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[金黄色葡萄球菌蛋白A显示的改良方法(作者译)]

[Improved method for the demonstration of protein A of Staphylococcus aureus (author's transl)].

作者信息

Schaeg W, Brückler J, Blobel H

出版信息

Zentralbl Bakteriol Orig A. 1979 Dec;245(4):442-9.

PMID:44938
Abstract

Protein A (PA) could be extracted completely from Staphylococcus aureus by treatment with concentrated formic acid. This led to the development of a semi-quantitative determination of PA by hemagglutination (fig. 1). The treatment with formic acid yielded PA more effectively than the commonly used extraction by boiling (table 1). It could be conducted directly on a loopfull of staphylococci obtained from blood agar. It required no additional cultivation in a fluid medium. Most suitable for the hemagglutination was a commercial preparation of Rh-positive human erythrocytes, blood group O, loaded with Rh-antibodies from humans. This relatively stable preparation had also a higher susceptibility for PA in the slide-test and served for a better detection of PA-positive staphylococci (table 2).

摘要

用浓甲酸处理可从金黄色葡萄球菌中完全提取出蛋白A(PA)。这促使通过血凝反应(图1)对PA进行半定量测定。与常用的煮沸提取法相比,用甲酸处理能更有效地获得PA(表1)。该方法可直接对从血琼脂平板上取一环的葡萄球菌进行操作,无需在液体培养基中进行额外培养。最适合用于血凝反应的是一种商业制备的O型Rh阳性人红细胞,其负载有人源Rh抗体。这种相对稳定的制剂在玻片试验中对PA的敏感性也更高,有助于更好地检测PA阳性葡萄球菌(表2)。

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