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Different sensitivity levels to norspermidine on biofilm formation in clinical and commensal Staphylococcus epidermidis strains

机译:临床和普通表皮葡萄球菌菌株对去甲精胺对生物膜形成的不同敏感性水平

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摘要

Biofilm formation on medical and surgical devices is the main virulence factor of Staphylococcus epidermidis. A recent study has shown that norspermidine inhibits and disassembles the biofilm in the wildtype Bacillus subtilis NCBI3610 strain. In this study, the effect of norspermidine on S. epidermidis biofilm formation of clinical or commensal strains was tested. Biofilm producing strains of S. epidermidis were isolated from healthy skin (HS; n = 3), healthy conjunctiva (HC; n = 9) and ocular infection (01; n = 19). All strains were treated with different concentrations of norspermidine, spermidine, putrescine, and cadaverine (1, 10, 25, 50 and 100 mu M), and the biofilm formation was tested on microtiter plate. Besides, cell-free supernatants of S. epidermidis growth at 4 h and 40 h were analyzed by gas chromatography coupled to mass spectrometry (GC-MS) to detect norspermidine. Results showed that norspermidine at 25 mu M and 100 mu M prevented the biofilm formation in 45.16% (14/31) and 16.13% (5/31), respectively; only in one isolate from 01, norspermidine did not have effect. Other polyamines as spermidine, putrescine and cadaverine did not have effect on the biofilm formation of the strains tested. Norspermidine was also capable to disassemble a biofilm already formed. Norspermidine was detected in the 40 h cell-free supernatant of S. epidermidis by GC-MS. Norspermidine inhibited the biofilm development of S. epidermidis on the surface of contact lens. In this work, it was demonstrated that S. epidermidis produces and releases norspermidine causing an inhibitory effect on biofilm formation. Moreover, this is the first time showing that clinical S. epidermidis strains have different sensitivity to norspermidine, which suggest that the composition and structure of the biofilms is varied. We propose that norspermidine could potentially be used in the pre-treating of medical and surgical devices to inhibit the biofilm formation. (C) 2015 Elsevier Ltd. All rights reserved.
机译:医用和外科手术器械上生物膜的形成是表皮葡萄球菌的主要致病因子。最近的研究表明,去甲精胺可抑制和分解野生型枯草芽孢杆菌NCBI3610菌株中的生物膜。在这项研究中,测试了去甲精idine对临床或普通菌株表皮葡萄球菌生物膜形成的影响。从健康的皮肤(HS; n = 3),健康的结膜(HC; n = 9)和眼部感染(01; n = 19)中分离出产生生物膜的表皮葡萄球菌菌株。所有菌株均用不同浓度的降鸟精,亚精胺,腐胺和尸胺(1、10、25、50和100μM)处理,并在微量滴定板上测试生物膜的形成。此外,通过气相色谱-质谱联用(GC-MS)分析了表皮葡萄球菌在4小时和40小时生长的无细胞上清液,以检测去甲鸟精。结果表明,在25μM和100μM的去甲精胺分别有45.16%(14/31)和16.13%(5/31)阻止了生物膜的形成。仅在来自01的一种分离物中,去甲精per没有作用。其他多胺(如亚精胺,腐胺和尸胺)对所测试菌株的生物膜形成没有影响。去甲精胺还能够分解已经形成的生物膜。通过GC-MS在表皮葡萄球菌的40小时无细胞上清液中检测到了去甲精胺。去甲精胺可抑制隐形眼镜表面上表皮葡萄球菌的生物膜发育。在这项工作中,证明了表皮葡萄球菌产生并释放去甲精胺,从而对生物膜的形成产生抑制作用。而且,这是首次表明临床表皮葡萄球菌菌株对去甲精胺具有不同的敏感性,这表明生物膜的组成和结构是变化的。我们建议诺斯帕啶可潜在地用于医疗和外科手术设备的预处理,以抑制生物膜的形成。 (C)2015 Elsevier Ltd.保留所有权利。

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