应用多组学方法预测热带性Blomia过敏原

IF 4.6 2区 医学 Q2 ALLERGY
Jan Hubert, Susanne Vrtala, Bruno Sopko, Scot E. Dowd, Qixin He, Pavel B. Klimov, Karel Harant, Pavel Talacko, Tomas Erban
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引用次数: 0

摘要

背景热带圆蚧是热带和亚热带地区的主要致敏源。尽管这种螨在医学上具有重要意义,但其致敏性尚未得到充分研究。到目前为止,在热带B.tropicalis中仅鉴定出14个过敏原组,尽管早期的放射免疫电泳技术(27种未表征的过敏原复合物)和基于40种由世界卫生组织(世界卫生组织)/IUIS正式认可的过敏原组的比较数据表明存在大量额外的过敏原。方法在这里,我们采用多组学方法,利用基因组和转录组序列数据评估热带双歧杆菌的致敏组,并进行高灵敏度的蛋白质丰度定量。结果在14个已知过敏原组中,我们确认了13个(未发现一个世界卫生组织/IUIS过敏原,Blo t 19),并根据序列相似性确定了16个潜在的新过敏原。这些数据表明热带B.tropicalis与焦纹屋尘螨(Dermachopoides属)共有27个已知/推断的过敏原组。在这些组中,有五个过敏原编码基因在转录物水平上高度表达:印迹1、印迹5、印迹21(已知)、印迹15和印迹18(预测)。然而,在蛋白质水平上,发现了一组不同的最丰富的过敏原:印迹2、10、11、20和21(螨体)或印迹3、4、6,并预测印迹13、14和36(螨粪)。解释我们报告了使用综合组学方法来识别和预测一系列螨类过敏原,并使用先进的无标记蛋白质组学来确定过敏原蛋白丰度。我们的研究确定了一大组新的假定过敏原,并表明过敏原编码基因的表达水平可能与螨体内实际的致敏蛋白丰度没有严格相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Predicting Blomia tropicalis allergens using a multiomics approach

Predicting Blomia tropicalis allergens using a multiomics approach

Background

The domestic mite Blomia tropicalis is a major source of allergens in tropical and subtropical regions. Despite its great medical importance, the allergome of this mite has not been sufficiently studied. Only 14 allergen groups have been identified in B. tropicalis thus far, even though early radioimmunoelectrophoresis techniques (27 uncharacterized allergen complexes) and comparative data based on 40 allergen groups officially recognized by the World Health Organization (WHO)/IUIS in domestic astigmatid mites suggest the presence of a large set of additional allergens.

Methods

Here, we employ a multiomics approach to assess the allergome of B. tropicalis using genomic and transcriptomic sequence data and perform highly sensitive protein abundance quantification.

Findings

Among the 14 known allergen groups, we confirmed 13 (one WHO/IUIS allergen, Blo t 19, was not found) and identified 16 potentially novel allergens based on sequence similarity. These data indicate that B. tropicalis shares 27 known/deduced allergen groups with pyroglyphid house dust mites (genus Dermatophagoides). Among these groups, five allergen-encoding genes are highly expressed at the transcript level: Blo t 1, Blo t 5, Blo t 21 (known), Blo t 15, and Blo t 18 (predicted). However, at the protein level, a different set of most abundant allergens was found: Blo t 2, 10, 11, 20 and 21 (mite bodies) or Blo t 3, 4, 6 and predicted Blo t 13, 14 and 36 (mite feces).

Interpretation

We report the use of an integrated omics method to identify and predict an array of mite allergens and advanced, label-free proteomics to determine allergen protein abundance. Our research identifies a large set of novel putative allergens and shows that the expression levels of allergen-encoding genes may not be strictly correlated with the actual allergenic protein abundance in mite bodies.

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来源期刊
Clinical and Translational Allergy
Clinical and Translational Allergy Immunology and Microbiology-Immunology
CiteScore
7.50
自引率
4.50%
发文量
117
审稿时长
12 weeks
期刊介绍: Clinical and Translational Allergy, one of several journals in the portfolio of the European Academy of Allergy and Clinical Immunology, provides a platform for the dissemination of allergy research and reviews, as well as EAACI position papers, task force reports and guidelines, amongst an international scientific audience. Clinical and Translational Allergy accepts clinical and translational research in the following areas and other related topics: asthma, rhinitis, rhinosinusitis, drug hypersensitivity, allergic conjunctivitis, allergic skin diseases, atopic eczema, urticaria, angioedema, venom hypersensitivity, anaphylaxis, food allergy, immunotherapy, immune modulators and biologics, animal models of allergic disease, immune mechanisms, or any other topic related to allergic disease.
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