Suppr超能文献

基于聚合酶链反应的牛尿液中问号钩端螺旋体哈德乔亚型博氏哈德乔半定量检测的样本制备方法

Sample preparation method for polymerase chain reaction-based semiquantitative detection of Leptospira interrogans serovar hardjo subtype hardjobovis in bovine urine.

作者信息

Gerritsen M J, Olyhoek T, Smits M A, Bokhout B A

机构信息

Department of Bacteriology, Central Veterinary Institute, Lelystad, The Netherlands.

出版信息

J Clin Microbiol. 1991 Dec;29(12):2805-8. doi: 10.1128/jcm.29.12.2805-2808.1991.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3815/270437/0661e05dc5b6/jcm00048-0142-a.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验