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Stool microbiota composition is associated with the prospective risk of Plasmodium falciparum infection
BACKGROUND: In humans it is unknown if the composition of the gut microbiota alters the risk of Plasmodium falciparum infection or the risk of developing febrile malaria once P. falciparum infection is established. Here we collected stool samples from a cohort composed of 195 Malian children and adu...
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/PMC4546150/ https://www.ncbi.nlm.nih.gov/pubmed/26296559 http://dx.doi.org/10.1186/s12864-015-1819-3 |
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author | Yooseph, Shibu Kirkness, Ewen F. Tran, Tuan M. Harkins, Derek M. Jones, Marcus B. Torralba, Manolito G. O’Connell, Elise Nutman, Thomas B. Doumbo, Safiatou Doumbo, Ogobara K. Traore, Boubacar Crompton, Peter D. Nelson, Karen E. |
author_facet | Yooseph, Shibu Kirkness, Ewen F. Tran, Tuan M. Harkins, Derek M. Jones, Marcus B. Torralba, Manolito G. O’Connell, Elise Nutman, Thomas B. Doumbo, Safiatou Doumbo, Ogobara K. Traore, Boubacar Crompton, Peter D. Nelson, Karen E. |
author_sort | Yooseph, Shibu |
collection | PubMed |
description | BACKGROUND: In humans it is unknown if the composition of the gut microbiota alters the risk of Plasmodium falciparum infection or the risk of developing febrile malaria once P. falciparum infection is established. Here we collected stool samples from a cohort composed of 195 Malian children and adults just prior to an intense P. falciparum transmission season. We assayed these samples using massively parallel sequencing of the 16S ribosomal RNA gene to identify the composition of the gut bacterial communities in these individuals. During the ensuing 6-month P. falciparum transmission season we examined the relationship between the stool microbiota composition of individuals in this cohort and their prospective risk of both P. falciparum infection and febrile malaria. RESULTS: Consistent with prior studies, stool microbial diversity in the present cohort increased with age, although the overall microbiota profile was distinct from cohorts in other regions of Africa, Asia and North America. Age-adjusted Cox regression analysis revealed a significant association between microbiota composition and the prospective risk of P. falciparum infection; however, no relationship was observed between microbiota composition and the risk of developing febrile malaria once P. falciparum infection was established. CONCLUSIONS: These findings underscore the diversity of gut microbiota across geographic regions, and suggest that strategic modulation of gut microbiota composition could decrease the risk of P. falciparum infection in malaria-endemic areas, potentially as an adjunct to partially effective malaria vaccines. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1819-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4546150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45461502015-08-23 Stool microbiota composition is associated with the prospective risk of Plasmodium falciparum infection Yooseph, Shibu Kirkness, Ewen F. Tran, Tuan M. Harkins, Derek M. Jones, Marcus B. Torralba, Manolito G. O’Connell, Elise Nutman, Thomas B. Doumbo, Safiatou Doumbo, Ogobara K. Traore, Boubacar Crompton, Peter D. Nelson, Karen E. BMC Genomics Research Article BACKGROUND: In humans it is unknown if the composition of the gut microbiota alters the risk of Plasmodium falciparum infection or the risk of developing febrile malaria once P. falciparum infection is established. Here we collected stool samples from a cohort composed of 195 Malian children and adults just prior to an intense P. falciparum transmission season. We assayed these samples using massively parallel sequencing of the 16S ribosomal RNA gene to identify the composition of the gut bacterial communities in these individuals. During the ensuing 6-month P. falciparum transmission season we examined the relationship between the stool microbiota composition of individuals in this cohort and their prospective risk of both P. falciparum infection and febrile malaria. RESULTS: Consistent with prior studies, stool microbial diversity in the present cohort increased with age, although the overall microbiota profile was distinct from cohorts in other regions of Africa, Asia and North America. Age-adjusted Cox regression analysis revealed a significant association between microbiota composition and the prospective risk of P. falciparum infection; however, no relationship was observed between microbiota composition and the risk of developing febrile malaria once P. falciparum infection was established. CONCLUSIONS: These findings underscore the diversity of gut microbiota across geographic regions, and suggest that strategic modulation of gut microbiota composition could decrease the risk of P. falciparum infection in malaria-endemic areas, potentially as an adjunct to partially effective malaria vaccines. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1819-3) contains supplementary material, which is available to authorized users. BioMed Central 2015-08-22 /pmc/articles/PMC4546150/ /pubmed/26296559 http://dx.doi.org/10.1186/s12864-015-1819-3 Text en © Yooseph et al. 2015 Open Access This 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 Yooseph, Shibu Kirkness, Ewen F. Tran, Tuan M. Harkins, Derek M. Jones, Marcus B. Torralba, Manolito G. O’Connell, Elise Nutman, Thomas B. Doumbo, Safiatou Doumbo, Ogobara K. Traore, Boubacar Crompton, Peter D. Nelson, Karen E. Stool microbiota composition is associated with the prospective risk of Plasmodium falciparum infection |
title | Stool microbiota composition is associated with the prospective risk of Plasmodium falciparum infection |
title_full | Stool microbiota composition is associated with the prospective risk of Plasmodium falciparum infection |
title_fullStr | Stool microbiota composition is associated with the prospective risk of Plasmodium falciparum infection |
title_full_unstemmed | Stool microbiota composition is associated with the prospective risk of Plasmodium falciparum infection |
title_short | Stool microbiota composition is associated with the prospective risk of Plasmodium falciparum infection |
title_sort | stool microbiota composition is associated with the prospective risk of plasmodium falciparum infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4546150/ https://www.ncbi.nlm.nih.gov/pubmed/26296559 http://dx.doi.org/10.1186/s12864-015-1819-3 |
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