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Trypsin-like serine peptidase profiles in the egg, larval, and pupal stages of Aedes albopictus

BACKGROUND: Aedes albopictus, a ubiquitous mosquito, is one of the main vectors of dengue and yellow fever, representing an important threat to public health worldwide. Peptidases play key roles in processes such as digestion, oogenesis, and metamorphosis of insects. However, most of the information...

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Autores principales: Saboia-Vahia, Leonardo, Borges-Veloso, André, Mesquita-Rodrigues, Camila, Cuervo, Patricia, Dias-Lopes, Geovane, Britto, Constança, Silva, Ana Paula de Barros, De Jesus, Jose B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606343/
https://www.ncbi.nlm.nih.gov/pubmed/23445661
http://dx.doi.org/10.1186/1756-3305-6-50
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author Saboia-Vahia, Leonardo
Borges-Veloso, André
Mesquita-Rodrigues, Camila
Cuervo, Patricia
Dias-Lopes, Geovane
Britto, Constança
Silva, Ana Paula de Barros
De Jesus, Jose B
author_facet Saboia-Vahia, Leonardo
Borges-Veloso, André
Mesquita-Rodrigues, Camila
Cuervo, Patricia
Dias-Lopes, Geovane
Britto, Constança
Silva, Ana Paula de Barros
De Jesus, Jose B
author_sort Saboia-Vahia, Leonardo
collection PubMed
description BACKGROUND: Aedes albopictus, a ubiquitous mosquito, is one of the main vectors of dengue and yellow fever, representing an important threat to public health worldwide. Peptidases play key roles in processes such as digestion, oogenesis, and metamorphosis of insects. However, most of the information on the proteolytic enzymes of mosquitoes is derived from insects in the adult stages and is often directed towards the understanding of blood digestion. The aim of this study was to investigate the expression of active peptidases from the preimaginal stages of Ae. albopictus. METHODS: Ae. albopictus eggs, larvae, and pupae were analyzed using zymography with susbtrate-SDS-PAGE. The pH, temperature and peptidase inhibitor sensitivity was evaluated. In addition, the proteolytic activities of larval instars were assayed using the fluorogenic substrate Z-Phe-Arg-AMC. RESULTS: The proteolytic profile of the larval stage was composed of 8 bands ranging from 17 to 130 kDa. These enzymes displayed activity in a broad range of pH values, from 5.5 to 10.0. The enzymatic profile of the eggs was similar to that of the larvae, although the proteolytic bands of the eggs showed lower intensities. The pupal stage showed a complex proteolytic pattern, with at least 6 bands with apparent molecular masses ranging from 30 to 150 kDa and optimal activity at pH 7.5. Peptidases from larval instars were active from 10°C to 60°C, with optimal activity at temperatures between 37°C and 50°C. The proteolytic profile of both the larval and pupal stages was inhibited by phenyl-methyl sulfonyl-fluoride (PMSF) and Nα-Tosyl L-lysine chloromethyl ketone hydrochloride (TLCK), indicating that the main peptidases expressed during these developmental stages are trypsin-like serine peptidases. CONCLUSION: The preimaginal stages of Ae. albopictus exhibited a complex profile of trypsin-like serine peptidase activities. A comparative analysis of the active peptidase profiles revealed differential expression of trypsin-like isoforms among the preimaginal stages, suggesting that some of these enzymes are stage specific. Additionally, a comparison of the peptidase expression between larvae from eggs collected in the natural environment and larvae obtained from the eggs of female mosquitoes maintained in colonies for a long period of time demonstrated that the proteolytic profile is invariable under such conditions.
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spelling pubmed-36063432013-03-23 Trypsin-like serine peptidase profiles in the egg, larval, and pupal stages of Aedes albopictus Saboia-Vahia, Leonardo Borges-Veloso, André Mesquita-Rodrigues, Camila Cuervo, Patricia Dias-Lopes, Geovane Britto, Constança Silva, Ana Paula de Barros De Jesus, Jose B Parasit Vectors Research BACKGROUND: Aedes albopictus, a ubiquitous mosquito, is one of the main vectors of dengue and yellow fever, representing an important threat to public health worldwide. Peptidases play key roles in processes such as digestion, oogenesis, and metamorphosis of insects. However, most of the information on the proteolytic enzymes of mosquitoes is derived from insects in the adult stages and is often directed towards the understanding of blood digestion. The aim of this study was to investigate the expression of active peptidases from the preimaginal stages of Ae. albopictus. METHODS: Ae. albopictus eggs, larvae, and pupae were analyzed using zymography with susbtrate-SDS-PAGE. The pH, temperature and peptidase inhibitor sensitivity was evaluated. In addition, the proteolytic activities of larval instars were assayed using the fluorogenic substrate Z-Phe-Arg-AMC. RESULTS: The proteolytic profile of the larval stage was composed of 8 bands ranging from 17 to 130 kDa. These enzymes displayed activity in a broad range of pH values, from 5.5 to 10.0. The enzymatic profile of the eggs was similar to that of the larvae, although the proteolytic bands of the eggs showed lower intensities. The pupal stage showed a complex proteolytic pattern, with at least 6 bands with apparent molecular masses ranging from 30 to 150 kDa and optimal activity at pH 7.5. Peptidases from larval instars were active from 10°C to 60°C, with optimal activity at temperatures between 37°C and 50°C. The proteolytic profile of both the larval and pupal stages was inhibited by phenyl-methyl sulfonyl-fluoride (PMSF) and Nα-Tosyl L-lysine chloromethyl ketone hydrochloride (TLCK), indicating that the main peptidases expressed during these developmental stages are trypsin-like serine peptidases. CONCLUSION: The preimaginal stages of Ae. albopictus exhibited a complex profile of trypsin-like serine peptidase activities. A comparative analysis of the active peptidase profiles revealed differential expression of trypsin-like isoforms among the preimaginal stages, suggesting that some of these enzymes are stage specific. Additionally, a comparison of the peptidase expression between larvae from eggs collected in the natural environment and larvae obtained from the eggs of female mosquitoes maintained in colonies for a long period of time demonstrated that the proteolytic profile is invariable under such conditions. BioMed Central 2013-02-27 /pmc/articles/PMC3606343/ /pubmed/23445661 http://dx.doi.org/10.1186/1756-3305-6-50 Text en Copyright ©2013 Saboia-Vahia 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
Saboia-Vahia, Leonardo
Borges-Veloso, André
Mesquita-Rodrigues, Camila
Cuervo, Patricia
Dias-Lopes, Geovane
Britto, Constança
Silva, Ana Paula de Barros
De Jesus, Jose B
Trypsin-like serine peptidase profiles in the egg, larval, and pupal stages of Aedes albopictus
title Trypsin-like serine peptidase profiles in the egg, larval, and pupal stages of Aedes albopictus
title_full Trypsin-like serine peptidase profiles in the egg, larval, and pupal stages of Aedes albopictus
title_fullStr Trypsin-like serine peptidase profiles in the egg, larval, and pupal stages of Aedes albopictus
title_full_unstemmed Trypsin-like serine peptidase profiles in the egg, larval, and pupal stages of Aedes albopictus
title_short Trypsin-like serine peptidase profiles in the egg, larval, and pupal stages of Aedes albopictus
title_sort trypsin-like serine peptidase profiles in the egg, larval, and pupal stages of aedes albopictus
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3606343/
https://www.ncbi.nlm.nih.gov/pubmed/23445661
http://dx.doi.org/10.1186/1756-3305-6-50
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