Beyond the Standard Antibiogram: Unveiling the Roles of pH and Salinity in Modulating Gentamicin Efficacy Against Escherichia coli in Urinary Tract Infections

IF 3.6 3区 生物学 Q2 MICROBIOLOGY
Abdelwahab Rai, Mahdia El-djohra El-amina Saoud, Nesrine Tabchouche, Hamdi Bendif, Stefania Garzoli, Lotfi Mouni
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引用次数: 0

Abstract

Urinary tract infections are highly prevalent diseases with a broad spectrum of clinical manifestations. This study investigates the influence of two key abiotic factors, pH and salinity, on the growth and antibiotic susceptibility of Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 27853, and a clinical E. coli isolate obtained from a human urine sample. Growth kinetics and gentamicin susceptibility were evaluated across a pH range (4.5–11.0) and NaCl concentrations (0–1000 mM) using Luria–Bertani and Mueller–Hinton (MH) media. In parallel, real urine was analyzed, and urine-mimicking MH media were prepared by adjusting pH and salinity independently and in combination. Gentamicin susceptibility was strongly influenced by environmental conditions. Salinity pre-exposure increased E. coli and P. aeruginosa resistance from 23.0 to 19.0 mm and from 25.5 to 18.5 mm at 800 mM, respectively. Direct pH modification enhanced gentamicin activity at extreme pH (up to 34.33 mm in E. coli and 33.5 mm in P. aeruginosa). In standard MH medium, the clinical E. coli isolate exhibited a 32.5-mm inhibition zone and a gentamicin minimum inhibitory concentration (MIC) of 4 µg/mL. Under urine-mimicking conditions, the inhibition zone decreased to 22.5 mm, while the MIC increased eightfold to 32 µg/mL, indicating a marked reduction in gentamicin efficacy under physiologically relevant urinary conditions. These findings demonstrate that environmental stress profoundly influences gentamicin efficacy and suggest that this effect may involve physiological adaptations, including RpoS-mediated stress responses, membrane remodeling, and osmoprotective mechanisms previously described in the literature.

超越标准抗生素谱:揭示pH和盐度在调节庆大霉素对尿路感染大肠杆菌的功效中的作用。
尿路感染是一种非常普遍的疾病,具有广泛的临床表现。本研究探讨了pH和盐度这两个关键的非生物因素对大肠杆菌ATCC 25922、铜绿假单胞菌ATCC 27853和从人尿样本中获得的临床大肠杆菌分离株生长和抗生素敏感性的影响。使用Luria-Bertani和Mueller-Hinton (MH)培养基,在pH范围(4.5-11.0)和NaCl浓度(0-1000 mM)下评估生长动力学和庆大霉素敏感性。同时,对真实尿液进行分析,并通过单独和联合调节pH和盐度制备模拟尿液的MH培养基。庆大霉素敏感性受环境条件的强烈影响。盐度预暴露使大肠杆菌和铜绿假单胞菌的抗性分别从23.0 mm增加到19.0 mm和从25.5 mm增加到18.5 mm。直接的pH修饰增强了极端pH下庆大霉素的活性(大肠杆菌达到34.33 mm,铜绿假单胞菌达到33.5 mm)。在标准MH培养基中,临床大肠杆菌分离物表现出32.5 mm的抑制带,庆大霉素最低抑制浓度(MIC)为4µg/mL。在模拟尿液条件下,抑制带减少到22.5 mm,而MIC增加了8倍,达到32µg/mL,表明在生理相关的尿液条件下庆大霉素的功效显着降低。这些发现表明,环境应激深刻地影响庆大霉素的疗效,并表明这种影响可能涉及生理适应,包括rpos介导的应激反应、膜重塑和先前文献中描述的渗透保护机制。
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来源期刊
MicrobiologyOpen
MicrobiologyOpen MICROBIOLOGY-
CiteScore
8.00
自引率
0.00%
发文量
78
审稿时长
20 weeks
期刊介绍: MicrobiologyOpen is a peer reviewed, fully open access, broad-scope, and interdisciplinary journal delivering rapid decisions and fast publication of microbial science, a field which is undergoing a profound and exciting evolution in this post-genomic era. The journal aims to serve the research community by providing a vehicle for authors wishing to publish quality research in both fundamental and applied microbiology. Our goal is to publish articles that stimulate discussion and debate, as well as add to our knowledge base and further the understanding of microbial interactions and microbial processes. MicrobiologyOpen gives prompt and equal consideration to articles reporting theoretical, experimental, applied, and descriptive work in all aspects of bacteriology, virology, mycology and protistology, including, but not limited to: - agriculture - antimicrobial resistance - astrobiology - biochemistry - biotechnology - cell and molecular biology - clinical microbiology - computational, systems, and synthetic microbiology - environmental science - evolutionary biology, ecology, and systematics - food science and technology - genetics and genomics - geobiology and earth science - host-microbe interactions - infectious diseases - natural products discovery - pharmaceutical and medicinal chemistry - physiology - plant pathology - veterinary microbiology We will consider submissions across unicellular and cell-cluster organisms: prokaryotes (bacteria, archaea) and eukaryotes (fungi, protists, microalgae, lichens), as well as viruses and prions infecting or interacting with microorganisms, plants and animals, including genetic, biochemical, biophysical, bioinformatic and structural analyses. The journal features Original Articles (including full Research articles, Method articles, and Short Communications), Commentaries, Reviews, and Editorials. Original papers must report well-conducted research with conclusions supported by the data presented in the article. We also support confirmatory research and aim to work with authors to meet reviewer expectations. MicrobiologyOpen publishes articles submitted directly to the journal and those referred from other Wiley journals.
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