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Understanding the evolutionary structural variability and target specificity of tick salivary Kunitz peptides using next generation transcriptome data
BACKGROUND: Ticks are blood-sucking arthropods and a primary function of tick salivary proteins is to counteract the host’s immune response. Tick salivary Kunitz-domain proteins perform multiple functions within the feeding lesion and have been classified as venoms; thereby, constituting them as one...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3890586/ https://www.ncbi.nlm.nih.gov/pubmed/24397261 http://dx.doi.org/10.1186/1471-2148-14-4 |
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author | Schwarz, Alexandra Cabezas-Cruz, Alejandro Kopecký, Jan Valdés, James J |
author_facet | Schwarz, Alexandra Cabezas-Cruz, Alejandro Kopecký, Jan Valdés, James J |
author_sort | Schwarz, Alexandra |
collection | PubMed |
description | BACKGROUND: Ticks are blood-sucking arthropods and a primary function of tick salivary proteins is to counteract the host’s immune response. Tick salivary Kunitz-domain proteins perform multiple functions within the feeding lesion and have been classified as venoms; thereby, constituting them as one of the important elements in the arms race with the host. The two main mechanisms advocated to explain the functional heterogeneity of tick salivary Kunitz-domain proteins are gene sharing and gene duplication. Both do not, however, elucidate the evolution of the Kunitz family in ticks from a structural dynamic point of view. The Red Queen hypothesis offers a fruitful theoretical framework to give a dynamic explanation for host-parasite interactions. Using the recent salivary gland Ixodes ricinus transcriptome we analyze, for the first time, single Kunitz-domain encoding transcripts by means of computational, structural bioinformatics and phylogenetic approaches to improve our understanding of the structural evolution of this important multigenic protein family. RESULTS: Organizing the I. ricinus single Kunitz-domain peptides based on their cysteine motif allowed us to specify a putative target and to relate this target specificity to Illumina transcript reads during tick feeding. We observe that several of these Kunitz peptide groups vary in their translated amino acid sequence, secondary structure, antigenicity, and intrinsic disorder, and that the majority of these groups are subject to a purifying (negative) selection. We finalize by describing the evolution and emergence of these Kunitz peptides. The overall interpretation of our analyses discloses a rapidly emerging Kunitz group with a distinct disulfide bond pattern from the I. ricinus salivary gland transcriptome. CONCLUSIONS: We propose a model to explain the structural and functional evolution of tick salivary Kunitz peptides that we call target-oriented evolution. Our study reveals that combining analytical approaches (transcriptomes, computational, bioinformatics and phylogenetics) improves our understanding of the biological functions of important salivary gland mediators during tick feeding. |
format | Online Article Text |
id | pubmed-3890586 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38905862014-01-23 Understanding the evolutionary structural variability and target specificity of tick salivary Kunitz peptides using next generation transcriptome data Schwarz, Alexandra Cabezas-Cruz, Alejandro Kopecký, Jan Valdés, James J BMC Evol Biol Research Article BACKGROUND: Ticks are blood-sucking arthropods and a primary function of tick salivary proteins is to counteract the host’s immune response. Tick salivary Kunitz-domain proteins perform multiple functions within the feeding lesion and have been classified as venoms; thereby, constituting them as one of the important elements in the arms race with the host. The two main mechanisms advocated to explain the functional heterogeneity of tick salivary Kunitz-domain proteins are gene sharing and gene duplication. Both do not, however, elucidate the evolution of the Kunitz family in ticks from a structural dynamic point of view. The Red Queen hypothesis offers a fruitful theoretical framework to give a dynamic explanation for host-parasite interactions. Using the recent salivary gland Ixodes ricinus transcriptome we analyze, for the first time, single Kunitz-domain encoding transcripts by means of computational, structural bioinformatics and phylogenetic approaches to improve our understanding of the structural evolution of this important multigenic protein family. RESULTS: Organizing the I. ricinus single Kunitz-domain peptides based on their cysteine motif allowed us to specify a putative target and to relate this target specificity to Illumina transcript reads during tick feeding. We observe that several of these Kunitz peptide groups vary in their translated amino acid sequence, secondary structure, antigenicity, and intrinsic disorder, and that the majority of these groups are subject to a purifying (negative) selection. We finalize by describing the evolution and emergence of these Kunitz peptides. The overall interpretation of our analyses discloses a rapidly emerging Kunitz group with a distinct disulfide bond pattern from the I. ricinus salivary gland transcriptome. CONCLUSIONS: We propose a model to explain the structural and functional evolution of tick salivary Kunitz peptides that we call target-oriented evolution. Our study reveals that combining analytical approaches (transcriptomes, computational, bioinformatics and phylogenetics) improves our understanding of the biological functions of important salivary gland mediators during tick feeding. BioMed Central 2014-01-07 /pmc/articles/PMC3890586/ /pubmed/24397261 http://dx.doi.org/10.1186/1471-2148-14-4 Text en Copyright © 2014 Schwarz et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Schwarz, Alexandra Cabezas-Cruz, Alejandro Kopecký, Jan Valdés, James J Understanding the evolutionary structural variability and target specificity of tick salivary Kunitz peptides using next generation transcriptome data |
title | Understanding the evolutionary structural variability and target specificity of tick salivary Kunitz peptides using next generation transcriptome data |
title_full | Understanding the evolutionary structural variability and target specificity of tick salivary Kunitz peptides using next generation transcriptome data |
title_fullStr | Understanding the evolutionary structural variability and target specificity of tick salivary Kunitz peptides using next generation transcriptome data |
title_full_unstemmed | Understanding the evolutionary structural variability and target specificity of tick salivary Kunitz peptides using next generation transcriptome data |
title_short | Understanding the evolutionary structural variability and target specificity of tick salivary Kunitz peptides using next generation transcriptome data |
title_sort | understanding the evolutionary structural variability and target specificity of tick salivary kunitz peptides using next generation transcriptome data |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3890586/ https://www.ncbi.nlm.nih.gov/pubmed/24397261 http://dx.doi.org/10.1186/1471-2148-14-4 |
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