Host and Parasite Transcriptomic Changes upon Successive <named-content content-type="genus-species">Plasmodium falciparum</named-content> Infections in Early Childhood

ABSTRACT Children are highly susceptible to clinical malaria, and in regions where malaria is endemic, their immune systems must face successive encounters with Plasmodium falciparum parasites before they develop immunity, first against severe disease and later against uncomplicated malaria. Underst...

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Autores principales: Katie R. Bradwell, Drissa Coulibaly, Abdoulaye K. Koné, Matthew B. Laurens, 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
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Publicado: American Society for Microbiology 2020
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spelling oai:doaj.org-article:4e3104401ead46c1a245fe5ab39d23c32021-12-02T18:44:37ZHost and Parasite Transcriptomic Changes upon Successive <named-content content-type="genus-species">Plasmodium falciparum</named-content> Infections in Early Childhood10.1128/mSystems.00116-202379-5077https://doaj.org/article/4e3104401ead46c1a245fe5ab39d23c32020-08-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mSystems.00116-20https://doaj.org/toc/2379-5077ABSTRACT Children are highly susceptible to clinical malaria, and in regions where malaria is endemic, their immune systems must face successive encounters with Plasmodium falciparum parasites before they develop immunity, first against severe disease and later against uncomplicated malaria. Understanding cellular and molecular interactions between host and parasites during an infection could provide insights into the processes underlying this gradual acquisition of immunity, as well as to how parasites adapt to infect hosts that are successively more malaria experienced. Here, we describe methods to analyze the host and parasite gene expression profiles generated simultaneously from blood samples collected from five consecutive symptomatic P. falciparum infections in three Malian children. We show that the data generated enable statistical assessment of the proportions of (i) each white blood cell subset and (ii) the parasite developmental stages, as well as investigations of host-parasite gene coexpression. We also use the sequences generated to analyze allelic variations in transcribed regions and determine the complexity of each infection. While limited by the modest sample size, our analyses suggest that host gene expression profiles primarily clustered by individual, while the parasite gene expression profiles seemed to differentiate early from late infections. Overall, this study provides a solid framework to examine the mechanisms underlying acquisition of immunity to malaria infections using whole-blood transcriptome sequencing (RNA-seq). IMPORTANCE We show that dual RNA-seq from patient blood samples allows characterization of host/parasite interactions during malaria infections and can provide a solid framework to study the acquisition of antimalarial immunity, as well as the adaptations of P. falciparum to malaria-experienced hosts.Katie R. BradwellDrissa CoulibalyAbdoulaye K. KonéMatthew B. LaurensAhmadou DembéléYoussouf ToloKarim TraoréAmadou NiangalyAndrea A. BerryBourema KouribaChristopher V. PloweOgobara K. DoumboKirsten E. LykeShannon Takala-HarrisonMahamadou A. TheraMark A. TravassosDavid SerreAmerican Society for MicrobiologyarticlemalariatranscriptomicsMicrobiologyQR1-502ENmSystems, Vol 5, Iss 4 (2020)
institution DOAJ
collection DOAJ
language EN
topic malaria
transcriptomics
Microbiology
QR1-502
spellingShingle malaria
transcriptomics
Microbiology
QR1-502
Katie R. Bradwell
Drissa Coulibaly
Abdoulaye K. Koné
Matthew B. Laurens
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
Host and Parasite Transcriptomic Changes upon Successive <named-content content-type="genus-species">Plasmodium falciparum</named-content> Infections in Early Childhood
description ABSTRACT Children are highly susceptible to clinical malaria, and in regions where malaria is endemic, their immune systems must face successive encounters with Plasmodium falciparum parasites before they develop immunity, first against severe disease and later against uncomplicated malaria. Understanding cellular and molecular interactions between host and parasites during an infection could provide insights into the processes underlying this gradual acquisition of immunity, as well as to how parasites adapt to infect hosts that are successively more malaria experienced. Here, we describe methods to analyze the host and parasite gene expression profiles generated simultaneously from blood samples collected from five consecutive symptomatic P. falciparum infections in three Malian children. We show that the data generated enable statistical assessment of the proportions of (i) each white blood cell subset and (ii) the parasite developmental stages, as well as investigations of host-parasite gene coexpression. We also use the sequences generated to analyze allelic variations in transcribed regions and determine the complexity of each infection. While limited by the modest sample size, our analyses suggest that host gene expression profiles primarily clustered by individual, while the parasite gene expression profiles seemed to differentiate early from late infections. Overall, this study provides a solid framework to examine the mechanisms underlying acquisition of immunity to malaria infections using whole-blood transcriptome sequencing (RNA-seq). IMPORTANCE We show that dual RNA-seq from patient blood samples allows characterization of host/parasite interactions during malaria infections and can provide a solid framework to study the acquisition of antimalarial immunity, as well as the adaptations of P. falciparum to malaria-experienced hosts.
format article
author Katie R. Bradwell
Drissa Coulibaly
Abdoulaye K. Koné
Matthew B. Laurens
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 Katie R. Bradwell
Drissa Coulibaly
Abdoulaye K. Koné
Matthew B. Laurens
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 Katie R. Bradwell
title Host and Parasite Transcriptomic Changes upon Successive <named-content content-type="genus-species">Plasmodium falciparum</named-content> Infections in Early Childhood
title_short Host and Parasite Transcriptomic Changes upon Successive <named-content content-type="genus-species">Plasmodium falciparum</named-content> Infections in Early Childhood
title_full Host and Parasite Transcriptomic Changes upon Successive <named-content content-type="genus-species">Plasmodium falciparum</named-content> Infections in Early Childhood
title_fullStr Host and Parasite Transcriptomic Changes upon Successive <named-content content-type="genus-species">Plasmodium falciparum</named-content> Infections in Early Childhood
title_full_unstemmed Host and Parasite Transcriptomic Changes upon Successive <named-content content-type="genus-species">Plasmodium falciparum</named-content> Infections in Early Childhood
title_sort host and parasite transcriptomic changes upon successive <named-content content-type="genus-species">plasmodium falciparum</named-content> infections in early childhood
publisher American Society for Microbiology
publishDate 2020
url https://doaj.org/article/4e3104401ead46c1a245fe5ab39d23c3
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