Gut microbiota composition is associated with SARS-CoV-2 vaccine immunogenicity and adverse events

Siew C. Ng(Chinese University of Hong Kong), Ye Peng(HKU-Pasteur Research Pole), Lin Zhang(Chinese University of Hong Kong), Chris KP Mok(Chinese University of Hong Kong), Shilin Zhao(HKU-Pasteur Research Pole), Amy Li(Chinese University of Hong Kong), Jessica Y. L. Ching(Chinese University of Hong Kong), Yingzhi Liu(Chinese University of Hong Kong), Shuai Yan(Chinese University of Hong Kong), Dream L S Chan(Chinese University of Hong Kong), Jie Zhu(HKU-Pasteur Research Pole), Chunke Chen(Chinese University of Hong Kong), Adrian Chi Heng Fung(University of Hong Kong), Kenneth KY Wong(University of Hong Kong), David S.C. Hui(Chinese University of Hong Kong), Francis K.L. Chan(Chinese University of Hong Kong), Hein M. Tun(HKU-Pasteur Research Pole)
Gut
February 9, 2022
Cited by 178Open Access
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Abstract

Objective The gut microbiota plays a key role in modulating host immune response. We conducted a prospective, observational study to examine gut microbiota composition in association with immune responses and adverse events in adults who have received the inactivated vaccine (CoronaVac; Sinovac) or the mRNA vaccine (BNT162b2; BioNTech; Comirnaty). Design We performed shotgun metagenomic sequencing in stool samples of 138 COVID-19 vaccinees (37 CoronaVac and 101 BNT162b2 vaccinees) collected at baseline and 1 month after second dose of vaccination. Immune markers were measured by SARS-CoV-2 surrogate virus neutralisation test and spike receptor-binding domain IgG ELISA. Results We found a significantly lower immune response in recipients of CoronaVac than BNT162b2 vaccines (p<0.05). Bifidobacterium adolescentis was persistently higher in subjects with high neutralising antibodies to CoronaVac vaccine (p=0.023) and their baseline gut microbiome was enriched in pathways related to carbohydrate metabolism (linear discriminant analysis (LDA) scores >2 and p<0.05). Neutralising antibodies in BNT162b2 vaccinees showed a positive correlation with the total abundance of bacteria with flagella and fimbriae including Roseburia faecis (p=0.028). The abundance of Prevotella copri and two Megamonas species were enriched in individuals with fewer adverse events following either of the vaccines indicating that these bacteria may play an anti-inflammatory role in host immune response (LDA scores>3 and p<0.05). Conclusion Our study has identified specific gut microbiota markers in association with improved immune response and reduced adverse events following COVID-19 vaccines. Microbiota-targeted interventions have the potential to complement effectiveness of COVID-19 vaccines.


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