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通过相对定量实时 PCR 监测伴放线放线杆菌 rcpA 基因表达与抗菌光动力疗法的关系。

Monitoring gene expression of rcpA from Aggregatibacter actinomycetemcomitans versus antimicrobial photodynamic therapy by relative quantitative real-time PCR.

机构信息

Department of Microbiology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran; Dental Research Center, Dentistry Research Institute, Tehran University of Medical Sciences, Tehran, Iran; Dental Implant Research Center, Dentistry Research Institute, Tehran University of Medical Sciences, Tehran, Iran.

Laser Research Center of Dentistry (LRCD), Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Photodiagnosis Photodyn Ther. 2017 Sep;19:51-55. doi: 10.1016/j.pdpdt.2017.04.011. Epub 2017 Apr 24.

DOI:10.1016/j.pdpdt.2017.04.011
PMID:28450261
Abstract

BACKGROUND

Aggregatibacter actinomycetemcomitans is an important pathogen that is frequently found in various infections, particularly aggressive periodontitis. In this study, we described the outcome of the expression level of A. actinomycetemcomitans virulence factor following treatment by antimicrobial photodynamic therapy (aPDT) with indocyanine green (ICG) as a photosensitizing agent.

MATERIALS AND METHODS

To determine the aPDT effect on the cell-surviving assay and expression ratio of the rcpA gene in A. actinomycetemcomitans by a colony-forming unit and relative quantitative (q) real-time PCR (qRT-PCR) assays, respectively, the proper dosing of sub-lethal aPDT was specified.

RESULTS

The results of the current study showed that ICG-mediated aPDT, using 250-1000μg/mL, showed a significant reduction in A. actinomycetemcomitans growth when compared to the control group (P<0.05). Also, a sub-lethal dose of aPDT against A. actinomycetemcomitans was 125μg/mL ICG, with a 30s diode laser irradiation time at fluency of 15.6J/cm that could reduce the expression of rcpA gene approximately 6-fold.

DISCUSSION

aPDT with ICG could reduce the cell survival and the virulence agent of A. actinomycetemcomitans. Thus, use of the appropriate aPDT dosage can be used for the successful treatment of periodontitis in vivo.

摘要

背景

伴放线放线杆菌是一种重要的病原体,常存在于各种感染中,尤其是侵袭性牙周炎。在这项研究中,我们描述了使用作为光敏剂的吲哚菁绿(ICG)进行抗菌光动力疗法(aPDT)后,伴放线放线杆菌毒力因子表达水平的结果。

材料和方法

为了确定 aPDT 对细胞存活测定和 rcpA 基因表达比率的影响,分别使用平板计数法和相对定量(q)实时 PCR(qRT-PCR)法,确定亚致死剂量的 aPDT。

结果

本研究结果表明,与对照组相比,250-1000μg/mL 的 ICG 介导的 aPDT 显著降低了伴放线放线杆菌的生长(P<0.05)。此外,亚致死剂量的 aPDT 对伴放线放线杆菌的抑制作用为 125μg/mL 的 ICG,二极管激光辐照时间为 30 秒,通量为 15.6J/cm,可使 rcpA 基因的表达降低约 6 倍。

讨论

ICG 的 aPDT 可以降低伴放线放线杆菌的细胞存活和毒力因子。因此,使用适当的 aPDT 剂量可以成功治疗体内牙周炎。

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