Effects of chelating agent and environmental stresses on microbial biofilms: relevance to clinical microbiology

被引:17
作者
Al-Azemi, A. [1 ]
Fielder, M. D. [2 ]
Abuknesha, R. A. [1 ]
Price, R. G. [1 ,2 ]
机构
[1] Kings Coll London, Pharmaceut Sci Res Div, Analyt Sci Res Grp, Sch Biomed Sci, London SE1 9NH, England
[2] Kingston Univ, Sch Life Sci, Surrey, England
关键词
biofilms; chelating agents; environmental stress; PVL plus ve CA-MSSA; BACTERIAL BIOFILMS; STAPHYLOCOCCUS-AUREUS; ESCHERICHIA-COLI; MECHANISMS; EDTA; RESISTANCE; DISPERSAL; GROWTH; CELLS;
D O I
10.1111/j.1365-2672.2011.04983.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aims: To determine the effect of pH, temperature, desiccation, ethylenediaminetetraacetic acid (EDTA) and desferrioxamine B (DFO) on Panton-Valentine leukocidin-positive community acquired methicillin-susceptible Staphylococcus aureus (PVL +ve CA-MSSA) biofilm formation. Methods and Results: Biofilms from PVL +ve CA-MSSA (clinical isolate) were subjected to pH, temperature, desiccation, EDTA and DFO. PVL +ve CA-MSSA were more resistant to pH and heat than their planktonic equivalents. Desiccation studies demonstrated that PVL +ve CA-MSSA biofilms were more refractory to the treatment than planktonic cells. Significant inhibition of PVL +ve CA-MSSA biofilm formation was observed in the presence of 1 mmol l-1 EDTA. Low concentrations (2 center dot 5 mu mol l-1) of DFO enhanced the growth of PVL +ve CA-MSSA biofilms. At higher concentrations (1 mmol l-1), DFO did inhibit the growth but not as much as EDTA. A combination of EDTA and DFO inhibited PVL +ve CA-MSSA biofilm formation at lower concentrations than either alone. Conclusions: This study demonstrates that PVL +ve CA-MSSA biofilms are resistant to environmental stress but their growth can inhibited effectively by a mixture of EDTA and DFO. Significance and Impact of the Study: The inhibition of biofilm formation by PVL +ve CA-MSSA using chelating agents has not been previously reported and provides a practical approach to achieve the disruption of these potentially important biofilms formed by an emerging pathogen.
引用
收藏
页码:1307 / 1313
页数:7
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