Al-Sherbiny Maged M, Farrag Abd-Al Magid M K, Fayad Mohamed H, Makled Mohamed K, Tawfeek Gihan M, Ali Nehad M S
Department of Zoology, Faculty of Science, Cairo University, 12311, Cairo, Egypt.
Parasitol Res. 2004 Jun;93(2):87-95. doi: 10.1007/s00436-004-1076-x. Epub 2004 Apr 22.
The aim of the present work was to apply and evaluate a dipstick assay for the serodiagnosis of human hydatidosis as well as human and experimental trichinosis using camel hydatid cyst fluid (HCF) and Trichinella spiralis muscle larval (TSML) antigens, respectively, and compare this to enzyme-linked immunoelectrotransfer blot (EITB) and Falcon assay screening test-enzyme-linked immunosorbent assay (FAST-ELISA). Sera samples were collected from patients with confirmed hydatidosis and trichinosis and with other parasitic diseases as well as from normal healthy individuals. Also, sera samples were collected from mice experimentally infected with T. spiralis which were sacrificed at different time points post-infection (PI). HCF and TSML antigens were used in EITB after separation and characterization of their antigenic components using 5-22.5% sodium dodecyl sulphate-polyacrylamide gel electrophoresis under non-reducing condition. For the diagnosis of hydatidosis, the sensitivity, specificity and diagnostic accuracy of the dipstick assay and EITB were 100, 91.4 and 95.1% while those of FAST-ELISA were 96.2, 100 and 98.4%, respectively. For the diagnosis of human trichinosis, the sensitivity, specificity and diagnostic accuracy of the dipstick assay and EITB were 100% while those of FAST-ELISA were 85.7%. FAST-ELISA proved to be more sensitive in the early diagnosis of experimental T. spiralis infection (100% sensitivity from the second week PI) than the dipstick and EITB (100% sensitivity from the third week PI). All tests retained their sensitivity till the 12th week PI. Since the dipstick assay is extremely easy to perform with a visually interpreted result within 15 min, in addition to being both sensitive and specific, the test could be an acceptable alternative for use in clinical laboratories lacking specialized equipment and the technological expertise needed for EITB and FAST-ELISA.
本研究的目的是分别应用骆驼包虫囊肿液(HCF)和旋毛虫肌肉幼虫(TSML)抗原,评估用于人体包虫病以及人体和实验性旋毛虫病血清学诊断的试纸条检测方法,并将其与酶联免疫电转移印迹法(EITB)和猎鹰试验筛选试验 - 酶联免疫吸附测定法(FAST - ELISA)进行比较。血清样本采集自确诊为包虫病和旋毛虫病的患者、患有其他寄生虫病的患者以及正常健康个体。此外,还采集了实验感染旋毛虫的小鼠在感染后不同时间点处死时的血清样本。在非还原条件下,使用5 - 22.5%十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳对HCF和TSML抗原的抗原成分进行分离和表征后,将其用于EITB。对于包虫病的诊断,试纸条检测法和EITB的敏感性、特异性和诊断准确性分别为100%、91.4%和95.1%,而FAST - ELISA的相应数值分别为96.2%、100%和98.4%。对于人体旋毛虫病的诊断,试纸条检测法和EITB的敏感性、特异性和诊断准确性均为100%,而FAST - ELISA的为85.7%。事实证明,FAST - ELISA在实验性旋毛虫感染的早期诊断中(感染后第二周敏感性为100%)比试纸条检测法和EITB(感染后第三周敏感性为100%)更敏感。所有检测方法在感染后第12周前均保持其敏感性。由于试纸条检测法操作极其简便,15分钟内即可获得肉眼可判读的结果,且兼具敏感性和特异性,因此对于缺乏EITB和FAST - ELISA所需专业设备和技术专长的临床实验室而言,该检测方法可能是一种可接受的替代方法。