RNA viruses alter house dust mite physiology and allergen production with no detected consequences for allergenicity

被引:3
作者
Vidal-Quist, Jose Cristian [1 ,8 ]
Declercq, Jozefien [2 ,3 ]
Vanhee, Stijn [2 ,3 ]
Lambrecht, Bart N. [2 ,3 ]
Gomez-Rial, Jose [4 ]
Vidal, Carmen [5 ]
Aydogdu, Eylem [6 ,7 ]
Rombauts, Stephane [6 ,7 ]
Hernandez-Crespo, Pedro [1 ]
机构
[1] Ctr Invest Biol Margarita Salas CIB, Dept Biotecnol Microbiana & Plantas, Entomol Aplicada Agr & Salud, CSIC, Madrid, Spain
[2] VIB Ctr Inflammat Res, Lab Immunoregulat & Mucosal Immunol, Ghent, Belgium
[3] Univ Ghent, Dept Internal Med & Pediat, Ghent, Belgium
[4] Complejo Hosp Univ Santiago, Un Inmunol, Lab Inmunogenet, Santiago De Compostela, Spain
[5] Complejo Hosp Univ Santiago, Serv Alergol, Santiago De Compostela, Spain
[6] Ctr Plant Syst Biol VIB, Ghent, Belgium
[7] Univ Ghent, Dept Plant Biotechnol & Bioinformat, Ghent, Belgium
[8] Ctr InvestigacionesBiol Margarita Salas CIB, Dept Biotecnol Microbiana Yde Plantas, Entomol Aplicada Agr & Salud, CSIC, Ramirode Maeztu 9, Madrid 28040, Spain
基金
欧洲研究理事会;
关键词
allergen; Dermatophagoides; house dust mites; physiology; RNA virus; DERMATOPHAGOIDES-PTERONYSSINUS; FARINAE; IDENTIFICATION; MECHANISMS; EXPRESSION; DIVERSITY; REVEALS; DEFENSE; UPDATE; GUT;
D O I
10.1111/imb.12822
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
RNA viruses have recently been detected in association with house dust mites, including laboratory cultures, dust samples, and mite-derived pharmaceuticals used for allergy diagnosis. This study aimed to assess the incidence of viral infection on Dermatophagoides pteronyssinus physiology and on the allergenic performance of extracts derived from its culture. Transcriptional changes between genetically identical control and virus-infected mite colonies were analysed by RNAseq with the support of a new D. pteronyssinus high-quality annotated genome (56.8 Mb, 108 scaffolds, N50 = 2.73 Mb, 96.7% BUSCO-completeness). Extracts of cultures and bodies from both colonies were compared by inspecting major allergen accumulation by enzyme-linked immunosorbent assay (ELISA), allergen-related enzymatic activities by specific assays, airway inflammation in a mouse model of allergic asthma, and binding to allergic patient's sera IgE by ImmunoCAP. Viral infection induced a significant transcriptional response, including several immunity and stress-response genes, and affected the expression of seven allergens, putative isoallergens and allergen orthologs. Major allergens were unaffected except for Der p 23 that was upregulated, increasing ELISA titers up to 29% in infected-mite extracts. By contrast, serine protease allergens Der p 3, 6 and 9 were downregulated, being trypsin and chymotrypsin enzymatic activities reduced up to 21% in extracts. None of the parameters analysed in our mouse model, nor binding to human IgE were significantly different when comparing control and infected-mite extracts. Despite the described physiological impact of viral infection on the mites, no significant consequences for the allergenicity of derived extracts or their practical use in allergy diagnosis have been detected.
引用
收藏
页码:173 / 186
页数:14
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