Zhang S, Li B W, Weil G J
Department of Internal Medicine, Barnes-Jewish Hospital and Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Am J Trop Med Hyg. 2000 Jul-Aug;63(1-2):85-9. doi: 10.4269/ajtmh.2000.63.85.
Prior studies have shown that Onchocerca volvulus DNA can be detected in skin snips and in black flies after polymerase chain reaction (PCR) with primers specific for repeated "O-150" DNA sequences. We have adapted a paper chromatography hybridization assay (PCHA) to detect amplified O-150 DNA and compared this method to two established methods, namely agarose gel electrophoresis (AGE) and hybridization enzyme-linked immunosorbent assay (ELISA). The minimum amounts of purified O-150 DNA detected by PCHA, AGE, and ELISA were 5, 10, and 2 ng, respectively. The three methods had similar estimated sensitivities for detecting O. volvulus DNA amplified from skin snips from African subjects with onchocerciasis (88%, 84%, and 91%, respectively). No false positive results were observed with skin snips from uninfected control subjects. The paper chromatography hybridization assay detects PCR products in 30 minutes without electricity or special equipment. This technology brings DNA detection a step closer to widespread use in field settings.
先前的研究表明,在用针对重复的“O-150”DNA序列的引物进行聚合酶链反应(PCR)后,可在皮肤切片和黑蝇中检测到盘尾丝虫DNA。我们采用了一种纸层析杂交试验(PCHA)来检测扩增的O-150 DNA,并将该方法与两种既定方法,即琼脂糖凝胶电泳(AGE)和杂交酶联免疫吸附测定(ELISA)进行了比较。PCHA、AGE和ELISA检测到的纯化O-150 DNA的最小量分别为5、10和2 ng。这三种方法对检测从患有盘尾丝虫病的非洲受试者的皮肤切片中扩增出的盘尾丝虫DNA的估计灵敏度相似(分别为88%、84%和91%)。未感染对照受试者的皮肤切片未观察到假阳性结果。纸层析杂交试验无需电力或特殊设备,在30分钟内即可检测PCR产物。这项技术使DNA检测更接近在现场广泛应用。