Background: -butylhydroquinone (tBHQ) is an antioxidant commonly used as a food additive. Studies suggest that tBHQ could modulate immune responses to influenza and SARS-CoV-2 infection. In our transcriptomic analysis we explored the molecular mechanisms behind tBHQ's modulatory properties and the relationships to respiratory viral infections.
Methods: tBHQ was administered to BALB/c mice (1.5% [/]) for 20 days. Splenic T cells were isolated with magnetic separation and subjected to transcriptomic analysis. Gene-set enrichment analysis and g:Profiler was conducted to provide a functional interpretation of significantly changed genes. Further analysis for AHR/NRF2 binding sites was performed with GeneHancer.
Results: In CD4 cells, we found significantly altered expression of 269 genes by tBHQ. Of them, many had relevance in influenza infection such as genes responsible for virus entry (, ), interferon signaling (, ), or prostaglandin synthesis (Ptgs1/2). In SARS-CoV-2 infections, interferon signaling (1), proteolytic enzymes (), and also cell-surface proteins (, ) were among the prominent alterations after tBHQ exposure. Of these genes, many had one or more binding sites for AHR and NRF2, two major xenosensors triggered by tBHQ.
Conclusions: Our results strongly suggest that a common food additive, tBHQ, can modulate virus-dependent processes in both influenza and SARS-CoV-2 infections.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9147452 | PMC |
http://dx.doi.org/10.3390/life12050642 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!