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2
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本文引用的文献

1
Voriconazole inhibits biofilm formation in different species of the genus Candida.伏立康唑抑制不同种属念珠菌的生物膜形成。
J Antimicrob Chemother. 2012 Oct;67(10):2418-23. doi: 10.1093/jac/dks242. Epub 2012 Jun 25.
2
A recently evolved transcriptional network controls biofilm development in Candida albicans.近期进化出的转录调控网络控制白念珠菌生物膜的形成。
Cell. 2012 Jan 20;148(1-2):126-38. doi: 10.1016/j.cell.2011.10.048.
3
Epidemiology of Candida blood stream infections in patients with hematological malignancies or solid tumors.血液系统恶性肿瘤或实体瘤患者中念珠菌血流感染的流行病学。
Med Mycol. 2012 Jan;50(1):50-5. doi: 10.3109/13693786.2011.587211. Epub 2011 Jun 22.
4
Micafungin alters the expression of genes related to cell wall integrity in Candida albicans biofilms.米卡芬净改变白念珠菌生物膜中与细胞壁完整性相关的基因表达。
Jpn J Infect Dis. 2010 Sep;63(5):355-7.
5
The transcriptional regulator Nrg1p controls Candida albicans biofilm formation and dispersion.转录调节因子Nrg1p控制白色念珠菌生物膜的形成与分散。
Eukaryot Cell. 2010 Oct;9(10):1531-7. doi: 10.1128/EC.00111-10. Epub 2010 Aug 13.
6
Inappropriate empiric antifungal therapy for candidemia in the ICU and hospital resource utilization: a retrospective cohort study.ICU 和医院资源利用中不适当的经验性抗真菌治疗与念珠菌血症:一项回顾性队列研究。
BMC Infect Dis. 2010 Jun 3;10:150. doi: 10.1186/1471-2334-10-150.
7
Anti-Candida-biofilm activity of micafungin is attenuated by voriconazole but restored by pharmacological inhibition of Hsp90-related stress responses.棘白菌素类药物米卡芬净的抗假丝酵母菌生物膜活性被伏立康唑减弱,但通过抑制与热休克蛋白 90 相关的应激反应可恢复其活性。
Med Mycol. 2010 Jun;48(4):606-12. doi: 10.3109/13693780903426721.
8
Patients with long-term oral carriage harbor high-persister mutants of Candida albicans.长期口腔携带的患者携带高耐唑类药物的白色念珠菌突变体。
Antimicrob Agents Chemother. 2010 Jan;54(1):39-44. doi: 10.1128/AAC.00860-09. Epub 2009 Oct 19.
9
Quantitative analysis of proliferation and excretion of Bartonella quintana in body lice, Pediculus humanus L.五日热巴尔通体在人体虱子(人虱)体内增殖与排泄的定量分析
Am J Trop Med Hyg. 2007 Sep;77(3):562-6.
10
How to build a biofilm: a fungal perspective.如何构建生物膜:真菌视角
Curr Opin Microbiol. 2006 Dec;9(6):588-94. doi: 10.1016/j.mib.2006.10.003. Epub 2006 Oct 20.

实时观察米卡芬净和氟康唑对念珠菌生物膜形成的影响

Real-time microscopic observation of Candida biofilm development and effects due to micafungin and fluconazole.

机构信息

Department of Chemotherapy and Mycoses, National Institute of Infectious Diseases, Tokyo, Japan.

出版信息

Antimicrob Agents Chemother. 2013 May;57(5):2226-30. doi: 10.1128/AAC.02290-12. Epub 2013 Mar 4.

DOI:10.1128/AAC.02290-12
PMID:23459484
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3632923/
Abstract

To understand the process of Candida biofilm development and the effects of antifungal agents on biofilms, we analyzed real-time data comprising time-lapse images taken at times separated by brief intervals. The growth rate was calculated by measuring the change of biofilm thickness every hour. For the antifungal study, 5-h-old biofilms of Candida albicans were treated with either micafungin (MCFG) or fluconazole (FLCZ). MCFG began to suppress biofilm growth a few minutes after the initiation of the treatment, and this effect was maintained over the course of the observation period. In contrast, the suppressive effects of FLCZ on biofilm growth took longer to manifest: biofilms grew in the first 5 h after treatment, and then their growth was suppressed over the next 10 h, finally producing results similar to those observed with MCFG. MCFG was also involved in the disruption of cells in the biofilms, releasing string-like structures (undefined extracellular component) from the burst hyphae. Thus, MCFG inhibited the detachment of yeast cell clusters from the tips of hyphae. In contrast, FLCZ did not disrupt biofilm cells. MCFG also showed fast antifungal activity against Candida parapsilosis biofilms. In conclusion, our results show that inhibition of glucan synthesis due to MCFG contributed not only to fungicidal activity but also to the immediate suppression of biofilm growth, while FLCZ suppressed growth by inhibiting ergosterol synthesis. Therefore, those characteristic differences should be considered when treating clinical biofilm infections.

摘要

为了理解念珠菌生物膜的形成过程以及抗真菌药物对生物膜的影响,我们分析了实时数据,这些数据由每隔很短时间拍摄的延时图像组成。通过每小时测量生物膜厚度的变化来计算生长速率。在抗真菌研究中,用米卡芬净(MCFG)或氟康唑(FLCZ)处理 5 小时龄的白念珠菌生物膜。MCFG 在治疗开始后几分钟就开始抑制生物膜的生长,这种作用在观察期内持续。相比之下,FLCZ 对生物膜生长的抑制作用需要更长的时间才能显现:生物膜在治疗后的前 5 小时内生长,然后在接下来的 10 小时内被抑制,最终产生与 MCFG 观察到的相似的结果。MCFG 还参与了生物膜中细胞的破坏,从爆发的菌丝中释放出线状结构(未定义的细胞外成分)。因此,MCFG 抑制了酵母细胞簇从菌丝尖端的脱落。相比之下,FLCZ 不会破坏生物膜细胞。MCFG 对近平滑念珠菌生物膜也表现出快速的抗真菌活性。总之,我们的研究结果表明,MCFG 抑制葡聚糖合成不仅有助于杀菌活性,还能立即抑制生物膜的生长,而 FLCZ 通过抑制麦角固醇合成来抑制生长。因此,在治疗临床生物膜感染时,应该考虑这些特征差异。