Aiyer Aditi, Visser Simone K, Bye Peter, Britton Warwick J, Whiteley Gregory S, Glasbey Trevor, Kriel Frederik H, Farrell Jessica, Das Theerthankar, Manos Jim
Charles Perkins Centre, Infection, Immunity and Inflammation, School of Medical Sciences, The University of Sydney, Sydney, NSW 2006, Australia.
Royal Prince Alfred Hospital, 12 Missenden Road, Sydney, NSW 2050, Australia.
Antibiotics (Basel). 2021 Sep 27;10(10):1176. doi: 10.3390/antibiotics10101176.
Cystic fibrosis (CF) is a genetic disorder causing dysfunctional ion transport resulting in accumulation of viscous mucus that fosters chronic bacterial biofilm-associated infection in the airways. and are increasingly prevalent CF pathogens and while is slowly decreasing; all are complicated by multidrug resistance that is enhanced by biofilm formation. This study investigates potential synergy between the antibiotics ciprofloxacin (0.5-128 µg/mL), colistin (0.5-128 µg/mL) and tobramycin (0.5-128 µg/mL) when combined with the neutral pH form of -Acetylcysteine (NAC) (0.5-16.3 mg/mL) against 11 cystic fibrosis strains of and sp. in planktonic and biofilm cultures. We screened for potential synergism using checkerboard assays from which fraction inhibitory concentration indices (FICI) were calculated. Synergistic (FICI ≤ 0.5) and additive (0.5 > FICI ≥ 1) combinations were tested on irreversibly attached bacteria and 48 h mature biofilms via time-course and colony forming units (CFU/mL) assays. This study suggests that planktonic FICI analysis does not necessarily translate to reduction in bacterial loads in a biofilm model. Future directions include refining synergy testing and determining further mechanisms of action of NAC to understand how it may interact with antibiotics to better predict synergy.
囊性纤维化(CF)是一种遗传性疾病,会导致离子转运功能失调,进而使黏稠黏液积聚,促使气道中形成与慢性细菌生物膜相关的感染。[具体细菌名称1]和[具体细菌名称2]是越来越常见的CF病原体,虽然[具体细菌名称3]的感染率在缓慢下降;但所有这些病原体都因生物膜形成而导致的多重耐药性变得更加复杂。本研究调查了抗生素环丙沙星(0.5 - 128 µg/mL)、黏菌素(0.5 - 128 µg/mL)和妥布霉素(0.5 - 128 µg/mL)与中性pH形式的N - 乙酰半胱氨酸(NAC)(0.5 - 16.3 mg/mL)联合使用时,对11株囊性纤维化患者的[具体细菌名称1]和[具体细菌名称2]菌株在浮游和生物膜培养中的潜在协同作用。我们使用棋盘法筛选潜在协同作用,并据此计算分数抑菌浓度指数(FICI)。通过时间进程和菌落形成单位(CFU/mL)测定,对不可逆附着细菌和48小时成熟生物膜上的协同(FICI ≤ 0.5)和相加(0.5 > FICI ≥ 1)组合进行了测试。本研究表明,浮游FICI分析不一定能转化为生物膜模型中细菌载量的降低。未来的方向包括完善协同作用测试,以及确定NAC的进一步作用机制,以了解它如何与抗生素相互作用,从而更好地预测协同作用。