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Mammalian cell growth versus biofilm formation on biomaterial surfaces in an in vitro post-operative contamination model

机译:哺乳动物细胞生长对体外后污染模型的生物材料表面上的生物膜形成

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Biomaterial-associated infections are the major cause of implant failure and can develop many years after implantation. Success or failure of an implant depends on the balance between host tissue integration and bacterial colonization. Here, we describe a new in vitro model for the post-operative bacterial contamination of implant surfaces and investigate the effects of contamination on the balance between mammalian cell growth and bacterial biofilm formation. U2OS osteosarcoma cells were seeded on poly(methyl methacrylate) in different densities and allowed to grow for 24?h in a parallel-plate flow chamber at a low shear rate (0.14?s?1), followed by contamination with Staphylococcus epidermidis ATCC 35983 at a shear rate of 11?s?1. The U2OS cells and staphylococci were allowed to grow simultaneously for another 24?h under low-shear conditions (0.14?s?1). Mammalian cell growth was severely impaired when the bacteria were introduced to surfaces with a low initial cell density (2.5×104 cells cm?2), but in the presence of higher initial cell densities (8.2×104 cells cm?2 and 17×104 cells cm?2), contaminating staphylococci did not affect cell growth. This study is believed to be the first to show that a critical coverage by mammalian cells is needed to effectively protect a biomaterial implant against contaminating bacteria.
机译:生物材料相关的感染是植入物失败的主要原因,并且在植入后可能发展多年。植入物的成功或失败取决于宿主组织整合与细菌定植之间的平衡。在这里,我们描述了一种新的体外模型,用于植入物表面的术后细菌污染,并调查污染对哺乳动物细胞生长和细菌生物膜形成平衡的影响。将U2OS骨肉瘤细胞接种在不同密度的聚(甲基丙烯酸甲酯)上,并以低剪切速率(0.14Ω·1)在平行板流量室中生长24·h,然后用葡萄球菌的污染ATCC 35983以11?s?1的剪切速度。使U2OS细胞和葡萄球菌在低剪切条件下同时生长24℃(0.14Ω·1)。当细菌引入具有低初始细胞密度的表面时(2.5×104个细胞Cm 2),但在初始初始细胞密度(8.2×104个细胞cm 2和17×104)存在下,哺乳动物细胞生长严重受损细胞cm?2),污染葡萄球菌不会影响细胞生长。该研究被认为是首先表明需要哺乳动物细胞的关键覆盖以有效保护生物材料植入物免受污染细菌。

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