Centre of advanced study in Marine Biology, Annamalai University, Parangipettai - 608 502, Tamil Nadu, India.
Department of Biotechnology, Karpagam academy of higher education, Eachanari, Coimbatore-641 021, Tamil Nadu, India.
J Med Microbiol. 2020 Nov;69(11):1308-1318. doi: 10.1099/jmm.0.001253.
is a diverse virulent synthesis pathogen responsible for invasive systemic infections. Establishment of antibiotic resistance in the pathogen has produced a need for new antibiofilm agents to control the biofilm formation and reduce biofilm-associated resistance development. The present study investigates the antibiofilm activity of eucalyptol against . The antibiofilm potential of eucalyptol was assessed using a microdilution method and their biofilm inhibition efficacy was visualized by microscopic analysis. The biochemical assays were performed to assess the influence of eucalyptol on virulence productions. Real-time PCR analysis was performed to evaluate the expression profile of the virulence genes. Eucalyptol showed significant antibiofilm potential in a dose-dependent manner without affecting bacterial growth. Eucalyptol at 300 µg ml (biofilm inhibitory concentration) significantly inhibited the initial stage of biofilm formation in . However, eucalyptol failed to diminish the mature biofilms of at biofilm inhibitory concentration and it effectively reduced the biofilm formation on stainless steel, titanium, and silicone surfaces. The biochemical assay results revealed that eucalyptol greatly affects the cell-surface hydrophobicity, auto-aggregation, extracellular protease, haemolysis and hyaluronic acid synthesis. Further, the gene-expression analysis results showed significant downregulation of virulence gene expression upon eucalyptol treatment. The present study suggests that eucalyptol applies its antibiofilm assets by intruding the initial biofilm formation of . Supplementary studies are needed to understand the mode of action involved in biofilm inhibition.
是一种具有多种毒力的合成病原体,可导致侵袭性全身感染。病原体对抗生素耐药性的建立产生了对新的抗生物膜剂的需求,以控制生物膜的形成并降低生物膜相关的耐药性发展。本研究调查了桉叶油醇对 的抗生物膜活性。使用微量稀释法评估桉叶油醇的抗生物膜潜力,并通过显微镜分析观察其生物膜抑制效果。进行生化测定以评估桉叶油醇对毒力产物的影响。进行实时 PCR 分析以评估毒力基因的表达谱。桉叶油醇以剂量依赖性方式表现出显著的抗生物膜潜力,而不影响细菌生长。桉叶油醇在 300μg/ml(生物膜抑制浓度)时可显著抑制 生物膜形成的初始阶段。然而,在生物膜抑制浓度下,桉叶油醇未能减少 的成熟生物膜,并且有效减少了不锈钢、钛和硅树脂表面的生物膜形成。生化测定结果表明,桉叶油醇极大地影响细胞表面疏水性、自动聚集、细胞外蛋白酶、溶血和透明质酸合成。此外,基因表达分析结果表明,桉叶油醇处理后毒力基因表达显著下调。本研究表明,桉叶油醇通过侵入 生物膜形成的初始阶段发挥其抗生物膜作用。需要进一步的研究来了解涉及生物膜抑制的作用模式。