Microbiota-derived acetate is associated with functionally optimal virus-specific CD8+ T cell responses to influenza virus infection via GPR43-dependent metabolic reprogramming
Jingjing Qiu,
Chunwei Shi,
Yanan Zhang,
Tianming Niu,
Shuxian Chen,
Guilian Yang,
Shu Jeffrey Zhu,
Chunfeng Wang
Affiliations
Jingjing Qiu
College of Veterinary Medicine, Jilin Agricultural University, Changchun, P. R. China
Chunwei Shi
College of Veterinary Medicine, Jilin Agricultural University, Changchun, P. R. China
Yanan Zhang
Department of Veterinary Medicine, College of Animal Sciences, Zhejiang University, Hangzhou, Zhejiang, P. R. China
Tianming Niu
College of Veterinary Medicine, Jilin Agricultural University, Changchun, P. R. China
Shuxian Chen
Department of Veterinary Medicine, College of Animal Sciences, Zhejiang University, Hangzhou, Zhejiang, P. R. China
Guilian Yang
College of Veterinary Medicine, Jilin Agricultural University, Changchun, P. R. China
Shu Jeffrey Zhu
Department of Veterinary Medicine, College of Animal Sciences, Zhejiang University, Hangzhou, Zhejiang, P. R. China
Chunfeng Wang
College of Veterinary Medicine, Jilin Agricultural University, Changchun, P. R. China
The microbiota-associated factors that affect host susceptibility and adaptive immunity to influenza A virus (IAV) infection have not been fully elucidated. By comparing the microbiota composition between survivors and mice that succumbed to IAV strain PR8 infection, we identified that the commensal bacterium Blautia coccoides protects antibiotics (Abx)-treated or germ-free (GF) mice from PR8 infection by inducing functionally optimal virus-specific CD8+ T cell responses. Administration of exogenous acetate reproduced the protective effect of B. coccoides monocolonization in Abx and GF mice, enhancing oxidative phosphorylation and glycolysis as well as secretion of IFN-γ and granzyme B in virus-specific CD8+ T cells, dependent on GPR43 signaling and acetyl-CoA synthetase 2. Thus, we have demonstrated that microbiota-derived acetate possesses an antiviral effect that induces an optimal virus-specific CD8+ T cell response to IAV PR8 infection via GPR43-dependent metabolic reprogramming.
