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通过酶联免疫吸附测定法研究金黄色葡萄球菌败血症和心内膜炎患者针对全株金黄色葡萄球菌的抗体反应。

Antibody response against whole Staphylococcus aureus in patients with staphylococcal septicaemia and endocarditis investigated by ELISA.

作者信息

Jarløv J O, Christensson B, Espersen F, Hertz J B, Hedström S A

出版信息

Acta Pathol Microbiol Immunol Scand B. 1985 Aug;93(4):307-13. doi: 10.1111/j.1699-0463.1985.tb02893.x.

Abstract

A whole cell Staphylococcus aureus enzyme-linked immunosorbent assay (ELISA) for the detection of IgG antibodies against S. aureus has been developed. To avoid non-specific binding of IgG to protein A, the protein A-poor strains of S. aureus, E 1369 and Wood 46, were used as antigens. One-hundred and eighty serum samples from 120 patients with S. aureus endocarditis, non S. aureus endocarditis, S. aureus septicaemia and non S. aureus septicaemia were tested together with sera from 155 healthy controls. The sensitivity was similar for the E 1369 ELISA and the Wood 46 ELISA and positive test values were detected in 84.2% of patients with S. aureus endocarditis and 41.2% of patients with complicated S. aureus septicaemia. No distinction could be found between complicated and uncomplicated S. aureus septicaemia. The E 1369 ELISA was more specific showing cross reactions with sera from patients infected with other bacteria than S. aureus in 3.6%. Furthermore, the reproducibility was better for the E 1369 ELISA with a coefficient of variation at 0.054. The absence of need for purified antigens makes the whole S. aureus ELISA easy, rapid and cheap. Therefore, we suggest the whole S. aureus ELISA as a good alternative to previously reported assays using purified cell wall antigens.

摘要

已开发出一种用于检测抗金黄色葡萄球菌IgG抗体的全细胞金黄色葡萄球菌酶联免疫吸附测定(ELISA)。为避免IgG与蛋白A的非特异性结合,使用蛋白A含量低的金黄色葡萄球菌菌株E 1369和Wood 46作为抗原。对120例患有金黄色葡萄球菌性心内膜炎、非金黄色葡萄球菌性心内膜炎、金黄色葡萄球菌败血症和非金黄色葡萄球菌败血症患者的180份血清样本以及155名健康对照者的血清进行了检测。E 1369 ELISA和Wood 46 ELISA的敏感性相似,在84.2%的金黄色葡萄球菌性心内膜炎患者和41.2%的复杂性金黄色葡萄球菌败血症患者中检测到阳性测试值。在复杂性和非复杂性金黄色葡萄球菌败血症之间未发现差异。E 1369 ELISA更具特异性,与感染除金黄色葡萄球菌外其他细菌患者的血清发生交叉反应的比例为3.6%。此外,E 1369 ELISA的重复性更好,变异系数为0.054。无需纯化抗原使得全细胞金黄色葡萄球菌ELISA简便、快速且成本低廉。因此,我们建议将全细胞金黄色葡萄球菌ELISA作为先前报道的使用纯化细胞壁抗原的检测方法的良好替代方法。

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