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Fluorescence In Situ Hybridization (FISH) Assays for Diagnosing Malaria in Endemic Areas
Malaria is a responsible for approximately 600 thousand deaths worldwide every year. Appropriate and timely treatment of malaria can prevent deaths but is dependent on accurate and rapid diagnosis of the infection. Currently, microscopic examination of the Giemsa stained blood smears is the method o...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4558036/ https://www.ncbi.nlm.nih.gov/pubmed/26333092 http://dx.doi.org/10.1371/journal.pone.0136726 |
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author | Shah, Jyotsna Mark, Olivia Weltman, Helena Barcelo, Nicolas Lo, Wai Wronska, Danuta Kakkilaya, Srinivas Rao, Aravinda Bhat, Shalia T. Sinha, Ruchi Omar, Sabah O’bare, Peter Moro, Manuel Gilman, Robert H. Harris, Nick |
author_facet | Shah, Jyotsna Mark, Olivia Weltman, Helena Barcelo, Nicolas Lo, Wai Wronska, Danuta Kakkilaya, Srinivas Rao, Aravinda Bhat, Shalia T. Sinha, Ruchi Omar, Sabah O’bare, Peter Moro, Manuel Gilman, Robert H. Harris, Nick |
author_sort | Shah, Jyotsna |
collection | PubMed |
description | Malaria is a responsible for approximately 600 thousand deaths worldwide every year. Appropriate and timely treatment of malaria can prevent deaths but is dependent on accurate and rapid diagnosis of the infection. Currently, microscopic examination of the Giemsa stained blood smears is the method of choice for diagnosing malaria. Although it has limited sensitivity and specificity in field conditions, it still remains the gold standard for the diagnosis of malaria. Here, we report the development of a fluorescence in situ hybridization (FISH) based method for detecting malaria infection in blood smears and describe the use of an LED light source that makes the method suitable for use in resource-limited malaria endemic countries. The Plasmodium Genus (P-Genus) FISH assay has a Plasmodium genus specific probe that detects all five species of Plasmodium known to cause the disease in humans. The P. falciparum (PF) FISH assay and P. vivax (PV) FISH assay detect and differentiate between P. falciparum and P. vivax respectively from other Plasmodium species. The FISH assays are more sensitive than Giemsa. The sensitivities of P-Genus, PF and PV FISH assays were found to be 98.2%, 94.5% and 98.3%, respectively compared to 89.9%, 83.3% and 87.9% for the detection of Plasmodium, P. falciparum and P. vivax by Giemsa staining respectively. |
format | Online Article Text |
id | pubmed-4558036 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-45580362015-09-10 Fluorescence In Situ Hybridization (FISH) Assays for Diagnosing Malaria in Endemic Areas Shah, Jyotsna Mark, Olivia Weltman, Helena Barcelo, Nicolas Lo, Wai Wronska, Danuta Kakkilaya, Srinivas Rao, Aravinda Bhat, Shalia T. Sinha, Ruchi Omar, Sabah O’bare, Peter Moro, Manuel Gilman, Robert H. Harris, Nick PLoS One Research Article Malaria is a responsible for approximately 600 thousand deaths worldwide every year. Appropriate and timely treatment of malaria can prevent deaths but is dependent on accurate and rapid diagnosis of the infection. Currently, microscopic examination of the Giemsa stained blood smears is the method of choice for diagnosing malaria. Although it has limited sensitivity and specificity in field conditions, it still remains the gold standard for the diagnosis of malaria. Here, we report the development of a fluorescence in situ hybridization (FISH) based method for detecting malaria infection in blood smears and describe the use of an LED light source that makes the method suitable for use in resource-limited malaria endemic countries. The Plasmodium Genus (P-Genus) FISH assay has a Plasmodium genus specific probe that detects all five species of Plasmodium known to cause the disease in humans. The P. falciparum (PF) FISH assay and P. vivax (PV) FISH assay detect and differentiate between P. falciparum and P. vivax respectively from other Plasmodium species. The FISH assays are more sensitive than Giemsa. The sensitivities of P-Genus, PF and PV FISH assays were found to be 98.2%, 94.5% and 98.3%, respectively compared to 89.9%, 83.3% and 87.9% for the detection of Plasmodium, P. falciparum and P. vivax by Giemsa staining respectively. Public Library of Science 2015-09-02 /pmc/articles/PMC4558036/ /pubmed/26333092 http://dx.doi.org/10.1371/journal.pone.0136726 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Shah, Jyotsna Mark, Olivia Weltman, Helena Barcelo, Nicolas Lo, Wai Wronska, Danuta Kakkilaya, Srinivas Rao, Aravinda Bhat, Shalia T. Sinha, Ruchi Omar, Sabah O’bare, Peter Moro, Manuel Gilman, Robert H. Harris, Nick Fluorescence In Situ Hybridization (FISH) Assays for Diagnosing Malaria in Endemic Areas |
title | Fluorescence In Situ Hybridization (FISH) Assays for Diagnosing Malaria in Endemic Areas |
title_full | Fluorescence In Situ Hybridization (FISH) Assays for Diagnosing Malaria in Endemic Areas |
title_fullStr | Fluorescence In Situ Hybridization (FISH) Assays for Diagnosing Malaria in Endemic Areas |
title_full_unstemmed | Fluorescence In Situ Hybridization (FISH) Assays for Diagnosing Malaria in Endemic Areas |
title_short | Fluorescence In Situ Hybridization (FISH) Assays for Diagnosing Malaria in Endemic Areas |
title_sort | fluorescence in situ hybridization (fish) assays for diagnosing malaria in endemic areas |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4558036/ https://www.ncbi.nlm.nih.gov/pubmed/26333092 http://dx.doi.org/10.1371/journal.pone.0136726 |
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