Alem Mohammed A S, Douglas L Julia
Division of Infection and Immunity, Institute of Biomedical and Life Sciences, University of Glasgow, Glasgow G12 8QQ, United Kingdom.
Antimicrob Agents Chemother. 2004 Jan;48(1):41-7. doi: 10.1128/AAC.48.1.41-47.2004.
Prostaglandins are now known to be produced by Candida albicans and may play an important role in fungal colonization. Their synthesis in mammalian cells is decreased by inhibitors of the cyclooxygenase isoenzymes required for prostaglandin formation. In the present study, a catheter disk model system was used to investigate the effects of nonsteroidal anti-inflammatory drugs (all cyclooxygenase inhibitors) on biofilm formation by three strains of C. albicans. Seven of nine drugs tested at a concentration of 1 mM inhibited biofilm formation. Aspirin, etodolac, and diclofenac produced the greatest effects, with aspirin causing up to 95% inhibition. Celecoxib, nimesulide, ibuprofen, and meloxicam also inhibited biofilm formation, but to a lesser extent. Aspirin was active against growing and fully mature (48-h) biofilms; its effect was dose related, and it produced significant inhibition (20 to 80%) at pharmacological concentrations. Simultaneous addition of prostaglandin E(2) abolished the inhibitory effect of 25 or 50 micro M aspirin. At 1 mM, aspirin reduced the viability of biofilm organisms to 1.9% of that of controls. Surviving cells had a wrinkled appearance, as judged by scanning electron microscopy, and consisted of both yeasts and hyphae. Treatment with other cyclooxygenase inhibitors, such as etodolac, resulted in biofilms that consisted almost entirely of yeast cells. In conventional assays for germ tube formation, these drugs produced significant inhibition, whereas aspirin had little effect. Our findings suggest that cyclooxygenase-dependent synthesis of fungal prostaglandin(s) is important for both biofilm development and morphogenesis in C. albicans and may act as a regulator in these physiological processes. Our results also demonstrate that aspirin possesses potent antibiofilm activity in vitro and could be useful in combined therapy with conventional antifungal agents in the management of some biofilm-associated Candida infections.
现已知道,白色念珠菌可产生前列腺素,且其可能在真菌定植过程中发挥重要作用。前列腺素在哺乳动物细胞中的合成会被前列腺素形成所需的环氧化酶同工酶抑制剂所抑制。在本研究中,使用导管盘模型系统来研究非甾体抗炎药(所有环氧化酶抑制剂)对三株白色念珠菌生物膜形成的影响。在1 mM浓度下测试的9种药物中有7种抑制了生物膜形成。阿司匹林、依托度酸和双氯芬酸的效果最为显著,阿司匹林可导致高达95%的抑制率。塞来昔布、尼美舒利、布洛芬和美洛昔康也抑制了生物膜形成,但程度较小。阿司匹林对生长中的和完全成熟(48小时)的生物膜均有活性;其作用与剂量相关,且在药理浓度下产生显著抑制(20%至80%)。同时添加前列腺素E2可消除25或50 μM阿司匹林的抑制作用。在1 mM时,阿司匹林将生物膜微生物的活力降低至对照的1.9%。通过扫描电子显微镜判断,存活细胞外观皱缩,由酵母细胞和菌丝组成。用其他环氧化酶抑制剂(如依托度酸)处理后,生物膜几乎完全由酵母细胞组成。在传统的芽管形成试验中,这些药物产生显著抑制,而阿司匹林几乎没有作用。我们的研究结果表明,真菌前列腺素的环氧化酶依赖性合成对于白色念珠菌的生物膜发育和形态发生均很重要,并且可能在这些生理过程中起调节作用。我们的结果还表明,阿司匹林在体外具有强大的抗生物膜活性,在某些生物膜相关念珠菌感染的治疗中,与传统抗真菌药物联合使用可能会有帮助。