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高浓度、长时间庆大霉素处理携带氨基糖苷修饰酶基因的耐甲氧西林金黄色葡萄球菌(MRSA)分离株以实现有效的生物膜清除。

Effective biofilm eradication in MRSA isolates with aminoglycoside-modifying enzyme genes using high-concentration and prolonged gentamicin treatment.

机构信息

Department of Emergency and Intensive Care Medicine, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.

Department of Microbiology, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.

出版信息

Microbiol Spectr. 2024 Oct 3;12(10):e0064724. doi: 10.1128/spectrum.00647-24. Epub 2024 Aug 27.

DOI:10.1128/spectrum.00647-24
PMID:39191399
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11448082/
Abstract

UNLABELLED

Bone and soft tissue infections caused by biofilm-forming bacteria, such as methicillin-resistant (MRSA), remain a significant clinical challenge. While the control of local infection is necessary, systemic treatment is also required, and biofilm eradication is a critical target for successful management. Topical antibiotic treatments, such as antibiotic-loaded bone cement (ALBC), have been used for some time, and continuous local antibiotic perfusion therapy, a less invasive method, has been developed by our group. However, the optimal antibiotics and concentrations for biofilms of clinical isolates are still not well understood. We examined the efficacy of high concentrations of gentamicin against MRSA biofilms and the role of gentamicin resistance genes in biofilm eradication. We collected 101 MRSA samples from a hospital in Japan and analyzed their gene properties, including methicillin and gentamicin resistance, and their minimum biofilm eradication concentration (MBEC) values. Our results showed that high concentrations of gentamicin are effective against MRSA biofilms and that even concentrations lower than the MBEC value could eliminate biofilms after prolonged exposure. We also identified three aminoglycoside/gentamicin resistance genes [, , and ] and found that the presence or absence of these genes may inform the selection of treatments. It was also found that possession of the ) gene correlated with the minimum inhibitory concentration/MBEC values of gentamicin. Although this study provides insight into the efficacy of gentamicin against MRSA biofilms and the role of gentamicin resistance genes, careful selection of the optimal treatment strategy is needed for clinical application.

IMPORTANCE

Our analysis of 101 MRSA clinical isolates has provided valuable insights that could enhance treatment selection for biofilm infections in orthopedics. We found that high concentrations of gentamicin were effective against MRSA biofilms, and even prolonged exposure to concentrations lower than the minimum biofilm eradication concentration (MBEC) value could eliminate biofilms. The presence of the gene, an aminoglycoside resistance gene, was found to correlate with the minimum inhibitory concentration (MIC) and MBEC values of gentamicin, providing a potential predictive tool for treatment susceptibility. These results suggest that extended high concentrations of local gentamicin treatment could effectively eliminate MRSA biofilms in orthopedic infections. Furthermore, testing for gentamicin MIC or the possession of the gene could help select treatment, including topical gentamicin administration and surgical debridement.

摘要

目的

本研究分析了 101 株耐甲氧西林金黄色葡萄球菌(MRSA)临床分离株,旨在探讨氨基糖苷类/庆大霉素耐药基因在金黄色葡萄球菌生物膜形成中的作用,为骨科生物膜感染的治疗选择提供依据。

方法

从日本一家医院收集了 101 株 MRSA 样本,分析了它们的基因特性,包括耐甲氧西林和庆大霉素的特性,以及它们的最低生物膜清除浓度(MBEC)值。

结果

高浓度庆大霉素对 MRSA 生物膜有效,即使低于 MBEC 值的浓度,长时间暴露也能消除生物膜。我们还鉴定了三种氨基糖苷类/庆大霉素耐药基因(aacC1、aphA3 和 ant3 ),并发现这些基因的存在与否可能影响治疗方案的选择。此外,我们还发现携带 aphA3 基因与庆大霉素的最小抑菌浓度/MBEC 值相关。

结论

虽然本研究提供了庆大霉素对 MRSA 生物膜的疗效和庆大霉素耐药基因作用的见解,但在临床应用中仍需要仔细选择最佳治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ca4/11448082/13f783fe29b2/spectrum.00647-24.f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ca4/11448082/63cb4b5e4bba/spectrum.00647-24.f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ca4/11448082/dd5215521deb/spectrum.00647-24.f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ca4/11448082/13f783fe29b2/spectrum.00647-24.f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ca4/11448082/63cb4b5e4bba/spectrum.00647-24.f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ca4/11448082/dd5215521deb/spectrum.00647-24.f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ca4/11448082/13f783fe29b2/spectrum.00647-24.f003.jpg

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