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A Simple Isothermal DNA Amplification Method to Screen Black Flies for Onchocerca volvulus Infection
Onchocerciasis is a debilitating neglected tropical disease caused by infection with the filarial parasite Onchocerca volvulus. Adult worms live in subcutaneous tissues and produce large numbers of microfilariae that migrate to the skin and eyes. The disease is spread by black flies of the genus Sim...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4191976/ https://www.ncbi.nlm.nih.gov/pubmed/25299656 http://dx.doi.org/10.1371/journal.pone.0108927 |
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author | Alhassan, Andy Makepeace, Benjamin L. LaCourse, Elwyn James Osei-Atweneboana, Mike Y. Carlow, Clotilde K. S. |
author_facet | Alhassan, Andy Makepeace, Benjamin L. LaCourse, Elwyn James Osei-Atweneboana, Mike Y. Carlow, Clotilde K. S. |
author_sort | Alhassan, Andy |
collection | PubMed |
description | Onchocerciasis is a debilitating neglected tropical disease caused by infection with the filarial parasite Onchocerca volvulus. Adult worms live in subcutaneous tissues and produce large numbers of microfilariae that migrate to the skin and eyes. The disease is spread by black flies of the genus Simulium following ingestion of microfilariae that develop into infective stage larvae in the insect. Currently, transmission is monitored by capture and dissection of black flies and microscopic examination of parasites, or using the polymerase chain reaction to determine the presence of parasite DNA in pools of black flies. In this study we identified a new DNA biomarker, encoding O. volvulus glutathione S-transferase 1a (OvGST1a), to detect O. volvulus infection in vector black flies. We developed an OvGST1a-based loop-mediated isothermal amplification (LAMP) assay where amplification of specific target DNA is detectable using turbidity or by a hydroxy naphthol blue color change. The results indicated that the assay is sensitive and rapid, capable of detecting DNA equivalent to less than one microfilaria within 60 minutes. The test is highly specific for the human parasite, as no cross-reaction was detected using DNA from the closely related and sympatric cattle parasite Onchocerca ochengi. The test has the potential to be developed further as a field tool for use in the surveillance of transmission before and after implementation of mass drug administration programs for onchocerciasis. |
format | Online Article Text |
id | pubmed-4191976 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41919762014-10-14 A Simple Isothermal DNA Amplification Method to Screen Black Flies for Onchocerca volvulus Infection Alhassan, Andy Makepeace, Benjamin L. LaCourse, Elwyn James Osei-Atweneboana, Mike Y. Carlow, Clotilde K. S. PLoS One Research Article Onchocerciasis is a debilitating neglected tropical disease caused by infection with the filarial parasite Onchocerca volvulus. Adult worms live in subcutaneous tissues and produce large numbers of microfilariae that migrate to the skin and eyes. The disease is spread by black flies of the genus Simulium following ingestion of microfilariae that develop into infective stage larvae in the insect. Currently, transmission is monitored by capture and dissection of black flies and microscopic examination of parasites, or using the polymerase chain reaction to determine the presence of parasite DNA in pools of black flies. In this study we identified a new DNA biomarker, encoding O. volvulus glutathione S-transferase 1a (OvGST1a), to detect O. volvulus infection in vector black flies. We developed an OvGST1a-based loop-mediated isothermal amplification (LAMP) assay where amplification of specific target DNA is detectable using turbidity or by a hydroxy naphthol blue color change. The results indicated that the assay is sensitive and rapid, capable of detecting DNA equivalent to less than one microfilaria within 60 minutes. The test is highly specific for the human parasite, as no cross-reaction was detected using DNA from the closely related and sympatric cattle parasite Onchocerca ochengi. The test has the potential to be developed further as a field tool for use in the surveillance of transmission before and after implementation of mass drug administration programs for onchocerciasis. Public Library of Science 2014-10-09 /pmc/articles/PMC4191976/ /pubmed/25299656 http://dx.doi.org/10.1371/journal.pone.0108927 Text en © 2014 Alhassan et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Alhassan, Andy Makepeace, Benjamin L. LaCourse, Elwyn James Osei-Atweneboana, Mike Y. Carlow, Clotilde K. S. A Simple Isothermal DNA Amplification Method to Screen Black Flies for Onchocerca volvulus Infection |
title | A Simple Isothermal DNA Amplification Method to Screen Black Flies for Onchocerca volvulus Infection |
title_full | A Simple Isothermal DNA Amplification Method to Screen Black Flies for Onchocerca volvulus Infection |
title_fullStr | A Simple Isothermal DNA Amplification Method to Screen Black Flies for Onchocerca volvulus Infection |
title_full_unstemmed | A Simple Isothermal DNA Amplification Method to Screen Black Flies for Onchocerca volvulus Infection |
title_short | A Simple Isothermal DNA Amplification Method to Screen Black Flies for Onchocerca volvulus Infection |
title_sort | simple isothermal dna amplification method to screen black flies for onchocerca volvulus infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4191976/ https://www.ncbi.nlm.nih.gov/pubmed/25299656 http://dx.doi.org/10.1371/journal.pone.0108927 |
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