Krasteva D, Toubiana M, Hartati Sri, Kusumawati Asmarani, Dubremetz J F, Widada J Sri
UMR 5119, CNRS-UM2, Université Montpellier II, 34095 Montpellier Cedex 05, France.
Vet Parasitol. 2009 Jun 10;162(3-4):327-31. doi: 10.1016/j.vetpar.2009.03.014. Epub 2009 Mar 17.
Infection with Toxoplasma gondii is one of the most common parasitic infections in humans and other warm-blooded animals. This paper describes the development of loop-mediated isothermal amplification (LAMP) specific to the single-copy gene SAG1 as a diagnostic tool of toxoplasmosis. A set of primers, composed of outer primers, inner primers and loop primers was designed from a published sequence data (GeneBank Acc. no. AY651825). Experiments showed that when LAMP was applied to sample organs, amplification absolutely required the loop primers to complete. SAG1-based LAMP turned out to be very sensitive, exhibiting a degree of sensitivity higher than the conventional PCR. LAMP is a convenient and sensitive diagnostic tool for routine health control of toxoplasmosis.
弓形虫感染是人类和其他温血动物中最常见的寄生虫感染之一。本文描述了针对单拷贝基因SAG1的环介导等温扩增(LAMP)技术的开发,作为一种弓形虫病的诊断工具。根据已发表的序列数据(基因库登录号AY651825)设计了一组引物,包括外引物、内引物和环引物。实验表明,当将LAMP应用于样本器官时,扩增绝对需要环引物才能完成。基于SAG1的LAMP非常灵敏,其灵敏度高于传统PCR。LAMP是一种用于弓形虫病常规健康监测的便捷且灵敏的诊断工具。