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Volatile biomarkers of symptomatic and asymptomatic malaria infection in humans
Malaria remains among the world’s deadliest diseases, and control efforts depend critically on the availability of effective diagnostic tools, particularly for the identification of asymptomatic infections, which play a key role in disease persistence and may account for most instances of transmissi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5984526/ https://www.ncbi.nlm.nih.gov/pubmed/29760095 http://dx.doi.org/10.1073/pnas.1801512115 |
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author | De Moraes, Consuelo M. Wanjiku, Caroline Stanczyk, Nina M. Pulido, Hannier Sims, James W. Betz, Heike S. Read, Andrew F. Torto, Baldwyn Mescher, Mark C. |
author_facet | De Moraes, Consuelo M. Wanjiku, Caroline Stanczyk, Nina M. Pulido, Hannier Sims, James W. Betz, Heike S. Read, Andrew F. Torto, Baldwyn Mescher, Mark C. |
author_sort | De Moraes, Consuelo M. |
collection | PubMed |
description | Malaria remains among the world’s deadliest diseases, and control efforts depend critically on the availability of effective diagnostic tools, particularly for the identification of asymptomatic infections, which play a key role in disease persistence and may account for most instances of transmission but often evade detection by current screening methods. Research on humans and in animal models has shown that infection by malaria parasites elicits changes in host odors that influence vector attraction, suggesting that such changes might yield robust biomarkers of infection status. Here we present findings based on extensive collections of skin volatiles from human populations with high rates of malaria infection in Kenya. We report broad and consistent effects of malaria infection on human volatile profiles, as well as significant divergence in the effects of symptomatic and asymptomatic infections. Furthermore, predictive models based on machine learning algorithms reliably determined infection status based on volatile biomarkers. Critically, our models identified asymptomatic infections with 100% sensitivity, even in the case of low-level infections not detectable by microscopy, far exceeding the performance of currently available rapid diagnostic tests in this regard. We also identified a set of individual compounds that emerged as consistently important predictors of infection status. These findings suggest that volatile biomarkers may have significant potential for the development of a robust, noninvasive screening method for detecting malaria infections under field conditions. |
format | Online Article Text |
id | pubmed-5984526 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-59845262018-06-07 Volatile biomarkers of symptomatic and asymptomatic malaria infection in humans De Moraes, Consuelo M. Wanjiku, Caroline Stanczyk, Nina M. Pulido, Hannier Sims, James W. Betz, Heike S. Read, Andrew F. Torto, Baldwyn Mescher, Mark C. Proc Natl Acad Sci U S A Biological Sciences Malaria remains among the world’s deadliest diseases, and control efforts depend critically on the availability of effective diagnostic tools, particularly for the identification of asymptomatic infections, which play a key role in disease persistence and may account for most instances of transmission but often evade detection by current screening methods. Research on humans and in animal models has shown that infection by malaria parasites elicits changes in host odors that influence vector attraction, suggesting that such changes might yield robust biomarkers of infection status. Here we present findings based on extensive collections of skin volatiles from human populations with high rates of malaria infection in Kenya. We report broad and consistent effects of malaria infection on human volatile profiles, as well as significant divergence in the effects of symptomatic and asymptomatic infections. Furthermore, predictive models based on machine learning algorithms reliably determined infection status based on volatile biomarkers. Critically, our models identified asymptomatic infections with 100% sensitivity, even in the case of low-level infections not detectable by microscopy, far exceeding the performance of currently available rapid diagnostic tests in this regard. We also identified a set of individual compounds that emerged as consistently important predictors of infection status. These findings suggest that volatile biomarkers may have significant potential for the development of a robust, noninvasive screening method for detecting malaria infections under field conditions. National Academy of Sciences 2018-05-29 2018-05-14 /pmc/articles/PMC5984526/ /pubmed/29760095 http://dx.doi.org/10.1073/pnas.1801512115 Text en Copyright © 2018 the Author(s). Published by PNAS. http://creativecommons.org/licenses/by/4.0/ This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Biological Sciences De Moraes, Consuelo M. Wanjiku, Caroline Stanczyk, Nina M. Pulido, Hannier Sims, James W. Betz, Heike S. Read, Andrew F. Torto, Baldwyn Mescher, Mark C. Volatile biomarkers of symptomatic and asymptomatic malaria infection in humans |
title | Volatile biomarkers of symptomatic and asymptomatic malaria infection in humans |
title_full | Volatile biomarkers of symptomatic and asymptomatic malaria infection in humans |
title_fullStr | Volatile biomarkers of symptomatic and asymptomatic malaria infection in humans |
title_full_unstemmed | Volatile biomarkers of symptomatic and asymptomatic malaria infection in humans |
title_short | Volatile biomarkers of symptomatic and asymptomatic malaria infection in humans |
title_sort | volatile biomarkers of symptomatic and asymptomatic malaria infection in humans |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5984526/ https://www.ncbi.nlm.nih.gov/pubmed/29760095 http://dx.doi.org/10.1073/pnas.1801512115 |
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