Experimental evolution of Escherichia coli on semi-dry silver, copper, stainless steel, and glass surfaces.

IF 3.7 2区 生物学 Q2 MICROBIOLOGY
Microbiology spectrum Pub Date : 2025-04-01 Epub Date: 2025-02-14 DOI:10.1128/spectrum.02173-24
Merilin Rosenberg, Sandra Park, Sigrit Umerov, Angela Ivask
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引用次数: 0

Abstract

To study bacterial adaptation to antimicrobial metal surfaces in application-relevant conditions, Escherichia coli was exposed to copper and silver surfaces for 30 exposure cycles in low-organic dry or high-organic humid conditions. The evolved populations demonstrated increased metal surface tolerance without concurrent increase in minimal biocidal concentration (MBC) and minimal inhibitory concentration (MIC) values of respective metal ions or selected antibiotics. Mutation analysis did not detect increased mutation accumulation nor mutations in cop, cus, cue, sil, pco, or general efflux genes known to actively maintain copper/silver homeostasis. Instead, during cyclic exposure, mutations in genes related to cellular barrier functions and sulfur metabolism were enriched, potentially suggesting that reducing bioavailability and passively restricting uptake of the toxic metals rather than active efflux is selected for on copper and silver surfaces. The changes detected in the evolved populations did not indicate an increased risk of antibiotic cross-resistance as a result of copper or silver surface exposure. However, rapid emergence of mutations in silS activated the cryptic sil efflux locus during silver ion challenge in liquid MBC assay with the evolved populations. The silS mutants showed no benefit on copper and silver surfaces but demonstrated decreased sensitivity to ampicillin and ciprofloxacin, as well as copper and silver ions in liquid tests, indicating that efflux might be specific to granting heavy metal tolerance in liquid but not surface exposure format. Our findings highlight the critical importance of appropriate exposure conditions not only in efficacy testing but also in risk assessment of antimicrobial surface applications.

Importance: This study examines the evolutionary adaptations of Escherichia coli after semi-dry exposure to copper and silver surfaces, leading to an increase in surface tolerance but no increase in mutation accumulation or substantially enhanced metal ion tolerance in standard tests. Notably, enriched mutations indicate a shift toward more energy-passive mechanisms of metal tolerance. Additionally, while enhanced silver efflux was rapidly selected for in a single round of silver exposure in liquid tests and substantially increased copper and silver ion tolerance in conventional test formats, the causal mutations did not improve viability on silver and copper surfaces, underscoring the different fitness scenarios of tolerance mechanisms dependent on exposure conditions. These findings emphasize the need for appropriate exposure conditions in evaluating of both efficacy and the potential risks of using antimicrobial surfaces, as the results from conventional liquid-based tests may not apply in solid contexts.

半干燥的银、铜、不锈钢和玻璃表面上大肠杆菌的实验进化。
为了研究细菌在应用相关条件下对抗菌金属表面的适应性,研究人员在低有机干燥或高有机潮湿条件下,将大肠杆菌暴露于铜和银表面30个暴露周期。进化后的种群表现出金属表面耐受性的增强,而各自金属离子或选定抗生素的最小杀菌浓度(MBC)和最小抑菌浓度(MIC)值并未同时增加。突变分析没有发现突变积累增加,也没有发现cop、cus、cue、sil、pco或已知的积极维持铜/银稳态的一般外排基因的突变。相反,在循环暴露期间,与细胞屏障功能和硫代谢相关的基因突变富集,可能表明铜和银表面选择降低生物利用度和被动限制有毒金属的吸收,而不是主动外排。在进化种群中检测到的变化并不表明由于铜或银表面暴露而增加抗生素交叉抗性的风险。然而,在进化后的种群中,在液体MBC试验中,silS突变的迅速出现激活了银离子攻击时的隐sil外排位点。silS突变体在铜和银表面没有表现出任何益处,但在液体试验中对氨苄西林和环丙沙星以及铜和银离子的敏感性降低,这表明外排可能特定于在液体中给予重金属耐受性,而不是表面暴露形式。我们的研究结果强调了适当的暴露条件不仅在功效测试中至关重要,而且在抗菌药物表面应用的风险评估中也至关重要。重要性:本研究考察了大肠杆菌在半干燥暴露于铜和银表面后的进化适应性,导致表面耐受性增加,但在标准试验中没有增加突变积累或大幅增强金属离子耐受性。值得注意的是,富集突变表明金属耐受性向能量被动机制转变。此外,尽管在液体试验中,单轮银暴露迅速增强了银外排,并在常规试验中大幅增加了铜和银离子的耐受性,但因果突变并没有提高银和铜表面的生存能力,强调了依赖于暴露条件的耐受性机制的不同适应度情景。这些发现强调,在评估使用抗菌表面的功效和潜在风险时,需要适当的暴露条件,因为传统的基于液体的测试结果可能不适用于固体环境。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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