Laboratório de Pesquisa em Ciências da Saúde, Universidade Federal da Grande Dourados-UFGD, Dourados, Mato Grasso do Sul, Brazil.
Hospital Universitário de Dourados, Universidade Federal da Grande Dourados-UFGD, Dourados, Mato Grosso do Sul, Brazil.
PLoS One. 2020 Jul 23;15(7):e0236505. doi: 10.1371/journal.pone.0236505. eCollection 2020.
Multidrug resistance prompts the search for new sources of antibiotics with new targets at bacteria cell. To investigate the antibacterial activity of Cinnamomum cassia L. essential oil (CCeo) alone and in combination with antibiotics against carbapenemase-producing Klebsiella pneumoniae and Serratia marcescens. The antimicrobial susceptibility of the strains was determined by Vitek® 2 and confirmed by MALDI-TOF/TOF. The antibacterial activity of CCeo and its synergism with antibiotics was determined using agar disk diffusion, broth microdilution, time-kill, and checkboard methods. The integrity of the bacterial cell membrane in S. marcescens was monitored by protein leakage assay. CCeo exhibited inhibitory effects with MIC = 281.25 μg.mL-1. The association between CCeo and polymyxin B showed a decrease in terms of viable cell counts on survival curves over time after a 4 hour-treatment with a FIC index value of 0.006. Protein leakage was observed with increasing concentrations for CCeo and CCeo + polymyxin B treatments. CCeo showed antibacterial activity against the studied strains. When associated with polymyxin B, a synergistic effect was able to inhibit bacterial growth rapidly and consistently, making it a potential candidate for the development of an alternative treatment and drug delivery system for carbapenemase-producing strains.
多药耐药性促使人们寻找新的抗生素来源,以针对细菌细胞的新靶标。本研究旨在探讨肉桂精油(CCeo)单独使用和联合抗生素对产碳青霉烯酶肺炎克雷伯菌和粘质沙雷氏菌的抗菌活性。采用 Vitek® 2 系统和 MALDI-TOF/TOF 对菌株的药敏性进行测定。采用琼脂扩散、肉汤微量稀释、时间杀伤和棋盘试验法测定 Cceo 的抗菌活性及其与抗生素的协同作用。通过蛋白渗漏试验监测粘质沙雷氏菌的细菌细胞膜完整性。CCeo 的 MIC 值为 281.25 μg.mL-1。CCeo 与多粘菌素 B 联合使用时,在 4 小时处理后,存活曲线的活菌计数随时间减少,FIC 指数值为 0.006。随着 Cceo 和 Cceo+多粘菌素 B 处理浓度的增加,观察到蛋白渗漏。CCeo 对研究菌株表现出抗菌活性。当与多粘菌素 B 联合使用时,协同作用能够快速且持续地抑制细菌生长,使其成为开发针对产碳青霉烯酶菌株的替代治疗方法和药物输送系统的潜在候选药物。