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Rhipicephalus microplus serine protease inhibitor family: annotation, expression and functional characterisation assessment
BACKGROUND: Rhipicephalus (Boophilus) microplus evades the host’s haemostatic system through a complex protein array secreted into tick saliva. Serine protease inhibitors (serpins) conform an important component of saliva which are represented by a large protease inhibitor family in Ixodidae. These...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4322644/ https://www.ncbi.nlm.nih.gov/pubmed/25564202 http://dx.doi.org/10.1186/s13071-014-0605-4 |
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author | Rodriguez-Valle, Manuel Xu, Tao Kurscheid, Sebastian Lew-Tabor, Ala E |
author_facet | Rodriguez-Valle, Manuel Xu, Tao Kurscheid, Sebastian Lew-Tabor, Ala E |
author_sort | Rodriguez-Valle, Manuel |
collection | PubMed |
description | BACKGROUND: Rhipicephalus (Boophilus) microplus evades the host’s haemostatic system through a complex protein array secreted into tick saliva. Serine protease inhibitors (serpins) conform an important component of saliva which are represented by a large protease inhibitor family in Ixodidae. These secreted and non-secreted inhibitors modulate diverse and essential proteases involved in different physiological processes. METHODS: The identification of R. microplus serpin sequences was performed through a web-based bioinformatics environment called Yabi. The database search was conducted on BmiGi V1, BmiGi V2.1, five SSH libraries, Australian tick transcriptome libraries and RmiTR V1 using bioinformatics methods. Semi quantitative PCR was carried out using different adult tissues and tick development stages. The cDNA of four identified R. microplus serpins were cloned and expressed in Pichia pastoris in order to determine biological targets of these serpins utilising protease inhibition assays. RESULTS: A total of four out of twenty-two serpins identified in our analysis are new R. microplus serpins which were named as RmS-19 to RmS-22. The analyses of DNA and predicted amino acid sequences showed high conservation of the R. microplus serpin sequences. The expression data suggested ubiquitous expression of RmS except for RmS-6 and RmS-14 that were expressed only in nymphs and adult female ovaries, respectively. RmS-19, and -20 were expressed in all tissues samples analysed showing their important role in both parasitic and non-parasitic stages of R. microplus development. RmS-21 was not detected in ovaries and RmS-22 was not identified in ovary and nymph samples but were expressed in the rest of the samples analysed. A total of four expressed recombinant serpins showed protease specific inhibition for Chymotrypsin (RmS-1 and RmS-6), Chymotrypsin / Elastase (RmS-3) and Thrombin (RmS-15). CONCLUSION: This study constitutes an important contribution and improvement to the knowledge about the physiologic role of R. microplus serpins during the host-tick interaction. |
format | Online Article Text |
id | pubmed-4322644 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43226442015-02-11 Rhipicephalus microplus serine protease inhibitor family: annotation, expression and functional characterisation assessment Rodriguez-Valle, Manuel Xu, Tao Kurscheid, Sebastian Lew-Tabor, Ala E Parasit Vectors Research BACKGROUND: Rhipicephalus (Boophilus) microplus evades the host’s haemostatic system through a complex protein array secreted into tick saliva. Serine protease inhibitors (serpins) conform an important component of saliva which are represented by a large protease inhibitor family in Ixodidae. These secreted and non-secreted inhibitors modulate diverse and essential proteases involved in different physiological processes. METHODS: The identification of R. microplus serpin sequences was performed through a web-based bioinformatics environment called Yabi. The database search was conducted on BmiGi V1, BmiGi V2.1, five SSH libraries, Australian tick transcriptome libraries and RmiTR V1 using bioinformatics methods. Semi quantitative PCR was carried out using different adult tissues and tick development stages. The cDNA of four identified R. microplus serpins were cloned and expressed in Pichia pastoris in order to determine biological targets of these serpins utilising protease inhibition assays. RESULTS: A total of four out of twenty-two serpins identified in our analysis are new R. microplus serpins which were named as RmS-19 to RmS-22. The analyses of DNA and predicted amino acid sequences showed high conservation of the R. microplus serpin sequences. The expression data suggested ubiquitous expression of RmS except for RmS-6 and RmS-14 that were expressed only in nymphs and adult female ovaries, respectively. RmS-19, and -20 were expressed in all tissues samples analysed showing their important role in both parasitic and non-parasitic stages of R. microplus development. RmS-21 was not detected in ovaries and RmS-22 was not identified in ovary and nymph samples but were expressed in the rest of the samples analysed. A total of four expressed recombinant serpins showed protease specific inhibition for Chymotrypsin (RmS-1 and RmS-6), Chymotrypsin / Elastase (RmS-3) and Thrombin (RmS-15). CONCLUSION: This study constitutes an important contribution and improvement to the knowledge about the physiologic role of R. microplus serpins during the host-tick interaction. BioMed Central 2015-01-07 /pmc/articles/PMC4322644/ /pubmed/25564202 http://dx.doi.org/10.1186/s13071-014-0605-4 Text en © Rodriguez-Valle et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Rodriguez-Valle, Manuel Xu, Tao Kurscheid, Sebastian Lew-Tabor, Ala E Rhipicephalus microplus serine protease inhibitor family: annotation, expression and functional characterisation assessment |
title | Rhipicephalus microplus serine protease inhibitor family: annotation, expression and functional characterisation assessment |
title_full | Rhipicephalus microplus serine protease inhibitor family: annotation, expression and functional characterisation assessment |
title_fullStr | Rhipicephalus microplus serine protease inhibitor family: annotation, expression and functional characterisation assessment |
title_full_unstemmed | Rhipicephalus microplus serine protease inhibitor family: annotation, expression and functional characterisation assessment |
title_short | Rhipicephalus microplus serine protease inhibitor family: annotation, expression and functional characterisation assessment |
title_sort | rhipicephalus microplus serine protease inhibitor family: annotation, expression and functional characterisation assessment |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4322644/ https://www.ncbi.nlm.nih.gov/pubmed/25564202 http://dx.doi.org/10.1186/s13071-014-0605-4 |
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