中产生的NO有反应,以调节细胞形态。了解厌氧条件下NahK在代谢中的作用对于确定其在异质代谢环境(如生物膜)中的作用具有更大的意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Bacteriology
Journal of Bacteriology 生物-微生物学
CiteScore
6.10
自引率
9.40%
发文量
324
审稿时长
1.3 months
期刊介绍: The Journal of Bacteriology (JB) publishes research articles that probe fundamental processes in bacteria, archaea and their viruses, and the molecular mechanisms by which they interact with each other and with their hosts and their environments.
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