Microbiology Department, Theodor Bilharz Research Institute (TBRI), Giza, Egypt.
Biochemistry and Molecular Biology Department, Theodor Bilharz Research Institute (TBRI), Giza, Egypt.
Infect Genet Evol. 2021 Apr;89:104722. doi: 10.1016/j.meegid.2021.104722. Epub 2021 Jan 11.
Methicillin-resistant Staphylococcus aureus (MRSA) biofilm infection is a major threat in Healthcare facilities. The search for biofilm inhibitors is essential to overcome the antibiotic resistance. Eugenol is a phyto-compound that possesses many biological properties. In this study, the aim was to estimate the effect of eugenol on biofilms of MRSA through quantifying the level of gene expression of three genes (IcaA, IcaD and SarA) involved in biofilm development.. Fifty MRSA biofilm producers collected from the microbiology lab at Theodor Bilharz Research Institute were incubated with different concentrations of eugenol for 24 h. The minimum inhibitory concentration of eugenol (MIC) that eradicates the biofilms growth was detected. mRNA was extracted from all isolates before and after the application of eugenol at 0.5 x MIC, and then subjected to quantitative real-time PCR (qPCR). Results showed that fourteen isolates out of 50 (28%) exhibited intermediate biofilm formation ability, and 36 out of 50 (72%) were strong biofilm producers. The MIC values of eugenol for MRSA ranged from 3.125% to 0.01%. The mean values of MIC in both strong and intermediate biofilm forming MRSA isolates were statistically comparable (p = 0.202). qPCR results revealed that the levels of expression of the studied genes IcaA, IcaD, and SarA were decreased after eugenol treatment when compared with their corresponding values before treatment (p = 0.001). Eugenol inhibited the formation of biofilm of MRSA isolates, indicating it could be used to control infections associated with MRSA biofilms.
耐甲氧西林金黄色葡萄球菌(MRSA)生物膜感染是医疗机构的主要威胁。寻找生物膜抑制剂对于克服抗生素耐药性至关重要。丁香酚是一种植物化合物,具有许多生物学特性。在这项研究中,目的是通过定量测定参与生物膜发育的三个基因(IcaA、IcaD 和 SarA)的基因表达水平来评估丁香酚对 MRSA 生物膜的影响。从 Theodor Bilharz 研究所的微生物实验室收集了 50 株 MRSA 生物膜生产者,并用不同浓度的丁香酚孵育 24 小时。检测出消除生物膜生长的丁香酚最小抑菌浓度(MIC)。在应用 0.5 x MIC 的丁香酚前后,从所有分离株中提取 mRNA,然后进行实时定量 PCR(qPCR)。结果表明,在 50 株分离株中,有 14 株(28%)表现出中等生物膜形成能力,有 36 株(72%)是强生物膜生产者。MRSA 对丁香酚的 MIC 值范围为 3.125%至 0.01%。强和中等生物膜形成 MRSA 分离株的 MIC 值平均值在统计学上无差异(p=0.202)。qPCR 结果显示,与治疗前相比,丁香酚处理后研究基因 IcaA、IcaD 和 SarA 的表达水平降低(p=0.001)。丁香酚抑制了 MRSA 分离株生物膜的形成,表明它可用于控制与 MRSA 生物膜相关的感染。