Kengne-Ouafo Jonas A, Morang'a Collins M, Nyakoe Nancy K, Dosoo Daniel, Tackie Richmond, Mutungi Joe K, Bah Saikou Y, Amenga-Etego Lucas N, Urban Britta, Awandare Gordon A, Dinko Bismarck, Aniweh Yaw
West African Centre for Cell Biology of Infectious Pathogens, College of Basic and Applied Sciences, University of Ghana, Legon, Accra P.O. Box LG 56, Ghana.
Department of Clinical Microbiology, School of Medicine and Dentistry College of Health Sciences, Kwame Nkrumah University of Science and Technology, Kumasi 00233, Ashanti Region, Ghana.
Cells. 2025 Jul 31;14(15):1184. doi: 10.3390/cells14151184.
With the increasing detection of artemisinin resistance to front-line antimalarials in Africa and notwithstanding the planned roll-out of RTS'S and R21 in Africa, the search for new vaccines with high efficacy remains an imperative. Towards this endeavour, we performed in silico screening to identify gametocyte stage genes that could be targets of protection or diagnosis. Through the analysis we identified a gene, Pf3D7_1105800, coding for a subtilisin-like domain-containing protein (PfSDP) and thus dubbed the gene . Genetic diversity assessment revealed the gene to be relatively conserved across continents with signs of directional selection. Using RT qPCR and Western blots, we observed that is expressed in all developmental stages of the parasite both at the transcript and protein level. Immunofluorescence assays found PfSDP protein co-localizing with PfMSP-1 and partially with Pfs48/45 at the asexual and sexual stages, respectively. Further, we demonstrated that anti-PfSDP peptide-specific antibodies inhibited erythrocyte invasion by 20-60% in a dose-dependent manner, suggesting that PfSDP protein might play a role in merozoite invasion. We also discovered that PfSDP protein is immunogenic in children from different endemic areas with antibody levels increasing from acute infection to day 7 post-treatment, followed by a gradual decay. The limited effect of antibodies on erythrocyte invasion could imply that it might be more involved in other processes in the development of the parasite.
随着非洲青蒿素对一线抗疟药物耐药性的日益发现,尽管计划在非洲推广RTS'S和R21,但寻找高效的新疫苗仍然势在必行。为了实现这一目标,我们进行了计算机模拟筛选,以确定可能作为保护或诊断靶点的配子体阶段基因。通过分析,我们鉴定出一个基因Pf3D7_1105800,它编码一种含枯草杆菌蛋白酶样结构域的蛋白质(PfSDP),因此将该基因命名为 。遗传多样性评估显示,该基因在各大洲相对保守,并有定向选择的迹象。使用RT qPCR和蛋白质免疫印迹法,我们观察到 在寄生虫的所有发育阶段均在转录本和蛋白质水平上表达。免疫荧光分析发现,PfSDP蛋白在无性和有性阶段分别与PfMSP-1共定位,并与Pfs48/45部分共定位。此外,我们证明抗PfSDP肽特异性抗体以剂量依赖的方式抑制红细胞入侵20%-60%,这表明PfSDP蛋白可能在裂殖子入侵中发挥作用。我们还发现,PfSDP蛋白在来自不同流行地区的儿童中具有免疫原性,抗体水平从急性感染到治疗后第7天升高,随后逐渐下降。抗体对红细胞入侵的有限作用可能意味着它可能更多地参与寄生虫发育的其他过程。