Excretory-secretory products of the fish-borne parasite Anisakis simplex L3 larvae possess allergens and unusual glycan modifications.

IF 3.9 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Isabella Adduci, Xiaoxu Wang, Katharina Paschinger, Iain B H Wilson, Guofeng Cheng, Shi Yan
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引用次数: 0

Abstract

Anisakis simplex is a parasitic aquatic nematode, which may cause mild-to-severe gastrointestinal allergic reactions (anisakiasis) with clinical symptoms, such as rhinitis and urticaria, in humans who accidentally consume raw or undercooked marine products contaminated with infective L3 Anisakis larvae. Several Anisakis excretory-secretory (E/S) products and somatic proteins are known to be involved in IgE-mediated allergic reactions. In comparison with vertebrates, nematodes have a distinct machinery to glycosylate their proteins, and unusual glycan structures have been reported previously, many of which play immunogenic and immunomodulatory roles in host-parasite interactions. While an early study indicated that O-glycans participate in the cross-reactivity of antibodies in allergy patients to A. simplex somatic antigens, the N-glycosylation pattern of Anisakis and the potential role of N-glycans in allergic reactions remained unknown. The aim of the present study was to characterise N-glycans and the associated glycoproteins from Anisakis E/S products using mass spectrometry. We collected E/S products from larvae culture and released N-glycans from trypsinised proteins using PNGase Ar. Native glycans were pyridylaminated prior to HPLC separation and MALDI-TOF-MS/MS analysis. In addition, hydrofluoric acid and glycosidase digestions were performed to aid structural characterisation. MS data of 5 h and 24 h E/S products indicated the presence of pauci-mannose and core fucosylated N-glycans as major species; tri-fucosylated and methylated glycans as well as complex-type and phosphorylcholine-substituted glycans were also detected. In addition, E/S products were subject to proteomics analysis, which revealed a set of proteins with conserved domains associated with allergens. Our study provides the first insight into the N-glycosylation machinery of Anisakis and highlights the need for investigating whether and which N-glycans are indubitably involved in the modulation of allergic responses.

鱼媒寄生虫单一异尖线虫L3幼虫的排泄-分泌产物具有过敏原和不寻常的聚糖修饰。
单纯异尖线虫是一种水生寄生虫,意外食用被感染L3异尖线虫幼虫污染的生的或未煮熟的海产品,可引起轻度至重度胃肠道过敏反应(异尖线虫病),并伴有鼻炎和荨麻疹等临床症状。已知一些异尖线虫的排泄/分泌(E/S)产物和体细胞蛋白参与ige介导的过敏反应。与脊椎动物相比,线虫具有独特的蛋白质糖基化机制,并且以前报道过不寻常的聚糖结构,其中许多在宿主-寄生虫相互作用中起免疫原性和免疫调节作用。虽然早期的研究表明o -聚糖参与了过敏患者对单形单胞杆菌体细胞抗原抗体的交叉反应性,但异尖线虫的n -糖基化模式和n -聚糖在过敏反应中的潜在作用尚不清楚。本研究的目的是利用质谱法对异尖线虫E/S产物中的n -聚糖和相关糖蛋白进行表征。我们从幼虫培养中收集E/S产物,并使用PNGase Ar从胰蛋白酶化蛋白中释放n -聚糖。在HPLC分离和MALDI-TOF-MS/MS分析之前,对天然聚糖进行pyridylaminated。此外,氢氟酸和糖苷酶消化进行了帮助结构表征。5h和24h E/S产物的MS数据表明,主要存在低糖甘露糖和核心集中的n -聚糖;三聚焦化和甲基化聚糖以及络合物型和磷胆碱取代的聚糖也被检测到。此外,对E/S产物进行蛋白质组学分析,发现了一组与过敏原相关的保守结构域的蛋白质。我们的研究首次深入了解了异尖线虫的n -糖基化机制,并强调了研究n -聚糖是否以及哪些无疑参与了过敏反应的调节的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biochemical Journal
Biochemical Journal 生物-生化与分子生物学
CiteScore
8.00
自引率
0.00%
发文量
255
审稿时长
1 months
期刊介绍: Exploring the molecular mechanisms that underpin key biological processes, the Biochemical Journal is a leading bioscience journal publishing high-impact scientific research papers and reviews on the latest advances and new mechanistic concepts in the fields of biochemistry, cellular biosciences and molecular biology. The Journal and its Editorial Board are committed to publishing work that provides a significant advance to current understanding or mechanistic insights; studies that go beyond observational work using in vitro and/or in vivo approaches are welcomed. Painless publishing: All papers undergo a rigorous peer review process; however, the Editorial Board is committed to ensuring that, if revisions are recommended, extra experiments not necessary to the paper will not be asked for. Areas covered in the journal include: Cell biology Chemical biology Energy processes Gene expression and regulation Mechanisms of disease Metabolism Molecular structure and function Plant biology Signalling
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