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

Emma Roux, Reegan J. Willms, Jana Van Dycke, Álvaro Cortes Calabuig, Lore Van Espen, Geert Schoofs, Jelle Matthijnssens, Johan Neyts, Peter de Witte, Edan Foley, Joana Rocha-Pereira

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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.

Original languageEnglish
Article number2431167
JournalGut Microbes
Volume16
Issue number1
Early online date25 Nov 2024
DOIs
Publication statusPublished - 31 Dec 2024

Data Availability Statement

The single-cell RNA-seq data discussed in this publication have been deposited in NCBI’s Gene Expression Omnibus(Edgar et al., 2002) and are accessible throughGEOSeriesaccessionnumberGSE261163 (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE261163). Any additional information required to re-analyze the data reported in this paper is available upon request to the corresponding author.

Funding

This work was supported by the Research Foundation Flanders (FWO) under [grant 11K7922N] to ER; the National Science and Engineering Research Council(NSERC) Canada Graduate Scholarships and Alberta Innovates Graduate Student Scholarships to RJW;GUTVIBRATIONS, a project funded by the European Commission in the Call Next Generation Organ-On-Chip Call (DT-NMBP-23) to JVD; KU Leuven internal funds (C2project), a KU Leuven starting grant under grant STG/21/028,and FWO junior project funding under [grant G065623N] to JRP.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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