Department of Microbiology and Immunology- Faculty of Pharmacy- Zagazig University- Zagazig, 44519, Egypt.
Department of Medicinal Chemistry- Faculty of Pharmacy- Kafrelsheikh University- Kafr El Sheikh 33516, Egypt.
Microb Pathog. 2021 Sep;158:105097. doi: 10.1016/j.micpath.2021.105097. Epub 2021 Jul 17.
The current failure of antimicrobials in treating life-threatening diseases, the high rate of multidrug resistant pathogens and the slow progress in the development of new antibiotics directed scientists to develop antivirulence drugs that targets quorum sensing (QS). In many microbes, QS acts as a communication system which control pathogenicity of microbes. Analgesics can be beneficial in controlling virulence traits of microbes and hence they may augment the efficacy of antimicrobials. In this study, two analgesics were screened for the inhibition of QS in Chromobacterium violaceum CV026 and their effects on virulence production in Pseudomonas aeruginosa PAO1 strain and clinical isolates of Acinetobacter baumannii were evaluated. The traits investigated were biofilm formation, pyocyanin and rhamnolipid production, twitching, swarming or surface associated motilities, production of protease, phospholipase and gelatinase enzymes and sensitivity to oxidative stress. Relative expression of abaI gene was calculated by performing qRT-PCR. Docking analysis of paracetamol as QSI (quorum sensing inhibitor) of AbaI and AbaR proteins was performed. Paracetamol inhibited QS in CV026, but indomethacin devoids anti-QS activity. Paracetamol inhibited virulence factors of PAO1. It strongly inhibited biofilm formation, and swarming by 66.4% and 57.1%, respectively. While, it moderately to slightly inhibited rhamnolipid, pyocyanin, gelatinase, resistance to oxidative stress, protease and twitching motility by 33.3%, 33.1% 17.5%, 9.1%, 8.7% and 7.7%, respectively. For A. baumannii, paracetamol strongly inhibited biofilm by 39.7-93% and phospholipase enzyme by 8.7-100%, reduced twitching and surface motility by 6.7-82.5% and 7.7-29.4%, respectively, And slightly reduced sensitivity to oxidative stress by 3.3-36.4%. Paracetamol at sub-MIC suppressed the expression of abaI gene by 32% in A. baumannii. Docking studies suggested that paracetamol can bind to AbaR and AbaI proteins and bind more to AbaR, hence it may act by inhibiting AHL signal reception. As a conclusion, paracetamol, beside its analgesic activity, has anti-QS activity and could be used in the eradication of P. aeruginosa and A. baumannii infections in combination with antibiotics.
目前,抗生素在治疗危及生命的疾病方面已经失效,多种耐药病原体的高比率以及新抗生素开发进展缓慢,促使科学家们开发针对群体感应(QS)的抗病毒药物。在许多微生物中,QS 充当一种控制微生物致病性的通信系统。镇痛药可用于控制微生物的毒力特征,因此它们可能增强抗生素的疗效。在这项研究中,筛选了两种镇痛药,以抑制 Chromobacterium violaceum CV026 中的 QS,并评估了它们对铜绿假单胞菌 PAO1 菌株和鲍曼不动杆菌临床分离株的毒力产生的影响。研究的特征是生物膜形成、绿脓菌素和鼠李糖脂的产生、菌毛运动、迁徙或表面相关运动、蛋白酶、磷脂酶和明胶酶的产生以及对氧化应激的敏感性。通过 qRT-PCR 计算 abaI 基因的相对表达。对扑热息痛作为 AbaI 和 AbaR 蛋白的 QSI(群体感应抑制剂)进行了对接分析。扑热息痛抑制了 CV026 中的 QS,但吲哚美辛缺乏抗 QS 活性。扑热息痛抑制了 PAO1 的毒力因子。它强烈抑制生物膜形成和菌毛运动,分别为 66.4%和 57.1%。而对鼠李糖脂、绿脓菌素、明胶酶、氧化应激抗性、蛋白酶和菌毛运动的抑制作用分别为 33.3%、33.1%、17.5%、8.7%和 7.7%。对于鲍曼不动杆菌,扑热息痛强烈抑制生物膜形成,抑制率为 39.7-93%,抑制磷脂酶的抑制率为 8.7-100%,降低菌毛运动和表面运动,抑制率分别为 6.7-82.5%和 7.7-29.4%,对氧化应激的敏感性降低 3.3-36.4%。扑热息痛在亚 MIC 下抑制鲍曼不动杆菌的 abaI 基因表达 32%。对接研究表明,扑热息痛可以与 AbaR 和 AbaI 蛋白结合,并与 AbaR 结合更多,因此它可能通过抑制 AHL 信号接收而起作用。总之,扑热息痛除了具有镇痛活性外,还具有抗 QS 活性,可与抗生素联合用于根除铜绿假单胞菌和鲍曼不动杆菌感染。