Antwi-Baffour Samuel, Adjei Jonathan Kofi, Agyemang-Yeboah Francis, Annani-Akollor Max, Kyeremeh Ransford, Asare George Awuku, Gyan Ben
Department of Medical Laboratory Sciences, School of Biomedical and Allied Health Sciences, College of Health Sciences, University of Ghana, P. O. Box KB 143, Korle-Bu, Accra, Ghana.
Department of Molecular Medicine, School of Medical Sciences Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.
Proteome Sci. 2017 Mar 24;15:5. doi: 10.1186/s12953-017-0113-5. eCollection 2016.
Malaria continues to be a great public health concern due to the significant mortality and morbidity associated with the disease especially in developing countries. Microparticles (MPs), also called plasma membrane derived extracellular vesicles (PMEVs) are subcellular structures that are generated when they bud off the plasma membrane. They can be found in healthy individuals but the numbers tend to increase in pathological conditions including malaria. Although, various studies have been carried out on the protein content of specific cellular derived MPs, there seems to be paucity of information on the protein content of circulating MPs in malaria and their association with the various signs and symptoms of the disease. The aim of this study was therefore to carry out proteomic analyses of MPs isolated from malaria positive samples and compare them with proteins of MPs from malaria parasite culture supernatant and healthy controls in order to ascertain the role of MPs in malaria infection.
Plasma samples were obtained from forty-three (43) malaria diagnosed patients (cases) and ten (10) healthy individuals (controls). Malaria parasite culture supernatant was obtained from our laboratory and MPs were isolated from them and confirmed using flow cytometry. 2D LC-MS was done to obtain their protein content. Resultant data were analyzed using SPSS Ver. 21.0 statistical software, Kruskal Wallis test and Spearman's correlation coefficient .
In all, 1806 proteins were isolated from the samples. The MPs from malaria positive samples recorded 1729 proteins, those from culture supernatant were 333 while the control samples recorded 234 proteins. The mean number of proteins in MPs of malaria positive samples was significantly higher than that in the control samples. Significantly, higher quantities of haemoglobin subunits were seen in MPs from malaria samples and culture supernatant compared to control samples.
A great number of proteins were observed to be carried in the microparticles (MPs) from malaria samples and culture supernatant compared to controls. The greater loss of haemoglobin from erythrocytes via MPs from malaria patients could serve as the initiation and progression of anaemia in infection. Also while some proteins were upregulated in circulating MPs in malaria samples, others were down regulated.
疟疾仍然是一个重大的公共卫生问题,因为该疾病尤其是在发展中国家会导致显著的死亡率和发病率。微颗粒(MPs),也称为质膜衍生细胞外囊泡(PMEVs),是从质膜上芽生时产生的亚细胞结构。它们可以在健康个体中发现,但在包括疟疾在内的病理状况下数量往往会增加。尽管已经对特定细胞衍生的微颗粒的蛋白质含量进行了各种研究,但关于疟疾中循环微颗粒的蛋白质含量及其与疾病各种体征和症状的关联似乎缺乏信息。因此,本研究的目的是对从疟疾阳性样本中分离的微颗粒进行蛋白质组学分析,并将它们与来自疟原虫培养上清液和健康对照的微颗粒蛋白质进行比较,以确定微颗粒在疟疾感染中的作用。
从四十三(43)名经疟疾诊断的患者(病例)和十(10)名健康个体(对照)中获取血浆样本。从我们的实验室获得疟原虫培养上清液,并从中分离微颗粒,并用流式细胞术进行确认。进行二维液相色谱 - 质谱分析以获得它们的蛋白质含量。使用SPSS Ver. 21.0统计软件、Kruskal Wallis检验和Spearman相关系数对所得数据进行分析。
总共从样本中分离出1806种蛋白质。疟疾阳性样本的微颗粒记录到1729种蛋白质,培养上清液的微颗粒有333种,而对照样本记录到234种蛋白质。疟疾阳性样本微颗粒中的蛋白质平均数量显著高于对照样本。值得注意的是,与对照样本相比,在来自疟疾样本和培养上清液的微颗粒中观察到更高量的血红蛋白亚基。
与对照相比,在来自疟疾样本和培养上清液的微颗粒(MPs)中观察到携带大量蛋白质。通过疟疾患者的微颗粒导致红细胞中血红蛋白的大量损失可能是感染中贫血发生和进展的原因。此外,虽然疟疾样本中循环微颗粒中的一些蛋白质上调,但其他蛋白质下调