Kotani H, McGarrity G J
J Immunol Methods. 1985 Dec 27;85(2):257-67. doi: 10.1016/0022-1759(85)90136-x.
A simple and rapid method of species identification of mycoplasmas by immunobinding assay is described. Small amounts of antigen of supernatant from cell cultures, broth cultures or clinical specimens were spotted onto nitrocellulose paper. This was followed by application of specific anti-mycoplasma antisera. After incubation, an enzyme-conjugated antiserum against the first antiserum was applied. A positive reaction was indicated by the development of intense blue color reaction when substrate was added. This method identified mycoplasma species with monoclonal and polyclonal antibodies. It detected 9.3 X 10(3) - 7.5 X 10(4) CFU/ml of organisms depending on mycoplasma species. For identification of mycoplasma, ureaplasma, acholeplasma and spiroplasma species, this assay is useful and rapid compared with other serological methods. In limited studies, the method correlated with microbiological assay of clinical specimens for Mycoplasma pneumoniae.
本文描述了一种通过免疫结合试验快速简便地鉴定支原体种类的方法。将细胞培养物、肉汤培养物或临床标本上清液中的少量抗原点样于硝酸纤维素纸上。随后加入特异性抗支原体抗血清。孵育后,加入针对第一种抗血清的酶标记抗血清。加入底物后出现强烈的蓝色反应表明为阳性反应。该方法可使用单克隆抗体和多克隆抗体鉴定支原体种类。根据支原体种类的不同,它能检测到9.3×10³ - 7.5×10⁴ CFU/ml的支原体。与其他血清学方法相比,该试验对于鉴定支原体、脲原体、无胆甾原体和螺原体种类既实用又快速。在有限的研究中,该方法与肺炎支原体临床标本的微生物学检测结果相关。