Department of Microbiology and Immunology, Faculty of Pharmacy, Zagazig University, Zagazig, Egypt.
PLoS One. 2022 Jul 29;17(7):e0272417. doi: 10.1371/journal.pone.0272417. eCollection 2022.
Staphylococcus aureus is an opportunistic pathogen that causes wide range of nosocomial and community-acquired infections which have spread worldwide leading to an urgent need for developing effective anti-staphylococcal agents. Efflux is an important resistance mechanism that bacteria used to fight the antimicrobial action. This study aimed to investigate the efflux mechanism in S. aureus and assess diclofenac, domperidone, glyceryl trinitrate and metformin as potential efflux pump inhibitors that can be used in combination with antibiotics for treating topical infections caused by S. aureus.
Efflux was detected qualitatively by the ethidium bromide Cart-Wheel method followed by investigating the presence of efflux genes by polymerase chain reaction. Twenty-six isolates were selected for further investigation of efflux by Cart-Wheel method in absence and presence of tested compounds followed by quantitative efflux assay. Furthermore, antibiotics minimum inhibitory concentrations in absence and presence of tested compounds were determined. The effects of tested drugs on expression levels of efflux genes norA, fexA and tetK were determined by quantitative real time-polymerase chain reaction.
Efflux was found in 65.3% of isolates, the prevalence of norA, tetK, fexA and msrA genes were 91.7%, 77.8%, 27.8% and 6.9%. Efflux assay revealed that tested drugs had potential efflux inhibitory activities, reduced the antibiotic's MICs and significantly decreased the relative expression of efflux genes.
Diclofenac sodium, domperidone and glyceryl trinitrate showed higher efflux inhibitory activities than verapamil and metformin. To our knowledge, this is the first report that shows that diclofenac sodium, glyceryl trinitrate and domperidone have efflux pump inhibitory activities against S. aureus.
金黄色葡萄球菌是一种机会致病菌,可引起广泛的医院获得性和社区获得性感染,这些感染已在全球范围内传播,因此迫切需要开发有效的抗葡萄球菌药物。外排是细菌用来对抗抗菌作用的一种重要耐药机制。本研究旨在研究金黄色葡萄球菌的外排机制,并评估双氯芬酸钠、多潘立酮、甘油三硝酸酯和二甲双胍作为潜在的外排泵抑制剂,可与抗生素联合用于治疗金黄色葡萄球菌引起的局部感染。
通过溴化乙锭车轮法定性检测外排,然后通过聚合酶链反应检测外排基因的存在。选择 26 株分离株进一步通过车轮法在无和有测试化合物的情况下进行外排研究,然后进行定量外排测定。此外,还测定了无和有测试化合物时抗生素的最小抑菌浓度。通过实时定量聚合酶链反应测定测试药物对norA、fexA 和 tetK 外排基因表达水平的影响。
发现 65.3%的分离株存在外排,norA、tetK、fexA 和 msrA 基因的流行率分别为 91.7%、77.8%、27.8%和 6.9%。外排测定表明,测试药物具有潜在的外排抑制活性,降低了抗生素的 MICs,并显著降低了外排基因的相对表达。
双氯芬酸钠、多潘立酮和甘油三硝酸酯显示出比维拉帕米和二甲双胍更高的外排抑制活性。据我们所知,这是首次报道双氯芬酸钠、甘油三硝酸酯和多潘立酮对金黄色葡萄球菌具有外排泵抑制活性。