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Simple, sensitive and quantitative bioluminescence assay for determination of malaria pre-patent period
BACKGROUND: The first phase of malaria infection occurs in the liver and is clinically silent. Inside hepatocytes each Plasmodium sporozoite replicate into thousands of erythrocyte-infectious merozoites that when released into the blood stream result in clinical symptoms of the disease. The time bet...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3893453/ https://www.ncbi.nlm.nih.gov/pubmed/24400642 http://dx.doi.org/10.1186/1475-2875-13-15 |
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author | Zuzarte-Luis, Vanessa Sales-Dias, Joana Mota, Maria M |
author_facet | Zuzarte-Luis, Vanessa Sales-Dias, Joana Mota, Maria M |
author_sort | Zuzarte-Luis, Vanessa |
collection | PubMed |
description | BACKGROUND: The first phase of malaria infection occurs in the liver and is clinically silent. Inside hepatocytes each Plasmodium sporozoite replicate into thousands of erythrocyte-infectious merozoites that when released into the blood stream result in clinical symptoms of the disease. The time between sporozoite inoculation and the appearance of parasites in the blood is defined as the pre-patent period, which is classically analysed by time-consuming and labor-intensive techniques, such as microscopy and PCR. METHODS: Luciferase-expressing Plasmodium berghei parasites were used to measure pre-patent period of malaria infection in rodents using a bioluminescence assay that requires only one microliter of blood collected from the tail-vein. The accuracy and sensitivity of this new method was compared with conventional microscopy and PCR based techniques, and its capacity to measure the impact of anti-malarial interventions against the liver evaluated. RESULTS: The described method is very sensitive allowing the detection of parasites during the first cycles of blood stage replication. It accurately translates differences in liver load due to inoculation of different sporozoite doses as well as a result of treatment with different primaquine regimens. CONCLUSIONS: A novel, simple, fast, and sensitive method to measure pre-patent period of malaria infection in rodents is described here. The sensitivity and accuracy of this new method is comparable to standard PCR and microscopy-based techniques, respectively. |
format | Online Article Text |
id | pubmed-3893453 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38934532014-01-17 Simple, sensitive and quantitative bioluminescence assay for determination of malaria pre-patent period Zuzarte-Luis, Vanessa Sales-Dias, Joana Mota, Maria M Malar J Methodology BACKGROUND: The first phase of malaria infection occurs in the liver and is clinically silent. Inside hepatocytes each Plasmodium sporozoite replicate into thousands of erythrocyte-infectious merozoites that when released into the blood stream result in clinical symptoms of the disease. The time between sporozoite inoculation and the appearance of parasites in the blood is defined as the pre-patent period, which is classically analysed by time-consuming and labor-intensive techniques, such as microscopy and PCR. METHODS: Luciferase-expressing Plasmodium berghei parasites were used to measure pre-patent period of malaria infection in rodents using a bioluminescence assay that requires only one microliter of blood collected from the tail-vein. The accuracy and sensitivity of this new method was compared with conventional microscopy and PCR based techniques, and its capacity to measure the impact of anti-malarial interventions against the liver evaluated. RESULTS: The described method is very sensitive allowing the detection of parasites during the first cycles of blood stage replication. It accurately translates differences in liver load due to inoculation of different sporozoite doses as well as a result of treatment with different primaquine regimens. CONCLUSIONS: A novel, simple, fast, and sensitive method to measure pre-patent period of malaria infection in rodents is described here. The sensitivity and accuracy of this new method is comparable to standard PCR and microscopy-based techniques, respectively. BioMed Central 2014-01-08 /pmc/articles/PMC3893453/ /pubmed/24400642 http://dx.doi.org/10.1186/1475-2875-13-15 Text en Copyright © 2014 Zuzarte-Luis et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Methodology Zuzarte-Luis, Vanessa Sales-Dias, Joana Mota, Maria M Simple, sensitive and quantitative bioluminescence assay for determination of malaria pre-patent period |
title | Simple, sensitive and quantitative bioluminescence assay for determination of malaria pre-patent period |
title_full | Simple, sensitive and quantitative bioluminescence assay for determination of malaria pre-patent period |
title_fullStr | Simple, sensitive and quantitative bioluminescence assay for determination of malaria pre-patent period |
title_full_unstemmed | Simple, sensitive and quantitative bioluminescence assay for determination of malaria pre-patent period |
title_short | Simple, sensitive and quantitative bioluminescence assay for determination of malaria pre-patent period |
title_sort | simple, sensitive and quantitative bioluminescence assay for determination of malaria pre-patent period |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3893453/ https://www.ncbi.nlm.nih.gov/pubmed/24400642 http://dx.doi.org/10.1186/1475-2875-13-15 |
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