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Development and clinical performance of high throughput loop-mediated isothermal amplification for detection of malaria

BACKGROUND: Accurate and efficient detection of sub-microscopic malaria infections is crucial for enabling rapid treatment and interruption of transmission. Commercially available malaria LAMP kits have excellent diagnostic performance, though throughput is limited by the need to prepare samples ind...

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Autores principales: Perera, Rushini S., Ding, Xavier C., Tully, Frank, Oliver, James, Bright, Nigel, Bell, David, Chiodini, Peter L., Gonzalez, Iveth J., Polley, Spencer D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5293265/
https://www.ncbi.nlm.nih.gov/pubmed/28166235
http://dx.doi.org/10.1371/journal.pone.0171126
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author Perera, Rushini S.
Ding, Xavier C.
Tully, Frank
Oliver, James
Bright, Nigel
Bell, David
Chiodini, Peter L.
Gonzalez, Iveth J.
Polley, Spencer D.
author_facet Perera, Rushini S.
Ding, Xavier C.
Tully, Frank
Oliver, James
Bright, Nigel
Bell, David
Chiodini, Peter L.
Gonzalez, Iveth J.
Polley, Spencer D.
author_sort Perera, Rushini S.
collection PubMed
description BACKGROUND: Accurate and efficient detection of sub-microscopic malaria infections is crucial for enabling rapid treatment and interruption of transmission. Commercially available malaria LAMP kits have excellent diagnostic performance, though throughput is limited by the need to prepare samples individually. Here, we evaluate the clinical performance of a newly developed high throughput (HTP) sample processing system for use in conjunction with the Eiken malaria LAMP kit. METHODS: The HTP system utilised dried blood spots (DBS) and liquid whole blood (WB), with parallel sample processing of 94 samples per run. The system was evaluated using 699 samples of known infection status pre-determined by gold standard nested PCR. RESULTS: The sensitivity and specificity of WB-HTP-LAMP was 98.6% (95% CI, 95.7–100), and 99.7% (95% CI, 99.2–100); sensitivity of DBS-HTP-LAMP was 97.1% (95% CI, 93.1–100), and specificity 100% against PCR. At parasite densities greater or equal to 2 parasites/μL, WB and DBS HTP-LAMP showed 100% sensitivity and specificity against PCR. At densities less than 2 p/μL, WB-HTP-LAMP sensitivity was 88.9% (95% CI, 77.1–100) and specificity was 99.7% (95% CI, 99.2–100); sensitivity and specificity of DBS-HTP-LAMP was 77.8% (95% CI, 54.3–99.5) and 100% respectively. CONCLUSIONS: The HTP-LAMP system is a highly sensitive diagnostic test, with the potential to allow large scale population screening in malaria elimination campaigns.
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spelling pubmed-52932652017-02-17 Development and clinical performance of high throughput loop-mediated isothermal amplification for detection of malaria Perera, Rushini S. Ding, Xavier C. Tully, Frank Oliver, James Bright, Nigel Bell, David Chiodini, Peter L. Gonzalez, Iveth J. Polley, Spencer D. PLoS One Research Article BACKGROUND: Accurate and efficient detection of sub-microscopic malaria infections is crucial for enabling rapid treatment and interruption of transmission. Commercially available malaria LAMP kits have excellent diagnostic performance, though throughput is limited by the need to prepare samples individually. Here, we evaluate the clinical performance of a newly developed high throughput (HTP) sample processing system for use in conjunction with the Eiken malaria LAMP kit. METHODS: The HTP system utilised dried blood spots (DBS) and liquid whole blood (WB), with parallel sample processing of 94 samples per run. The system was evaluated using 699 samples of known infection status pre-determined by gold standard nested PCR. RESULTS: The sensitivity and specificity of WB-HTP-LAMP was 98.6% (95% CI, 95.7–100), and 99.7% (95% CI, 99.2–100); sensitivity of DBS-HTP-LAMP was 97.1% (95% CI, 93.1–100), and specificity 100% against PCR. At parasite densities greater or equal to 2 parasites/μL, WB and DBS HTP-LAMP showed 100% sensitivity and specificity against PCR. At densities less than 2 p/μL, WB-HTP-LAMP sensitivity was 88.9% (95% CI, 77.1–100) and specificity was 99.7% (95% CI, 99.2–100); sensitivity and specificity of DBS-HTP-LAMP was 77.8% (95% CI, 54.3–99.5) and 100% respectively. CONCLUSIONS: The HTP-LAMP system is a highly sensitive diagnostic test, with the potential to allow large scale population screening in malaria elimination campaigns. Public Library of Science 2017-02-06 /pmc/articles/PMC5293265/ /pubmed/28166235 http://dx.doi.org/10.1371/journal.pone.0171126 Text en © 2017 Perera 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Perera, Rushini S.
Ding, Xavier C.
Tully, Frank
Oliver, James
Bright, Nigel
Bell, David
Chiodini, Peter L.
Gonzalez, Iveth J.
Polley, Spencer D.
Development and clinical performance of high throughput loop-mediated isothermal amplification for detection of malaria
title Development and clinical performance of high throughput loop-mediated isothermal amplification for detection of malaria
title_full Development and clinical performance of high throughput loop-mediated isothermal amplification for detection of malaria
title_fullStr Development and clinical performance of high throughput loop-mediated isothermal amplification for detection of malaria
title_full_unstemmed Development and clinical performance of high throughput loop-mediated isothermal amplification for detection of malaria
title_short Development and clinical performance of high throughput loop-mediated isothermal amplification for detection of malaria
title_sort development and clinical performance of high throughput loop-mediated isothermal amplification for detection of malaria
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5293265/
https://www.ncbi.nlm.nih.gov/pubmed/28166235
http://dx.doi.org/10.1371/journal.pone.0171126
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