Suppr超能文献

建立一种新型的环介导等温扩增(LAMP)诊断方法,用于肉眼检测猪多杀性巴氏杆菌。

Development of a novel LAMP diagnostic method for visible detection of swine Pasteurella multocida.

机构信息

College of Animal Science and Veterinary Medicine, Heilongjiang Bayi Agricultural University, Daqing High-tech Industrial Development Zone, Daqing, 163319, People's Republic of China.

出版信息

Vet Res Commun. 2010 Dec;34(8):649-57. doi: 10.1007/s11259-010-9433-y. Epub 2010 Aug 19.

Abstract

A set of four specific primers for six regions of kmt1 gene from a species specific region was designed for developing the loop-mediated isothermal amplification diagnostic method of swine Pasteurella multocida (Pm-LAMP). After the Pm-LAMP was carried out at 63°C for 1 h, the LAMP products could be visually confirmed using fluorescent dyes as detection reagent under UV-illumination. In sensitivity, the detection limit of the Pm-LAMP was 10 cfu/mL, and was 1 log less than that of the PCR method. In specificity, the Pm-LAMP did not amplify genomic DNA of swine common respiratory pathogens. Furthermore, based on results for clinical swab samples (n = 31) using PCR detection as golden standard, relative sensitivity of the Pm-LAMP was 100%, relative specificity of the Pm-LAMP was 90.9%, and percentage of observation agreement was 93.5% (Kappa = 0.85). The Pm-LAMP method should be a useful diagnostic tool for rapid and visible detection of swine Pasteurella multocida.

摘要

设计了一组针对 kmt1 基因六个区域的特定引物,用于开发猪多杀性巴氏杆菌(Pm-LAMP)的环介导等温扩增诊断方法。在 63°C 下进行 1 小时的 Pm-LAMP 后,使用荧光染料作为检测试剂,在紫外光照射下可以目视确认 LAMP 产物。在灵敏度方面,Pm-LAMP 的检测限为 10cfu/mL,比 PCR 方法低 1 个对数。在特异性方面,Pm-LAMP 不会扩增猪常见呼吸道病原体的基因组 DNA。此外,基于使用 PCR 检测作为金标准的临床拭子样本(n=31)的结果,Pm-LAMP 的相对灵敏度为 100%,相对特异性为 90.9%,观察一致性百分比为 93.5%(Kappa=0.85)。Pm-LAMP 方法应该是一种快速、可见的检测猪多杀性巴氏杆菌的有用诊断工具。

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