Department of Microbiology, School of Biology, College of Science, University of Tehran, Tehran, Iran.
Department of Photo Healing and Regeneration, Medical Laser Research Center, Yara Institute, Academic Center for Education, Culture and Research (ACECR), Tehran, Iran.
Lasers Med Sci. 2019 Aug;34(6):1159-1165. doi: 10.1007/s10103-018-02707-y. Epub 2019 Jan 3.
During antimicrobial photodynamic inactivation (APDI) in the treatment of an infection, it is likely that microorganisms would be exposed to sub-lethal doses of APDI (sAPDI). Although sAPDI cannot kill microorganisms, it can significantly affect microbial virulence. In this study, we evaluated the effect of sAPDI using methylene blue (MB) on the expression of genes belonging to two quorum sensing (QS) operons (rhl and las systems) and two genes necessary for biofilm formation (pelF and pslA) under QS control in Pseudomonas aeruginosa. Biofilm formation ability of P. aeruginosa ATCC 27853 exposed to sAPDI (MB at 0.012 mM and light dose of 23 J/cm) was evaluated using triphenyl tetrazolium chloride (TTC) assay and scanning electron microscopy (SEM). The effect of sAPDI on expression of rhlI, rhlR, lasI, lasR, pelF, and pslA were also evaluated by quantitative real-time polymerase chain reaction. Quantitative assay (TTC) results and morphological observations (SEM) indicated that a single sAPDI treatment resulted in a significant decrease in biofilm formation ability of P. aeruginosa ATCC 27853 compared to their non-treated controls (P = 0.012). These results were consistent with the expression of genes belonging to rhl and las systems and pelF and pslA genes. The results suggested that the transcriptional decreases caused by MB-sAPDI did lead to phenotypic changes.
在抗菌光动力灭活 (APDI) 治疗感染的过程中,微生物可能会暴露于亚致死剂量的 APDI(sAPDI)下。虽然 sAPDI 不能杀死微生物,但它可以显著影响微生物的毒力。在这项研究中,我们使用亚甲蓝 (MB) 评估了 sAPDI 对铜绿假单胞菌中两个群体感应 (QS) 操纵子(rhl 和 las 系统)和两个与生物膜形成相关的基因(pelF 和 pslA)表达的影响,这些基因受 QS 调控。通过三苯基四氮唑氯化物 (TTC) 测定法和扫描电子显微镜 (SEM) 评估了 sAPDI(MB 浓度为 0.012 mM,光照剂量为 23 J/cm)对铜绿假单胞菌 ATCC 27853 生物膜形成能力的影响。通过定量实时聚合酶链反应评估了 sAPDI 对 rhlI、rhlR、lasI、lasR、pelF 和 pslA 表达的影响。定量测定(TTC)结果和形态观察(SEM)表明,与未处理对照组相比,单次 sAPDI 处理显著降低了铜绿假单胞菌 ATCC 27853 的生物膜形成能力(P=0.012)。这些结果与 rhl 和 las 系统以及 pelF 和 pslA 基因的表达一致。结果表明,MB-sAPDI 引起的转录下降确实导致了表型变化。