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Series GSE252828 Query DataSets for GSE252828
Status Public on Jan 11, 2024
Title Cell atlas of the Atlantic salmon spleen reveals immune cell heterogeneity and cell-specific responses to bacterial infection
Organism Salmo salar
Experiment type Expression profiling by high throughput sequencing
Summary The spleen is a conserved secondary lymphoid organ that emerged in parallel to adaptive immunity in early jawed vertebrates. Recent studies have applied single cell transcriptomics to reveal the cellular composition of spleen in several species, cataloguing diverse immune cell types and subpopulations. In this study, 51,119 spleen nuclei transcriptomes were comprehensively investigated in the commercially important teleost Atlantic salmon (Salmo salar L.), contrasting control animals with those challenged with the bacterial pathogen Aeromonas salmonicida. We identified clusters of nuclei representing the expected major cell types, namely T cells, B cells, natural killer-like cells, granulocytes, mononuclear phagocytes, endothelial cells, mesenchymal cells, erythrocytes and thrombocytes. We discovered heterogeneity within several immune lineages, providing evidence for resident macrophages and melanomacrophages, infiltrating monocytes, several candidate dendritic cell subpopulations, and B cells at distinct stages of differentiation, including plasma cells and an igt+ B subset. We provide evidence for twelve candidate T cell subsets, including cd4+ T helper and regulatory T cells, one cd8+ subset, three γδT subsets, and populations double negative for cd4 and cd8. The number of genes showing differential expression during the early stages of infection with Aeromonas was highly variable across cell types, with the largest changes observed in resident macrophages and infiltrating monocytes, followed by resting mature B cells. Our differential expression analysis offers evidence for a strong inflammatory response to bacteria in the spleen driven by macrophages and monocytes, and the recruitment of splenic igt+ B cells to the gut. Overall, this study provides a new cell-resolved perspective of the immune actions of Atlantic salmon spleen, highlighting extensive heterogeneity hidden to bulk transcriptomics. We further provide a large catalogue of cell-specific marker genes that can be leveraged to further explore the function and structural organization of the salmonid immune system.
 
Overall design Twenty Atlantic salmon were anaesthetized and given an intraperitoneal injection of either PBS (n=10), or the pathogenic Hooke strain of A. salmonicida (n=10). Sampling was performed 24 h post-injection and control (n=2) and infected (n=2) fish were selected based on immune response validated with qPCR. Single nucleus libraries were constructed according using the 10x Genomics Chromium platform.
 
Contributor(s) Sun J, Daniels RR, Balic A, Andresen AM, Bjørgen H, Dobie R, Henderson NC, Koppang EO, Martin SA, Hol Fosse J, Taylor RS, Macqueen DJ
Citation(s) 38176627
Submission date Jan 09, 2024
Last update date Apr 11, 2024
Contact name Jianxuan Sun
E-mail(s) J.Sun-52@sms.ed.ac.uk
Organization name Roslin Institute
Lab Macqueen lab
Street address The University of Edinburgh, Easter Bush Campus
City Edinburgh
State/province Midlothian
ZIP/Postal code EH25 9RG
Country United Kingdom
 
Platforms (1)
GPL24981 Illumina NovaSeq 6000 (Salmo salar)
Samples (4)
GSM8008589 Spleen, PBS treated, replicate 1
GSM8008590 Spleen, PBS treated, replicate 2
GSM8008591 Spleen, AS treated, replicate 1
Relations
BioProject PRJNA1062782

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Supplementary file Size Download File type/resource
GSE252828_RAW.tar 1.8 Gb (http)(custom) TAR (of MTX, TSV)
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Raw data are available in SRA

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