Burg J L, Grover C M, Pouletty P, Boothroyd J C
Department of Microbiology and Immunology, Stanford University School of Medicine, California 94305-5402.
J Clin Microbiol. 1989 Aug;27(8):1787-92. doi: 10.1128/jcm.27.8.1787-1792.1989.
We applied the polymerase chain reaction to detection of the pathogenic protozoan Toxoplasma gondii based on our identification of a 35-fold-repetitive gene (the B1 gene) as a target. Using this procedure, we were able to amplify and detect the DNA of a single organism directly from a crude cell lysate. This level of sensitivity also allowed us to detect the B1 gene from purified DNA samples containing as few as 10 parasites in the presence of 100,000 human leukocytes. This is representative of the maximal cellular infiltration (10(5)/ml) in 1 ml of cerebrospinal fluid obtained from patients with toxoplasmic encephalitis. The B1 gene is present and conserved in all six T. gondii strains tested to date, including two isolates from patients with acquired immunodeficiency syndrome. No signal was detected by using this assay and DNAs from a variety of other organisms, including several which might be found in the central nervous system of an immunocompromised host. This combination of sensitivity and specificity should make detection of the B1 gene based on polymerase chain reaction amplification a very useful method for diagnosis of toxoplasmosis both in immunocompromised hosts and in congenitally infected fetuses.
基于我们对一个35倍重复基因(B1基因)作为靶标的鉴定,我们应用聚合酶链反应来检测致病性原生动物刚地弓形虫。使用该程序,我们能够直接从粗细胞裂解物中扩增并检测单个生物体的DNA。这种灵敏度水平还使我们能够在存在100,000个人类白细胞的情况下,从含有低至10个寄生虫的纯化DNA样品中检测B1基因。这代表了从弓形虫性脑炎患者获得的1 ml脑脊液中的最大细胞浸润(10⁵/ml)。B1基因在迄今为止测试的所有六种刚地弓形虫菌株中均存在且保守,包括来自获得性免疫缺陷综合征患者的两个分离株。使用该检测方法以及来自多种其他生物体的DNA未检测到信号,这些生物体包括免疫受损宿主中枢神经系统中可能发现的几种。这种灵敏度和特异性的结合应使基于聚合酶链反应扩增检测B1基因成为免疫受损宿主和先天性感染胎儿弓形虫病诊断的非常有用的方法。