Department of Veterinary Biosciences, Melbourne Veterinary School, The University of Melbourne, Parkville, VIC, 3010, Australia.
Parasit Vectors. 2019 Apr 29;12(1):187. doi: 10.1186/s13071-019-3419-6.
Signalling pathways have been extensively investigated in the free-living nematode Caenorhabditis elegans, but very little is known about these pathways in parasitic nematodes. Here, we constructed a model for the dauer-associated signalling pathways in an economically highly significant parasitic worm, Haemonchus contortus.
Guided by data and information available for C. elegans, we used extensive genomic and transcriptomic datasets to infer gene homologues in the dauer-associated pathways, explore developmental transcriptomic, proteomic and phosphoproteomic profiles in H. contortus and study selected molecular structures.
The canonical cyclic guanosine monophosphate (cGMP), transforming growth factor-β (TGF-β), insulin-like growth factor 1 (IGF-1) and steroid hormone signalling pathways of H. contortus were inferred to represent a total of 61 gene homologues. Compared with C. elegans, H. contortus has a reduced set of genes encoding insulin-like peptides, implying evolutionary and biological divergences between the parasitic and free-living nematodes. Similar transcription profiles were found for all gene homologues between the infective stage of H. contortus and dauer stage of C. elegans. High transcriptional levels for genes encoding G protein-coupled receptors (GPCRs), TGF-β, insulin-like ligands (e.g. ins-1, ins-17 and ins-18) and transcriptional factors (e.g. daf-16) in the infective L3 stage of H. contortus were suggestive of critical functional roles in this stage. Conspicuous protein expression patterns and extensive phosphorylation of some components of these pathways suggested marked post-translational modifications also in the L3 stage. The high structural similarity in the DAF-12 ligand binding domain among nematodes indicated functional conservation in steroid (i.e. dafachronic acid) signalling linked to worm development.
Taken together, this pathway model provides a basis to explore hypotheses regarding biological processes and regulatory mechanisms (via particular microRNAs, phosphorylation events and/or lipids) associated with the development of H. contortus and related nematodes as well as parasite-host cross talk, which could aid the discovery of new therapeutic targets.
信号通路在自由生活的线虫秀丽隐杆线虫中得到了广泛研究,但对于寄生线虫中的这些通路知之甚少。在这里,我们构建了一个经济上非常重要的寄生蠕虫旋毛虫 dauer 相关信号通路的模型。
根据秀丽隐杆线虫的数据和信息,我们使用广泛的基因组和转录组数据集来推断 dauer 相关通路中的基因同源物,探索旋毛虫的发育转录组、蛋白质组和磷酸化蛋白质组谱,并研究选定的分子结构。
我们推断旋毛虫的经典环鸟苷酸 (cGMP)、转化生长因子-β (TGF-β)、胰岛素样生长因子 1 (IGF-1) 和类固醇激素信号通路代表了总共 61 个基因同源物。与秀丽隐杆线虫相比,旋毛虫具有一组减少的胰岛素样肽编码基因,这表明寄生和自由生活线虫之间存在进化和生物学差异。在旋毛虫的感染阶段和秀丽隐杆线虫的 dauer 阶段之间,所有基因同源物的转录谱都相似。在旋毛虫的感染 L3 阶段,编码 G 蛋白偶联受体 (GPCR)、TGF-β、胰岛素样配体 (如 ins-1、ins-17 和 ins-18) 和转录因子 (如 daf-16) 的基因具有高转录水平,表明它们在该阶段具有关键的功能作用。这些通路中一些成分的显著蛋白表达模式和广泛磷酸化表明,在 L3 阶段也存在显著的翻译后修饰。线虫中 DAF-12 配体结合域的高结构相似性表明,与蠕虫发育相关的类固醇(即达法库林酸)信号传导的功能保守性。
综上所述,该通路模型为探索与旋毛虫和相关线虫发育以及寄生虫-宿主相互作用相关的生物学过程和调节机制(通过特定的 microRNAs、磷酸化事件和/或脂质)的假设提供了基础,这可能有助于发现新的治疗靶点。