León-Janampa Nancy, Liendo Ruddy, Gilman Robert H, Padilla Carlos, García Hector H, Gonzales Armando, Sheen Patricia, Pajuelo Mónica J, Zimic Mirko
Laboratorio de Bioinformática y Biología Molecular, Facultad de Ciencias y Filosofía, Universidad Peruana Cayetano Heredia, Lima, Peru.
Department of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
Vet Parasitol. 2019 Mar;267:9-16. doi: 10.1016/j.vetpar.2019.01.004. Epub 2019 Jan 29.
Porcine cysticercosis is an endemic parasitic disease caused by infection with Taenia solium that is found predominantly in developing countries. In order to aid in the development of simple diagnostic approaches, identification and characterization of potential new antigens for immunodiagnostic purposes is desired. The cysteine protease family has previously been found to have important immunodiagnostic properties. These proteases are expressed as zymogens which contain a signal peptide, pro-peptide, and an active domain. Subsequent catalytic cleavage of the pro-peptide converts these zymogens into enzymes. With the use of bioinformatic tools we identified an active domain of a novel cathepsin L-like cysteine protease (TsolCL) in the T. solium genome. The TsolCL gene includes 705 nucleotides (nt) within a single intron and a 633 nt exonic sequence encoding an active protein of 211 amino acids. Sequence alignment and phylogenetic analysis suggest that the TsolCL gene is closely related to genes found in Echinoccocus granulosus and E. multiloculars. In addition, TsolCL was found to have a 61.9%-99.0% similarity to other cathepsin L proteins found in other helminths and mammals. We cloned, expressed, purified, and characterized the recombinant active TsolCL (27 kDa) using the baculovirus-insect cell expression system. TsolCL showed cysteine protease enzymatic activity with the capacity to hydrolyze the Z-Phe-Arg-AMC substrate as well as bovine serum albumin. However, TsolCL was not able to hydrolyze human immunoglobulin. In addition, TsolCL has cathepsin L conserved amino acid residues in the catalytic site (Gln8, Cys14, His159, Asn179 and Trp181) and the motif GCNGG. Using ELISA, TsolCL was able to distinguish circulating IgG antibodies between healthy animals and naturally infected pigs with cysticercosis, showing a moderate sensitivity of 83.33% (40/48; 95% CI: [69.8%-92.5 %]), and a specificity of 83.78% (31/37; 95% CI: [67.9%-93.8%]). In conclusion, a novel cathepsin L-like cysteine protease from a T. solium metacestode was expressed successfully in Baculovirus system and was evaluated as a candidate antigen to diagnose porcine cysticercosis using the ELISA immunoassay.
猪囊尾蚴病是一种由猪带绦虫感染引起的地方性寄生虫病,主要见于发展中国家。为了有助于开发简单的诊断方法,需要鉴定和表征用于免疫诊断的潜在新抗原。此前已发现半胱氨酸蛋白酶家族具有重要的免疫诊断特性。这些蛋白酶以酶原形式表达,其包含信号肽、前肽和活性结构域。前肽的后续催化裂解将这些酶原转化为酶。利用生物信息学工具,我们在猪带绦虫基因组中鉴定了一种新型组织蛋白酶L样半胱氨酸蛋白酶(TsolCL)的活性结构域。TsolCL基因在单个内含子内包含705个核苷酸(nt)和一个633 nt的外显子序列,编码一个211个氨基酸的活性蛋白。序列比对和系统发育分析表明,TsolCL基因与细粒棘球绦虫和多房棘球绦虫中的基因密切相关。此外,发现TsolCL与其他蠕虫和哺乳动物中发现的其他组织蛋白酶L蛋白具有61.9%-99.0%的相似性。我们使用杆状病毒-昆虫细胞表达系统克隆、表达、纯化并表征了重组活性TsolCL(27 kDa)。TsolCL表现出半胱氨酸蛋白酶酶活性,能够水解Z-苯丙氨酸-精氨酸-7-氨基-4-甲基香豆素底物以及牛血清白蛋白。然而,TsolCL不能水解人免疫球蛋白。此外,TsolCL在催化位点(Gln8、Cys14、His159、Asn179和Trp181)和基序GCNGG中具有组织蛋白酶L保守氨基酸残基。使用酶联免疫吸附测定(ELISA),TsolCL能够区分健康动物和自然感染囊尾蚴病的猪之间的循环IgG抗体,显示出83.33%(40/48;95%置信区间:[69.8%-92.5%])的中等敏感性和83.78%(31/37;95%置信区间:[67.9%-93.8%])的特异性。总之,一种来自猪带绦虫中绦期幼虫的新型组织蛋白酶L样半胱氨酸蛋白酶在杆状病毒系统中成功表达,并作为使用ELISA免疫测定诊断猪囊尾蚴病的候选抗原进行了评估。