在夹心酶联免疫吸附试验(ELISA)中使用抗凝血酶相关顶端裂殖蛋白(TRAMP)多克隆抗体检测克雷西疟原虫的可能性。

W S M Wan Nazri, Y L Lau, F W Cheong
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引用次数: 0

摘要

知更鸟疟原虫主要是人畜共患疟疾的一种,是东南亚地区最常见的疟疾病原体,尤其是在马来西亚婆罗洲。由于知更鸟疟原虫与其他人类疟原虫形态相似,显微镜检测知更鸟疟原虫的灵敏度受到影响,而显微镜检测是检测知更鸟疟原虫的黄金标准。因此,人们一直在努力寻找疾病诊断的替代方法。本研究描述了在夹心酶联免疫吸附试验中使用抗 PkTRAMP 多克隆抗体检测 P. knowlesi 的可能性。首先用 Western 印迹法评估了从小鼠和兔子身上提取的抗 PkTRAMP 多克隆抗体与 P. knowlesi 裂解液中的原生蛋白的结合能力。然后将这些小鼠和兔多克隆抗体分别作为捕获抗体和检测抗体用于夹心酶联免疫吸附试验。用柯莱斯病菌 A1H1 培养物来确定该检测方法的检测限(LOD)。通过对存档的人类疟疾样本和未感染样本进行检测,确定了该检测方法的临床性能。Western 印迹分析证实了多克隆抗体对柯莱西疟原虫的反应性。通过三次重复检测得出的 LOD 值为 0.015%。该检测方法对柯莱斯虫的敏感性为 76%,特异性为 75%。其阳性和阴性预测值分别为 76% 和 75%。与恶性疟原虫和健康样本没有交叉反应,但对间日疟原虫有交叉反应,12 个样本中有 10 个样本检测到了间日疟原虫。总之,抗 PkTRAMP 多克隆抗体可用于检测克雷西疟原虫。尽管如此,抗PkTRAMP抗体用于诊断的全部潜力仍有待进一步探索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Potential use of anti-thrombospondin-related apical merozoite protein (TRAMP) polyclonal antibodies in sandwich enzyme-linked immunosorbent assay (ELISA) for detection of Plasmodium knowlesi.

Plasmodium knowlesi, primarily a zoonotic malaria species is the most common malaria pathogen in the Southeast Asia especially in Malaysian Borneo, Malaysia. Due to morphological resemblance of P. knowlesi to other human Plasmodium, the sensitivity for microscopic detection of P. knowlesi, which is the gold standard, is compromised. Thus, efforts have been made in finding alternatives for the disease diagnosis. This study described the potential use of anti-PkTRAMP polyclonal antibodies in sandwich ELISA for P. knowlesi detection. Anti-PkTRAMP polyclonal antibodies raised from mice and rabbit were first evaluated for their binding capability towards native proteins in P. knowlesi lysates using Western blot. These mice and rabbit polyclonal antibodies were then used in the sandwich ELISA as capture and detection antibodies, respectively. P. knowlesi A1H1 culture was utilised to determine the limit of detection (LOD) of this assay. Its clinical performance was determined by testing with archived human malaria and uninfected samples. Western blot analysis affirmed the polyclonal antibodies reactivity to P. knowlesi. The LOD obtained from three replicated assays was at 0.015% parasitaemia. The assay has 76% sensitivity and 75% specificity for P. knowlesi. Its positive and negative predictive values were 76% and 75%, respectively. No cross reactivity with P. falciparum and healthy samples was observed, except for P. vivax where 10 out of 12 samples were detected. In conclusion, anti-PkTRAMP polyclonal antibodies can be useful in detecting P. knowlesi. Regardless, the full potential of anti-PkTRAMP antibodies for diagnostic purposes need to be explored further.

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