BMC Genomics | |
Stool microbiota composition is associated with the prospective risk of Plasmodium falciparum infection | |
Research Article | |
Marcus B. Jones1  Shibu Yooseph1  Karen E. Nelson1  Derek M. Harkins2  Ewen F. Kirkness2  Manolito G. Torralba2  Tuan M. Tran3  Peter D. Crompton3  Elise O’Connell4  Thomas B. Nutman4  Boubacar Traore5  Safiatou Doumbo5  Ogobara K. Doumbo5  | |
[1] J. Craig Venter Institute, 4120 Capricorn Lane, 92037, La Jolla, CA, USA;J. Craig Venter Institute, 9704 Medical Center Drive, 20850, Rockville, MD, USA;Laboratory of Immunogenetics, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 20852, Rockville, MD, USA;Laboratory of Parasitic Diseases, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 20892, Bethesda, MD, USA;Malaria Research and Training Centre, Department of Epidemiology of Parasitic Diseases, International Center of Excellence in Research, University of Sciences, Technique and Technology of Bamako, Bamako, Mali; | |
关键词: Stool microbiota; Gut microbiota; Malaria; 16S rRNA gene sequencing; Plasmodium falciparum; Human; Prospective cohort; | |
DOI : 10.1186/s12864-015-1819-3 | |
received in 2015-04-22, accepted in 2015-08-05, 发布年份 2015 | |
来源: Springer | |
【 摘 要 】
BackgroundIn 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.ResultsConsistent 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.ConclusionsThese 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.
【 授权许可】
CC BY
© Yooseph et al. 2015
【 预 览 】
Files | Size | Format | View |
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RO202311100592213ZK.pdf | 1532KB | download |
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