Arsenic-induced modulation of virulence and drug resistance in Pseudomonas aeruginosa

IF 11.3 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL Journal of Hazardous Materials Pub Date : 2025-05-05 Epub Date: 2025-01-23 DOI:10.1016/j.jhazmat.2025.137352
Yingjie Song , Tao Li , Fang Zhao , Ze Li , Rui Bao
{"title":"Arsenic-induced modulation of virulence and drug resistance in Pseudomonas aeruginosa","authors":"Yingjie Song ,&nbsp;Tao Li ,&nbsp;Fang Zhao ,&nbsp;Ze Li ,&nbsp;Rui Bao","doi":"10.1016/j.jhazmat.2025.137352","DOIUrl":null,"url":null,"abstract":"<div><div>Arsenic contamination of water sources, whether from natural or industrial origins, represents a significant risk to human health. However, its impact on waterborne pathogens remains understudied. This research explores the effects of arsenic exposure on the opportunistic pathogen <em>Pseudomonas aeruginosa</em>, a bacterium found in diverse environments. The arsenic exposure at concentrations of 0.12–20 mg/L As(III) resulted in rapid growth arrest of <em>P. aeruginosa</em>. Moreover, arsenic exposure significantly reduced the production of key virulence factors such as elastase (by 1.48- to 9.24-fold), pyocyanin, and flagella while increasing siderophore and extracellular polysaccharide production (by 1.44–1.75 and 1.36–2.59 times, respectively). Proteomic analysis revealed that both low (0.12 mg/L) and high (1.2 mg/L) As(III) levels activated an antioxidant defense response, with upregulation of Fnr-2, TrxB2, and Ohr. Furthermore, arsenic-induced the overexpression of multidrug resistance efflux proteins MexAB-OprM, MexCD-OprJ, and MexEF-OprN. At the same time, proteins associated with quorum sensing (QS), type III secretion system (T3SS), pyocyanin biosynthesis, and flagellar assembly were downregulated. In vitro assays confirmed that arsenic reduced bacterial virulence and significantly enhanced survival and proliferation under antibiotic treatment. These results indicate that arsenic exposure modulates the virulence and antibiotic resistance of <em>P. aeruginosa</em>, raising concerns about the public health risks posed by the convergence of arsenic-contaminated water and multidrug-resistant bacteria.</div></div>","PeriodicalId":361,"journal":{"name":"Journal of Hazardous Materials","volume":"488 ","pages":"Article 137352"},"PeriodicalIF":11.3000,"publicationDate":"2025-05-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Hazardous Materials","FirstCategoryId":"93","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S030438942500264X","RegionNum":1,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/23 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"ENGINEERING, ENVIRONMENTAL","Score":null,"Total":0}
引用次数: 0

Abstract

Arsenic contamination of water sources, whether from natural or industrial origins, represents a significant risk to human health. However, its impact on waterborne pathogens remains understudied. This research explores the effects of arsenic exposure on the opportunistic pathogen Pseudomonas aeruginosa, a bacterium found in diverse environments. The arsenic exposure at concentrations of 0.12–20 mg/L As(III) resulted in rapid growth arrest of P. aeruginosa. Moreover, arsenic exposure significantly reduced the production of key virulence factors such as elastase (by 1.48- to 9.24-fold), pyocyanin, and flagella while increasing siderophore and extracellular polysaccharide production (by 1.44–1.75 and 1.36–2.59 times, respectively). Proteomic analysis revealed that both low (0.12 mg/L) and high (1.2 mg/L) As(III) levels activated an antioxidant defense response, with upregulation of Fnr-2, TrxB2, and Ohr. Furthermore, arsenic-induced the overexpression of multidrug resistance efflux proteins MexAB-OprM, MexCD-OprJ, and MexEF-OprN. At the same time, proteins associated with quorum sensing (QS), type III secretion system (T3SS), pyocyanin biosynthesis, and flagellar assembly were downregulated. In vitro assays confirmed that arsenic reduced bacterial virulence and significantly enhanced survival and proliferation under antibiotic treatment. These results indicate that arsenic exposure modulates the virulence and antibiotic resistance of P. aeruginosa, raising concerns about the public health risks posed by the convergence of arsenic-contaminated water and multidrug-resistant bacteria.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
砷诱导的铜绿假单胞菌毒力和耐药性调控
水源的砷污染,无论是自然来源还是工业来源,都对人类健康构成重大风险。然而,它对水传播病原体的影响仍未得到充分研究。本研究探讨砷暴露对机会致病菌铜绿假单胞菌的影响,这是一种在不同环境中发现的细菌。砷暴露浓度为0.12 ~ 20 mg/L As(III)时,铜绿假单胞菌生长迅速停止。此外,砷暴露显著降低了关键毒力因子的产生,如弹性酶(1.48- 9.24倍)、花青素和鞭毛,同时增加了铁载体和细胞外多糖的产生(分别为1.44-1.75倍和1.36-2.59倍)。蛋白质组学分析显示,低(0.12 mg/L)和高(1.2 mg/L) As(III)水平均激活了抗氧化防御反应,并上调了Fnr-2、TrxB2和Ohr。此外,砷诱导多药耐药外排蛋白MexAB-OprM、mexd - oprj和MexEF-OprN过表达。与此同时,与群体感应(QS)、III型分泌系统(T3SS)、花青素生物合成和鞭毛组装相关的蛋白下调。体外试验证实,砷可降低细菌毒力,并显著提高抗生素治疗下的存活和增殖。这些结果表明,砷暴露调节了铜绿假单胞菌的毒力和抗生素耐药性,引起了人们对砷污染水和多重耐药细菌汇合所带来的公共卫生风险的关注。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
文献相关原料
公司名称
产品信息
麦克林
paraformaldehyde
来源期刊
Journal of Hazardous Materials
Journal of Hazardous Materials 工程技术-工程:环境
CiteScore
25.40
自引率
5.90%
发文量
3059
审稿时长
58 days
期刊介绍: The Journal of Hazardous Materials serves as a global platform for promoting cutting-edge research in the field of Environmental Science and Engineering. Our publication features a wide range of articles, including full-length research papers, review articles, and perspectives, with the aim of enhancing our understanding of the dangers and risks associated with various materials concerning public health and the environment. It is important to note that the term "environmental contaminants" refers specifically to substances that pose hazardous effects through contamination, while excluding those that do not have such impacts on the environment or human health. Moreover, we emphasize the distinction between wastes and hazardous materials in order to provide further clarity on the scope of the journal. We have a keen interest in exploring specific compounds and microbial agents that have adverse effects on the environment.
期刊最新文献
A Trojan Horse in the soil: Tetracycline hijacks plant organellar ribosomes to stunt growth and unbalance the rhizosphere microecology Pesticide fate and transport in the atmosphere and implications for risk assessment Selecting emergent wetland plants for constructed wetlands under microplastic stress: Physiological performance and transcriptomic mechanisms Probabilistic risk assessment of hazardous VOCs and carbonyl compounds in mainstream and secondhand cigarette smoke using mechanistic exposure modeling and Korean-specific parameters Differential distribution characteristics of heavy metal resistance genes and driving mechanisms of heavy metal speciation in river-lake system sediments
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1