Cheun Hyeng-Il, Chung Byung-Suk, Ma Da-Won, Goo Bo-La, Cho Shin-Hyeong, Ji Mi-Jung, Lee Won-Ja
Division of Malaria and Parasitic Diseases, Korea National Institute of Health, Osong, Korea ; Division of Epidemic Intelligence Service, Korea Centers for Disease Control and Prevention, Osong, Korea.
Osong Public Health Res Perspect. 2013 Jun;4(3):146-51. doi: 10.1016/j.phrp.2013.04.006. Epub 2013 May 4.
This study aims to develop a high-sensitivity antibody diagnostic kit that will enable a rapid and accurate detection of Cryptospofidium parvum and Giardia lamblia in patients with diarrhea.
The cultivated C. parvum oocysts and G. lamblia cysts in each calf and dog were injected to mice to obtain antibodies, which were titrated. Spleen cells of the immunized mouse were separated and blended with myelomas to produce hybrid cell lines that form monoclonal antibodies. Using ELISA method, antibodies that specifically respond to C. parvum and G.lamblia were then selected. The cells were injected into the abdominal cavity of a BALB/c mouse to isolate hydrops abdominis containing high level of antibodies. The IgG antibody was purified using protein G gel.
The detection limit of monoclonal antibodies for Cryptosporidium parvum and Giardia lamblia was 125 oocysts/mL and 1250 cysts/mL, respectively. In addition, during testing they did not show cross-reactivity to viruses (n = 15), bacteria (n =17), and parasites (n = 9).
The rapid diagnostic antibody kit developed in this study, which specifically responds to C. parvum and G. lamblia, will be useful in detecting and monitoring diarrheal infections.
本研究旨在开发一种高灵敏度抗体诊断试剂盒,能够快速、准确地检测腹泻患者中的微小隐孢子虫和蓝氏贾第鞭毛虫。
将每只小牛和狗体内培养的微小隐孢子虫卵囊和蓝氏贾第鞭毛虫包囊注射到小鼠体内以获取抗体,并进行滴定。分离免疫小鼠的脾细胞并与骨髓瘤细胞融合,以产生形成单克隆抗体的杂交细胞系。然后使用酶联免疫吸附测定(ELISA)方法,筛选出对微小隐孢子虫和蓝氏贾第鞭毛虫有特异性反应的抗体。将细胞注射到BALB/c小鼠的腹腔中,以分离出含有高水平抗体的腹水。使用蛋白G凝胶纯化IgG抗体。
针对微小隐孢子虫和蓝氏贾第鞭毛虫的单克隆抗体的检测限分别为125个卵囊/毫升和1250个包囊/毫升。此外,在测试过程中,它们对病毒(n = 15)、细菌(n = 17)和寄生虫(n = 9)均未表现出交叉反应。
本研究开发的快速诊断抗体试剂盒对微小隐孢子虫和蓝氏贾第鞭毛虫具有特异性反应,将有助于检测和监测腹泻感染。