Modulation of Quorum Sensing and Virulence Gene Expression in Escherichia coli by Extracts of Physalis alkekengi.

IF 3.1 4区 生物学 Q2 ENVIRONMENTAL SCIENCES
Mansoureh Esfandiyari Doolaby, Mohammad Javad Mehdipour Moghaddam, Akbar Norastehnia
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Abstract

The rise of multidrug-resistant (MDR) bacteria underscores the need for new antimicrobials. In uropathogenic Escherichia coli, quorum sensing and adhesion play central roles in pathogenicity; therefore, luxS and fimH were selected as virulence targets. This study examined the antibacterial, antibiofilm and gene-modulating effects of ethanolic and aqueous root extracts of Physalis alkekengi L. against three E. coli isolates (EC1, EC2, EC3). Phytochemical analysis confirmed the presence of phenolics, flavonoids, flavonols and anthocyanins, along with measurable antioxidant capacity. Antimicrobial activity was assessed using agar well diffusion, disk diffusion and broth microdilution on the MDR isolate EC2. Biofilm inhibition was quantified using a microtiter plate, and changes in luxS and fimH expression were evaluated by real-time PCR. The ethanolic extract contained higher flavonoid and flavonol levels, whereas the aqueous extract was richer in phenolics. Anthocyanins and DPPH activity were undetectable in both extracts. The ethanolic extract completely inhibited EC3 at 10 mg/mL, although no MBC was observed for EC1, EC2 or any isolate exposed to the aqueous extract. In EC2, the ethanolic extract produced larger but variable inhibition zones, reduced biofilm by approximately 63% and significantly downregulated luxS and fimH (p < 0.05), supporting the potential of P. alkekengi as a natural antivirulence agent.

酸浆菌提取物对大肠杆菌群体感应及毒力基因表达的调控。
耐多药细菌(MDR)的增加强调了对新型抗菌剂的需求。在尿路致病性大肠杆菌中,群体感应和粘附在致病性中起核心作用;因此,选择luxS和fimH作为毒力靶点。本研究考察了泡Physalis alkekengi L.乙醇提取物和水提取物对3株大肠杆菌(EC1, EC2, EC3)的抑菌、抗生物膜和基因调控作用。植物化学分析证实了酚类物质、类黄酮、类黄酮醇和花青素的存在,并具有可测量的抗氧化能力。采用琼脂孔扩散法、圆盘扩散法和肉汤微量稀释法对MDR分离菌EC2进行抑菌活性评价。采用微滴板定量测定生物膜抑制作用,实时荧光定量PCR检测luxS和fimH表达变化。乙醇提取物的类黄酮和黄醇含量较高,而水提取物的酚类物质含量较高。两种提取物均未检测到花青素和DPPH活性。乙醇提取物在10 mg/mL浓度下完全抑制EC3,但没有观察到EC1、EC2或任何暴露于水提取物的分离物的MBC。在EC2中,乙醇提取物产生了更大但可变的抑制区,减少了约63%的生物膜,并显著下调了luxS和fimH (p
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来源期刊
Environmental Microbiology Reports
Environmental Microbiology Reports ENVIRONMENTAL SCIENCES-MICROBIOLOGY
CiteScore
6.00
自引率
3.00%
发文量
91
审稿时长
3.0 months
期刊介绍: The journal is identical in scope to Environmental Microbiology, shares the same editorial team and submission site, and will apply the same high level acceptance criteria. The two journals will be mutually supportive and evolve side-by-side. Environmental Microbiology Reports provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following: the structure, activities and communal behaviour of microbial communities microbial community genetics and evolutionary processes microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors microbes in the tree of life, microbial diversification and evolution population biology and clonal structure microbial metabolic and structural diversity microbial physiology, growth and survival microbes and surfaces, adhesion and biofouling responses to environmental signals and stress factors modelling and theory development pollution microbiology extremophiles and life in extreme and unusual little-explored habitats element cycles and biogeochemical processes, primary and secondary production microbes in a changing world, microbially-influenced global changes evolution and diversity of archaeal and bacterial viruses new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens.
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