Departamento de Medicina Veterinária Preventiva, Universidade Estadual Paulista "Júlio de Mesquita Filho", Jaboticabal, SP, Brazil.
Braz J Microbiol. 2013 May 17;44(1):119-24. doi: 10.1590/S1517-83822013005000031. eCollection 2013.
Biofilm formation is considered to be a selective advantage for Staphylococcus aureus mastitis isolates by facilitating bacterial persistence in the udder. It requires attachment to mammary epithelium, proliferation and accumulation of cells in multilayers. The objective of this study was to determine the sensitivity and specificity of three techniques for the detection of S. aureus biofilm-positive strains. Two phenotypic tests, including growth on microtitre plates and Congo red agar, were compared with a PCR technique using 94 S. aureus strains obtained from cows with subclinical mastitis from two farms in the state of São Paulo. These strains were characterised by in vitro slime production on Congo red agar, biofilm formation on microtitre plates and the presence of the icaA and icaD genes. The results revealed that 85% of the isolates tested produced slime on the Congo red agar, 98.9% of the isolates produced biofilms in vitro by adhering to sterile 96-well "U" bottom polystyrene tissue culture plates, and 95.7% of the isolates carried the icaA and icaD genes. The results of the phenotypic tests for biofilm formation were compared with those of the molecular analysis, and the sensitivity and specificity of the Congo red agar test were 88.9% and 100%, respectively, while those of the microtitre plate test were 100% and 25%, respectively. When the phenotypic methods for the detection of biofilm producers, namely growth on microtitre plates and Congo red agar, were compared, the sensitivity and specificity were 86% and 100%, respectively. Therefore, growth on Congo red agar and the microtitre plate test are methods that could be used to determine whether an isolate has the potential for biofilm production.
生物膜形成被认为是金黄色葡萄球菌乳腺炎分离株的选择性优势,因为它有助于细菌在乳房中持续存在。它需要附着在乳腺上皮细胞上,在多层细胞中增殖和积累。本研究的目的是确定三种检测金黄色葡萄球菌生物膜阳性菌株的技术的敏感性和特异性。两种表型试验,包括微量滴定板和刚果红琼脂上的生长,与使用从来自圣保罗州两个农场的亚临床乳腺炎奶牛获得的 94 株金黄色葡萄球菌的 PCR 技术进行了比较。这些菌株通过在刚果红琼脂上产生粘液、在微量滴定板上形成生物膜以及存在 icaA 和 icaD 基因来表征。结果表明,85%的测试分离株在刚果红琼脂上产生粘液,98.9%的分离株通过附着在无菌 96 孔“U”底聚苯乙烯组织培养板上体外产生生物膜,95.7%的分离株携带 icaA 和 icaD 基因。生物膜形成的表型试验结果与分子分析结果进行了比较,刚果红琼脂试验的敏感性和特异性分别为 88.9%和 100%,而微量滴定板试验的敏感性和特异性分别为 100%和 25%。当比较用于检测生物膜产生菌的表型方法,即微量滴定板和刚果红琼脂上的生长时,敏感性和特异性分别为 86%和 100%。因此,刚果红琼脂和微量滴定板试验的生长是可以用来确定分离株是否具有生物膜产生潜力的方法。