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Towards environmental detection of Chagas disease vectors and pathogen

Chagas disease vector control relies on prompt, accurate identification of houses infested with triatomine bugs for targeted insecticide spraying. However, most current detection methods are laborious, lack standardization, have substantial operational costs and limited sensitivity, especially when...

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Autores principales: Gysin, Grace, Urbano, Plutarco, Brandner-Garrod, Luke, Begum, Shahida, Kristan, Mojca, Walker, Thomas, Hernández, Carolina, Ramírez, Juan David, Messenger, Louisa A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9194887/
https://www.ncbi.nlm.nih.gov/pubmed/35701602
http://dx.doi.org/10.1038/s41598-022-14051-x
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author Gysin, Grace
Urbano, Plutarco
Brandner-Garrod, Luke
Begum, Shahida
Kristan, Mojca
Walker, Thomas
Hernández, Carolina
Ramírez, Juan David
Messenger, Louisa A.
author_facet Gysin, Grace
Urbano, Plutarco
Brandner-Garrod, Luke
Begum, Shahida
Kristan, Mojca
Walker, Thomas
Hernández, Carolina
Ramírez, Juan David
Messenger, Louisa A.
author_sort Gysin, Grace
collection PubMed
description Chagas disease vector control relies on prompt, accurate identification of houses infested with triatomine bugs for targeted insecticide spraying. However, most current detection methods are laborious, lack standardization, have substantial operational costs and limited sensitivity, especially when triatomine bug densities are low or highly focal. We evaluated the use of FTA cards or cotton-tipped swabs to develop a low-technology, non-invasive method of detecting environmental DNA (eDNA) from both triatomine bugs and Trypanosoma cruzi for use in household surveillance in eastern Colombia, an endemic region for Chagas disease. Study findings demonstrated that Rhodnius prolixus eDNA, collected on FTA cards, can be detected at temperatures between 21 and 32 °C, when deposited by individual, recently blood-fed nymphs. Additionally, cotton-tipped swabs are a feasible tool for field sampling of both T. cruzi and R. prolixus eDNA in infested households and may be preferable due to their lower cost. eDNA detection should not yet replace current surveillance tools, but instead be evaluated in parallel as a more sensitive, higher-throughput, lower cost alternative. eDNA collection requires virtually no skills or resources in situ and therefore has the potential to be implemented in endemic communities as part of citizen science initiatives to control Chagas disease transmission.
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spelling pubmed-91948872022-06-16 Towards environmental detection of Chagas disease vectors and pathogen Gysin, Grace Urbano, Plutarco Brandner-Garrod, Luke Begum, Shahida Kristan, Mojca Walker, Thomas Hernández, Carolina Ramírez, Juan David Messenger, Louisa A. Sci Rep Article Chagas disease vector control relies on prompt, accurate identification of houses infested with triatomine bugs for targeted insecticide spraying. However, most current detection methods are laborious, lack standardization, have substantial operational costs and limited sensitivity, especially when triatomine bug densities are low or highly focal. We evaluated the use of FTA cards or cotton-tipped swabs to develop a low-technology, non-invasive method of detecting environmental DNA (eDNA) from both triatomine bugs and Trypanosoma cruzi for use in household surveillance in eastern Colombia, an endemic region for Chagas disease. Study findings demonstrated that Rhodnius prolixus eDNA, collected on FTA cards, can be detected at temperatures between 21 and 32 °C, when deposited by individual, recently blood-fed nymphs. Additionally, cotton-tipped swabs are a feasible tool for field sampling of both T. cruzi and R. prolixus eDNA in infested households and may be preferable due to their lower cost. eDNA detection should not yet replace current surveillance tools, but instead be evaluated in parallel as a more sensitive, higher-throughput, lower cost alternative. eDNA collection requires virtually no skills or resources in situ and therefore has the potential to be implemented in endemic communities as part of citizen science initiatives to control Chagas disease transmission. Nature Publishing Group UK 2022-06-14 /pmc/articles/PMC9194887/ /pubmed/35701602 http://dx.doi.org/10.1038/s41598-022-14051-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Gysin, Grace
Urbano, Plutarco
Brandner-Garrod, Luke
Begum, Shahida
Kristan, Mojca
Walker, Thomas
Hernández, Carolina
Ramírez, Juan David
Messenger, Louisa A.
Towards environmental detection of Chagas disease vectors and pathogen
title Towards environmental detection of Chagas disease vectors and pathogen
title_full Towards environmental detection of Chagas disease vectors and pathogen
title_fullStr Towards environmental detection of Chagas disease vectors and pathogen
title_full_unstemmed Towards environmental detection of Chagas disease vectors and pathogen
title_short Towards environmental detection of Chagas disease vectors and pathogen
title_sort towards environmental detection of chagas disease vectors and pathogen
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9194887/
https://www.ncbi.nlm.nih.gov/pubmed/35701602
http://dx.doi.org/10.1038/s41598-022-14051-x
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