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Rapid molecular assays for the detection of the four dengue viruses in infected mosquitoes
The pantropic emergence of severe dengue disease can partly be attributed to the co-circulation of different dengue viruses (DENVs) in the same geographical location. Effective monitoring for circulation of each of the four DENVs is critical to inform disease mitigation strategies. In low resource s...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000 Research Limited
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816563/ https://www.ncbi.nlm.nih.gov/pubmed/36636741 http://dx.doi.org/10.12688/gatesopenres.13534.2 |
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author | Ahmed, Madeeha Pollak, Nina M. Hugo, Leon E. van den Hurk, Andrew F. Hobson-Peters, Jody Macdonald, Joanne |
author_facet | Ahmed, Madeeha Pollak, Nina M. Hugo, Leon E. van den Hurk, Andrew F. Hobson-Peters, Jody Macdonald, Joanne |
author_sort | Ahmed, Madeeha |
collection | PubMed |
description | The pantropic emergence of severe dengue disease can partly be attributed to the co-circulation of different dengue viruses (DENVs) in the same geographical location. Effective monitoring for circulation of each of the four DENVs is critical to inform disease mitigation strategies. In low resource settings, this can be effectively achieved by utilizing inexpensive, rapid, sensitive and specific assays to detect viruses in mosquito populations. In this study, we developed four rapid DENV tests with direct applicability for low-resource virus surveillance in mosquitoes. The test protocols utilize a novel sample preparation step, a single-temperature isothermal amplification, and a simple lateral flow detection. Analytical sensitivity testing demonstrated tests could detect down to 1,000 copies/µL of virus-specific DENV RNA, and analytical specificity testing indicated tests were highly specific for their respective virus, and did not detect closely related flaviviruses. All four DENV tests showed excellent diagnostic specificity and sensitivity when used for detection of both individually infected mosquitoes and infected mosquitoes in pools of uninfected mosquitoes. With individually infected mosquitoes, the rapid DENV-1, -2 and -3 tests showed 100% diagnostic sensitivity (95% CI = 69% to 100%, n=8 for DENV-1; n=10 for DENV 2,3) and the DENV-4 test showed 92% diagnostic sensitivity (CI: 62% to 100%, n=12) along with 100% diagnostic specificity (CI: 48–100%) for all four tests. Testing infected mosquito pools, the rapid DENV-2, -3 and -4 tests showed 100% diagnostic sensitivity (95% CI = 69% to 100%, n=10) and the DENV-1 test showed 90% diagnostic sensitivity (55.50% to 99.75%, n=10) together with 100% diagnostic specificity (CI: 48–100%). Our tests reduce the operational time required to perform mosquito infection status surveillance testing from > two hours to only 35 minutes, and have potential to improve accessibility of mosquito screening, improving monitoring and control strategies in low-income countries most affected by dengue outbreaks. |
format | Online Article Text |
id | pubmed-9816563 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | F1000 Research Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-98165632023-01-11 Rapid molecular assays for the detection of the four dengue viruses in infected mosquitoes Ahmed, Madeeha Pollak, Nina M. Hugo, Leon E. van den Hurk, Andrew F. Hobson-Peters, Jody Macdonald, Joanne Gates Open Res Method Article The pantropic emergence of severe dengue disease can partly be attributed to the co-circulation of different dengue viruses (DENVs) in the same geographical location. Effective monitoring for circulation of each of the four DENVs is critical to inform disease mitigation strategies. In low resource settings, this can be effectively achieved by utilizing inexpensive, rapid, sensitive and specific assays to detect viruses in mosquito populations. In this study, we developed four rapid DENV tests with direct applicability for low-resource virus surveillance in mosquitoes. The test protocols utilize a novel sample preparation step, a single-temperature isothermal amplification, and a simple lateral flow detection. Analytical sensitivity testing demonstrated tests could detect down to 1,000 copies/µL of virus-specific DENV RNA, and analytical specificity testing indicated tests were highly specific for their respective virus, and did not detect closely related flaviviruses. All four DENV tests showed excellent diagnostic specificity and sensitivity when used for detection of both individually infected mosquitoes and infected mosquitoes in pools of uninfected mosquitoes. With individually infected mosquitoes, the rapid DENV-1, -2 and -3 tests showed 100% diagnostic sensitivity (95% CI = 69% to 100%, n=8 for DENV-1; n=10 for DENV 2,3) and the DENV-4 test showed 92% diagnostic sensitivity (CI: 62% to 100%, n=12) along with 100% diagnostic specificity (CI: 48–100%) for all four tests. Testing infected mosquito pools, the rapid DENV-2, -3 and -4 tests showed 100% diagnostic sensitivity (95% CI = 69% to 100%, n=10) and the DENV-1 test showed 90% diagnostic sensitivity (55.50% to 99.75%, n=10) together with 100% diagnostic specificity (CI: 48–100%). Our tests reduce the operational time required to perform mosquito infection status surveillance testing from > two hours to only 35 minutes, and have potential to improve accessibility of mosquito screening, improving monitoring and control strategies in low-income countries most affected by dengue outbreaks. F1000 Research Limited 2022-12-22 /pmc/articles/PMC9816563/ /pubmed/36636741 http://dx.doi.org/10.12688/gatesopenres.13534.2 Text en Copyright: © 2022 Ahmed M et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Method Article Ahmed, Madeeha Pollak, Nina M. Hugo, Leon E. van den Hurk, Andrew F. Hobson-Peters, Jody Macdonald, Joanne Rapid molecular assays for the detection of the four dengue viruses in infected mosquitoes |
title | Rapid molecular assays for the detection of the four dengue viruses in infected mosquitoes |
title_full | Rapid molecular assays for the detection of the four dengue viruses in infected mosquitoes |
title_fullStr | Rapid molecular assays for the detection of the four dengue viruses in infected mosquitoes |
title_full_unstemmed | Rapid molecular assays for the detection of the four dengue viruses in infected mosquitoes |
title_short | Rapid molecular assays for the detection of the four dengue viruses in infected mosquitoes |
title_sort | rapid molecular assays for the detection of the four dengue viruses in infected mosquitoes |
topic | Method Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816563/ https://www.ncbi.nlm.nih.gov/pubmed/36636741 http://dx.doi.org/10.12688/gatesopenres.13534.2 |
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