群体感应调控的sRNA Lrs1参与了铜绿假单胞菌对低铁的适应

IF 3.6 4区 生物学 Q2 ENVIRONMENTAL SCIENCES
Dimitra Panagiotopoulou, Natalia Romo Catalán, Max Wilcox, Nigel Halliday, Paolo Pantalone, James Lazenby, Miguel Cámara, Stephan Heeb
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引用次数: 0

摘要

铁是微生物生长所必需的营养物质。机会致病菌铜绿假单胞菌可以在多种条件下生存,包括在小非编码rna (sRNAs)的帮助下缺铁环境。铜绿假单胞菌还使用三种群体感应系统:Las、Rhl和Pqs来协调种群水平上的毒力和感染建立。本研究的目的是研究sRNA Lrs1的作用,该基因位于Pqs生物合成操纵子pqsABCDE的启动子内。转录组学和表型分析表明,Lrs1下调铁载体pyochelin的产生,但不下调pyoverdine的产生,并且Lrs1调节本身依赖于铁的可用性。虽然Lrs1在菌株PA14中与转录调节因子LasR存在正反馈回路,但目前的研究结果表明,在测试条件下,pa01 - l的情况并非如此。Lrs1的转录依赖于群体感应,主要依赖于RhlR, PqsE的辅助作用。此外,Pqs系统和非那嗪的生产仅在铁限制下由Lrs1调节。本研究发现Lrs1在低铁条件下是一种新的qs依赖性转录后调节因子,强调了其在铜绿假单胞菌环境适应中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Quorum Sensing Regulated sRNA Lrs1 Is Involved in the Adaptation to Low Iron in Pseudomonas aeruginosa

The Quorum Sensing Regulated sRNA Lrs1 Is Involved in the Adaptation to Low Iron in Pseudomonas aeruginosa

Iron is an essential nutrient for microbial growth. The opportunistic pathogen Pseudomonas aeruginosa can survive under diverse conditions, including iron-depleted environments with the aid of small non-coding RNAs (sRNAs). P. aeruginosa also uses three quorum sensing (QS) systems: Las, Rhl and Pqs, to coordinate virulence and infection establishment at the population level. The aim of this study is to investigate the role of the sRNA Lrs1, the gene of which is positioned within the promoter of the Pqs biosynthetic operon pqsABCDE. Transcriptomics and phenotypic assays indicate that Lrs1 downregulates the production of the siderophore pyochelin but not pyoverdine, and that lrs1 regulation itself is dependent on iron availability. Although Lrs1 has been implicated in a positive feedback loop with the transcriptional regulator LasR in the strain PA14, the present findings indicate that this is not the case in PAO1-L in the tested conditions. Transcription of Lrs1 is dependent on quorum sensing, predominantly on RhlR with an auxiliary effect by PqsE. Furthermore, the Pqs system and phenazine production are modulated by Lrs1 only under iron limitation. This study identifies Lrs1 as a new QS-dependent post-transcriptional regulator in low iron, highlighting its importance in environmental adaptation in P. aeruginosa.

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来源期刊
Environmental Microbiology Reports
Environmental Microbiology Reports ENVIRONMENTAL SCIENCES-MICROBIOLOGY
CiteScore
6.00
自引率
3.00%
发文量
91
审稿时长
3.0 months
期刊介绍: The journal is identical in scope to Environmental Microbiology, shares the same editorial team and submission site, and will apply the same high level acceptance criteria. The two journals will be mutually supportive and evolve side-by-side. Environmental Microbiology Reports provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following: the structure, activities and communal behaviour of microbial communities microbial community genetics and evolutionary processes microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors microbes in the tree of life, microbial diversification and evolution population biology and clonal structure microbial metabolic and structural diversity microbial physiology, growth and survival microbes and surfaces, adhesion and biofouling responses to environmental signals and stress factors modelling and theory development pollution microbiology extremophiles and life in extreme and unusual little-explored habitats element cycles and biogeochemical processes, primary and secondary production microbes in a changing world, microbially-influenced global changes evolution and diversity of archaeal and bacterial viruses new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens.
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