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Updated: Jul 11, 2025

Contact-Free Co-Culture Model for the Study of Innate Immune Cell Activation During Respiratory Virus Infection
Published on: February 28, 2021
GlcNac produced by the gut microbiome enhances host influenza resistance by modulating NK cells
Xiaotong Hu1,2,3, Xiaolu Sun1,2,3, Ya Zhao1,2,3
1State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan, China.
Abstract:
Microbiota are known to modulate the host response to influenza infection, but the mechanisms remain largely unknown. Gut metabolites are the key mediators through which gut microbes play anti-influenza effect. Transferring fecal metabolites from mice with high influenza resistance into antibiotic-treated recipient mice conferred resistance to influenza infections. By comparing the metabolites of different individuals with high or low influenza resistance, we identified and validated N-acetyl-D-glucosamine (GlcNAc) and adenosine showed strong positive correlations with influenza resistance and exerted anti-influenza effects in vivo or in vitro, respectively. Especially, GlcNAc mediated the anti-influenza effect by increasing the proportion and activity of NK cells. Several gut microbes, including Clostridium sp., Phocaeicola sartorii, and Akkermansia muciniphila, were positively correlated with influenza resistance, and can upregulate the level of GlcNAc in the mouse gut by exogenous supplementation. Subsequent studies confirmed that administering a combination of the three bacteria to mice via gavage resulted in similar modulation of NK cell responses as observed with GlcNAc. This study demonstrates that gut microbe-produced GlcNAc protects the host against influenza by regulating NK cells, facilitating the elucidation of the action mechanism of gut microbes mediating host influenza resistance.
Insights
Gut microbes and their metabolites, like N-acetyl-D-glucosamine (GlcNAc), enhance host resistance to influenza. Specific bacteria boost GlcNAc levels, which modulate NK cells to fight influenza infection.
Area of Science:
- Microbiology
- Immunology
- Metabolomics
Background:
- Gut microbiota influence host responses to influenza, but underlying mechanisms are unclear.
- Gut microbial metabolites are key mediators of the anti-influenza effects of the microbiota.
Purpose of the Study:
- To elucidate the mechanisms by which gut microbes confer resistance to influenza.
- To identify specific gut metabolites and microbes associated with influenza resistance.
Main Methods:
- Comparative metabolomic analysis of mice with varying influenza resistance.
- In vivo and in vitro validation of identified metabolites (N-acetyl-D-glucosamine and adenosine).
- Gavage administration of specific gut bacteria (Clostridium sp., Phocaeicola sartorii, Akkermansia muciniphila) to mice.
Main Results:
- N-acetyl-D-glucosamine (GlcNAc) and adenosine were positively correlated with influenza resistance.
- GlcNAc mediated anti-influenza effects by enhancing Natural Killer (NK) cell activity and proportion.
- Administration of Clostridium sp., P. sartorii, and A. muciniphila increased gut GlcNAc levels and modulated NK cell responses.
Conclusions:
- Gut microbe-derived GlcNAc protects against influenza by regulating host NK cell responses.
- This study reveals a key mechanism of gut microbiota-mediated influenza resistance.
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