Wu Junlin, Peng Yunping, Liu Xiaoyun, Li Wenmei, Tang Shixing
Guangdong Institute of Microbiology; State Key Laboratory of Applied Microbiology Southern China, Guangdong Provincial Key Laboratory of Microbial Culture Collection and Application, Guangzhou, 510070, China.
Acta Parasitol. 2014 Jun;59(2):267-71. doi: 10.2478/s11686-014-0238-y. Epub 2014 May 15.
Prompt and accurate diagnosis is necessary to start adequate treatment for different affecting species including P. falciparum and P. vivax. Here we described the Wondfo Rapid diagnostic Kit (Pf-HRP2/PAN-pLDH) for the detection of P. falciparum and pan-plasmodium in patient specimen by using a nano-gold immunochromatographic assay. Our rapid assay adapted nano-gold labeling techniques and the monoclonal antibodies (mAbs) against both histidine rich protein-2 (Pf HRP-2) of P. falciparum and pan plasmodium-specific pLDH (pan pLDH). The established two-antibody sandwich immunochromatographic assay could detect P. falciparum and pan-plasmodium. The sensitivity and specificity of Wondfo rapid diagnostic kit were determined by comparing with the "gold standard" of microscopic examination of blood smears. In this study1023 blood samples were collected from outpatient clinics in China and Burma, and detected by both Wondfo kit and microscopic examination. The detection sensitivity and specificity of Wondfo rapid diagnostic kit were 96.46% and 99.67% for P. falciparum (HRP2), 95.03% and 99.24% for pLDH, 96.83% and 99.74% for non-falciparum species, 96.70% and 99.74% for P. vivax, respectively. These results indicate that Wondfo rapid diagnostic assay may be useful for detecting P. falciparum and non-P. falciparum (especially P.v.) in patient specimen.
及时准确的诊断对于启动针对不同感染物种(包括恶性疟原虫和间日疟原虫)的适当治疗至关重要。在此,我们描述了万孚快速诊断试剂盒(Pf-HRP2/PAN-pLDH),其通过纳米金免疫层析法检测患者样本中的恶性疟原虫和泛疟原虫。我们的快速检测采用了纳米金标记技术以及针对恶性疟原虫富含组氨酸蛋白-2(Pf HRP-2)和泛疟原虫特异性pLDH(泛pLDH)的单克隆抗体(mAbs)。所建立的双抗体夹心免疫层析法能够检测恶性疟原虫和泛疟原虫。通过与血涂片显微镜检查这一“金标准”进行比较,确定了万孚快速诊断试剂盒的敏感性和特异性。在本研究中,从中国和缅甸的门诊收集了1023份血样,并分别用万孚试剂盒和显微镜检查进行检测。万孚快速诊断试剂盒对恶性疟原虫(HRP2)的检测敏感性和特异性分别为96.46%和99.67%,对pLDH的检测敏感性和特异性分别为95.03%和99.24%,对非恶性疟原虫物种的检测敏感性和特异性分别为96.83%和99.74%,对间日疟原虫的检测敏感性和特异性分别为96.70%和99.74%。这些结果表明,万孚快速诊断检测方法可能有助于检测患者样本中的恶性疟原虫和非恶性疟原虫(尤其是间日疟原虫)。