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Molecular Signature of Pseudomonas aeruginosa with Simultaneous Nanomolar Detection of Quorum Sensing Signaling Molecules at a Boron-Doped Diamond Electrode

机译:铜掺杂金刚石电极上同时感测信号感应分子的铜纳米假单胞菌的分子特征

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摘要

Electroanalysis was performed using a boron-doped diamond (BDD) electrode for the simultaneous detection of 2-heptyl-3-hydroxy-4-quinolone (PQS), 2-heptyl-4-hydroxyquinoline (HHQ) and pyocyanin (PYO). PQS and its precursor HHQ are two important signal molecules produced by Pseudomonas aeruginosa, while PYO is a redox active toxin involved in virulence and pathogenesis. This Gram-negative and opportunistic human pathogen is associated with a hospital-acquired infection particularly in patients with compromised immunity and is the primary cause of morbidity and mortality in cystic fibrosis (CF) patients. Early detection is crucial in the clinical management of this pathogen, with established infections entering a biofilm lifestyle that is refractory to conventional antibiotic therapies. Herein, a detection procedure was optimized and proven for the simultaneous detection of PYO, HHQ and PQS in standard mixtures, biological samples, and P. aeruginosa spiked CF sputum samples with remarkable sensitivity, down to nanomolar levels. Differential pulse voltammetry (DPV) scans were also applicable for monitoring the production of PYO, HHQ and PQS in P. aeruginosa PA14 over 8 h of cultivation. The simultaneous detection of these three compounds represents a molecular signature specific to this pathogen.
机译:使用硼掺杂金刚石(BDD)电极进行电分析,以同时检测2-庚基-3-羟基-4-喹诺酮(PQS),2-庚基-4-羟基喹啉(HHQ)和绿脓素(PYO)。 PQS及其前体HHQ是铜绿假单胞菌产生的两个重要信号分子,而PYO是涉及毒力和发病机理的氧化还原活性毒素。这种革兰氏阴性和机会性人类病原体与医院获得性感染有关,尤其是在免疫力受损的患者中,并且是囊性纤维化(CF)患者发病和死亡的主要原因。早期检测对于这种病原体的临床管理至关重要,因为已建立的感染进入了生物膜的生活方式,而传统的抗生素治疗对此没有影响。本文对检测程序进行了优化,并证明了该方法可同时检测标准混合物,生物样品和铜绿假单胞菌加标CF痰样品中的PYO,HHQ和PQS,具有极低的灵敏度,低至纳摩尔水平。差分脉冲伏安法(DPV)扫描也可用于监测在8小时的培养时间内铜绿假单胞菌PA14中PYO,HHQ和PQS的产生。同时检测这三种化合物代表了对该病原体特有的分子特征。

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