Ochola-Oyier Lynette Isabella, Okombo John, Wagatua Njoroge, Ochieng Jacob, Tetteh Kevin K, Fegan Greg, Bejon Philip, Marsh Kevin
KEMRI-Wellcome Trust Collaborative Programme, P.O. Box 230, Kilifi, 80108, Kenya.
Department of Immunology and Infection, Faculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK.
Malar J. 2016 May 6;15(1):261. doi: 10.1186/s12936-016-1304-8.
Plasmodium falciparum merozoite antigens elicit antibody responses in malaria-endemic populations, some of which are clinically protective, which is one of the reasons why merozoite antigens are the focus of malaria vaccine development efforts. Polymorphisms in several merozoite antigen-encoding genes are thought to arise as a result of selection by the human immune system.
The allele frequency distribution of 15 merozoite antigens over a two-year period, 2007 and 2008, was examined in parasites obtained from children with uncomplicated malaria. In the same population, allele frequency changes pre- and post-anti-malarial treatment were also examined. Any gene which showed a significant shift in allele frequencies was also assessed longitudinally in asymptomatic and complicated malaria infections.
Fluctuating allele frequencies were identified in codons 147 and 148 of reticulocyte-binding homologue (Rh) 5, with a shift from HD to YH haplotypes over the two-year period in uncomplicated malaria infections. However, in both the asymptomatic and complicated malaria infections YH was the dominant and stable haplotype over the two-year and ten-year periods, respectively. A logistic regression analysis of all three malaria infection populations between 2007 and 2009 revealed, that the chance of being infected with the HD haplotype decreased with time from 2007 to 2009 and increased in the uncomplicated and asymptomatic infections.
Rh5 codons 147 and 148 showed heterogeneity at both an individual and population level and may be under some degree of immune selection.
恶性疟原虫裂殖子抗原可在疟疾流行地区人群中引发抗体反应,其中一些具有临床保护作用,这是裂殖子抗原成为疟疾疫苗研发重点的原因之一。几种裂殖子抗原编码基因中的多态性被认为是人类免疫系统选择的结果。
对2007年和2008年两年间从患单纯性疟疾儿童体内获取的疟原虫中15种裂殖子抗原的等位基因频率分布进行了检测。在同一人群中,还检测了抗疟治疗前后等位基因频率的变化。对任何等位基因频率出现显著变化的基因,也在无症状和复杂性疟疾感染中进行了纵向评估。
在网织红细胞结合同源物(Rh)5的第147和148密码子中发现了波动的等位基因频率,在单纯性疟疾感染中,两年间从HD单倍型转变为YH单倍型。然而,在无症状和复杂性疟疾感染中,YH分别在两年和十年期间是主要且稳定的单倍型。对2007年至2009年所有三种疟疾感染人群进行的逻辑回归分析显示,感染HD单倍型的几率从2007年到2009年随时间下降,在单纯性和无症状感染中则增加。
Rh5的第147和148密码子在个体和群体水平上均表现出异质性,可能受到一定程度的免疫选择。