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New rapid one-step PCR diagnostic assay for Plasmodium falciparum infective mosquitoes
An essential component of malaria vector control programmes is the detection of Plasmodium falciparum within its mosquito vectors, particularly in the salivary glands where the infective sporozoites reside. Several protocols have been developed for this purpose; however they require dissection of mo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5780459/ https://www.ncbi.nlm.nih.gov/pubmed/29362379 http://dx.doi.org/10.1038/s41598-018-19780-6 |
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author | Kefi, Mary Mavridis, Konstantinos Simões, Maria L. Dimopoulos, George Siden-Kiamos, Inga Vontas, John |
author_facet | Kefi, Mary Mavridis, Konstantinos Simões, Maria L. Dimopoulos, George Siden-Kiamos, Inga Vontas, John |
author_sort | Kefi, Mary |
collection | PubMed |
description | An essential component of malaria vector control programmes is the detection of Plasmodium falciparum within its mosquito vectors, particularly in the salivary glands where the infective sporozoites reside. Several protocols have been developed for this purpose; however they require dissection of mosquito specimens prior to analysis. Here, a novel one-step RT-qPCR TaqMan diagnostic assay was developed for mosquitoes with infective Plasmodium falciparum sporozoites in the salivary glands. It is based on detection of the sporozoite-specific Pfslarp and Pfplp1 gene transcripts. These transcripts were chosen based on bioinformatics analysis, and experimentally verified to be overexpressed in the salivary gland sporozoite stage of the parasite compared to other mosquito parasite stages. The proof of principle and the performance of the assay were demonstrated using RNAlater preserved mosquito samples. Tests of analytical sensitivity showed the novel TaqMan assay to be 100% accurate, although its performance in the field needs to be further demonstrated. This method has no requirement for dissection and post-PCR processing and thus is simple and rapid to perform in individual mosquitoes or mosquito pools. It can be used in single or multiplex formats also targeting additional markers expressed in different tissues, such as detoxification enzymes associated with insecticide resistance. |
format | Online Article Text |
id | pubmed-5780459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57804592018-02-06 New rapid one-step PCR diagnostic assay for Plasmodium falciparum infective mosquitoes Kefi, Mary Mavridis, Konstantinos Simões, Maria L. Dimopoulos, George Siden-Kiamos, Inga Vontas, John Sci Rep Article An essential component of malaria vector control programmes is the detection of Plasmodium falciparum within its mosquito vectors, particularly in the salivary glands where the infective sporozoites reside. Several protocols have been developed for this purpose; however they require dissection of mosquito specimens prior to analysis. Here, a novel one-step RT-qPCR TaqMan diagnostic assay was developed for mosquitoes with infective Plasmodium falciparum sporozoites in the salivary glands. It is based on detection of the sporozoite-specific Pfslarp and Pfplp1 gene transcripts. These transcripts were chosen based on bioinformatics analysis, and experimentally verified to be overexpressed in the salivary gland sporozoite stage of the parasite compared to other mosquito parasite stages. The proof of principle and the performance of the assay were demonstrated using RNAlater preserved mosquito samples. Tests of analytical sensitivity showed the novel TaqMan assay to be 100% accurate, although its performance in the field needs to be further demonstrated. This method has no requirement for dissection and post-PCR processing and thus is simple and rapid to perform in individual mosquitoes or mosquito pools. It can be used in single or multiplex formats also targeting additional markers expressed in different tissues, such as detoxification enzymes associated with insecticide resistance. Nature Publishing Group UK 2018-01-23 /pmc/articles/PMC5780459/ /pubmed/29362379 http://dx.doi.org/10.1038/s41598-018-19780-6 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kefi, Mary Mavridis, Konstantinos Simões, Maria L. Dimopoulos, George Siden-Kiamos, Inga Vontas, John New rapid one-step PCR diagnostic assay for Plasmodium falciparum infective mosquitoes |
title | New rapid one-step PCR diagnostic assay for Plasmodium falciparum infective mosquitoes |
title_full | New rapid one-step PCR diagnostic assay for Plasmodium falciparum infective mosquitoes |
title_fullStr | New rapid one-step PCR diagnostic assay for Plasmodium falciparum infective mosquitoes |
title_full_unstemmed | New rapid one-step PCR diagnostic assay for Plasmodium falciparum infective mosquitoes |
title_short | New rapid one-step PCR diagnostic assay for Plasmodium falciparum infective mosquitoes |
title_sort | new rapid one-step pcr diagnostic assay for plasmodium falciparum infective mosquitoes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5780459/ https://www.ncbi.nlm.nih.gov/pubmed/29362379 http://dx.doi.org/10.1038/s41598-018-19780-6 |
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