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The draft genome, transcriptome, and microbiome of Dermatophagoides farinae reveal a broad spectrum of dust mite allergens

机译:粉尘螨(Dermatophagoides farinae)的基因组,转录组和微生物组草案揭示了广谱的尘螨过敏原

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摘要

© 2014 The Authors. Published by Elsevier Inc. Background A sequenced house dust mite (HDM) genome would advance our understanding of HDM allergens, a common cause of human allergies. Objective We sought to produce an annotated Dermatophagoides farinae draft genome and develop a combined genomic-transcriptomic-proteomic approach for elucidation of HDM allergens. Methods A D farinae draft genome and transcriptome were assembled with high-throughput sequencing, accommodating microbiome sequences. The allergen gene structures were validated by means of Sanger sequencing. The mite's microbiome composition was determined, and the predominant genus was validated immunohistochemically. The allergenicity of a ubiquinol-cytochrome c reductase binding protein homologue was evaluated with immunoblotting, immunosorbent assays, and skin prick tests. Results The full gene structures of 20 canonical allergens and 7 noncanonical allergen homologues were produced. A novel major allergen, ubiquinol-cytochrome c reductase binding protein-like protein, was found and designated Der f 24. All 40 sera samples from patients with mite allergy had IgE antibodies against rDer f 24. Of 10 patients tested, 5 had positive skin reactions. The predominant bacterial genus among 100 identified species was Enterobacter (63.4%). An intron was found in the 13.8-kDa D farinae bacteriolytic enzyme gene, indicating that it is of HDM origin. The Kyoto Encyclopedia of Genes and Genomes pathway analysis revealed a phototransduction pathway in D farinae, as well as thiamine and amino acid synthesis pathways, which is suggestive of an endosymbiotic relationship between D farinae and its microbiome. Conclusion An HDM genome draft produced from genomic, transcriptomic, and proteomic experiments revealed allergen genes and a diverse endosymbiotic microbiome, providing a tool for further identification and characterization of HDM allergens and development of diagnostics and immunotherapeutic vaccines.
机译:©2014作者。背景房尘螨(HDM)测序基因组将加深我们对人类过敏的常见病因-HDM过敏原的理解。目的我们试图产生一种带注释的粉红色皮肤癣菌的基因组草图,并开发出一种结合基因组-转录组-蛋白质组学的方法来阐明HDM过敏原。方法采用高通量测序技术组装D farinae草案基因组和转录组,以容纳微生物组序列。过敏原基因结构通过Sanger测序验证。确定了螨的微生物组组成,并对主要属进行了免疫组织化学验证。通过免疫印迹,免疫吸附测定和皮肤点刺试验评估了泛醇-细胞色素C还原酶结合蛋白同源物的变应原性。结果产生了20个典型变应原和7个非典型变应原同系物的完整基因结构。发现了一种新的主​​要过敏原,即泛醇-细胞色素C还原酶结合蛋白样蛋白,命名为Der f24。来自螨虫过敏患者的所有40份血清样品均具有针对rDer f 24的IgE抗体。在测试的10例患者中,有5例皮肤阳性反应。在100个已鉴定物种中,细菌属最主要的是肠杆菌(63.4%)。在13.8-kDa D farinae细菌分解酶基因中发现了一个内含子,表明它是HDM来源。 《京都议定书》的基因和基因组百科全书通路分析揭示了D粉菌的光转导途径以及硫胺素和氨基酸合成途径,这表明D粉菌与其微生物组之间存在共生关系。结论通过基因组,转录组和蛋白质组学实验产生的HDM基因组草图揭示了过敏原基因和多种内共生微生物组,为进一步鉴定和表征HDM过敏原以及开发诊断和免疫治疗疫苗提供了工具。

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