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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American Society for Microbiology
2020
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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) |
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malaria transcriptomics Microbiology QR1-502 |
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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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