Hogan S, Zapotoczna M, Stevens N T, Humphreys H, O'Gara J P, O'Neill E
Department of Clinical Microbiology, Royal College of Surgeons in Ireland, Beaumont Hospital, Dublin, Ireland.
Department of Clinical Microbiology, Royal College of Surgeons in Ireland, Beaumont Hospital, Dublin, Ireland Department of Microbiology, Beaumont Hospital, Dublin, Ireland.
Antimicrob Agents Chemother. 2016 Sep 23;60(10):5968-75. doi: 10.1128/AAC.00910-16. Print 2016 Oct.
Staphylococci are a leading cause of catheter-related infections (CRIs) due to biofilm formation. CRIs are typically managed by either device removal or systemic antibiotics, often in combination with catheter lock solutions (CLSs). CLSs provide high concentrations of the antimicrobial agent at the site of infection. However, the most effective CLSs against staphylococcal biofilm-associated infections have yet to be determined. The purpose of this study was to evaluate the efficacy and suitability of two newly described antimicrobial agents, ML:8 and Citrox, as CLSs against Staphylococcus aureus biofilms. ML:8 (1% [vol/vol]) and Citrox (1% [vol/vol]), containing caprylic acid and flavonoids, respectively, were used to treat S. aureus biofilms grown in vitro using newly described static and flow biofilm assays. Both agents reduced biofilm viability >97% after 24 h of treatment. Using a rat model of CRI, ML:8 was shown to inactivate early-stage S. aureus biofilms in vivo, while Citrox inactivated established, mature in vivo biofilms. Cytotoxicity and hemolytic activity of ML:8 and Citrox were equivalent to those of other commercially available CLSs. Neither ML:8 nor Citrox induced a cytokine response in human whole blood, and exposure of S. aureus to either agent for 90 days was not associated with any increase in resistance. Taken together, these data reveal the therapeutic potential of these agents for the treatment of S. aureus catheter-related biofilm infections.
葡萄球菌是导管相关感染(CRIs)的主要病因,这是由生物膜形成导致的。CRIs通常通过移除装置或全身使用抗生素来处理,常常还会结合导管封管溶液(CLSs)。CLSs可在感染部位提供高浓度的抗菌剂。然而,针对葡萄球菌生物膜相关感染的最有效CLSs尚未确定。本研究的目的是评估两种新描述的抗菌剂ML:8和Citrox作为CLSs对抗金黄色葡萄球菌生物膜的疗效和适用性。分别含有辛酸和类黄酮的ML:8(1%[体积/体积])和Citrox(1%[体积/体积]),被用于使用新描述的静态和流动生物膜检测方法来处理体外培养的金黄色葡萄球菌生物膜。两种试剂在处理24小时后均使生物膜活力降低>97%。使用CRI大鼠模型,结果显示ML:8可在体内使早期金黄色葡萄球菌生物膜失活,而Citrox可使已形成的、成熟的体内生物膜失活。ML:8和Citrox的细胞毒性和溶血活性与其他市售CLSs相当。ML:8和Citrox均未在人全血中诱导细胞因子反应,并且将金黄色葡萄球菌暴露于任何一种试剂90天均未导致耐药性增加。综上所述,这些数据揭示了这些试剂在治疗金黄色葡萄球菌导管相关生物膜感染方面的治疗潜力。