Mone Nishigandha S, Syed Sahil, Ravichandiran Palanisamy, Kamble Ekta E, Pardesi Karishma R, Salunke-Gawali Sunita, Rai Mansi, Vikram Singh Ajay, Prasad Dakua Sarada, Park Byung-Hyun, Yoo Dong Jin, Satpute Surekha K
Department of Microbiology, Savitribai Phule Pune University, Pune, Maharashtra, 411007, India.
Department of Energy Storage/Conversion Engineering (BK21 FOUR) of Graduate School, Hydrogen and Fuel Cell Research Center, Jeonbuk National University, Jeonju, Jeollabuk-do, 54896, Republic of Korea.
ChemMedChem. 2023 Dec 14;18(24):e202300328. doi: 10.1002/cmdc.202300328. Epub 2023 Nov 10.
Antimicrobial resistance (AMR) interferes with the effective treatment of infections and increases the risk of microbial spread and infection-related illness and death. The synergistic activities of combinations of antimicrobial compounds offer satisfactory approaches to some extent. Structurally diverse naphthoquinones (NQs) including menadione (-CH group at C2) exhibit substantial antimicrobial activities against multidrug-resistant (MDR) pathogens. We explored the combinations of menadione with antibiotic ciprofloxacin or ampicillin against Staphylococcus aureus and its biofilms. We found an additive (0.5<FICI 1.0) and synergistic (FICI≤0.5) effect of menadione with ciprofloxacin and ampicillin, respectively. High reactive oxygen species (ROS) activity and inhibition of biofilm formation (>90 %) were also observed. However, preformed biofilms were not affected. Dent formation was also evident in S. aureus treated with the test compounds. The structure-function relationship (SFR) of NQs was used to determine and predict their activity pattern against pathogens. Analysis of 10 structurally distinct NQs revealed that the compounds with -Cl, -Br, -CH , or -OH groups displayed the lowest MICs (32-256 μg/mL). Furthermore, 1,4-NQs possessing a halogen or -CH moiety showed elevated ROS activity, whereas molecules with an -OH group affected cell integrity. Improved activity of antimicrobial combinations and SFR approaches are significant in antimicrobial therapies.
抗菌药物耐药性(AMR)干扰感染的有效治疗,并增加微生物传播以及感染相关疾病和死亡的风险。抗菌化合物组合的协同活性在一定程度上提供了令人满意的方法。包括甲萘醌(C2处为-CH基团)在内的结构多样的萘醌(NQs)对多重耐药(MDR)病原体表现出显著的抗菌活性。我们研究了甲萘醌与抗生素环丙沙星或氨苄西林联合对金黄色葡萄球菌及其生物膜的作用。我们发现甲萘醌分别与环丙沙星和氨苄西林联合具有相加作用(0.5<FICI≤1.0)和协同作用(FICI≤0.5)。还观察到高活性氧(ROS)活性以及生物膜形成受到抑制(>90%)。然而,预先形成的生物膜不受影响。在用测试化合物处理的金黄色葡萄球菌中也明显出现了凹陷形成。利用萘醌的构效关系(SFR)来确定和预测它们对病原体的活性模式。对10种结构不同的萘醌的分析表明,具有-Cl、-Br、-CH₃或-OH基团的化合物显示出最低的最低抑菌浓度(MICs)(32 - 256μg/mL)。此外,具有卤素或-CH₃部分的1,4-萘醌显示出升高的ROS活性,而具有-OH基团的分子影响细胞完整性。抗菌组合活性的提高和SFR方法在抗菌治疗中具有重要意义。