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Anti-complement activity in salivary glands and midgut of Chagas disease vector, Panstrongylus megistus (Hemiptera, Triatominae)
The triatomine insect Panstrongylus megistus , one of the most important Chagas disease vectors in Brazil, presents salivary molecules pharmacologically active to counteract homeostatic responses from the host, including inhibitors of the human complement system, a major effector of immune responses...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Instituto de Medicina Tropical
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6690578/ https://www.ncbi.nlm.nih.gov/pubmed/31411268 http://dx.doi.org/10.1590/S1678-9946201961038 |
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author | Mendes-Sousa, Antonio Ferreira Rocha, Elias de Almeida Macêdo, Mateus Almeida Barros, Veruska Cavalcanti |
author_facet | Mendes-Sousa, Antonio Ferreira Rocha, Elias de Almeida Macêdo, Mateus Almeida Barros, Veruska Cavalcanti |
author_sort | Mendes-Sousa, Antonio Ferreira |
collection | PubMed |
description | The triatomine insect Panstrongylus megistus , one of the most important Chagas disease vectors in Brazil, presents salivary molecules pharmacologically active to counteract homeostatic responses from the host, including inhibitors of the human complement system, a major effector of immune responses. The aim of the present study was to investigate the effect of P. megistus salivary gland extract (SGE) on the complement system from different host species and characterize the inhibitory effect of SGE and intestinal contents on human complement. Glands and midguts from fourth instar nymphs were used. Hemolytic assays were performed with sheep erythrocytes as complement activators by using human, rats and chickens sera in the presence or absence of SGE. An ELISA assay was carried out detect deposition of the C3b component on IgG- or agarose-sensitized microplates, in the presence or absence of SGE or midgut contents. P. megistus SGE was able to significantly inhibit the complement of the three studied species (human, rat and chiken). Both, SGE and midgut contents inhibited C3b deposition in either the classical or the alternative pathways. As conclusions, SGE and midgut from P. megistus possess anti-complement activity. The inhibitors are effective against different host species and act on the initial steps of the complement system cascade. These inhibitors may have a role in blood feeding and Trypanosoma cruzi transmission by the vector. |
format | Online Article Text |
id | pubmed-6690578 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Instituto de Medicina Tropical |
record_format | MEDLINE/PubMed |
spelling | pubmed-66905782019-08-23 Anti-complement activity in salivary glands and midgut of Chagas disease vector, Panstrongylus megistus (Hemiptera, Triatominae) Mendes-Sousa, Antonio Ferreira Rocha, Elias de Almeida Macêdo, Mateus Almeida Barros, Veruska Cavalcanti Rev Inst Med Trop Sao Paulo Original Article The triatomine insect Panstrongylus megistus , one of the most important Chagas disease vectors in Brazil, presents salivary molecules pharmacologically active to counteract homeostatic responses from the host, including inhibitors of the human complement system, a major effector of immune responses. The aim of the present study was to investigate the effect of P. megistus salivary gland extract (SGE) on the complement system from different host species and characterize the inhibitory effect of SGE and intestinal contents on human complement. Glands and midguts from fourth instar nymphs were used. Hemolytic assays were performed with sheep erythrocytes as complement activators by using human, rats and chickens sera in the presence or absence of SGE. An ELISA assay was carried out detect deposition of the C3b component on IgG- or agarose-sensitized microplates, in the presence or absence of SGE or midgut contents. P. megistus SGE was able to significantly inhibit the complement of the three studied species (human, rat and chiken). Both, SGE and midgut contents inhibited C3b deposition in either the classical or the alternative pathways. As conclusions, SGE and midgut from P. megistus possess anti-complement activity. The inhibitors are effective against different host species and act on the initial steps of the complement system cascade. These inhibitors may have a role in blood feeding and Trypanosoma cruzi transmission by the vector. Instituto de Medicina Tropical 2019-08-08 /pmc/articles/PMC6690578/ /pubmed/31411268 http://dx.doi.org/10.1590/S1678-9946201961038 Text en https://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Mendes-Sousa, Antonio Ferreira Rocha, Elias de Almeida Macêdo, Mateus Almeida Barros, Veruska Cavalcanti Anti-complement activity in salivary glands and midgut of Chagas disease vector, Panstrongylus megistus (Hemiptera, Triatominae) |
title | Anti-complement activity in salivary glands and midgut of Chagas
disease vector, Panstrongylus megistus (Hemiptera,
Triatominae) |
title_full | Anti-complement activity in salivary glands and midgut of Chagas
disease vector, Panstrongylus megistus (Hemiptera,
Triatominae) |
title_fullStr | Anti-complement activity in salivary glands and midgut of Chagas
disease vector, Panstrongylus megistus (Hemiptera,
Triatominae) |
title_full_unstemmed | Anti-complement activity in salivary glands and midgut of Chagas
disease vector, Panstrongylus megistus (Hemiptera,
Triatominae) |
title_short | Anti-complement activity in salivary glands and midgut of Chagas
disease vector, Panstrongylus megistus (Hemiptera,
Triatominae) |
title_sort | anti-complement activity in salivary glands and midgut of chagas
disease vector, panstrongylus megistus (hemiptera,
triatominae) |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6690578/ https://www.ncbi.nlm.nih.gov/pubmed/31411268 http://dx.doi.org/10.1590/S1678-9946201961038 |
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