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单细胞转录组分析揭示甲病毒感染期间肥胖相关的免疫细胞动力学变化

Obesity-Associated Changes in Immune Cell Dynamics During Alphavirus Infection Revealed by Single Cell Transcriptomic Analysis.

作者信息

Hameed Muddassar, Daamen Andrea R, Hossain Md Shakhawat, Coutermarsh-Ott Sheryl, Lipsky Peter E, Weger-Lucarelli James

机构信息

Department of Biomedical Sciences and Pathobiology, Virginia-Maryland College of Veterinary Medicine, Virginia Tech, Blacksburg, VA 24061, USA.

Center for Zoonotic and Arthropod-borne Pathogens, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061, USA.

出版信息

bioRxiv. 2024 Oct 13:2024.10.10.617696. doi: 10.1101/2024.10.10.617696.

Abstract

Obesity induces diverse changes in host immunity, resulting in worse disease outcomes following infection with various pathogens, including arthritogenic alphaviruses. However, the impact of obesity on the functional landscape of immune cells during arthritogenic alphavirus infection remains unexplored. Here, we used single-cell RNA sequencing (scRNA-seq) to dissect the blood and tissue immune responses to Mayaro virus (MAYV) infection in lean and obese mice. Footpad injection of MAYV caused significant shifts in immune cell populations and induced robust expression of interferon response and proinflammatory cytokine genes and related pathways in both blood and tissue. In MAYV-infected lean mice, analysis of the local tissue response revealed a unique macrophage subset with high expression of IFN response genes that was not found in obese mice. This was associated with less severe inflammation in lean mice. These results provide evidence for a unique macrophage population that may contribute to the superior capacity of lean mice to control arthritogenic alphavirus infection.

摘要

肥胖会引起宿主免疫的多种变化,导致在感染包括致关节炎甲病毒在内的各种病原体后疾病预后更差。然而,肥胖对致关节炎甲病毒感染期间免疫细胞功能格局的影响仍未得到探索。在此,我们使用单细胞RNA测序(scRNA-seq)来剖析瘦小鼠和肥胖小鼠对马亚罗病毒(MAYV)感染的血液和组织免疫反应。足垫注射MAYV导致免疫细胞群体发生显著变化,并在血液和组织中诱导干扰素反应、促炎细胞因子基因及相关通路的强烈表达。在感染MAYV的瘦小鼠中,对局部组织反应的分析揭示了一个独特的巨噬细胞亚群,其IFN反应基因高表达,而在肥胖小鼠中未发现。这与瘦小鼠中炎症较轻有关。这些结果为一个独特的巨噬细胞群体提供了证据,该群体可能有助于瘦小鼠控制致关节炎甲病毒感染的卓越能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/667d/11482886/44558f68662f/nihpp-2024.10.10.617696v1-f0001.jpg

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