Yang See Hoon, Park Jung-Ok, Lee John Hwa, Jeon Byung Hun, Kim Won Sin, Kim Suk-Il, Yun Ki-Jung, Jeong Eun Taik, Lee Kil-Whoan, Kim Yong Man, Lee Mi Hyang, Park Hyun
Departments of Internal Medicine, Pathology, and Parasitology, College of Medicine, Department of Pathology, College of Oriental Medicine, Wonkwang University, Iksan 570-749, Korea.
Am J Trop Med Hyg. 2004 Jul;71(1):87-92.
The cysteine proteinases of Paragonimus westermani are known to play important roles in invasion and pathogenesis to hosts and in immune modulation and nutrient uptake. In this study, we have cloned a new cysteine proteinase of P. westermani, PwCP2, from adult worms and tested its diagnostic usefulness. The PwCP2 gene had an open reading frame of 816 base pairs and a conserved catalytic triad of cysteine, histidine, and asparagine residues. The mature form of recombinant PwCP2 (rPwCP2) lacking a proregion was overexpressed in Escherichia coli and used to produce antiserum. Western blot and immunohistochemical analyses using this antiserum showed that PwCP2 was expressed as a mature form, 24-kD product in a crude extract and in the excretory-secretory product of P. westermani, and was localized mainly in the intestinal epithelium of the adult worm. Western blot analysis using the rPwCP2 showed not only high sensitivity (90%) and specificity (100%) to sera from patients with paragonimiasis westermani, but also no cross-reactivity with sera from patients with clonorchiasis, sparganosis, or cysticercosis. Furthermore, an enzyme-linked immunosorbent assay using rPwCP2 exhibited a sensitivity of 93% and a specificity of 93% with sera of rats infected with P. westermani metacercariae. These results suggest that the excretory-secretory PwCP2 can be used for the diagnosis of paragonimiasis.
已知卫氏并殖吸虫的半胱氨酸蛋白酶在对宿主的侵袭和致病过程以及免疫调节和营养摄取中发挥重要作用。在本研究中,我们从成虫中克隆了一种新的卫氏并殖吸虫半胱氨酸蛋白酶PwCP2,并测试了其诊断效用。PwCP2基因有一个816个碱基对的开放阅读框以及一个由半胱氨酸、组氨酸和天冬酰胺残基组成的保守催化三联体。缺乏前区的重组PwCP2(rPwCP2)成熟形式在大肠杆菌中过表达,并用于制备抗血清。使用该抗血清进行的蛋白质印迹和免疫组织化学分析表明,PwCP2以成熟形式表达,为24-kD产物,存在于卫氏并殖吸虫的粗提物和排泄-分泌产物中,且主要定位于成虫的肠上皮中。使用rPwCP2进行的蛋白质印迹分析显示,其不仅对卫氏并殖吸虫病患者血清具有高敏感性(90%)和特异性(100%),而且与华支睾吸虫病、裂头蚴病或囊尾蚴病患者血清无交叉反应。此外,使用rPwCP2进行的酶联免疫吸附测定对感染卫氏并殖吸虫后尾蚴的大鼠血清显示出93%的敏感性和93%的特异性。这些结果表明,排泄-分泌型PwCP2可用于卫氏并殖吸虫病的诊断。