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Methods and compositions for detecting serotypes of Chlamydia trachomatis capable of causing lymphogranuloma venereum

机译:用于检测能引起性病性淋巴肉芽肿的沙眼衣原体血清型的方法和组合物

摘要

Disclosed are methods and compositions for conducting assays utilizing real-time polymerase chain reactions (“PCRs”) in detection of serotypes L I, L II, and L III, but not stereotype B, of Chlamydia trachomatis, capable of causing lymphogranuloma venereum (“LGV”). These assays take advantage of a deletion occurring in the cytotoxin gene locus specific to the L I, L II, and L III serotypes. Each assay employs a first primer having a nucleotide sequence flanking one side of the deletion point and a second primer having a nucleotide sequence flanking the other side of the deletion point, wherein the first primer and the second primer are capable of hybridizing respectively to the plus strand and the minus strand of the genome of Chlamydia trachomatis during PCR. Synthesis during PCR of a sequence-specific amplicon containing this deletion point indicates that the sample contains nucleic acid specific to an LGV-causing serotype of Chlamydia trachomatis.
机译:公开了利用实时聚合酶链反应(“ PCR”)进行检测以检测沙眼衣原体的血清型LI,L II和L III但不是定型B的方法和组合物,引起性病性淋巴肉芽肿(“ LGV”)的原因。这些测定利用了在针对L I,L II和L III血清型的细胞毒素基因位点中发生的缺失。每种测定法均使用具有在缺失点的一侧侧翼的核苷酸序列的第一引物和具有在缺失点的另一侧侧翼的核苷酸序列的第二引物,其中第一引物和第二引物能够分别与正末端杂交。 PCR过程中沙眼衣原体基因组的负链和负链。在PCR期间包含该缺失点的序列特异性扩增子的合成表明该样品含有对导致沙眼衣原体的LGV血清型特异性的核酸。

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