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Cloning and characterization of a mannose binding C-type lectin gene from salivary gland of Aedes albopictus
BACKGROUND: The studies on sialomes have shown that hematophagous mosquito saliva consists of a lot of pharmacologically active proteins, in which C-type lectins have been identified and regarded as an important component of saliva. The previous studies showed that C-type lectins play crucial roles...
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/PMC4223726/ https://www.ncbi.nlm.nih.gov/pubmed/25051984 http://dx.doi.org/10.1186/1756-3305-7-337 |
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author | Cheng, Jinzhi Wang, Yu Li, Fangzhan Liu, Jian Sun, Yu Wu, Jiahong |
author_facet | Cheng, Jinzhi Wang, Yu Li, Fangzhan Liu, Jian Sun, Yu Wu, Jiahong |
author_sort | Cheng, Jinzhi |
collection | PubMed |
description | BACKGROUND: The studies on sialomes have shown that hematophagous mosquito saliva consists of a lot of pharmacologically active proteins, in which C-type lectins have been identified and regarded as an important component of saliva. The previous studies showed that C-type lectins play crucial roles not only in innate immunity but also in promoting disease transmission in mammals. However, the function and mechanism of C-type lectins from the mosquito sialome is still elusive. METHODS: A putative C-type lectin gene (Aalb_CTL1) was cloned and expressed from Aedes albopictus by RT-PCR. The deduced amino acid sequence was analyzed by bioinformatic methods. The gene expression profiles in different tissues and various blood-fed stages of Ae. albopictus were examined by Real-Time qRT-PCR and the biological functions of the recombined mature Aalb_CTL1 were tested by hemagglutination and sugar inhibitory agglutination assays. Moreover, the capabilities of rAalb_CTL1 against microorganisms were measured by microbial-agglutination assay. RESULTS: The full-length Open reading frame (ORF) of Aalb_CTL1 consisted of 462 bp, encoding 153 amino acid residues. The deduced amino acid sequence contained a putative signal peptide of 19 amino acids. It also contained a CRD domain with a WND (Trp(137)-Asn(138)-Asp-(139)) motif that needed calcium for the hemagglutinating activity and an imperfect EPS (Glu(128)-Pro(129)-Ser(130)) motif that had a predicted ligand binding specificity for mannose. The mRNA level of Aalb_CTL1 was much higher in female mosquito salivary gland than those in fat body and midgut which was down-regulated in salivary gland after blood feeding. The rAalb_CTL1 contained not only hemagglutinating activity and a high affinity with mannose but also agglutinating activity against yeast C. albicans and Gram-positive bacteria S. aureus in Ca(2+) dependent manner. CONCLUSION: Aalb_CTL1 was a mannose-binding C-type lectin and constituted one of the important components in saliva of Ae. albopictus, which could be involved in the defense against yeast and Gram-positive bacteria infection. |
format | Online Article Text |
id | pubmed-4223726 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42237262014-11-08 Cloning and characterization of a mannose binding C-type lectin gene from salivary gland of Aedes albopictus Cheng, Jinzhi Wang, Yu Li, Fangzhan Liu, Jian Sun, Yu Wu, Jiahong Parasit Vectors Research BACKGROUND: The studies on sialomes have shown that hematophagous mosquito saliva consists of a lot of pharmacologically active proteins, in which C-type lectins have been identified and regarded as an important component of saliva. The previous studies showed that C-type lectins play crucial roles not only in innate immunity but also in promoting disease transmission in mammals. However, the function and mechanism of C-type lectins from the mosquito sialome is still elusive. METHODS: A putative C-type lectin gene (Aalb_CTL1) was cloned and expressed from Aedes albopictus by RT-PCR. The deduced amino acid sequence was analyzed by bioinformatic methods. The gene expression profiles in different tissues and various blood-fed stages of Ae. albopictus were examined by Real-Time qRT-PCR and the biological functions of the recombined mature Aalb_CTL1 were tested by hemagglutination and sugar inhibitory agglutination assays. Moreover, the capabilities of rAalb_CTL1 against microorganisms were measured by microbial-agglutination assay. RESULTS: The full-length Open reading frame (ORF) of Aalb_CTL1 consisted of 462 bp, encoding 153 amino acid residues. The deduced amino acid sequence contained a putative signal peptide of 19 amino acids. It also contained a CRD domain with a WND (Trp(137)-Asn(138)-Asp-(139)) motif that needed calcium for the hemagglutinating activity and an imperfect EPS (Glu(128)-Pro(129)-Ser(130)) motif that had a predicted ligand binding specificity for mannose. The mRNA level of Aalb_CTL1 was much higher in female mosquito salivary gland than those in fat body and midgut which was down-regulated in salivary gland after blood feeding. The rAalb_CTL1 contained not only hemagglutinating activity and a high affinity with mannose but also agglutinating activity against yeast C. albicans and Gram-positive bacteria S. aureus in Ca(2+) dependent manner. CONCLUSION: Aalb_CTL1 was a mannose-binding C-type lectin and constituted one of the important components in saliva of Ae. albopictus, which could be involved in the defense against yeast and Gram-positive bacteria infection. BioMed Central 2014-07-22 /pmc/articles/PMC4223726/ /pubmed/25051984 http://dx.doi.org/10.1186/1756-3305-7-337 Text en Copyright © 2014 Cheng 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 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 Cheng, Jinzhi Wang, Yu Li, Fangzhan Liu, Jian Sun, Yu Wu, Jiahong Cloning and characterization of a mannose binding C-type lectin gene from salivary gland of Aedes albopictus |
title | Cloning and characterization of a mannose binding C-type lectin gene from salivary gland of Aedes albopictus |
title_full | Cloning and characterization of a mannose binding C-type lectin gene from salivary gland of Aedes albopictus |
title_fullStr | Cloning and characterization of a mannose binding C-type lectin gene from salivary gland of Aedes albopictus |
title_full_unstemmed | Cloning and characterization of a mannose binding C-type lectin gene from salivary gland of Aedes albopictus |
title_short | Cloning and characterization of a mannose binding C-type lectin gene from salivary gland of Aedes albopictus |
title_sort | cloning and characterization of a mannose binding c-type lectin gene from salivary gland of aedes albopictus |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4223726/ https://www.ncbi.nlm.nih.gov/pubmed/25051984 http://dx.doi.org/10.1186/1756-3305-7-337 |
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