Biofouling and Biofilm Processes Section, Water and Steam Chemistry Division, BARC Facilities, Kalpakkam, India.
J Antibiot (Tokyo). 2013 Feb;66(2):55-60. doi: 10.1038/ja.2012.98. Epub 2012 Nov 14.
The dominant role of biofilm-associated protein (Bap) in Staphylococcus aureus biofilm development prompted us to investigate Bap as a potential target for proteinase-mediated biofilm dispersion. Biofilm assay in microtitre plates showed that proteinase K hampered the early adhesion of cells as well as biofilm development. Proteinase K treatment of 24- and 48-h-old biofilms showed enhanced dispersion of bap-positive S. aureus biofilm; however, proteinase K did not affect the bap-negative S. aureus biofilm. When antibiotics were used in combination with proteinase K, significant enhancement in antibiotic action was noticed against bap-positive S. aureus biofilm. This study establishes that antibiotics in combination with proteinase K can be used for controlling S. aureus biofilms in whose development Bap surface protein has a major role. We propose that Bap protein could be a potential target for therapeutic control of S. aureus infections (for example, bovine mastitis).
生物膜相关蛋白(Bap)在金黄色葡萄球菌生物膜形成中起主要作用,这促使我们研究 Bap 是否可以作为蛋白酶介导的生物膜分散的潜在靶点。微孔板中的生物膜测定显示,蛋白酶 K 阻碍了细胞的早期黏附以及生物膜的形成。蛋白酶 K 处理 24 小时和 48 小时的生物膜显示出 bap 阳性金黄色葡萄球菌生物膜的分散增强;然而,蛋白酶 K 对 bap 阴性金黄色葡萄球菌生物膜没有影响。当抗生素与蛋白酶 K 联合使用时,发现对 bap 阳性金黄色葡萄球菌生物膜的抗生素作用有明显增强。这项研究表明,抗生素联合蛋白酶 K 可用于控制 Bap 表面蛋白在其形成中起主要作用的金黄色葡萄球菌生物膜。我们提出 Bap 蛋白可能是治疗金黄色葡萄球菌感染(例如牛乳腺炎)的潜在靶点。