Christensson B, Espersen F, Hedström S A, Kronvall G
J Clin Microbiol. 1984 May;19(5):680-6. doi: 10.1128/jcm.19.5.680-686.1984.
In the present studies we compared the ability of two commonly used assays, solid-phase radioimmunoassay and enzyme-linked immunosorbent assay (ELISA), to detect human antibodies to Staphylococcus aureus peptidoglycan. ELISA was superior, with a reproducibility of 12.0%, as compared with 18.1% in solid-phase radioimmunoassay. Much lower serum dilutions could be used in ELISA. We also studied the effects of solubilizing the antigen by lysostaphin, lysozyme, or ultrasonication. Lysostaphin-treated peptidoglycan cannot be recommended since solid-phase radioimmunoassay could not distinguish positive from negative serum samples with this preparation. On the other hand, the sensitivity in both assays was high when peptidoglycan treated with lysozyme for 240 min or with ultrasonication for 30 min was used as antigen. The interassay correlation between solid-phase radioimmunoassay and ELISA was slightly better with sonicated peptidoglycan (correlation coefficient = 0.94, P less than 0.01), as compared with lysozyme-treated peptidoglycan (correlation coefficient = 0.76, P less than 0.01). We recommend the ELISA with sonicated peptidoglycan as antigen for use in routine serology.
在本研究中,我们比较了两种常用检测方法——固相放射免疫测定法和酶联免疫吸附测定法(ELISA)检测人抗金黄色葡萄球菌肽聚糖抗体的能力。ELISA更具优势,其重复性为12.0%,而固相放射免疫测定法为18.1%。ELISA中使用的血清稀释度要低得多。我们还研究了用溶葡萄球菌酶、溶菌酶或超声处理使抗原溶解的效果。不推荐使用经溶葡萄球菌酶处理的肽聚糖,因为固相放射免疫测定法无法区分该制剂处理的血清样本的阳性和阴性。另一方面,当用溶菌酶处理240分钟或超声处理30分钟的肽聚糖作为抗原时,两种检测方法的灵敏度都很高。与经溶菌酶处理的肽聚糖(相关系数 = 0.76,P < 0.01)相比,超声处理的肽聚糖用于固相放射免疫测定法和ELISA时的测定间相关性稍好(相关系数 = 0.94,P < 0.01)。我们推荐以超声处理的肽聚糖为抗原的ELISA用于常规血清学检测。