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Development of a rapid loop-mediated isothermal amplification assay for diagnosis and assessment of cure of Leishmania infection

BACKGROUND: Leishmaniasis is a spectrum of diseases with great relevance to public health. Conventional diagnostic methods are time consuming, needing trained personnel. A robust, rapid and cost effective diagnostic test is warranted for on-time diagnosis and field application. METHODS: We have deve...

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Autores principales: Verma, Sandeep, Singh, Ruchi, Sharma, Vanila, Bumb, Ram Avtar, Negi, Narendra Singh, Ramesh, V, Salotra, Poonam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363003/
https://www.ncbi.nlm.nih.gov/pubmed/28335752
http://dx.doi.org/10.1186/s12879-017-2318-8
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author Verma, Sandeep
Singh, Ruchi
Sharma, Vanila
Bumb, Ram Avtar
Negi, Narendra Singh
Ramesh, V
Salotra, Poonam
author_facet Verma, Sandeep
Singh, Ruchi
Sharma, Vanila
Bumb, Ram Avtar
Negi, Narendra Singh
Ramesh, V
Salotra, Poonam
author_sort Verma, Sandeep
collection PubMed
description BACKGROUND: Leishmaniasis is a spectrum of diseases with great relevance to public health. Conventional diagnostic methods are time consuming, needing trained personnel. A robust, rapid and cost effective diagnostic test is warranted for on-time diagnosis and field application. METHODS: We have developed a loop mediated isothermal amplification (LAMP) assay with primers (n = 6) based on Leishmania donovani kDNA for detection of Leishmania infection, using a closed tube to prevent cross-contamination. The assay was used to detect Leishmania infection in biological samples obtained from patients of visceral leishmaniasis (VL), post kala-azar dermal leishmaniasis (PKDL) and cutaneous leishmaniasis (CL). RESULTS: The assay was positive for L. donovani, L. tropica and L. major parasites, with the highest sensitivity towards L. donovani (1 fg DNA). The high sensitivity of the assay for detection of L. donovani was reflected in its ability to detect parasite DNA within 30 min of amplification time with a threshold detection limit of ≥25 copies per reaction. The assay detected parasite in 64 of 66 VL blood samples (sensitivity, 96.9%; 95% CI: 89.6-99.2%), 15 of 15 VL bone marrow aspirate samples (sensitivity, 100%; 95% CI:79.6-100%), 65 of 67 PKDL tissue biopsy samples (sensitivity, 97%; 95% CI:89.7-99.2%). The assay was evaluated in a few cases of CL wherein it was found positive in 8 of 10 tissue biopsies (sensitivity, 80%; 95% CI: 49-94.3%). The assay was negative in all control blood (n = 76) and tissue biopsy (n = 24) samples (specificity, 100%; 95% CI: 96.3-100%). Further, the assay was evaluated for its utility in assessment of cure in treated VL and PKDL patients. The assay detected parasite DNA in 2 of 20VL blood samples and 2 of 21 PKDL tissue samples. Out of 4 cases that were positive for parasite DNA at post treatment stage, 2 patients (1VL and 1 PKDL) returned with relapse. CONCLUSIONS: The study demonstrated a Leishmania genus specific closed tube LAMP assay for reliable and rapid molecular diagnosis of VL and PKDL with potential for application in assessment of cure.
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spelling pubmed-53630032017-03-24 Development of a rapid loop-mediated isothermal amplification assay for diagnosis and assessment of cure of Leishmania infection Verma, Sandeep Singh, Ruchi Sharma, Vanila Bumb, Ram Avtar Negi, Narendra Singh Ramesh, V Salotra, Poonam BMC Infect Dis Research Article BACKGROUND: Leishmaniasis is a spectrum of diseases with great relevance to public health. Conventional diagnostic methods are time consuming, needing trained personnel. A robust, rapid and cost effective diagnostic test is warranted for on-time diagnosis and field application. METHODS: We have developed a loop mediated isothermal amplification (LAMP) assay with primers (n = 6) based on Leishmania donovani kDNA for detection of Leishmania infection, using a closed tube to prevent cross-contamination. The assay was used to detect Leishmania infection in biological samples obtained from patients of visceral leishmaniasis (VL), post kala-azar dermal leishmaniasis (PKDL) and cutaneous leishmaniasis (CL). RESULTS: The assay was positive for L. donovani, L. tropica and L. major parasites, with the highest sensitivity towards L. donovani (1 fg DNA). The high sensitivity of the assay for detection of L. donovani was reflected in its ability to detect parasite DNA within 30 min of amplification time with a threshold detection limit of ≥25 copies per reaction. The assay detected parasite in 64 of 66 VL blood samples (sensitivity, 96.9%; 95% CI: 89.6-99.2%), 15 of 15 VL bone marrow aspirate samples (sensitivity, 100%; 95% CI:79.6-100%), 65 of 67 PKDL tissue biopsy samples (sensitivity, 97%; 95% CI:89.7-99.2%). The assay was evaluated in a few cases of CL wherein it was found positive in 8 of 10 tissue biopsies (sensitivity, 80%; 95% CI: 49-94.3%). The assay was negative in all control blood (n = 76) and tissue biopsy (n = 24) samples (specificity, 100%; 95% CI: 96.3-100%). Further, the assay was evaluated for its utility in assessment of cure in treated VL and PKDL patients. The assay detected parasite DNA in 2 of 20VL blood samples and 2 of 21 PKDL tissue samples. Out of 4 cases that were positive for parasite DNA at post treatment stage, 2 patients (1VL and 1 PKDL) returned with relapse. CONCLUSIONS: The study demonstrated a Leishmania genus specific closed tube LAMP assay for reliable and rapid molecular diagnosis of VL and PKDL with potential for application in assessment of cure. BioMed Central 2017-03-23 /pmc/articles/PMC5363003/ /pubmed/28335752 http://dx.doi.org/10.1186/s12879-017-2318-8 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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 Research Article
Verma, Sandeep
Singh, Ruchi
Sharma, Vanila
Bumb, Ram Avtar
Negi, Narendra Singh
Ramesh, V
Salotra, Poonam
Development of a rapid loop-mediated isothermal amplification assay for diagnosis and assessment of cure of Leishmania infection
title Development of a rapid loop-mediated isothermal amplification assay for diagnosis and assessment of cure of Leishmania infection
title_full Development of a rapid loop-mediated isothermal amplification assay for diagnosis and assessment of cure of Leishmania infection
title_fullStr Development of a rapid loop-mediated isothermal amplification assay for diagnosis and assessment of cure of Leishmania infection
title_full_unstemmed Development of a rapid loop-mediated isothermal amplification assay for diagnosis and assessment of cure of Leishmania infection
title_short Development of a rapid loop-mediated isothermal amplification assay for diagnosis and assessment of cure of Leishmania infection
title_sort development of a rapid loop-mediated isothermal amplification assay for diagnosis and assessment of cure of leishmania infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363003/
https://www.ncbi.nlm.nih.gov/pubmed/28335752
http://dx.doi.org/10.1186/s12879-017-2318-8
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