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Multiplex DNase-free one-step reverse transcription PCR for Plasmodium 18S rRNA and spliced gametocyte-specific mRNAs

机译:疟原虫18S rRNA和剪接的配子体特异性mRNA的多重无DNase一步反转录PCR

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摘要

Background Plasmodium gametocytes are sexual stages transmitted to female Anopheles mosquitoes. While Plasmodium parasites can be differentiated microscopically on Giemsa-stained blood smears, molecular methods are increasingly used because of their increased sensitivity. Molecular detection of gametocytes requires methods that discriminate between asexual and sexual stage parasites. Commonly tested gametocyte-specific mRNAs are pfs25 and pfs230 detected by reverse transcription polymerase chain reaction (RT-PCR). However, detection of these unspliced mRNA targets requires preceding DNase treatment of nucleic acids to eliminate co-purified genomic DNA. If gametocyte-specific, spliced mRNAs could be identified, DNase treatment could be eliminated and one-step multiplexed molecular methods utilized.
机译:背景疟原虫配子体细胞是传递到雌性按蚊的性生活阶段。虽然可以在吉姆萨染色的血液涂片上通过显微镜区分疟原虫,但由于它们的敏感性增加,分子方法越来越多。配子细胞的分子检测需要区分无性和性阶段寄生虫的方法。常用测试的配子体特异性mRNA是通过逆转录聚合酶链反应(RT-PCR)检测到的pfs25和pfs230。但是,检测这些未剪接的mRNA靶标需要对核酸进行预先的DNase处理,以消除共纯化的基因组DNA。如果可以鉴定配子体特异性的剪接的mRNA,则可以消除DNase处理,并采用一步多路复用分子方法。

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