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首页> 外文期刊>Journal of Clinical Microbiology >Sample preparation method for polymerase chain reaction-based semiquantitative detection of Leptospira interrogans serovar hardjo subtype hardjobovis in bovine urine.
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Sample preparation method for polymerase chain reaction-based semiquantitative detection of Leptospira interrogans serovar hardjo subtype hardjobovis in bovine urine.

机译:基于聚合酶链反应的牛尿钩端螺旋体血清型Hardjo亚型Hardjobovis半定量检测的样品制备方法。

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摘要

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.
机译:开发了一种改进的制备牛尿液样品的方法,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血清型hardjobovis(hardjobovis亚型)DNA。总共使用了100头无钩端螺旋体的母牛,4头经实验感染的母牛和2头阴性对照母牛。通过(i)使用10 ml尿液样品代替1 ml样品来改善PCR结果,(ii)将10(7)加入10(8)钩端螺旋体血清型patoc细胞作为载体至每个处理的样品,(iii)防止沉淀的钩端螺旋体丢失,并且(iv)尽量减少样品中PCR抑制因子的存在。制备方法使我们能够使用PCR重复检测每毫升尿液中5至10个钩端螺旋体,而无需斑点印迹杂交。此外,我们能够估算出被实验感染的牛脱落的钩藤螺数量。

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