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纳米银与浮游生物和生物膜培养物中的大肠杆菌细胞的相互作用。

Interactions of nanosilver with Escherichia coli cells in planktonic and biofilm cultures.

机构信息

Department of Civil and Environmental Engineering, University of Missouri, E2509 Lafferre Hall, Columbia, MO 65211, USA.

出版信息

Water Res. 2010 Dec;44(20):6095-103. doi: 10.1016/j.watres.2010.06.069. Epub 2010 Jul 7.

DOI:10.1016/j.watres.2010.06.069
PMID:20659752
Abstract

Biofilms are often more resistant to toxic chemicals such as heavy metals and antimicrobial agents than planktonic cells. Nanosilver has a broad range of applications with strong antimicrobial activity. However, biofilm susceptibility to nanosilver toxicity is not well understood. We studied the bacterial activity in planktonic or biofilm cultures after nanosilver exposure using oxygen quenching fluorescence-based microrespirometry. We also determined the aggregation behavior and the spatial distribution of nanosilver having red fluorescence in biofilms of Escherichia coli expressing green fluorescent protein. At the same bacterial concentrations (3 × 10(8) CFU/mL), biofilms were about four times more resistant to nanosilver inhibition than planktonic cells. The minimum bactericidal concentrations (MBCs) of nanosilver (size from 15 to 21 nm), defined as the lowest concentration that kills at least 99.9% of a planktonic or biofilm bacterial population, were 38 and 10 mg/L Ag, respectively. For comparison, silver ions were more toxic to E. coli than nanosilver with MBCs of 2.4 and 1.2 mg/L Ag for planktonic and biofilm cultures, respectively. Nanosilver was aggregated in the presence of planktonic or biofilm-forming cells resulting in an increase of average particle size by a factor of 15 and 40, respectively. The nanosilver particles were able to penetrate to approximately 40 μm in a thick biofilm after 1-h exposure. These findings suggested that biofilm resistance to nanosilver could be at least partially due to nanoparticle aggregation and retarded silver ion/particle diffusion.

摘要

生物膜通常比浮游细胞更能抵抗重金属和抗菌剂等有毒化学物质。纳米银具有广泛的应用,具有很强的抗菌活性。然而,生物膜对纳米银毒性的敏感性还不是很清楚。我们使用基于氧猝灭荧光的微呼吸测定法研究了浮游或生物膜培养物在纳米银暴露后的细菌活性。我们还确定了在表达绿色荧光蛋白的大肠杆菌生物膜中具有红色荧光的纳米银的聚集行为和空间分布。在相同的细菌浓度(3×10(8) CFU/mL)下,生物膜对纳米银抑制的抵抗力比浮游细胞高约四倍。纳米银(尺寸为 15 至 21nm)的最小杀菌浓度(MBC)定义为杀死至少 99.9%浮游或生物膜细菌群体的最低浓度,分别为 38 和 10mg/L Ag。相比之下,银离子对大肠杆菌的毒性比纳米银强,浮游和生物膜培养物的 MBC 分别为 2.4 和 1.2mg/L Ag。在浮游或生物膜形成细胞存在的情况下,纳米银聚集导致平均粒径分别增加了 15 倍和 40 倍。纳米银颗粒在 1 小时暴露后能够穿透大约 40μm厚的生物膜。这些发现表明,生物膜对纳米银的抵抗力至少部分归因于纳米颗粒的聚集和银离子/颗粒的扩散受阻。

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