首页> 外文OA文献 >Genetic Diversity of Polymorphic Vaccine Candidate Antigens (Apical Membrane Antigen-1, Merozoite Surface Protein-3, and Erythrocyte Binding Antigen-175) in Plasmodium falciparum Isolates from Western and Central Africa
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Genetic Diversity of Polymorphic Vaccine Candidate Antigens (Apical Membrane Antigen-1, Merozoite Surface Protein-3, and Erythrocyte Binding Antigen-175) in Plasmodium falciparum Isolates from Western and Central Africa

机译:来自中西部非洲的恶性疟原虫分离株的多态性疫苗候选抗原(典型膜抗原-1,裂殖子表面蛋白-3和红细胞结合抗原-175)的遗传多样性。

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摘要

The malaria vaccine candidate antigens erythrocyte binding antigen 175 (EBA-175), merozoite surface protein 3 (MSP-3), and apical membrane antigen (AMA-1) from Plasmodium falciparum isolates from countries in central and west Africa were assessed for allelic diversity. Samples were collected on filter paper from 600 P. falciparum-infected symptomatic patients in Cameroon, Republic of Congo, Burkina Faso, Ghana, and Senegal and screened for class-specific amplification fragments. Genetic diversity, assessed by mean heterozygosity, was comparable among countries. We detected a clinical increase in eba 175 F-allele frequency from west to east across the study region. No statistical difference in msp-3 allele distribution between countries was observed. The ama-1 3D7 alleles were present at a lower frequency in central Africa than in West Africa. We also detected little to no genetic differentiation among sampling locations. This finding indicates that, at least at the level of resolution offered by restriction fragment length polymorphism analysis, these antigens showed remarkable genetic homogeneity throughout the region sampled, perhaps caused by balancing selection to maintain a diverse array of antigen haplotyes.
机译:对来自中非和西非国家的恶性疟原虫分离株的疟疾疫苗候选抗原红细胞结合抗原175(EBA-175),裂殖子表面蛋白3(MSP-3)和顶膜抗原(AMA-1)进行了等位基因多样性评估。在滤纸上收集了来自喀麦隆,刚果共和国,布基纳法索,加纳和塞内加尔的600例受恶性疟原虫感染的有症状患者的样品,并筛选了类特异性扩增片段。通过平均杂合度评估的遗传多样性在各国之间具有可比性。我们在整个研究区域内从西向东检测到eba 175 F等位基因频率的临床增加。在国家之间没有观察到msp-3等位基因分布的统计差异。 ama-1 3D7等位基因在中部非洲的出现频率低于在西非。我们还检测到采样点之间几乎没有遗传分化。该发现表明,至少在限制性片段长度多态性分析所提供的分辨率水平上,这些抗原在整个采样区域内显示出显着的遗传同质性,这可能是由于平衡选择以维持多种抗原单倍体而引起的。

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