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An. gambiae gSG6-P1 evaluation as a proxy for human-vector contact in the Americas: a pilot study
BACKGROUND: During blood meal, the female mosquito injects saliva able to elicit an immune response in the vertebrate. This immune response has been proven to reflect the intensity of exposure to mosquito bites and risk of infection for vector transmitted pathogens such as malaria. The peptide gSG6-...
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/PMC4605097/ https://www.ncbi.nlm.nih.gov/pubmed/26464073 http://dx.doi.org/10.1186/s13071-015-1160-3 |
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author | Londono-Renteria, Berlin Drame, Papa M. Weitzel, Thomas Rosas, Reinaldo Gripping, Crystal Cardenas, Jenny C. Alvares, Marcela Wesson, Dawn M Poinsignon, Anne Remoue, Franck Colpitts, Tonya M. |
author_facet | Londono-Renteria, Berlin Drame, Papa M. Weitzel, Thomas Rosas, Reinaldo Gripping, Crystal Cardenas, Jenny C. Alvares, Marcela Wesson, Dawn M Poinsignon, Anne Remoue, Franck Colpitts, Tonya M. |
author_sort | Londono-Renteria, Berlin |
collection | PubMed |
description | BACKGROUND: During blood meal, the female mosquito injects saliva able to elicit an immune response in the vertebrate. This immune response has been proven to reflect the intensity of exposure to mosquito bites and risk of infection for vector transmitted pathogens such as malaria. The peptide gSG6-P1 of An. gambiae saliva has been demonstrated to be antigenic and highly specific to Anopheles as a genus. However, the applicability of gSG6-P1 to measure exposure to different Anopheles species endemic in the Americas has yet to be evaluated. The purpose of this pilot study was to test whether human participants living in American countries present antibodies able to recognize the gSG6-P1, and whether these antibodies are useful as a proxy for mosquito bite exposure and malaria risk. METHODS: We tested human serum samples from Colombia, Chile, and the United States for the presence of IgG antibodies against gSG6-P1 by ELISA. Antibody concentrations were expressed as delta optical density (ΔOD) of each sera tested in duplicates. The difference in the antibody concentrations between groups was tested using the nonparametric Mann Whitney test (independent groups) and the nonparametric Wilcoxon matched-pairs signed rank test (dependent groups). All differences were considered significant with a P < 0.05. RESULTS: We found that the concentration of gSG6-P1 antibodies was significantly correlated with malaria infection status and mosquito bite exposure history. People with clinical malaria presented significantly higher concentrations of IgG anti-gSG6-P1 antibodies than healthy controls. Additionally, a significant raise in antibody concentrations was observed in subjects returning from malaria endemic areas. CONCLUSION: Our data shows that gSG6-P1 is a suitable candidate for the evaluation of exposure to Anopheles mosquito bites, risk of malaria transmission, and effectiveness of protection measures against mosquito bites in the Americas. |
format | Online Article Text |
id | pubmed-4605097 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46050972015-10-15 An. gambiae gSG6-P1 evaluation as a proxy for human-vector contact in the Americas: a pilot study Londono-Renteria, Berlin Drame, Papa M. Weitzel, Thomas Rosas, Reinaldo Gripping, Crystal Cardenas, Jenny C. Alvares, Marcela Wesson, Dawn M Poinsignon, Anne Remoue, Franck Colpitts, Tonya M. Parasit Vectors Research BACKGROUND: During blood meal, the female mosquito injects saliva able to elicit an immune response in the vertebrate. This immune response has been proven to reflect the intensity of exposure to mosquito bites and risk of infection for vector transmitted pathogens such as malaria. The peptide gSG6-P1 of An. gambiae saliva has been demonstrated to be antigenic and highly specific to Anopheles as a genus. However, the applicability of gSG6-P1 to measure exposure to different Anopheles species endemic in the Americas has yet to be evaluated. The purpose of this pilot study was to test whether human participants living in American countries present antibodies able to recognize the gSG6-P1, and whether these antibodies are useful as a proxy for mosquito bite exposure and malaria risk. METHODS: We tested human serum samples from Colombia, Chile, and the United States for the presence of IgG antibodies against gSG6-P1 by ELISA. Antibody concentrations were expressed as delta optical density (ΔOD) of each sera tested in duplicates. The difference in the antibody concentrations between groups was tested using the nonparametric Mann Whitney test (independent groups) and the nonparametric Wilcoxon matched-pairs signed rank test (dependent groups). All differences were considered significant with a P < 0.05. RESULTS: We found that the concentration of gSG6-P1 antibodies was significantly correlated with malaria infection status and mosquito bite exposure history. People with clinical malaria presented significantly higher concentrations of IgG anti-gSG6-P1 antibodies than healthy controls. Additionally, a significant raise in antibody concentrations was observed in subjects returning from malaria endemic areas. CONCLUSION: Our data shows that gSG6-P1 is a suitable candidate for the evaluation of exposure to Anopheles mosquito bites, risk of malaria transmission, and effectiveness of protection measures against mosquito bites in the Americas. BioMed Central 2015-10-13 /pmc/articles/PMC4605097/ /pubmed/26464073 http://dx.doi.org/10.1186/s13071-015-1160-3 Text en © Londono-Renteria et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Londono-Renteria, Berlin Drame, Papa M. Weitzel, Thomas Rosas, Reinaldo Gripping, Crystal Cardenas, Jenny C. Alvares, Marcela Wesson, Dawn M Poinsignon, Anne Remoue, Franck Colpitts, Tonya M. An. gambiae gSG6-P1 evaluation as a proxy for human-vector contact in the Americas: a pilot study |
title | An. gambiae gSG6-P1 evaluation as a proxy for human-vector contact in the Americas: a pilot study |
title_full | An. gambiae gSG6-P1 evaluation as a proxy for human-vector contact in the Americas: a pilot study |
title_fullStr | An. gambiae gSG6-P1 evaluation as a proxy for human-vector contact in the Americas: a pilot study |
title_full_unstemmed | An. gambiae gSG6-P1 evaluation as a proxy for human-vector contact in the Americas: a pilot study |
title_short | An. gambiae gSG6-P1 evaluation as a proxy for human-vector contact in the Americas: a pilot study |
title_sort | an. gambiae gsg6-p1 evaluation as a proxy for human-vector contact in the americas: a pilot study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4605097/ https://www.ncbi.nlm.nih.gov/pubmed/26464073 http://dx.doi.org/10.1186/s13071-015-1160-3 |
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