Wong Yide, Rosa Bruce A, Becker Luke, Camberis Mali, LeGros Graham, Zhan Bin, Bottazzi Maria Elena, Fujiwara Ricardo T, Ritmejeryte Edita, Laha Thewarach, Chaiyadet Sujittra, Taweethavonsawat Piyanan, Brindley Paul J, Bracken Bethany K, Giacomin Paul R, Mitreva Makedonka, Loukas Alex
Australian Institute of Tropical Health and Medicine, James Cook University, Cairns, Australia.
Centre for Tropical Bioinformatics and Molecular Biology, James Cook University, Cairns, Australia.
PLoS Negl Trop Dis. 2025 Jan 20;19(1):e0012780. doi: 10.1371/journal.pntd.0012780. eCollection 2025 Jan.
More than 470 million people globally are infected with the hookworms Ancylostoma ceylanicum and Necator americanus, resulting in an annual loss of 2.1 to 4 million disability-adjusted-life-years. Current infection management approaches are limited by modest drug efficacy, the costs associated with frequent mass drug administration campaigns, and the risk of reinfection and burgeoning drug resistance. Subunit vaccines based on proteins excreted and secreted (ES) by hookworms that reduce worm numbers and associated disease burden are a promising management strategy to overcome these limitations. However, studies on the ES proteomes of hookworms have mainly described proteins from the adult life stage which may preclude the opportunity to target the infective larva. Here, we employed high resolution mass spectrometry to identify 103 and 57 ES proteins from the infective third larvae stage (L3) as well as 106 and 512 ES proteins from the adult N. americanus and A. ceylanicum respectively. Comparisons between these developmental stages identified 91 and 41 proteins uniquely expressed in the L3 ES products of N. americanus and A. ceylanicum, respectively. We characterized these proteins based on functional annotation, KEGG pathway analysis, InterProScan signature and gene ontology. We also performed reciprocal BLAST analysis to identify orthologs across species for both the L3 and adult stages and identified five orthologous proteins in both life stages and 15 proteins that could be detected only in the L3 stage of both species. Last, we performed a three-way reciprocal BLAST on the L3 proteomes from both hookworm species together with a previously reported L3 proteome from the rodent hookworm Nippostrongylus brasiliensis, and identified eight L3 proteins that could be readily deployed for testing using well established rodent models. This novel characterization of L3 proteins and taxonomic conservation across hookworm species provides a raft of potential candidates for vaccine discovery for prevention of hookworm infection and disease.
全球有超过4.7亿人感染了钩虫锡兰钩虫和美洲板口线虫,导致每年损失210万至400万个伤残调整生命年。当前的感染管理方法受到药物疗效一般、频繁开展大规模药物给药运动的成本以及再感染风险和耐药性不断增加的限制。基于钩虫排泄和分泌(ES)蛋白的亚单位疫苗可以减少虫体数量和相关疾病负担,是克服这些限制的一种有前景的管理策略。然而,关于钩虫ES蛋白质组的研究主要描述了成虫阶段的蛋白质,这可能会错过针对感染性幼虫的机会。在这里,我们采用高分辨率质谱法分别从感染性第三幼虫期(L3)鉴定出103种和57种ES蛋白,以及从美洲板口线虫成虫和锡兰钩虫成虫中分别鉴定出106种和512种ES蛋白。这些发育阶段之间的比较分别确定了在美洲板口线虫和锡兰钩虫的L3 ES产物中独特表达的91种和41种蛋白质。我们基于功能注释、KEGG通路分析、InterProScan特征和基因本体对这些蛋白质进行了表征。我们还进行了双向BLAST分析,以鉴定L3期和成虫期跨物种的直系同源物,并在两个生命阶段鉴定出5种直系同源蛋白,以及仅在两个物种的L3期可检测到的15种蛋白。最后,我们对两种钩虫物种的L3蛋白质组与先前报道的巴西日圆线虫的L3蛋白质组进行了三方双向BLAST,并鉴定出8种L3蛋白,这些蛋白可以很容易地用于使用成熟的啮齿动物模型进行测试。这种对L3蛋白的新表征以及钩虫物种间的分类学保守性为预防钩虫感染和疾病的疫苗发现提供了大量潜在候选物。