Sub-Inhibitory Concentrations of Rifampicin Strongly Stimulated Biofilm Production in S. aureus.

Q3 Immunology and Microbiology
Open Microbiology Journal Pub Date : 2017-06-30 eCollection Date: 2017-01-01 DOI:10.2174/1874285801711010142
Agostinho Alves Lima-E-Silva, Renato Geraldo Silva-Filho, Henry Marcel Zalona Fernandes, Carmen Soares Meirelles Saramago, Alice Slotfeldt Viana, Maria José Souza, Eduardo Matos Nogueira
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引用次数: 18

Abstract

Background and objectives: Staphylococcus aureus is an important pathogen and a frequent cause of infections associated with biofilm production in implantable medical devices. Biofilm production can be induced by sub-inhibitory concentrations (sub-MICs) of certain antibiotics, but few studies have researched this occurrence in S. aureus. In this study, we investigated the effect of sub-MICs of rifampicin and minocycline on biofilm production by five clinical and five non-clinical S. aureus isolates.

Methods: Microtiter Plate assay and Congo Red Agar Test were used to analyze the biofilm production. The biofilm composition was evaluated by the detachment assay with sodium metaperiodate and proteinase K.

Results: Rifampicin sub-MICs induced very high biofilm formation in seven isolates that were non-producers in Tryptic Soy Broth. In one producer isolate, the biofilm formation level was not affected by sub-MICs of this drug. Sub-MICs of minocycline did not induce biofilm production in all isolates tested and in two producer isolates, instead, MIC/2 and MIC/4 inhibited biofilm production. The results of the drugs in combination were similar to those with rifampicin alone. The biofilm matrix was identified as polysaccharide, except for one producer isolate, classified as proteinaceous. Polysaccharide biofilm producer isolates, when grown on Congo Red Agar without sucrose, but with sub-MICs of rifampicin, showed results in agreement with those obtained in Microtiter Plate Test.

Conclusion: The high biofilm production induced by sub-MICs of rifampicin has potential clinical relevance, because this is one of the drugs commonly used in the impregnation of catheters. In addition, it is used adjunctively to treat certain S. aureus infections.

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利福平的亚抑制浓度强烈刺激金黄色葡萄球菌的生物膜生成。
背景和目的:金黄色葡萄球菌是一种重要的病原体,也是植入式医疗器械生物膜生产相关感染的常见原因。某些抗生素的亚抑制浓度(sub- mic)可以诱导生物膜的产生,但很少有研究研究这种情况在金黄色葡萄球菌中的发生。在这项研究中,我们研究了利福平和米诺环素亚mic对5株临床和5株非临床金黄色葡萄球菌生物膜生成的影响。方法:采用微滴板法和刚果红琼脂法对生物膜的生成进行分析。结果:利福平亚mic诱导7株非产菌在胰蛋白酶肉汤中形成非常高的生物膜。在一个生产者分离物中,该药物的亚mic不影响生物膜的形成水平。米诺环素的亚MIC在所有被试分离株和两个产生菌中都没有诱导生物膜的产生,相反,MIC/2和MIC/4抑制生物膜的产生。两种药物联合使用的结果与单独使用利福平的结果相似。生物膜基质被鉴定为多糖,除了一个生产者分离物外,被分类为蛋白质。当在刚果红琼脂上不加蔗糖,但含有亚mic的利福平时,多糖生物膜生产者分离物的结果与微滴板试验的结果一致。结论:利福平亚mic诱导的高生物膜生成具有潜在的临床意义,因为利福平是导管浸染中常用的药物之一。此外,它还用于辅助治疗某些金黄色葡萄球菌感染。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Open Microbiology Journal
Open Microbiology Journal Immunology and Microbiology-Immunology and Microbiology (all)
CiteScore
1.80
自引率
0.00%
发文量
24
期刊介绍: The Open Microbiology Journal is a peer-reviewed open access journal which publishes research articles, reviews/mini-reviews, case studies, guest edited thematic issues and short communications/letters covering theoretical and practical aspects of Microbial systematics, evolutionary microbiology, immunology, virology, parasitology , bacteriology, mycology, phycology, protozoology, microbial ecology, molecular biology, microbial physiology, biochemistry, microbial pathogenesis, host-microbe interaction, systems microbiology, synthetic microbiology, bioinformatics. The Open Microbiology Journal , a peer-reviewed journal, is an important and reliable source of current information on developments in the field. The emphasis will be on publishing quality papers rapidly and freely available to researchers worldwide.
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