Identification of broadly-conserved parasitic nematode proteins that activate immunity

B. Rosa, D. Zarlenga, V. Fournet, E. Beshah, D. Hill, Alexander Zarlenga, Angela Yee, Xiaowu Liang, Adam D. Shandling, Amit Oberai, J. Urban, M. Mitreva
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Abstract

Soil transmitted nematodes are impediments to human health and agricultural production. Poor anthelmintic efficiencies, the emergence of resistant strains, and the persistence of infective stages highlight the need for more effective control strategies. Parasitic nematodes elicit a Th2-type immune response that most often is not protective. Vaccination has thus far been unsuccessful due to unrealized antigenic characters and unknown mechanisms that nematodes use to circumvent host immunity.Here, we used a genomics/proteomics approach (including immunoblot experiments from pigs infected with T. suis) to prioritize putative immunogenic excretory/secretory (E/S) proteins conserved across and specific to several gastrointestinal (GI) parasitic nematode species. A cocktail of five recombinant proteins optimized for conserved GI nematode targets was used immunize pigs and test for active antibody responses in both the serum and intestinal ileal fluid of immunized pigs. An antibody-protein array of putative immunogenic proteins was developed from a combined bioinformatic, experimental, and literature-based prioritization of homologous parasite proteins.Screening the array with sera and ileal fluid samples from immunized pigs suggested cross-reactivity among homologous proteins and a general activation of immunity. PCA clustering showed that the overall immune responses were altered by immunization, but no substantial changes were observed following direct worm challenge with either Ascaris suum or Trichuris suis.Proteins that activated immunity are potential antigens for immunization and the multi-omics phylum-spanning prioritization database that was created is a valuable resource for identifying target proteins in a wide array of different parasitic nematodes. This research strongly supports future studies using a computational, comparative genomics/proteomics approach to produce an effective parasite vaccine.
广泛保守的激活免疫的寄生线虫蛋白的鉴定
土壤传播线虫是人类健康和农业生产的障碍。驱虫效果差、耐药菌株的出现以及感染阶段的持续性突出表明需要更有效的控制策略。寄生线虫引发Th2型免疫反应,这种免疫反应通常没有保护作用。到目前为止,由于线虫用来规避宿主免疫的抗原特性和未知机制,疫苗接种一直没有成功。在这里,我们使用了基因组学/蛋白质组学方法(包括从感染猪瘟的猪身上进行的免疫印迹实验)来优先考虑在几种胃肠道(GI)寄生线虫物种中保守并特异性的假定免疫原性排泄/分泌(E/S)蛋白。使用针对保守GI线虫靶标优化的五种重组蛋白的混合物免疫猪,并测试免疫猪的血清和肠回肠液中的活性抗体反应。根据同源寄生虫蛋白的生物信息学、实验和文献优先顺序,开发了一种推定免疫原性蛋白的抗体蛋白阵列。用免疫猪的血清和回肠液样品筛选该阵列表明同源蛋白之间的交叉反应性和免疫的普遍激活。PCA聚类显示,免疫改变了总体免疫反应,但在用猪蛔虫或猪鞭虫直接攻击蠕虫后没有观察到实质性变化。激活免疫的蛋白质是免疫的潜在抗原,创建的跨多组学门优先数据库是鉴定多种不同寄生线虫中靶蛋白的宝贵资源。这项研究有力地支持了未来使用计算、比较基因组学/蛋白质组学方法生产有效寄生虫疫苗的研究。
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