Cristina N, Derouin F, Pelloux H, Pierce R, Cesbron-Delauwn M F, Ambroise-Thomas P
Département de Parasitologie-Mycologie Médicale et Moléculaire, CNRS URA 1344, Faculté de Médecine, Université Joseph Fourier-Grenoble I, La Tronche, France.
Pathol Biol (Paris). 1992 Jan;40(1):52-5.
A repetitive original DNA sequence, TGR1E, was cloned and sequenced, then used to develop a polymerase chain reaction (PCR) test for detecting Toxoplasma gondii. Preliminary studies were performed using purified T. gondii DNA or a lysate of purified T. gondii cells [7], with or without a leukocyte lysate. A negative correlation was evidenced between sensitivity of the test and the amount of cellular debris contaminating the DNA to be amplified. Nevertheless, the method was tested on 100 clinical specimens subjected to lysis using the same method. Among the 88 specimens from AIDS patients, four were positive by conventional diagnostic tests and by PCR. Among the 12 specimens tested as part of evaluations for the prevention of congenital toxoplasmosis, PCR failed to detect the positive results yielded by conventional tests on two amniotic fluid specimens. No false positive result was seen with the PCR method.
一个重复的原始DNA序列TGR1E被克隆和测序,然后用于开发一种检测弓形虫的聚合酶链反应(PCR)检测方法。使用纯化的弓形虫DNA或纯化的弓形虫细胞裂解物进行了初步研究[7],有或没有白细胞裂解物。该检测方法的灵敏度与污染待扩增DNA的细胞碎片量之间呈负相关。尽管如此,该方法还是在100份使用相同方法进行裂解的临床标本上进行了测试。在88份艾滋病患者的标本中,有4份通过传统诊断测试和PCR检测呈阳性。在作为预防先天性弓形虫病评估一部分进行检测的12份标本中,PCR未能检测出两份羊水标本传统检测得出的阳性结果。PCR方法未出现假阳性结果。