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Development of Loop-Mediated Isothermal Amplification (LAMP) Assays for Rapid Detection of Ehrlichia ruminantium

BACKGROUND: The rickettsial bacterium Ehrlichia ruminantium is the causative agent of heartwater, a potential zoonotic disease of ruminants transmitted by ticks of the genus Amblyomma. The disease is distributed in nearly all of sub-Saharan Africa and some islands of the Caribbean, from where it thr...

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Autores principales: Nakao, Ryo, Stromdahl, Ellen Y, Magona, Joseph W, Faburay, Bonto, Namangala, Boniface, Malele, Imna, Inoue, Noboru, Geysen, Dirk, Kajino, Kiichi, Jongejan, Frans, Sugimoto, Chihiro
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3000401/
https://www.ncbi.nlm.nih.gov/pubmed/21087521
http://dx.doi.org/10.1186/1471-2180-10-296
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author Nakao, Ryo
Stromdahl, Ellen Y
Magona, Joseph W
Faburay, Bonto
Namangala, Boniface
Malele, Imna
Inoue, Noboru
Geysen, Dirk
Kajino, Kiichi
Jongejan, Frans
Sugimoto, Chihiro
author_facet Nakao, Ryo
Stromdahl, Ellen Y
Magona, Joseph W
Faburay, Bonto
Namangala, Boniface
Malele, Imna
Inoue, Noboru
Geysen, Dirk
Kajino, Kiichi
Jongejan, Frans
Sugimoto, Chihiro
author_sort Nakao, Ryo
collection PubMed
description BACKGROUND: The rickettsial bacterium Ehrlichia ruminantium is the causative agent of heartwater, a potential zoonotic disease of ruminants transmitted by ticks of the genus Amblyomma. The disease is distributed in nearly all of sub-Saharan Africa and some islands of the Caribbean, from where it threatens the American mainland. This report describes the development of two different loop-mediated isothermal amplification (LAMP) assays for sensitive and specific detection of E. ruminantium. RESULTS: Two sets of LAMP primers were designed from the pCS20 and sodB genes. The detection limits for each assay were 10 copies for pCS20 and 5 copies for sodB, which is at least 10 times higher than that of the conventional pCS20 PCR assay. DNA amplification was completed within 60 min. The assays detected 16 different isolates of E. ruminantium from geographically distinct countries as well as two attenuated vaccine isolates. No cross-reaction was observed with genetically related Rickettsiales, including zoonotic Ehrlichia species from the USA. LAMP detected more positive samples than conventional PCR but less than real-time PCR, when tested with field samples collected in sub-Saharan countries. CONCLUSIONS: Due to its simplicity and specificity, LAMP has the potential for use in resource-poor settings and also for active screening of E. ruminantium in both heartwater-endemic areas and regions that are at risk of contracting the disease.
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spelling pubmed-30004012010-12-10 Development of Loop-Mediated Isothermal Amplification (LAMP) Assays for Rapid Detection of Ehrlichia ruminantium Nakao, Ryo Stromdahl, Ellen Y Magona, Joseph W Faburay, Bonto Namangala, Boniface Malele, Imna Inoue, Noboru Geysen, Dirk Kajino, Kiichi Jongejan, Frans Sugimoto, Chihiro BMC Microbiol Research Article BACKGROUND: The rickettsial bacterium Ehrlichia ruminantium is the causative agent of heartwater, a potential zoonotic disease of ruminants transmitted by ticks of the genus Amblyomma. The disease is distributed in nearly all of sub-Saharan Africa and some islands of the Caribbean, from where it threatens the American mainland. This report describes the development of two different loop-mediated isothermal amplification (LAMP) assays for sensitive and specific detection of E. ruminantium. RESULTS: Two sets of LAMP primers were designed from the pCS20 and sodB genes. The detection limits for each assay were 10 copies for pCS20 and 5 copies for sodB, which is at least 10 times higher than that of the conventional pCS20 PCR assay. DNA amplification was completed within 60 min. The assays detected 16 different isolates of E. ruminantium from geographically distinct countries as well as two attenuated vaccine isolates. No cross-reaction was observed with genetically related Rickettsiales, including zoonotic Ehrlichia species from the USA. LAMP detected more positive samples than conventional PCR but less than real-time PCR, when tested with field samples collected in sub-Saharan countries. CONCLUSIONS: Due to its simplicity and specificity, LAMP has the potential for use in resource-poor settings and also for active screening of E. ruminantium in both heartwater-endemic areas and regions that are at risk of contracting the disease. BioMed Central 2010-11-19 /pmc/articles/PMC3000401/ /pubmed/21087521 http://dx.doi.org/10.1186/1471-2180-10-296 Text en Copyright © 2010 Nakao 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.
spellingShingle Research Article
Nakao, Ryo
Stromdahl, Ellen Y
Magona, Joseph W
Faburay, Bonto
Namangala, Boniface
Malele, Imna
Inoue, Noboru
Geysen, Dirk
Kajino, Kiichi
Jongejan, Frans
Sugimoto, Chihiro
Development of Loop-Mediated Isothermal Amplification (LAMP) Assays for Rapid Detection of Ehrlichia ruminantium
title Development of Loop-Mediated Isothermal Amplification (LAMP) Assays for Rapid Detection of Ehrlichia ruminantium
title_full Development of Loop-Mediated Isothermal Amplification (LAMP) Assays for Rapid Detection of Ehrlichia ruminantium
title_fullStr Development of Loop-Mediated Isothermal Amplification (LAMP) Assays for Rapid Detection of Ehrlichia ruminantium
title_full_unstemmed Development of Loop-Mediated Isothermal Amplification (LAMP) Assays for Rapid Detection of Ehrlichia ruminantium
title_short Development of Loop-Mediated Isothermal Amplification (LAMP) Assays for Rapid Detection of Ehrlichia ruminantium
title_sort development of loop-mediated isothermal amplification (lamp) assays for rapid detection of ehrlichia ruminantium
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3000401/
https://www.ncbi.nlm.nih.gov/pubmed/21087521
http://dx.doi.org/10.1186/1471-2180-10-296
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