The Histidine Kinase NahK Regulates Denitrification and Nitric Oxide Accumulation through RsmA inPseudomonas aeruginosa

Author:

Guercio Danielle,Boon ElizabethORCID

Abstract

AbstractPseudomonas aeruginosahave 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. aeruginosacan 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 inP. aeruginosa. In this study, we identify NahK as a novel regulator of denitrification under anaerobic conditions. Under anaerobic conditions, deletion ofnahKleads to a reduction of growth coupled with reduced transcriptional expression and activity of the denitrification reductases. Further, during stationary phase under anaerobic conditions, ΔnahKdoes not exhibit cell elongation, which is characteristic ofP. aeruginosa. We determine the loss of cell elongation is due to changes in NO accumulation inΔnahK. We further provide evidence that NahK may regulate denitrification through modification of RsmA activity.ImportanceP. aeruginosais an opportunistic multi-drug resistance pathogen that is associated with hospital acquired infections.P. aeruginosais 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 treatP. aeruginosainfections. The histidine kinase NahK has been previously shown to be involved in both 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 NahK’s role in metabolism under anaerobic conditions has larger implications in determining Nahk’s role in a heterogeneous metabolic environment such as a biofilm.

Publisher

Cold Spring Harbor Laboratory

Reference46 articles.

1. Pseudomonas aeruginosa: pathogenesis, virulence factors, antibiotic resistance, 455 interaction with host, technology advances and emerging therapeutics;Sig Transduct 456 Target Ther,2022

2. Invasion and diversity in Pseudomonas aeruginosa urinary tract infections;In Journal of Medical Microbiology,2022

3. Effect of Human Burn Wound Exudate on Pseudomonas aeruginosa Virulence;mSphere,2022

4. Cystic Fibrosis and Pseudomonas aeruginosa: the Host-Microbe Interface

5. Origin and Impact of Nitric Oxide in Pseudomonas aeruginosa Biofilms;J Bacteriol,2016

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3