Hall-Mendelin S, O'Donoghue P, Atwell R B, Lee R, Hall R A
School of Chemistry and Molecular Biosciences, The University of Queensland, St. Lucia, QLD 4072, Australia.
J Parasitol Res. 2011;2011:283416. doi: 10.1155/2011/283416. Epub 2011 May 18.
The Ixodes holocyclus tick causes paralysis in up to 10,000 companion and domestic animals each year in Australia. Treatment requires the removal of the parasite and the administration of a commercial tick antiserum that is prepared from hyperimmune dogs. Each batch of this serum is initially tested for toxin-neutralising potency in a mouse bioassay that is expensive, time consuming, and subjective. With the aim of developing a rapid in vitro assay to replace the bioassay, we used a partially purified antigen prepared from I. holocyclus salivary glands to develop an ELISA to detect toxin-reactive antibodies in hyperimmune dog sera. The optimised ELISA reliably detected antibodies reactive to I. holocyclus salivary gland antigens. Parallel testing of sera with a negative control antigen prepared from the salivary glands of the nontoxic tick Rhipicephalus (Boophilus) microplus provided further evidence that we were detecting toxin-specific antibodies in the assay. Using the ELISA, we could also detect antibodies induced in rats after experimental infestation with I. holocyclus. This assay shows promise as an alternative means of assessing the potency of batches of hyperimmune dog serum and to screen for toxin-reactive monoclonal antibodies produced from immunised rodents.
澳大利亚每年有多达10000只伴侣动物和家畜因全环硬蜱叮咬而瘫痪。治疗方法包括清除寄生虫,并注射一种由经超免疫处理的犬制备的商品化蜱抗血清。每一批这种血清最初都要在小鼠生物测定中检测毒素中和效力,该方法成本高、耗时且主观。为了开发一种快速的体外测定方法来取代生物测定,我们使用从全环硬蜱唾液腺制备的部分纯化抗原来开发一种酶联免疫吸附测定(ELISA),以检测经超免疫处理的犬血清中的毒素反应性抗体。优化后的ELISA能可靠地检测出与全环硬蜱唾液腺抗原反应的抗体。用从无毒蜱微小牛蜱唾液腺制备的阴性对照抗原对血清进行平行检测,进一步证明我们在该测定中检测到的是毒素特异性抗体。利用ELISA,我们还能检测实验性感染全环硬蜱的大鼠体内诱导产生的抗体。该测定方法有望作为评估经超免疫处理的犬血清批次效力的替代方法,并用于筛选免疫啮齿动物产生的毒素反应性单克隆抗体。