Department of Clinical Bacteriology, Parasitology, Zoonoses and Geographical Medicine, Medical School, University of Crete, Heraklion, Greece.
J Proteome Res. 2011 Feb 4;10(2):756-62. doi: 10.1021/pr100906v. Epub 2010 Dec 7.
The etiological agent of Q fever, Coxiella burnetii, is an obligate intracellular bacterium that multiplies within a phagosome-like parasitophorous vacuole. Fluoroquinolones have been used as an alternative therapy for Q fever. Resistance to fluoroquinolones can arise via several mechanisms utilized by pathogens to avoid killing. Until today, genome-based studies have shown that the main mechanism of C. burnetii to resist inhibition by fluoroquinolones is based on mutations in quinolone-resistance-determining region (QRDR). In this study, in a broader search at the protein level for C. burnetii mechanisms that confer resistance to fluoroquinolones, the proteomes of in vitro developed fluoroquinolone resistant bacteria and susceptible bacteria were compared using the MS-driven combined fractional diagonal chromatography (COFRADIC) proteomics technique. Quantitative comparison of the 381 proteins identified in both strains indicated the different expression of 15 bacterial proteins. These proteins are involved in different cellular processes indicating that the antibiotic resistance mechanism of the bacterium is a multifaceted process.
Q 热的病原体是柯克斯体,一种严格的细胞内细菌,在类似吞噬体的吞噬小泡内繁殖。氟喹诺酮类药物已被用作 Q 热的替代治疗方法。病原体通过几种机制来避免被杀死,从而产生对氟喹诺酮类药物的耐药性。直到今天,基于基因组的研究表明,C. burnetii 抵抗氟喹诺酮类药物抑制的主要机制是基于喹诺酮类药物耐药决定区 (QRDR) 的突变。在这项研究中,为了更广泛地在蛋白质水平上寻找赋予 C. burnetii 对氟喹诺酮类药物耐药的机制,使用 MS 驱动的联合分馏对角色谱 (COFRADIC) 蛋白质组学技术比较了体外诱导的氟喹诺酮耐药菌和敏感菌的蛋白质组。对两种菌株中鉴定的 381 种蛋白质进行定量比较表明,有 15 种细菌蛋白质的表达不同。这些蛋白质参与不同的细胞过程,表明细菌的抗生素耐药机制是一个多方面的过程。