De Sai Lata, Stanisic Danielle I, Rivera Fabian, Batzloff Michael R, Engwerda Christian, Good Michael F
Institute for Glycomics, Griffith University, Gold Coast, QLD, Australia.
QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
Malar J. 2016 Jan 4;15:3. doi: 10.1186/s12936-015-1027-2.
The spectrum of techniques to detect malaria parasites in whole blood is limited to measuring parasites in circulation. One approach that is currently used to enumerate total parasite bio-burden involves the use of bio-luminescent parasites. As an alternative approach, this study describes the use of a commercial ELISA human parasite lactate dehydrogenase (pLDH) detection kit to estimate total parasite bio-burden in murine malaria models.
The cross reactivity of pLDH in a commercial human malaria pLDH diagnostic kit was established in different components of blood for different murine malaria models. The use of pLDH as a measure of parasite bio-burden was evaluated by examining pLDH in relation to peripheral blood parasitaemia as determined by microscopy and calculating total parasite bio-burden using a bio-luminescent Plasmodium berghei ANKA luciferase parasite.
The pLDH antigen was detected in all four murine Plasmodium species and in all components of Plasmodium-infected blood. A significant correlation (r = 0.6922, P value <0.0001) was observed between total parasite bio-burden, measured as log average radiance, and concentration of pLDH units.
This high throughput assay is a suitable measure of total parasite bio-burden in murine malaria infections. Unlike existing methods, it permits the estimation of both circulating and sequestered parasites, allowing a more accurate assessment of parasite bio-burden.
检测全血中疟原虫的技术范围仅限于测量循环中的寄生虫。目前用于计数总寄生虫生物负荷的一种方法涉及使用生物发光寄生虫。作为一种替代方法,本研究描述了使用商业酶联免疫吸附测定(ELISA)人寄生虫乳酸脱氢酶(pLDH)检测试剂盒来估计小鼠疟疾模型中的总寄生虫生物负荷。
在不同小鼠疟疾模型的血液不同成分中确定了商业人类疟疾pLDH诊断试剂盒中pLDH的交叉反应性。通过检查与显微镜确定的外周血寄生虫血症相关的pLDH,并使用生物发光伯氏疟原虫ANKA荧光素酶寄生虫计算总寄生虫生物负荷,来评估使用pLDH作为寄生虫生物负荷指标的情况。
在所有四种小鼠疟原虫物种以及疟原虫感染血液的所有成分中均检测到pLDH抗原。以对数平均辐射度衡量的总寄生虫生物负荷与pLDH单位浓度之间存在显著相关性(r = 0.6922,P值<0.0001)。
这种高通量检测方法是衡量小鼠疟疾感染中总寄生虫生物负荷的合适方法。与现有方法不同,它可以估计循环中和隐匿的寄生虫,从而更准确地评估寄生虫生物负荷。