Noedl Harald, Wernsdorfer Walther H, Miller Robert Scott, Wongsrichanalai Chansuda
Department of Immunology and Medicine, Armed Forces Research Institute of Medical Sciences (USAMC-AFRIMS), Bangkok, Thailand.
Antimicrob Agents Chemother. 2002 Jun;46(6):1658-64. doi: 10.1128/AAC.46.6.1658-1664.2002.
The production of histidine-rich protein II (HRP2), a histidine- and alanine-rich protein produced by Plasmodium falciparum, is closely associated with the development and proliferation of the parasite and therefore is perfectly suited to reflect growth inhibition as a measure of drug susceptibility. It was the aim of the present study to develop a malaria drug sensitivity assay based on the measurement of HRP2 in a simple enzyme-linked immunosorbent assay (ELISA). The new test proved to be as reliable as traditional in vitro assays, while it was considerably easier to establish and perform. Parasites are incubated at an initial level of parasitemia of 0.01 to 0.1% on microculture plates predosed with ascending concentrations of antimalarial drugs. After incubation for 48 to 72 h, the samples are freeze-thawed and transferred to ELISA plates. The complete ELISA takes about 2.5 h to perform, may be carried out with commercially available test kits, and requires relatively little technical equipment. In correlation analysis, the results closely paralleled those obtained by the isotopic assay (R = 0.892; P < 0.0001) and World Health Organization schizont maturation tests (R = 0.959; P < 0.0001). The novel HRP2 drug susceptibility assay proved to be very sensitive, simple to establish, and highly reproducible. It can be used for a wide range of applications, from epidemiological studies to the screening of new drugs, and may have the potential to replace traditional in vitro techniques. Standard operating procedures, updated information, and analytical software are available from http://malaria.farch.net.
富含组氨酸蛋白II(HRP2)是由恶性疟原虫产生的一种富含组氨酸和丙氨酸的蛋白,其产生与该寄生虫的发育和增殖密切相关,因此非常适合作为反映生长抑制情况的药物敏感性指标。本研究的目的是基于简单的酶联免疫吸附测定(ELISA)法检测HRP2,开发一种疟疾药物敏感性检测方法。新检测方法经证明与传统体外检测方法一样可靠,同时其建立和操作要容易得多。将寄生虫以0.01%至0.1%的初始疟原虫血症水平接种于预先加入浓度递增的抗疟药物的微孔培养板中。孵育48至72小时后,将样本冻融并转移至ELISA板。完整的ELISA检测大约需要2.5小时完成,可使用市售检测试剂盒进行,并且所需技术设备相对较少。在相关性分析中,结果与同位素检测法(R = 0.892;P < 0.0001)和世界卫生组织裂殖体成熟试验(R = 0.959;P < 0.0001)的结果高度相似。新型HRP2药物敏感性检测方法经证明非常灵敏、易于建立且重复性高。它可用于广泛的应用,从流行病学研究到新药筛选,并且可能有潜力取代传统的体外技术。标准操作规程、更新信息及分析软件可从http://malaria.farch.net获取。