Figure S1 - Real-Time Loop-Mediated Isothermal Amplification (RealAmp) for the Species-Specific Identification of Plasmodium vivax

Comparison of the three sequences. The Pvr64 segment used to design the novel P. vivax primers was aligned with the P. knowlesi and P. falciparum sequences. The locations of the six LAMP primers are underlined (italicized sequences indicate location of the complementary sequences). Nucleotide differences found in the P. knowlesi (highlighted in green) and P. falciparum (highlighted in yellow) are shown. (DOCX)三种序列的比对分析。用于设计新型间日疟原虫（Plasmodium vivax）引物的Pvr64片段，与诺氏疟原虫（Plasmodium knowlesi）及恶性疟原虫（Plasmodium falciparum）的序列进行了比对。6条LAMP引物的结合位点已以下划线标注，其中斜体序列代表互补序列的所在位置。本图展示了诺氏疟原虫（以绿色高亮标注）与恶性疟原虫（以黄色高亮标注）序列中存在的核苷酸差异。（DOCX）