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鱼类肠道转录组分析鉴定巨噬细胞为人类诺如病毒感染的宿主细胞。

Transcriptional profiling of zebrafish intestines identifies macrophages as host cells for human norovirus infection.

机构信息

Department of Microbiology, Immunology and Transplantation, Rega Institute, Virus-Host Interactions & Therapeutic Approaches (VITA) Research Group, KU Leuven, Leuven, Belgium.

Department of Medical Microbiology and Immunology, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada.

出版信息

Gut Microbes. 2024 Jan-Dec;16(1):2431167. doi: 10.1080/19490976.2024.2431167. Epub 2024 Nov 25.

Abstract

Human noroviruses (HuNoVs) are a major cause of diarrheal disease, yet critical aspects of their biology, including cellular tropism, remain unclear. Although research has traditionally focused on the intestinal epithelium, the hypothesis that HuNoV infects macrophages has been recurrently discussed and is investigated here using a zebrafish larval model. Through single-cell RNA sequencing of dissected zebrafish intestines, we unbiasedly identified macrophages as host cells for HuNoV replication, with all three open reading frames mapped to individual macrophages. Notably, HuNoV preferentially infects actively phagocytosing inflammatory macrophages. HuNoV capsid proteins and double-stranded RNA colocalized within intestinal macrophages of infected zebrafish larvae, and the negative-strand RNA intermediate was detected within FACS-sorted macrophages. Flow cytometry confirmed viral replication within these macrophages, constituting approximately 23% of HuNoV's host cells. Identifying macrophages as host cells prompts a reevaluation of their role in HuNoV pathogenesis, offering new directions for understanding and controlling this infection.

摘要

人类诺如病毒(HuNoVs)是导致腹泻病的主要原因,但它们的生物学特性,包括细胞嗜性,仍不清楚。虽然研究传统上集中在肠上皮细胞,但 HuNoV 感染巨噬细胞的假说被反复讨论,本研究利用斑马鱼幼虫模型对此进行了研究。通过对分离的斑马鱼肠道进行单细胞 RNA 测序,我们在不偏倚的情况下鉴定出巨噬细胞是 HuNoV 复制的宿主细胞,三个开放阅读框均定位在单个巨噬细胞上。值得注意的是,HuNoV 优先感染活跃吞噬的炎症性巨噬细胞。HuNoV 衣壳蛋白和双链 RNA 在感染的斑马鱼幼虫肠道巨噬细胞中共定位,在 FACS 分选的巨噬细胞中检测到负链 RNA 中间体。流式细胞术证实了这些巨噬细胞中的病毒复制,约占 HuNoV 宿主细胞的 23%。将巨噬细胞鉴定为宿主细胞促使人们重新评估它们在 HuNoV 发病机制中的作用,为理解和控制这种感染提供了新的方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94ff/11591593/c571a72bbde1/KGMI_A_2431167_F0001_OC.jpg

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