Evangelista Francisco M D, van Vliet Arnoud H M, Lawton Scott P, Betson Martha
School of Veterinary Medicine, Faculty of Health and Medical Sciences, University of Surrey, Guildford, United Kingdom.
Centre for Epidemiology and Planetary Health, Department of Veterinary and Animal Sciences, Northern Faculty, Scotland's Rural University College (SRUC), An Lòchran, Inverness, United Kingdom.
Front Vet Sci. 2022 Nov 1;9:1014198. doi: 10.3389/fvets.2022.1014198. eCollection 2022.
Ascariasis is the most prevalent helminthic disease affecting both humans and pigs and is caused by the roundworms and . While preventive chemotherapy continues to be the most common control method, recent reports of anthelminthic resistance highlight the need for development of a vaccine against ascariasis. The aim of this study was to use a reverse vaccinology approach to identify potential vaccine candidates for . Three proteomes predicted from whole-genome sequences were analyzed. Candidate proteins were identified using open-access bioinformatic tools (e.g., Vacceed, VaxiJen, Bepipred 2.0) which test for different characteristics such as sub-cellular location, T-cell and B-cell molecular binding, antigenicity, allergenicity and phylogenetic relationship with other nematode proteins. From over 100,000 protein sequences analyzed, four transmembrane proteins were predicted to be non-allergen antigens and potential vaccine candidates. The four proteins are a Piezo protein, two voltage-dependent calcium channels and a protocadherin-like protein, are all expressed in either the muscle or ovaries of both species, and all contained high affinity epitopes for T-cells and B-cells. The use of a reverse vaccinology approach allowed the prediction of four new potential vaccination targets against ascariasis in humans and pigs. These targets can now be further tested in and assays to prove efficacy in both pigs and humans.
蛔虫病是影响人类和猪的最普遍的蠕虫病,由蛔虫引起。虽然预防性化疗仍然是最常见的控制方法,但最近关于抗蠕虫药耐药性的报道凸显了开发抗蛔虫病疫苗的必要性。本研究的目的是使用反向疫苗学方法来确定潜在的蛔虫病疫苗候选物。对从全基因组序列预测的三个蛋白质组进行了分析。使用开放获取的生物信息学工具(如Vacceed、VaxiJen、Bepipred 2.0)鉴定候选蛋白质,这些工具可检测不同特征,如亚细胞定位、T细胞和B细胞分子结合、抗原性、致敏性以及与其他线虫蛋白质的系统发育关系。在分析的超过100,000个蛋白质序列中,预测有四种跨膜蛋白为非变应原性抗原和潜在的疫苗候选物。这四种蛋白质分别是一种Piezo蛋白、两种电压依赖性钙通道和一种原钙黏蛋白样蛋白,它们均在两种蛔虫的肌肉或卵巢中表达,并且都含有T细胞和B细胞的高亲和力表位。使用反向疫苗学方法能够预测出针对人类和猪蛔虫病的四个新的潜在疫苗接种靶点。现在可以在猪和人体试验中进一步测试这些靶点,以证明其在猪和人类中的有效性。