Mu Alan Kang-Wai, Bee Ping Chong, Lau Yee Ling, Chen Yeng
Department of Oral Biology and Biomedical Sciences, Faculty of Dentistry, University of Malaya, Kuala Lumpur 50603, Malaysia.
Department of Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur 50603, Malaysia.
Int J Mol Sci. 2014 Nov 3;15(11):19952-61. doi: 10.3390/ijms151119952.
Malaria is caused by parasitic protozoans of the genus Plasmodium and is one of the most prevalent infectious diseases in tropical and subtropical regions. For this reason, effective and practical diagnostic methods are urgently needed to control the spread of malaria. The aim of the current study was to identify a panel of new malarial markers, which could be used to diagnose patients infected with various Plasmodium species, including P. knowlesi, P. vivax and P. falciparum. Sera from malaria-infected patients were pooled and compared to control sera obtained from healthy individuals using the isobaric tags for relative and absolute quantitation (iTRAQ) technique. Mass spectrometry was used to identify serum proteins and quantify their relative abundance. We found that the levels of several proteins were increased in pooled serum from infected patients, including cell adhesion molecule-4 and C-reactive protein. In contrast, the serum concentration of haptoglobin was reduced in malaria-infected individuals, which we verified by western blot assay. Therefore, these proteins might represent infectious markers of malaria, which could be used to develop novel diagnostic tools for detecting P. knowlesi, P. vivax and P. falciparum. However, these potential malarial markers will need to be validated in a larger population of infected individuals.
疟疾由疟原虫属的寄生原生动物引起,是热带和亚热带地区最普遍的传染病之一。因此,迫切需要有效且实用的诊断方法来控制疟疾的传播。本研究的目的是鉴定一组新的疟疾标志物,可用于诊断感染各种疟原虫物种的患者,包括诺氏疟原虫、间日疟原虫和恶性疟原虫。将疟疾感染患者的血清汇集起来,并使用相对和绝对定量等压标签(iTRAQ)技术与从健康个体获得的对照血清进行比较。采用质谱法鉴定血清蛋白并定量其相对丰度。我们发现,感染患者汇集血清中几种蛋白质的水平升高,包括细胞黏附分子-4和C反应蛋白。相比之下,疟疾感染个体的血清触珠蛋白浓度降低,我们通过蛋白质印迹分析进行了验证。因此,这些蛋白质可能代表疟疾的感染标志物,可用于开发检测诺氏疟原虫、间日疟原虫和恶性疟原虫的新型诊断工具。然而,这些潜在的疟疾标志物需要在更大规模的感染个体群体中进行验证。