Gerritsen M J, Olyhoek T, Smits M A, Bokhout B A
Department of Bacteriology, Central Veterinary Institute, Lelystad, The Netherlands.
J Clin Microbiol. 1991 Dec;29(12):2805-8. doi: 10.1128/jcm.29.12.2805-2808.1991.
An improved method of preparing bovine urine samples was developed for the rapid, specific, and sensitive detection of Leptospira interrogans serovar hardjo (subtype hardjobovis) DNA by the polymerase chain reaction (PCR). A total of 100 leptospire-free cows, 4 experimentally infected cows, and 2 negative control cows were used. PCR results were improved by (i) using 10-ml urine samples instead of 1-ml samples, (ii) adding 10(7) to 10(8) Leptospira biflexa serovar patoc cells as a carrier to each treated sample, (iii) preventing the loss of pelleted leptospires, and (iv) minimizing the presence of PCR-inhibiting factors in the samples. The preparation method enabled us to use the PCR to reproducibly detect as few as 5 to 10 leptospires per ml of urine without the need for dot blot hybridization. In addition, we were able to estimate the number of leptospires shed by experimentally infected cows.
开发了一种改进的牛尿液样本制备方法,用于通过聚合酶链反应(PCR)快速、特异性和灵敏地检测问号钩端螺旋体哈焦血清型(亚型哈焦波维斯)DNA。总共使用了100头无钩端螺旋体的奶牛、4头实验感染奶牛和2头阴性对照奶牛。通过以下方法改进了PCR结果:(i)使用10毫升尿液样本而非1毫升样本;(ii)向每个处理后的样本中添加10⁷至10⁸双曲钩端螺旋体帕托血清型细胞作为载体;(iii)防止沉淀的钩端螺旋体损失;(iv)尽量减少样本中PCR抑制因子的存在。该制备方法使我们能够使用PCR可重复地检测每毫升尿液中低至5至10条钩端螺旋体,而无需斑点印迹杂交。此外,我们能够估计实验感染奶牛排出的钩端螺旋体数量。