酸处理后刚地弓形虫速殖子和慢殖子的定量竞争聚合酶链反应鉴定。

H. Hata, F. Aosai, H. Mun, Mei Chen, Masashi Kobayashi, A. A. Khairul, H. Kubosawa, A. Yano
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引用次数: 1

摘要

结果表明,采用针对刚地弓形虫特异性SAG1基因的定量竞争性聚合酶链反应方法,可以定量分析由酸处理敏感性/抗性定义的刚地弓形虫速殖子和慢殖子。速殖子不仅被胃蛋白酶-HCl破坏,也被HCl或其他酸溶液破坏。在pH值低于1.8的条件下,酸致破坏发生。刚地弓形虫速殖子DNA易被酸处理破坏。这些DNA破坏使得通过QC-PCR区分速殖子和慢殖子成为可能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of Toxoplasma gondii Tachyzoites and Bradyzoites by a Quantitative Competitive Polymerase Chain Reaction Method after the Acid Treatment.
It was indicated that tachyzoites and bradyzoites of Toxoplasma gondii (T. gondii) defined by the susceptibility/resistance to acid treatment could be quantitatively analyzed by a quantitative competitive polymerase chain reaction method targeting SAG1 gene, specific for T. gondii. The tachyzoites were destroyed not only by pepsin-HCl but also by HCl or other acid solutions. The acid-induced destructions occurred under the pH conditions lower than pH 1.8. Tachyzoite DNA of T. gondii was easily destructed by acid treatment. These DNA destructions made it possible to differentiate between tachyzoites and bradyzoites by QC-PCR.
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