Alenazi Naifa A, Aleanizy Fadilah S, Alqahtani Fulwah Y, Aldossari Abdullah A, Alanazi Mohammed M, Alfaraj Rihaf
Department of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh 11495, Saudi Arabia.
Department of Pharmacology and Toxicology, College of Pharmacy, King Saud University, Riyadh 11495, Saudi Arabia.
Saudi Pharm J. 2024 Feb;32(2):101932. doi: 10.1016/j.jsps.2023.101932. Epub 2023 Dec 19.
Methicillin-resistant Staphylococcus aureus (MRSA) is a significant concern in both healthcare and community settings, as it causes numerous infections worldwide with high morbidity and mortality rates. One promising strategy is to target the quorum sensing (QS) system of MRSA using a dendrimer loaded with kinase inhibitor peptide. The present investigation has formulated a poly-amidoamine dendrimer (PAMAM) G5 dendrimer that is loaded with Quorum Quencher (QQ) peptide, which functions as a histidine kinase inhibitor. The particle average size of the formulated G5-QQ3 complex was determined to be 276 nm, and polydispersity index values of 0.33. The MIC for the formulated nanoparticles was 18 μM as demonstrated by a growth assay. Furthermore, the G5-QQ3 complex was able to inhibit the hemolysis activity of the MRSA with a concentration of 10 μM, and for was 3 μM. The G5-QQ3 complex possesses the ability to inhibit, penetrate, and eradicate biofilm in MRSA, , and different mutants with inhibition percentages ranging from 60 to 72%. Furthermore, live/dead viability assay confirmed the ability of the formulated nanoparticles to effectively kill all strains within the biofilm structure as evidenced by a confocal microscope, and the cytotoxicity of the G5-QQ3 complex was dose-dependent (p < 0.05). against RAW 264.7 cells. In general, the study confirmed that encapsulating QQ3 peptide within PAMAM G5 dendrimer results in a potent anti-virulence and anti-bacterial action and suggests a synergistic effect. The findings of this study have significant implications for the development of new treatments for MRSA infections, which are a major public health concern.
耐甲氧西林金黄色葡萄球菌(MRSA)在医疗保健和社区环境中都是一个重大问题,因为它在全球范围内引发了众多感染,发病率和死亡率都很高。一种有前景的策略是使用负载激酶抑制剂肽的树枝状大分子靶向MRSA的群体感应(QS)系统。本研究制备了一种负载群体猝灭(QQ)肽的聚酰胺胺树枝状大分子(PAMAM)G5树枝状大分子,该肽作为组氨酸激酶抑制剂发挥作用。所制备的G5-QQ3复合物的平均粒径测定为276 nm,多分散指数值为0.33。生长试验表明,所制备纳米颗粒的最低抑菌浓度(MIC)为18 μM。此外,G5-QQ3复合物能够在浓度为10 μM时抑制MRSA的溶血活性,而抑制浓度为3 μM。G5-QQ3复合物具有抑制、穿透和根除MRSA生物膜以及不同突变体的能力,抑制率在60%至72%之间。此外,活/死细胞活力测定证实了所制备的纳米颗粒能够有效杀死生物膜结构内的所有菌株,共聚焦显微镜也证明了这一点,并且G5-QQ3复合物的细胞毒性呈剂量依赖性(p < 0.05),对RAW 264.7细胞具有毒性。总体而言,该研究证实将QQ3肽包裹在PAMAM G5树枝状大分子中会产生强大的抗毒力和抗菌作用,并表明存在协同效应。本研究结果对开发针对MRSA感染的新疗法具有重要意义,MRSA感染是一个重大的公共卫生问题。