Asnoussi Abdouslam, Aibinu Ibukun E, Gasser Robin B, Lopata Andreas L, Smooker Peter M
Biosciences & Food Technology, School of Science, RMIT University, Bundoora West Campus, PO Box 71, Bundoora, VIC, 3083, Australia.
Department of Veterinary Biosciences, Melbourne Veterinary School, Faculty of Veterinary and Agricultural Sciences, The University of Melbourne, Parkville, VIC, 3010, Australia.
Parasitol Res. 2017 Dec;116(12):3291-3301. doi: 10.1007/s00436-017-5642-4. Epub 2017 Oct 16.
Tropomyosin (TM) is a major allergen in shellfish, known to cross-react with mite, cockroach and/or some roundworm (nematode) TM. In this study, we aimed to express and purify TM from the parasitic nematode Anisakis pegreffii and also to characterise its cross-reactivity with TM from shellfish. A. pegreffii was isolated from the flathead tiger fish (Neoplatycephalus richardsoni) and characterised using single-strand conformation polymorphism (SSCP)-based sequencing of the first and second internal transcribed spacers (ITS-1 and ITS-2) of nuclear ribosomal DNA. The recombinant tropomyosin (rTM) of A. pegreffii was expressed, purified and confirmed by immunohistochemistry, sequencing and LC-MS/MS analyses. Immunohistochemistry showed the muscle and the base layer of the third-stage larvae (L3) of A. pegreffii as the location of TM in A. pegreffii. The molecular relationship of TM of A. pegreffii with homologs from other nematodes and crustaceans was inferred from phylogenetic analysis. Immunogenicity of TM from A. pegreffii was tested by immunoblotting, which showed that rTM from A. pegreffii binds to IgE from sera of patients with allergy to crustaceans. Immunoblotting also showed that the anti-TM monoclonal antibody (MAb) did not recognise rTM from A. pegreffii. The rTM from A. pegreffii was, however, recognised by anti-TM polyclonal antibodies (PAbs) as well as anti-crustacean polyclonal antibodies (PAbs). The detection of specific serum IgE antibody against parasite TM has been proposed as a useful approach for the diagnosis of parasite-induced allergy. The findings of this study merit further exploration of the cross-reactive allergenic proteins of Anisakis for improved, future diagnosis of allergenic diseases.
原肌球蛋白(TM)是贝类中的一种主要过敏原,已知它会与螨虫、蟑螂和/或某些蛔虫(线虫)的TM发生交叉反应。在本研究中,我们旨在表达和纯化来自寄生线虫派氏异尖线虫的TM,并表征其与贝类TM的交叉反应性。从扁头虎鱼(Neoplatycephalus richardsoni)中分离出派氏异尖线虫,并使用基于单链构象多态性(SSCP)的核糖体DNA第一和第二内部转录间隔区(ITS-1和ITS-2)测序对其进行表征。通过免疫组织化学、测序和液相色谱-串联质谱(LC-MS/MS)分析对派氏异尖线虫的重组原肌球蛋白(rTM)进行了表达、纯化和确认。免疫组织化学显示派氏异尖线虫第三期幼虫(L3)的肌肉和基底层是TM在派氏异尖线虫中的定位部位。通过系统发育分析推断了派氏异尖线虫TM与其他线虫和甲壳类动物同源物的分子关系。通过免疫印迹测试了派氏异尖线虫TM的免疫原性,结果表明派氏异尖线虫的rTM与对甲壳类动物过敏患者血清中的IgE结合。免疫印迹还显示抗TM单克隆抗体(MAb)不能识别派氏异尖线虫的rTM。然而,派氏异尖线虫的rTM可被抗TM多克隆抗体(PAbs)以及抗甲壳类动物多克隆抗体(PAbs)识别。检测针对寄生虫TM的特异性血清IgE抗体已被提议作为诊断寄生虫诱导过敏的一种有用方法。本研究结果值得进一步探索异尖线虫的交叉反应性过敏原蛋白,以改进未来过敏性疾病的诊断。