一种新型小型化脉冲电磁场装置对植入物相关感染的微生物组调节。

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
João Gabriel S Souza, Fabio Azevedo, Maria Helena Rossy Borges, Raphael Cavalcante Costa, Takahiko Shiba, Shlomo Barak, Yaniv Mayer, Luciene Cristina de Figueiredo, Magda Feres, Valentim A R Barão, Jamil A Shibli
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引用次数: 0

摘要

由于缺乏有效的治疗策略,种植体相关感染被认为是导致治疗失败的主要原因。脉冲电磁场(PEMF)技术作为一种安全有效的增强生物反应的方式被引入。然而,PEMF在调节微生物多样性方面的作用尚未被探索。因此,我们测试了一种微型PEMF生物医学装置作为牙种植体的愈合组件。PEMF活化不会改变化学成分、表面粗糙度、润湿性和电化学性能。PEMF有效地控制了体外慢性多微生物积累。将设备插入患者口腔的体内研究和16S RNA测序分析证明,PEMF组的23种细菌种类减少了5倍或更多,并且该组中没有某些物种,包括与种植体相关感染相关的病原体。PEMF改变了细菌相互作用并促进了特定的细菌途径。PEMF已成为控制植入物相关感染的有效策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Microbiome modulation of implant-related infection by a novel miniaturized pulsed electromagnetic field device.

Dental implant-related infections, which lack effective therapeutic strategies, are considered the primary cause for treatment failure. Pulsed electromagnetic field (PEMF) technology has been introduced as a safe and effective modality for enhancing biological responses. However, the PEMF effect on modulating microbial diversity has not been explored. Thus, we tested a miniaturized PEMF biomedical device as a healing component for dental implants. PEMF activation did not alter the chemical composition, surface roughness, wettability, and electrochemical performance. PEMF effectively controlled chronic in vitro polymicrobial microbial accumulation. The in vivo study where devices were inserted in the patients' oral cavities and 16S RNA sequencing analysis evidenced a fivefold or more reduction in 23 bacterial species for PEMF group and the absence of some species for this group, including pathogens associated with implant-related infections. PEMF altered bacterial interactions and promoted specific bacterial pathways. PEMF has emerged as an effective strategy for controlling implant-related infections.

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来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
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