Sako Yasuhito, Nakao Minoru, Nakaya Kazuhiro, Yamasaki Hiroshi, Ito Akira
Department of Parasitology, Asahikawa Medical College, Japan.
Parasitol Int. 2006;55 Suppl:S69-73. doi: 10.1016/j.parint.2005.11.011. Epub 2005 Dec 13.
Diagnosis of cysticercosis/echinococcosis is primarily based on imaging techniques. These imaging techniques are sometimes limited by the small size of visualized lesions and atypical images, which are difficult to be distinguished from abscesses or neoplasms. Therefore, efforts have been directed toward identification and characterization of specific antigens of parasites for development of serodiagnostic method that can detect specific antibody. For cysticercosis, glycoproteins of 10-26 kDa in cyst fluid of Taenia solium have been widely accepted for serodiagnosis purpose. The glycoproteins consist of a very closely related family of 8-kDa proteins. We identified four genes (designated Ag1, Ag1V1, Ag2 and Ag2V1) encoding the 7- and 10-kDa polypeptides. Based on the antigenicities of these clones, Ag1V1 and Ag2 were chosen as ELISA antigens and the Ag1V1/Ag2 chimeric protein was expressed. The Ag1V1/Ag2 chimeric protein showed the similar sensitivity and specificity as the native glycoproteins. For alveolar echinococcosis, the 65-kDa protein of Echinococcus multilocularis protoscolices and Em18 has been considered as serodiagnostic antigens. The sensitivity and specificity of Em18 are very compatible to those of the recombinant 65-kDa protein. Recently, we demonstrated that Em18 was the proteolytic product of the 65-kDa protein following the action by cysteine proteinases. From the information of N-terminal amino acid sequences, molecular size and isoelectric point of Em18, recombinant Em18 ((349)K to (508)K of the 65-kDa protein, RecEm18) was expressed and evaluated for serodiagnostic value. RecEm18 has the potential for use in the differential serodiagnosis of alveolar echinococcosis.
囊尾蚴病/棘球蚴病的诊断主要基于影像学技术。这些影像学技术有时会受到可视化病变尺寸较小以及图像不典型的限制,这些不典型图像很难与脓肿或肿瘤区分开来。因此,人们致力于鉴定和表征寄生虫的特异性抗原,以开发能够检测特异性抗体的血清学诊断方法。对于囊尾蚴病,猪带绦虫囊液中10 - 26 kDa的糖蛋白已被广泛用于血清学诊断。这些糖蛋白由一个与8 kDa蛋白密切相关的家族组成。我们鉴定了四个编码7 kDa和10 kDa多肽的基因(命名为Ag1、Ag1V1、Ag2和Ag2V1)。基于这些克隆的抗原性,选择Ag1V1和Ag2作为酶联免疫吸附测定(ELISA)抗原,并表达了Ag1V1/Ag2嵌合蛋白。Ag1V1/Ag2嵌合蛋白显示出与天然糖蛋白相似的敏感性和特异性。对于泡型棘球蚴病,多房棘球绦虫原头节的65 kDa蛋白和Em18已被视为血清学诊断抗原。Em18的敏感性和特异性与重组65 kDa蛋白的非常匹配。最近,我们证明Em18是65 kDa蛋白在半胱氨酸蛋白酶作用后的蛋白水解产物。根据Em18的N端氨基酸序列、分子大小和等电点信息,表达了重组Em18(65 kDa蛋白的(349)K至(508)K,RecEm18)并评估其血清学诊断价值。RecEm18具有用于泡型棘球蚴病鉴别血清学诊断的潜力。