Bacterium–Phage Interactions Enhance Biofilm Resilience during Membrane Filtration Biofouling under Oxidative and Hydraulic Stresses

IF 11.3 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL 环境科学与技术 Pub Date : 2025-03-27 DOI:10.1021/acs.est.5c00490
Zijun Lin, Chujin Ruan, Rong Xia, Jingqiu Liao, Liang Zhu, Dongsheng Wang, Pedro J. J. Alvarez, Pingfeng Yu
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Abstract

Microbial interactions on membrane surfaces can facilitate biofilm formation and biofouling, which poses a significant challenge for pressure-driven membrane filtration systems. This multiomics study investigates the adaptive responses of bacterium–phage interactions under varying oxidative and hydraulic stress during membrane backwashing and their biological contributions to biofouling. Oxidative and hydraulic stress distinctly shaped bacteria and phage diversity and community composition. Under moderate oxidative backwashing (300 ppm of NaClO), diversity was maintained, with increased antioxidant enzyme activities, extracellular polymeric substance (EPS) production, and quorum sensing (QS) signaling, promoting bacterial resilience and biofilm formation. In contrast, excessive oxidative stress (600 ppm of NaClO) reduced bacteria and phage diversity, disrupted antioxidant responses, and increased microbial sensitivity. Hydraulic stress predominantly influenced viral diversity and co-occurrence network topology, favoring the expansion of broad host-range phages and lysogenic lifestyles under combined stresses. Phage–bacterium interaction analyses highlighted phages’ adaptive preferences for hosts with high network centrality and broad ecological niches, which enhanced microbial interactions and resilience. Transcriptomic profiling demonstrated the early enrichment of genes associated with energy metabolism, ROS detoxification, and biofilm formation, followed by stabilization as biofilms matured. Phage-encoded auxiliary metabolic genes were involved in DNA repair, QS, and EPS biosynthesis, contributing to microbial adaptation through oxidative stress resistance and biofilm stabilization. Overall, these findings provide mechanistic insights into biofouling dynamics and highlight the need to optimize chlorine dosing to prevent suboptimal levels of microbial adaptation and biofouling.

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细菌-噬菌体相互作用增强氧化和水力胁迫下膜过滤生物污染过程中的生物膜弹性
微生物在膜表面的相互作用可以促进生物膜的形成和生物污染,这对压力驱动的膜过滤系统提出了重大挑战。这项多组学研究探讨了膜反冲洗过程中细菌-噬菌体相互作用在不同氧化和水力胁迫下的适应性反应及其对生物污染的生物学贡献。氧化和水力胁迫明显影响细菌和噬菌体的多样性和群落组成。在中等氧化反冲洗(300 ppm NaClO)条件下,细菌多样性得以保持,抗氧化酶活性、胞外聚合物(EPS)生成和群体感应(QS)信号增强,促进了细菌的恢复力和生物膜的形成。相反,过度氧化应激(600 ppm NaClO)会降低细菌和噬菌体的多样性,破坏抗氧化反应,增加微生物的敏感性。水力胁迫主要影响病毒多样性和共发生的网络拓扑结构,有利于在联合胁迫下扩大宿主范围的噬菌体和溶原性生活方式。噬菌体-细菌相互作用分析强调了噬菌体对具有高网络中心性和广泛生态位的宿主的适应性偏好,这增强了微生物相互作用和恢复力。转录组学分析显示,与能量代谢、ROS解毒和生物膜形成相关的基因早期富集,随后随着生物膜成熟而稳定。噬菌体编码的辅助代谢基因参与DNA修复、QS和EPS的生物合成,通过抗氧化应激和生物膜稳定促进微生物适应。总的来说,这些发现为生物污染动力学提供了机理见解,并强调了优化氯剂量以防止微生物适应和生物污染的次优水平的必要性。
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来源期刊
环境科学与技术
环境科学与技术 环境科学-工程:环境
CiteScore
17.50
自引率
9.60%
发文量
12359
审稿时长
2.8 months
期刊介绍: Environmental Science & Technology (ES&T) is a co-sponsored academic and technical magazine by the Hubei Provincial Environmental Protection Bureau and the Hubei Provincial Academy of Environmental Sciences. Environmental Science & Technology (ES&T) holds the status of Chinese core journals, scientific papers source journals of China, Chinese Science Citation Database source journals, and Chinese Academic Journal Comprehensive Evaluation Database source journals. This publication focuses on the academic field of environmental protection, featuring articles related to environmental protection and technical advancements.
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