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Series GSE253835 Query DataSets for GSE253835
Status Public on May 01, 2024
Title Immunotyping of microglia and macrophages in the CNS during acute SIV infection: a single-cell study of rhesus macaque brains
Organism Macaca mulatta
Experiment type Expression profiling by high throughput sequencing
Summary Human immunodeficiency virus (HIV) is widely recognized for its striking impact on the immune system. Even though HIV is primarily known for the impairment of the peripheral CD4 T cells, its influence on the central nervous system (CNS) also cannot be neglected. The main immune constituents in the brain, microglia and macrophages, are the target for HIV in the brain, as well as for the simian immunodeficiency virus (SIV) in nonhuman primates. This infection can lead to neurological effects as well as the establishment of a virus reservoir. Given the gaps in our knowledge on how these cells respond in vivo to CNS infection, we performed single-cell RNA sequencing (scRNA-seq) on myeloid cells from the brains of 3 rhesus macaque with 12-day SIV infection as well as 3 uninfected controls. We identified six microglial clusters and two macrophage clusters by transcriptomic profiling. Intriguingly, there were two microglial clusters populated with the cells from infected animals. These two infection-specific clusters had significantly higher expression (p < 0.05) of MHC class I molecules, interferon-induced proteins, chemokines, and cytokines than did the other clusters. Although only a low proportion of SIV-infected cells were detected in microglia and macrophages (~0.14%), almost all the microglia and macrophages in infected animals were activated to certain extents. In addition, the clusters with higher expression of cytotoxic molecules increased their populations during the infection, suggesting their potential to cause HIV-associated neurological disorders.
 
Overall design 92T, 104T, 111T were non-infected control samples and other three (93T, 94T, 95T) were in acute-infected group. The rhesus macaques in the acut-infected group were infected with Simian Immunodeficiency Virus (SIV) for 12 days
 
Contributor(s) Xu X, Niu M, Lamberty BG, Emanuel K, Fox HS
Citation(s) 38617282, 39283947
Submission date Jan 22, 2024
Last update date Oct 10, 2024
Contact name Xiaoke Xu
E-mail(s) x.xu@unmc.edu
Organization name University of Nebraska Medical Center
Street address 42nd and Emile
City Omaha
State/province Nebraska
ZIP/Postal code 68198-7400
Country USA
 
Platforms (2)
GPL27943 Illumina NovaSeq 6000 (Macaca mulatta)
GPL29319 NextSeq 550 (Macaca mulatta)
Samples (20)
GSM8028494 92T_Micro1,Rhesus Macauqe,control,non-infection
GSM8028495 92T_Micro2,Rhesus Macauqe,control,non-infection
GSM8028496 92T_Micro3,Rhesus Macauqe,control,non-infection
Relations
BioProject PRJNA1067539

Download family Format
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Supplementary file Size Download File type/resource
GSE253835_RAW.tar 636.8 Mb (http)(custom) TAR (of H5)
SRA Run SelectorHelp
Raw data are available in SRA

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