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An ultrasensitive reverse transcription polymerase chain reaction assay to detect asymptomatic low-density Plasmodium falciparum and Plasmodium vivax infections in small volume blood samples
BACKGROUND: Highly sensitive, scalable diagnostic methods are needed to guide malaria elimination interventions. While traditional microscopy and rapid diagnostic tests (RDTs) are suitable for the diagnosis of symptomatic malaria infection, more sensitive tests are needed to screen for low-density,...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4690410/ https://www.ncbi.nlm.nih.gov/pubmed/26701778 http://dx.doi.org/10.1186/s12936-015-1038-z |
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author | Adams, Matthew Joshi, Sudhaunshu N. Mbambo, Gillian Mu, Amy Z. Roemmich, Shay M. Shrestha, Biraj Strauss, Kathy A. Johnson, Nicole Eddington Oo, Khine Zaw Hlaing, Tin Maung Han, Zay Yar Han, Kay Thwe Thura, Si Richards, Adam K. Huang, Fang Nyunt, Myaing M. Plowe, Christopher V. |
author_facet | Adams, Matthew Joshi, Sudhaunshu N. Mbambo, Gillian Mu, Amy Z. Roemmich, Shay M. Shrestha, Biraj Strauss, Kathy A. Johnson, Nicole Eddington Oo, Khine Zaw Hlaing, Tin Maung Han, Zay Yar Han, Kay Thwe Thura, Si Richards, Adam K. Huang, Fang Nyunt, Myaing M. Plowe, Christopher V. |
author_sort | Adams, Matthew |
collection | PubMed |
description | BACKGROUND: Highly sensitive, scalable diagnostic methods are needed to guide malaria elimination interventions. While traditional microscopy and rapid diagnostic tests (RDTs) are suitable for the diagnosis of symptomatic malaria infection, more sensitive tests are needed to screen for low-density, asymptomatic infections that are targeted by interventions aiming to eliminate the entire reservoir of malaria infection in humans. METHODS: A reverse transcription polymerase chain reaction (RT- PCR) was developed for multiplexed detection of the 18S ribosomal RNA gene and ribosomal RNA of Plasmodium falciparum and Plasmodium vivax. Simulated field samples stored for 14 days with sample preservation buffer were used to assess the analytical sensitivity and specificity. Additionally, 1750 field samples from Southeastern Myanmar were tested both by RDT and ultrasensitive RT-PCR. RESULTS: Limits of detection (LoD) were determined under simulated field conditions. When 0.3 mL blood samples were stored for 14 days at 28 °C and 80 % humidity, the LoD was less than 16 parasites/mL for P. falciparum and 19.7 copies/µL for P. vivax (using a plasmid surrogate), about 10,000-fold lower than RDTs. Of the 1739 samples successfully evaluated by both ultrasensitive RT-PCR and RDT, only two were RDT positive while 24 were positive for P. falciparum, 108 were positive for P. vivax, and 127 were positive for either P. vivax and/or P. falciparum using ultrasensitive RT-PCR. CONCLUSIONS: This ultrasensitive RT-PCR method is a robust, field-tested screening method that is vastly more sensitive than RDTs. Further optimization may result in a truly scalable tool suitable for widespread surveillance of low-level asymptomatic P. falciparum and P. vivax parasitaemia. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12936-015-1038-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4690410 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46904102015-12-25 An ultrasensitive reverse transcription polymerase chain reaction assay to detect asymptomatic low-density Plasmodium falciparum and Plasmodium vivax infections in small volume blood samples Adams, Matthew Joshi, Sudhaunshu N. Mbambo, Gillian Mu, Amy Z. Roemmich, Shay M. Shrestha, Biraj Strauss, Kathy A. Johnson, Nicole Eddington Oo, Khine Zaw Hlaing, Tin Maung Han, Zay Yar Han, Kay Thwe Thura, Si Richards, Adam K. Huang, Fang Nyunt, Myaing M. Plowe, Christopher V. Malar J Methodology BACKGROUND: Highly sensitive, scalable diagnostic methods are needed to guide malaria elimination interventions. While traditional microscopy and rapid diagnostic tests (RDTs) are suitable for the diagnosis of symptomatic malaria infection, more sensitive tests are needed to screen for low-density, asymptomatic infections that are targeted by interventions aiming to eliminate the entire reservoir of malaria infection in humans. METHODS: A reverse transcription polymerase chain reaction (RT- PCR) was developed for multiplexed detection of the 18S ribosomal RNA gene and ribosomal RNA of Plasmodium falciparum and Plasmodium vivax. Simulated field samples stored for 14 days with sample preservation buffer were used to assess the analytical sensitivity and specificity. Additionally, 1750 field samples from Southeastern Myanmar were tested both by RDT and ultrasensitive RT-PCR. RESULTS: Limits of detection (LoD) were determined under simulated field conditions. When 0.3 mL blood samples were stored for 14 days at 28 °C and 80 % humidity, the LoD was less than 16 parasites/mL for P. falciparum and 19.7 copies/µL for P. vivax (using a plasmid surrogate), about 10,000-fold lower than RDTs. Of the 1739 samples successfully evaluated by both ultrasensitive RT-PCR and RDT, only two were RDT positive while 24 were positive for P. falciparum, 108 were positive for P. vivax, and 127 were positive for either P. vivax and/or P. falciparum using ultrasensitive RT-PCR. CONCLUSIONS: This ultrasensitive RT-PCR method is a robust, field-tested screening method that is vastly more sensitive than RDTs. Further optimization may result in a truly scalable tool suitable for widespread surveillance of low-level asymptomatic P. falciparum and P. vivax parasitaemia. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12936-015-1038-z) contains supplementary material, which is available to authorized users. BioMed Central 2015-12-23 /pmc/articles/PMC4690410/ /pubmed/26701778 http://dx.doi.org/10.1186/s12936-015-1038-z Text en © Adams et al. 2015 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 | Methodology Adams, Matthew Joshi, Sudhaunshu N. Mbambo, Gillian Mu, Amy Z. Roemmich, Shay M. Shrestha, Biraj Strauss, Kathy A. Johnson, Nicole Eddington Oo, Khine Zaw Hlaing, Tin Maung Han, Zay Yar Han, Kay Thwe Thura, Si Richards, Adam K. Huang, Fang Nyunt, Myaing M. Plowe, Christopher V. An ultrasensitive reverse transcription polymerase chain reaction assay to detect asymptomatic low-density Plasmodium falciparum and Plasmodium vivax infections in small volume blood samples |
title | An ultrasensitive reverse transcription polymerase chain reaction assay to detect asymptomatic low-density Plasmodium falciparum and Plasmodium vivax infections in small volume blood samples |
title_full | An ultrasensitive reverse transcription polymerase chain reaction assay to detect asymptomatic low-density Plasmodium falciparum and Plasmodium vivax infections in small volume blood samples |
title_fullStr | An ultrasensitive reverse transcription polymerase chain reaction assay to detect asymptomatic low-density Plasmodium falciparum and Plasmodium vivax infections in small volume blood samples |
title_full_unstemmed | An ultrasensitive reverse transcription polymerase chain reaction assay to detect asymptomatic low-density Plasmodium falciparum and Plasmodium vivax infections in small volume blood samples |
title_short | An ultrasensitive reverse transcription polymerase chain reaction assay to detect asymptomatic low-density Plasmodium falciparum and Plasmodium vivax infections in small volume blood samples |
title_sort | ultrasensitive reverse transcription polymerase chain reaction assay to detect asymptomatic low-density plasmodium falciparum and plasmodium vivax infections in small volume blood samples |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4690410/ https://www.ncbi.nlm.nih.gov/pubmed/26701778 http://dx.doi.org/10.1186/s12936-015-1038-z |
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