Gene expression analyses reveal differences in children’s response to malaria according to their age

Abstract In Bandiagara, Mali, children experience on average two clinical malaria episodes per year. However, even in the same transmission area, the number of uncomplicated symptomatic infections, and their parasitemia, can vary dramatically among children. We simultaneously characterize host and p...

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Main Authors: Kieran Tebben, Salif Yirampo, Drissa Coulibaly, Abdoulaye K. Koné, Matthew B. Laurens, Emily M. Stucke, Ahmadou Dembélé, Youssouf Tolo, Karim Traoré, Amadou Niangaly, Andrea A. Berry, Bourema Kouriba, Christopher V. Plowe, Ogobara K. Doumbo, Kirsten E. Lyke, Shannon Takala-Harrison, Mahamadou A. Thera, Mark A. Travassos, David Serre
Format: Article
Language:English
Published: Nature Portfolio 2024-03-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-024-46416-3
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author Kieran Tebben
Salif Yirampo
Drissa Coulibaly
Abdoulaye K. Koné
Matthew B. Laurens
Emily M. Stucke
Ahmadou Dembélé
Youssouf Tolo
Karim Traoré
Amadou Niangaly
Andrea A. Berry
Bourema Kouriba
Christopher V. Plowe
Ogobara K. Doumbo
Kirsten E. Lyke
Shannon Takala-Harrison
Mahamadou A. Thera
Mark A. Travassos
David Serre
author_facet Kieran Tebben
Salif Yirampo
Drissa Coulibaly
Abdoulaye K. Koné
Matthew B. Laurens
Emily M. Stucke
Ahmadou Dembélé
Youssouf Tolo
Karim Traoré
Amadou Niangaly
Andrea A. Berry
Bourema Kouriba
Christopher V. Plowe
Ogobara K. Doumbo
Kirsten E. Lyke
Shannon Takala-Harrison
Mahamadou A. Thera
Mark A. Travassos
David Serre
author_sort Kieran Tebben
collection DOAJ
description Abstract In Bandiagara, Mali, children experience on average two clinical malaria episodes per year. However, even in the same transmission area, the number of uncomplicated symptomatic infections, and their parasitemia, can vary dramatically among children. We simultaneously characterize host and parasite gene expression profiles from 136 Malian children with symptomatic falciparum malaria and examine differences in the relative proportion of immune cells and parasite stages, as well as in gene expression, associated with infection and or patient characteristics. Parasitemia explains much of the variation in host and parasite gene expression, and infections with higher parasitemia display proportionally more neutrophils and fewer T cells, suggesting parasitemia-dependent neutrophil recruitment and/or T cell extravasation to secondary lymphoid organs. The child’s age also strongly correlates with variations in gene expression: Plasmodium falciparum genes associated with age suggest that older children carry more male gametocytes, while variations in host gene expression indicate a stronger innate response in younger children and stronger adaptive response in older children. These analyses highlight the variability in host responses and parasite regulation during P. falciparum symptomatic infections and emphasize the importance of considering the children’s age when studying and treating malaria infections.
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spelling doaj.art-447cb3bdd8454f21a2e4e8996ab940e32024-03-10T12:16:13ZengNature PortfolioNature Communications2041-17232024-03-0115111410.1038/s41467-024-46416-3Gene expression analyses reveal differences in children’s response to malaria according to their ageKieran Tebben0Salif Yirampo1Drissa Coulibaly2Abdoulaye K. Koné3Matthew B. Laurens4Emily M. Stucke5Ahmadou Dembélé6Youssouf Tolo7Karim Traoré8Amadou Niangaly9Andrea A. Berry10Bourema Kouriba11Christopher V. Plowe12Ogobara K. Doumbo13Kirsten E. Lyke14Shannon Takala-Harrison15Mahamadou A. Thera16Mark A. Travassos17David Serre18Institute for Genome Sciences, University of Maryland School of MedicineMalaria Research and Training Center, University of Sciences, Techniques and TechnologiesMalaria Research and Training Center, University of Sciences, Techniques and TechnologiesMalaria Research and Training Center, University of Sciences, Techniques and TechnologiesMalaria Research Program, Center for Vaccine Development and Global Health, University of Maryland School of MedicineMalaria Research Program, Center for Vaccine Development and Global Health, University of Maryland School of MedicineMalaria Research and Training Center, University of Sciences, Techniques and TechnologiesMalaria Research and Training Center, University of Sciences, Techniques and TechnologiesMalaria Research and Training Center, University of Sciences, Techniques and TechnologiesMalaria Research and Training Center, University of Sciences, Techniques and TechnologiesMalaria Research Program, Center for Vaccine Development and Global Health, University of Maryland School of MedicineMalaria Research and Training Center, University of Sciences, Techniques and TechnologiesMalaria Research Program, Center for Vaccine Development and Global Health, University of Maryland School of MedicineMalaria Research and Training Center, University of Sciences, Techniques and TechnologiesMalaria Research Program, Center for Vaccine Development and Global Health, University of Maryland School of MedicineMalaria Research Program, Center for Vaccine Development and Global Health, University of Maryland School of MedicineMalaria Research and Training Center, University of Sciences, Techniques and TechnologiesMalaria Research Program, Center for Vaccine Development and Global Health, University of Maryland School of MedicineInstitute for Genome Sciences, University of Maryland School of MedicineAbstract In Bandiagara, Mali, children experience on average two clinical malaria episodes per year. However, even in the same transmission area, the number of uncomplicated symptomatic infections, and their parasitemia, can vary dramatically among children. We simultaneously characterize host and parasite gene expression profiles from 136 Malian children with symptomatic falciparum malaria and examine differences in the relative proportion of immune cells and parasite stages, as well as in gene expression, associated with infection and or patient characteristics. Parasitemia explains much of the variation in host and parasite gene expression, and infections with higher parasitemia display proportionally more neutrophils and fewer T cells, suggesting parasitemia-dependent neutrophil recruitment and/or T cell extravasation to secondary lymphoid organs. The child’s age also strongly correlates with variations in gene expression: Plasmodium falciparum genes associated with age suggest that older children carry more male gametocytes, while variations in host gene expression indicate a stronger innate response in younger children and stronger adaptive response in older children. These analyses highlight the variability in host responses and parasite regulation during P. falciparum symptomatic infections and emphasize the importance of considering the children’s age when studying and treating malaria infections.https://doi.org/10.1038/s41467-024-46416-3
spellingShingle Kieran Tebben
Salif Yirampo
Drissa Coulibaly
Abdoulaye K. Koné
Matthew B. Laurens
Emily M. Stucke
Ahmadou Dembélé
Youssouf Tolo
Karim Traoré
Amadou Niangaly
Andrea A. Berry
Bourema Kouriba
Christopher V. Plowe
Ogobara K. Doumbo
Kirsten E. Lyke
Shannon Takala-Harrison
Mahamadou A. Thera
Mark A. Travassos
David Serre
Gene expression analyses reveal differences in children’s response to malaria according to their age
Nature Communications
title Gene expression analyses reveal differences in children’s response to malaria according to their age
title_full Gene expression analyses reveal differences in children’s response to malaria according to their age
title_fullStr Gene expression analyses reveal differences in children’s response to malaria according to their age
title_full_unstemmed Gene expression analyses reveal differences in children’s response to malaria according to their age
title_short Gene expression analyses reveal differences in children’s response to malaria according to their age
title_sort gene expression analyses reveal differences in children s response to malaria according to their age
url https://doi.org/10.1038/s41467-024-46416-3
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