Palmieri Nicola, Shrestha Aruna, Ruttkowski Bärbel, Beck Tomas, Vogl Claus, Tomley Fiona, Blake Damer P, Joachim Anja
Institute of Parasitology, Department of Pathobiology, University of Veterinary Medicine, Veterinärplatz 1, A-1210 Vienna, Austria.
Institute of Parasitology, Department of Pathobiology, University of Veterinary Medicine, Veterinärplatz 1, A-1210 Vienna, Austria.
Int J Parasitol. 2017 Mar;47(4):189-202. doi: 10.1016/j.ijpara.2016.11.007. Epub 2017 Feb 2.
Vaccine development targeting protozoan parasites remains challenging, partly due to the complex interactions between these eukaryotes and the host immune system. Reverse vaccinology is a promising approach for direct screening of genome sequence assemblies for new vaccine candidate proteins. Here, we applied this paradigm to Cystoisospora suis, an apicomplexan parasite that causes enteritis and diarrhea in suckling piglets and economic losses in pig production worldwide. Using Next Generation Sequencing we produced an ∼84Mb sequence assembly for the C. suis genome, making it the first available reference for the genus Cystoisospora. Then, we derived a manually curated annotation of more than 11,000 protein-coding genes and applied the tool Vacceed to identify 1,168 vaccine candidates by screening the predicted C. suis proteome. To refine the set of candidates, we looked at proteins that are highly expressed in merozoites and specific to apicomplexans. The stringent set of candidates included 220 proteins, among which were 152 proteins with unknown function, 17 surface antigens of the SAG and SRS gene families, 12 proteins of the apicomplexan-specific secretory organelles including AMA1, MIC6, MIC13, ROP6, ROP12, ROP27, ROP32 and three proteins related to cell adhesion. Finally, we demonstrated in vitro the immunogenic potential of a C. suis-specific 42kDa transmembrane protein, which might constitute an attractive candidate for further testing.
针对原生动物寄生虫开发疫苗仍然具有挑战性,部分原因是这些真核生物与宿主免疫系统之间存在复杂的相互作用。反向疫苗学是一种有前景的方法,可直接筛选基因组序列组装体以寻找新的疫苗候选蛋白。在此,我们将这种模式应用于猪等孢球虫,这是一种顶复门寄生虫,可导致哺乳仔猪肠炎和腹泻,并在全球养猪生产中造成经济损失。我们使用下一代测序技术为猪等孢球虫基因组生成了一个约84Mb的序列组装体,使其成为等孢球虫属的首个可用参考序列。然后,我们对11000多个蛋白质编码基因进行了人工整理注释,并应用Vacceed工具通过筛选预测的猪等孢球虫蛋白质组来鉴定1168个疫苗候选物。为了优化候选物集,我们研究了在裂殖子中高表达且顶复门特异性的蛋白质。严格筛选后的候选物集包括220种蛋白质,其中有152种功能未知的蛋白质、SAG和SRS基因家族的17种表面抗原、顶复门特异性分泌细胞器的12种蛋白质,包括AMA1、MIC6、MIC13、ROP6、ROP12、ROP27、ROP32以及三种与细胞黏附相关的蛋白质。最后,我们在体外证明了一种猪等孢球虫特异性42kDa跨膜蛋白的免疫原性潜力,它可能是进一步测试的有吸引力的候选物。