Rosa Bruce A, Townsend Reid, Jasmer Douglas P, Mitreva Makedonka
From the ‡The Genome Institute, Washington University in St Louis, Missouri 63108;
§Department of Cell Biology & Physiology and Department of Medicine, Washington University School of Medicine, St. Louis, Missouri 63108;
Mol Cell Proteomics. 2015 Apr;14(4):812-27. doi: 10.1074/mcp.M114.046227. Epub 2015 Jan 21.
The parasitic nematode intestine is responsible for nutrient digestion and absorption, and many other processes essential for reproduction and survival, making it a valuable target for anthelmintic drug treatment. However, nematodes display extreme biological diversity (including occupying distinct trophic habitats), resulting in limited knowledge of intestinal cell/protein functions of fundamental or adaptive significance. We developed a perfusion model for isolating intestinal proteins in Ascaris suum (a parasite of humans and swine), allowing for the identification of over 1000 intestinal A. suum proteins (using mass spectrometry), which were assigned to several different intestinal cell compartments (intestinal tissue, the integral and peripheral intestinal membranes, and the intestinal lumen). A multi-omics analysis approach identified a large diversity of biological functions across intestinal compartments, based on both functional enrichment analysis (identifying terms related to detoxification, proteolysis, and host-parasite interactions) and regulatory binding sequence analysis to identify putatively active compartment-specific transcription factors (identifying many related to intestinal sex differentiation or lifespan regulation). Orthologs of A. suum proteins in 15 other nematodes species, five host species, and two outgroups were identified and analyzed. Different cellular compartments demonstrated markedly different levels of protein conservation; e.g. integral intestinal membrane proteins were the most conserved among nematodes (up to 96% conservation), whereas intestinal lumen proteins were the most diverse (only 6% conservation across all nematodes, and 71% with no host orthologs). Finally, this integrated multi-omics analysis identified conserved nematode-specific intestinal proteins likely performing essential functions (including V-type ATPases and ABC transporters), which may serve as promising anthelmintic drug or vaccine targets in future research. Collectively, the findings provide valuable new insights on conserved and adaptive features of nematode intestinal cells, membranes and the intestinal lumen, and potential targets for parasite treatment and control.
寄生线虫的肠道负责营养物质的消化和吸收,以及许多其他对繁殖和生存至关重要的过程,使其成为驱虫药物治疗的重要靶点。然而,线虫表现出极端的生物多样性(包括占据不同的营养栖息地),导致对具有基本或适应性意义的肠道细胞/蛋白质功能的了解有限。我们开发了一种灌注模型,用于分离猪蛔虫(一种人和猪的寄生虫)的肠道蛋白质,通过质谱鉴定出1000多种猪蛔虫肠道蛋白质,这些蛋白质被分配到几个不同的肠道细胞区室(肠道组织、完整和外周肠膜以及肠腔)。一种多组学分析方法基于功能富集分析(识别与解毒、蛋白水解和宿主-寄生虫相互作用相关的术语)和调控结合序列分析来识别假定活跃的区室特异性转录因子(识别许多与肠道性别分化或寿命调节相关的因子),确定了肠道各区间生物功能的巨大多样性。鉴定并分析了15种其他线虫物种、5种宿主物种和2个外群中猪蛔虫蛋白质的直系同源物。不同的细胞区室显示出明显不同的蛋白质保守水平;例如,肠膜整合蛋白在线虫中最保守(高达96%的保守性),而肠腔蛋白则最多样化(所有线虫中只有6%的保守性,71%没有宿主直系同源物)。最后,这种综合的多组学分析确定了可能执行基本功能的保守线虫特异性肠道蛋白质(包括V型ATP酶和ABC转运蛋白),这些蛋白质可能在未来研究中作为有前景的驱虫药物或疫苗靶点。总的来说,这些发现为线虫肠道细胞、膜和肠腔的保守和适应性特征以及寄生虫治疗和控制的潜在靶点提供了有价值的新见解。