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Series GSE268112 Query DataSets for GSE268112
Status Public on Jun 03, 2024
Title A Spatial Transcriptomics Atlas of the Malaria-infected Liver Indicates a Crucial Role for Lipid Metabolism and Hotspots of Inflammatory Cell Infiltration
Organisms Plasmodium berghei ANKA; Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary During liver infection, the malaria parasite undergoes massive replication whilst remaining clinically silent. Spatial coordination of immune response regulation and metabolic zonation during malaria infection in the true tissue context remains unexplored. We perform spatial transcriptomics combined with snRNA-seq over multiple time points to delineate transcriptional programs of host-pathogen interactions across P. berghei-infected liver tissues. Our data suggest changes in gene expression related to lipid metabolism adjacent to infected hepatocytes, particularly modulation of the expression of genes involved in peroxisome proliferator-activated receptor pathway signaling. The data further indicates the presence of inflammatory hotspots with differential inflammation programs along the lobular axis in infected tissues. Additionally, upregulation of genes involved in inflammation is observed, but considerably delayed, in livers of control mice injected with mosquito salivary gland components. Our study establishes a benchmark for investigating host-parasite interactions, and can easily be implemented to validate de novo malaria drug and vaccine efforts.
 
Overall design For this study mice were infected with 400.000 sporozoites of P.berghei ANKA and their livers were collected after 12, 24 or 38h post-infection. Control mice were challenged with salivary gland lysate of the same number of mosquitos collected for P. berghei ANKA challenges and their livers were also collected after 12, 24 or 38h post-injection. Nuclei were isolated from the snap frozen liver tissues, and two biological replicates of each condition were pooled. Thus, the full single-nuclei RNA sequencing protocol, including sequencing and computational analysis, was performed for a total of 6 liver samples, of which 3 were infected with Plasmodium berghei parasites and 3 challenged with mosquito salivary gland lysate.
Web link https://pubmed.ncbi.nlm.nih.gov/39160174/
 
Contributor(s) Hildebrandt F, Urrutia Iturritza M, Zwicker C, Vanneste B, Van Hul N, Semle E, Quin J, Pascini T, Saarenpää S, He M, Andersson ER, Scott CL, Vega-Rodriguez J, Lundeberg J, Ankarklev J
Citation(s) 39160174
Submission date May 22, 2024
Last update date Sep 02, 2024
Contact name Miren Urrutia Iturritza
E-mail(s) miren.urrutiaiturritza@su.se
Organization name Stockholm University
Department The Department of Molecular Biosciences, The Wenner-Gren Institute (MBW)
Lab Ankarklev Lab
Street address Svante Arrhenius väg 20C
City Stockholm
ZIP/Postal code 114 18
Country Sweden
 
Platforms (2)
GPL24247 Illumina NovaSeq 6000 (Mus musculus)
GPL34512 Illumina NovaSeq 6000 (Mus musculus; Plasmodium berghei ANKA)
Samples (6)
GSM8285920 P. berghei Infected murine liver, 12h post infection, snRNAseq
GSM8285921 P. berghei Infected murine liver, 24h post infection, snRNAseq
GSM8285922 P. berghei Infected murine liver, 38h post infection, snRNAseq
Relations
BioProject PRJNA1114705

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Supplementary file Size Download File type/resource
GSE268112_RAW.tar 831.6 Mb (http)(custom) TAR (of MTX, TSV)
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Raw data are available in SRA

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