Molecular Assessment of Domain I of Apical Membrane Antigen I Gene in Plasmodium falciparum: Implications in Plasmodium Invasion, Taxonomy, Vaccine Development, and Drug Discovery.

IF 2.6 4区 医学 Q3 INFECTIOUS DISEASES Canadian Journal of Infectious Diseases & Medical Microbiology Pub Date : 2022-10-07 eCollection Date: 2022-01-01 DOI:10.1155/2022/1419998
Che Roland Achungu, Damian Nota Anong, Robert Adamu Shey, Cevie Jesenta Tabe
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Abstract

Given its global morbidity and mortality rates, malaria continues to be a major public health concern. Despite significant progress in the fight against malaria, efforts to control and eradicate the disease globally are in jeopardy due to lack of a universal vaccine. The conserved short peptide sequences found in Domain I of Plasmodium falciparum apical membrane antigen 1 (PfAMA1), which are exposed on the parasite cell surface and in charge of Plasmodium falciparum invasion of host cells, make PfAMA1 a promising vaccine candidate antigen. The precise amino acids that make up these conserved short peptides are still unknown, and it is still difficult to pinpoint the molecular processes by which PfAMA1 interacts with the human host cell during invasion. The creation of a universal malaria vaccine based on the AMA1 antigen is challenging due to these knowledge limitations. This study used genome mining techniques to look for these particular short peptides in PfAMA1. Thirty individuals with Plasmodium falciparum malaria had blood samples taken using Whatman's filter papers. DNA from the parasite was taken out using the Chelex technique. Domain I of the Plasmodium falciparum AMA1 gene was amplified using nested polymerase chain reactions, and the amplified products were removed, purified, and sequenced. The DNA sequence generated was converted into the matching amino acid sequence using bioinformatic techniques. These amino acid sequences were utilized to search for antigenic epitopes, therapeutic targets, and conserved short peptides in Domain I of PfAMA1. The results of this investigation shed important light on the molecular mechanisms behind Plasmodium invasion of host cells, a potential PfAMA1 vaccine antigen sequence, and prospective malaria treatment options in the future. Our work offers fresh information on malaria medication and vaccine research that has not been previously discussed.

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恶性疟原虫顶端膜抗原I基因I结构域的分子鉴定:在疟原虫入侵、分类、疫苗开发和药物发现中的意义
鉴于其全球发病率和死亡率,疟疾仍然是一个主要的公共卫生问题。尽管在防治疟疾方面取得了重大进展,但由于缺乏通用疫苗,全球控制和根除这一疾病的努力处于危险之中。恶性疟原虫根尖膜抗原1 (PfAMA1)结构域I中的保守短肽序列暴露在疟原虫细胞表面,负责恶性疟原虫对宿主细胞的侵袭,使PfAMA1成为一种有希望的疫苗候选抗原。构成这些保守短肽的精确氨基酸仍然未知,并且仍然难以确定PfAMA1在入侵过程中与人类宿主细胞相互作用的分子过程。由于这些知识限制,基于AMA1抗原的通用疟疾疫苗的研制具有挑战性。本研究使用基因组挖掘技术在PfAMA1中寻找这些特殊的短肽。30名恶性疟原虫疟疾患者使用Whatman的滤纸采集了血液样本。利用Chelex技术提取了寄生虫的DNA。采用巢式聚合酶链反应扩增恶性疟原虫AMA1基因的结构域I,并对扩增产物进行去除、纯化和测序。利用生物信息学技术将生成的DNA序列转化为匹配的氨基酸序列。这些氨基酸序列被用来寻找抗原表位、治疗靶点和PfAMA1结构域I中的保守短肽。这项研究的结果为疟原虫入侵宿主细胞的分子机制、潜在的PfAMA1疫苗抗原序列以及未来的疟疾治疗方案提供了重要的线索。我们的工作提供了以前没有讨论过的关于疟疾药物和疫苗研究的新信息。
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来源期刊
CiteScore
4.30
自引率
0.00%
发文量
108
审稿时长
>12 weeks
期刊介绍: Canadian Journal of Infectious Diseases and Medical Microbiology is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies related to infectious diseases of bacterial, viral and parasitic origin. The journal welcomes articles describing research on pathogenesis, epidemiology of infection, diagnosis and treatment, antibiotics and resistance, and immunology.
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