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Rhipicephalus microplus serine protease inhibitor family: annotation, expression and functional characterisation assessment
- Source :
- Parasites and Vectors, vol. 8, pp. 7, Parasites & Vectors
- Publication Year :
- 2015
-
Abstract
- 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.
- Subjects :
- Nymph
Proteases
Serine Proteinase Inhibitors
genetic structures
medicine.medical_treatment
Serpin
Complementary DNA
parasitic diseases
medicine
Rhipicephalus
Animals
DNA/genetics
DNA/metabolism
Gene Expression Regulation/physiology
Peptide Hydrolases/metabolism
Rhipicephalus/genetics
Rhipicephalus/metabolism
Saliva/chemistry
Serine Proteinase Inhibitors/genetics
Serine Proteinase Inhibitors/metabolism
Amino Acid Sequence
Cloning, Molecular
Saliva
Cattle tick
Serine protease
Protease
Genome
biology
Base Sequence
Research
Ovary
fungi
serpin
DNA
biology.organism_classification
Molecular biology
Protease inhibitor (biology)
Infectious Diseases
Biochemistry
Protease inhibitor
Rhipicephalus microplus
Gene Expression Regulation
biology.protein
Female
Parasitology
human activities
medicine.drug
Peptide Hydrolases
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Journal :
- Parasites and Vectors, vol. 8, pp. 7, Parasites & Vectors
- Accession number :
- edsair.doi.dedup.....55a7ad40f5c0aef6f6c0c4a6ed1a0c37