(p)ppGpp施加分级转录变化,损害生物膜的运动性并促进抗生素耐受性。

IF 9.2 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Florian Engelhardt, Kathryn Turnbull, Melisa Gür, Mathias Müsken, Matthias Preusse, Susanne Häussler, Mohammad Roghanian
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引用次数: 0

摘要

(p)ppGpp是细菌应激反应的主要调节因子,通过严格的反应来协调细胞生理,促进生存和适应。为了应对营养挑战和应激,(p)ppGpp广泛地重组转录组。在这里,我们证明(p)铜绿假单胞菌ppGpp的产生是渐进的,并且与应激严重程度有关,而不是二元的(开/关)。转录组学分析表明(p)ppGpp通过对基因表达的逐层调控确保了细胞对应激的相应反应。随着(p)ppGpp水平的上升,这些影响会加剧,高达四分之一的基因组在最高水平上受到差异调节。最初(p)ppGpp的增加会降低生长和代谢,同时抑制运动和花青素的产生。在较高水平上,生物膜相关基因以牺牲毒力基因为代价被上调,促进凝聚生物膜的形成。最后,(p) ppgpp驱动的重编程诱导抗菌素耐受性,特别是在生物膜条件下,独立于其对生长的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
(p)ppGpp imposes graded transcriptional changes to impair motility and promote antibiotic tolerance in biofilms.

(p)ppGpp is the master regulator of bacterial stress responses, orchestrating cellular physiology via the stringent response to promote survival and adaptation. In response to nutritional challenges and stress, (p)ppGpp extensively rewires the transcriptome. Here, we demonstrate that (p)ppGpp production in Pseudomonas aeruginosa is gradual and relative to stress severity, rather than binary (on/off). Transcriptomic analysis reveals that (p)ppGpp ensures proportionate cellular responses to stress by imposing a layer-by-layer regulation of gene expression. These effects intensify as (p)ppGpp levels rise, with up to a quarter of the genome differentially regulated at maximal levels. Initial increases in (p)ppGpp reduce growth and metabolism while suppressing motility and pyocyanin production. At higher levels, biofilm-related genes are upregulated at the expense of virulence genes, promoting the formation of condensed biofilms. Finally, (p)ppGpp-driven reprogramming induces antimicrobial tolerance, particularly under biofilm conditions, independently of its effects on growth.

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来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
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