Comparative analysis of cysteine proteases reveals gene family evolution of the group 1 allergens in astigmatic mites
Issued Date
2023-12-01
Resource Type
eISSN
20457022
Scopus ID
2-s2.0-85179698976
Journal Title
Clinical and Translational Allergy
Volume
13
Issue
12
Rights Holder(s)
SCOPUS
Bibliographic Citation
Clinical and Translational Allergy Vol.13 No.12 (2023)
Suggested Citation
Shi L., Xiong Q., Ao F.K., Wan T.Y., Xiao X., Liu X., Sun B., Tungtrongchitr A., Leung T.F., Tsui S.K.W. Comparative analysis of cysteine proteases reveals gene family evolution of the group 1 allergens in astigmatic mites. Clinical and Translational Allergy Vol.13 No.12 (2023). doi:10.1002/clt2.12324 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/95512
Title
Comparative analysis of cysteine proteases reveals gene family evolution of the group 1 allergens in astigmatic mites
Corresponding Author(s)
Other Contributor(s)
Abstract
Background: Astigmatic mites contain potent allergens that can trigger IgE-mediated immune responses, leading to allergic diseases such as asthma, allergic rhinitis and atopic dermatitis. In house dust mites Dermatophagoides pteronyssinus and Dermatophagoides farinae, group 1 allergens (Der p 1 and Der f 1), characterized as papain-like cysteine proteases, have been defined as the major allergens that have high prevalence and potency. Previous studies of mite group 1 allergens mainly focused on identification, comparison of sequence and structure, as well as the investigation of cross-reactivity. To achieve a comprehensive view of mite group 1 allergens, we performed a comparative genomic analysis of all the cysteine proteases in six astigmatic mite species to elucidate the evolutionary relationships of group 1 allergens. Methods: Based on the high-quality and annotated genomes, all the cysteine proteases in six astigmatic mite species were identified by sequence homology search. The phylogenetic relationships, gene synteny and expression levels were revealed by bioinformatic tools. The allergenicity of recombinant cysteine proteases was evaluated by enzyme-linked immunosorbent assay. Results: Tandem duplication was revealed as the major feature of cysteine protease gene evolution in astigmatic mites. The high IgE-binding capacity and the significant expression level of the cysteine protease DP_007902.01 suggested its potential as a novel group 1 allergen of D. pteronyssinus. In addition, gene decay events were identified in the skin-burrowing parasitic mite Sarcoptes scabiei. Conclusion: This comprehensive analysis provided insights into the evolution of cysteine proteases, as well as the component-resolved diagnosis of mite allergies.