Povlsen K, Jensen J S, Lind I
Mycoplasma Laboratory, Neisseria Department, Statens Serum Institut, Copenhagen, Denmark.
J Clin Microbiol. 1998 Nov;36(11):3211-6. doi: 10.1128/JCM.36.11.3211-3216.1998.
An assay which combines the direct detection of Ureaplasma urealyticum with biovar determination was developed and applied to 618 urogenital specimens. U. urealyticum was detected by inhibitor-controlled PCR. A 429-bp fragment of the urease gene was amplified. The amplicons were labelled with digoxigenin during PCR. Biovar determination was performed by liquid hybridization with biotin-labelled biovar-specific probes, and the hybrids were detected with peroxidase-conjugated sheep anti-digoxigenin immunoglobulin G Fab fragments. Results of PCR and culture for 453 urogenital specimens from women and 105 urethral specimens from men could be compared. Among the specimens from women, 63% were PCR positive as well as culture positive, 0.9% were positive only by PCR, and 4% were positive only by culture. Among the specimens from men, 15% were PCR positive as well as culture positive, 1% were positive only by PCR, and 9% were positive only by culture. By using culture as the reference method, the PCR had a sensitivity of 94% and a specificity of 98% when applied to specimens from women and a sensitivity of 64% and a specificity of 99% when applied to specimens from men. Overall, 80% of the PCR-positive specimens contained biovar 1,13.5% contained biovar 2, and 6.5% contained both biovars.
开发了一种将解脲脲原体的直接检测与生物变种测定相结合的检测方法,并将其应用于618份泌尿生殖系统标本。通过抑制剂控制的聚合酶链反应(PCR)检测解脲脲原体。扩增脲酶基因的一个429碱基对的片段。在PCR过程中用洋地黄毒苷标记扩增产物。通过与生物素标记的生物变种特异性探针进行液相杂交来进行生物变种测定,并用过氧化物酶偶联的羊抗洋地黄毒苷免疫球蛋白G Fab片段检测杂交体。可以比较来自女性的453份泌尿生殖系统标本和来自男性的105份尿道标本的PCR和培养结果。在女性标本中,63%的标本PCR和培养均为阳性,0.9%仅PCR阳性,4%仅培养阳性。在男性标本中,15%的标本PCR和培养均为阳性,1%仅PCR阳性,9%仅培养阳性。以培养作为参考方法,该PCR应用于女性标本时灵敏度为94%,特异性为98%;应用于男性标本时灵敏度为64%,特异性为99%。总体而言,80%的PCR阳性标本含有生物变种1,13.5%含有生物变种2,6.5%同时含有两种生物变种。