RelQ 介导的报警酮信号调节艰难梭菌的生长、压力诱导的生物膜形成和孢子积累。

IF 2.6 4区 生物学 Q3 MICROBIOLOGY
Areej Malik, Adenrele Oludiran, Asia Poudel, Orlando Berumen Alvarez, Charles Woodward, Erin B Purcell
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引用次数: 0

摘要

细菌严格反应(SR)是一种保守的转录重编程途径,由核苷酸信号警报素(pp)ppGpp 介导。难辨梭状芽孢杆菌是一种形成生物膜和孢子的病原体,会导致难辨梭状芽孢杆菌感染的顽固性和高度复发性。SR在其他过程中的作用及其调节艰难梭菌生理机能的效应器尚不清楚。艰难梭菌 RelQ 是一种梭菌报警酮合成酶。缺失 relQ 会使艰难梭菌在非应激条件下生长失调,影响对抗生素和氧化应激源的敏感性,并大大减少生物膜的形成。野生型艰难梭菌在亚致死压力下会增加生物膜的形成,而ΔrelQ菌株则不能上调生物膜的生成以应对压力。删除 relQ 会减缓浮游培养物中孢子的积累,但会加速生物膜中孢子的积累。这项工作确定了艰难梭菌的生物膜形成和孢子积累是由警报素介导的过程,并揭示了 RelQ 在应激诱导的生物膜调节中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RelQ-mediated alarmone signalling regulates growth, stress-induced biofilm formation and spore accumulation in Clostridioides difficile.

The bacterial stringent response (SR) is a conserved transcriptional reprogramming pathway mediated by the nucleotide signalling alarmones, (pp)pGpp. The SR has been implicated in antibiotic survival in Clostridioides difficile, a biofilm- and spore-forming pathogen that causes resilient, highly recurrent C. difficile infections. The role of the SR in other processes and the effectors by which it regulates C. difficile physiology are unknown. C. difficile RelQ is a clostridial alarmone synthetase. Deletion of relQ dysregulates C. difficile growth in unstressed conditions, affects susceptibility to antibiotic and oxidative stressors and drastically reduces biofilm formation. While wild-type C. difficile displays increased biofilm formation in the presence of sublethal stress, the ΔrelQ strain cannot upregulate biofilm production in response to stress. Deletion of relQ slows spore accumulation in planktonic cultures but accelerates it in biofilms. This work establishes biofilm formation and spore accumulation as alarmone-mediated processes in C. difficile and reveals the importance of RelQ in stress-induced biofilm regulation.

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来源期刊
Microbiology-Sgm
Microbiology-Sgm 生物-微生物学
CiteScore
4.60
自引率
7.10%
发文量
132
审稿时长
3.0 months
期刊介绍: We publish high-quality original research on bacteria, fungi, protists, archaea, algae, parasites and other microscopic life forms. Topics include but are not limited to: Antimicrobials and antimicrobial resistance Bacteriology and parasitology Biochemistry and biophysics Biofilms and biological systems Biotechnology and bioremediation Cell biology and signalling Chemical biology Cross-disciplinary work Ecology and environmental microbiology Food microbiology Genetics Host–microbe interactions Microbial methods and techniques Microscopy and imaging Omics, including genomics, proteomics and metabolomics Physiology and metabolism Systems biology and synthetic biology The microbiome.
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