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通过新的多重实时 PCR 检测法对光活化消毒后牙髓微生物进行快速检测和定量的实验研究。

An experimental study for rapid detection and quantification of endodontic microbiota following photo-activated disinfection via new multiplex real-time PCR assay.

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.

Legal Medicine Research Center, Legal Medicine Organization, Tehran, Iran.

出版信息

Photodiagnosis Photodyn Ther. 2018 Mar;21:344-350. doi: 10.1016/j.pdpdt.2018.01.006. Epub 2018 Jan 12.

Abstract

BACKGROUND

The infected root canal system harbors one of the highest accumulations of polymicrobial infections. Since the eradication of endopathogenic microbiota is a major goal in endodontic infection therapy, photo-activated disinfection (PAD) can be used as an alternative therapeutic method in endodontic treatment. Compared to cultivation-based approaches, molecular techniques are more reliable for identifying microbial agents associated with endodontic infections. The purpose of this study was to evaluate the ability of designed multiplex real-time PCR protocol for the rapid detection and quantification of six common microorganisms involved in endodontic infection before and after the PAD.

MATERIALS AND METHODS

Samples were taken from the root canals of 50 patients with primary and secondary/persistent endodontic infections using sterile paper points. PAD with toluidine blue O (TBO) plus diode laser was performed on root canals. Resampling was then performed, and the samples were transferred to transport medium. Then, six target microorganisms were detected using multiplex real-time PCR before and after the PAD.

RESULTS

Veillonella parvula was found using multiplex real-time PCR to have the highest frequency among samples collected before the PAD (29.4%), followed by Porphyromonas gingivalis (23.1%), Aggregatibacter actinomycetemcomitans (13.6%), Actinomyces naeslundii (13.0%), Enterococcus faecalis (11.5%), and Lactobacillus rhamnosus (9.4%). After TBO-mediated PAD, P. gingivalis strains, the most resistance microorganisms, were recovered in 41.7% of the samples using molecular approach (P > 0.05).

CONCLUSION

As the results shown, multiplex real-time PCR as an accurate detection approach with high-throughput and TBO-mediated PAD as an efficient antimicrobial strategy due to the significant reduction of the endopathogenic count can be used for detection and treatment of microbiota involved in infected root canals, respectively.

摘要

背景

感染的根管系统是多种微生物感染积累最多的地方之一。由于根除内源性微生物群是根管感染治疗的主要目标,因此光激活消毒 (PAD) 可以作为根管治疗的替代治疗方法。与基于培养的方法相比,分子技术更可靠地识别与根管感染相关的微生物。本研究旨在评估设计的多重实时 PCR 方案在 PAD 前后快速检测和定量六种常见参与根管感染的微生物的能力。

材料和方法

使用无菌纸尖从 50 名原发性和继发性/持续性根管感染患者的根管中采集样本。对根管进行 TBO 加二极管激光 PAD。然后进行重新取样,并将样本转移到运输培养基中。然后,在 PAD 前后使用多重实时 PCR 检测六种目标微生物。

结果

使用多重实时 PCR 发现,在 PAD 前采集的样本中,韦荣球菌属的检出率最高(29.4%),其次是牙龈卟啉单胞菌(23.1%)、伴放线放线杆菌(13.6%)、奈瑟放线菌(13.0%)、粪肠球菌(11.5%)和鼠李糖乳杆菌(9.4%)。在用 TBO 介导的 PAD 后,使用分子方法在 41.7%的样本中回收了最具耐药性的微生物牙龈卟啉单胞菌菌株(P > 0.05)。

结论

结果表明,多重实时 PCR 作为一种准确的检测方法,具有高通量和 TBO 介导的 PAD 作为一种有效的抗菌策略,由于内源性微生物计数的显著减少,可以分别用于检测和治疗感染根管中的微生物群。

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