SARS-CoV-2 Variant Delta Potently Suppresses Innate Immune Response and Evades Interferon-Activated Antiviral Responses
Tandel, D.; Sah, V.; Singh, N. K.; Potharaju, P. S.; Gupta, D.; Shrivastava, S.; Sowpati, D. T.; Harshan, K. H.
Show abstract
Delta variant of SARS-CoV-2 has caused more severe infections than its previous variants. We studied the host innate immune response to Delta, Alpha and two earlier variants to map the evolution of the recent ones. Our biochemical and transcriptomic studies reveal that Alpha and Delta have progressively evolved over the ancestral variants by silencing innate immune response, thereby limiting cytokine and chemokine production. Though Alpha silenced RLR pathway just as Delta, it failed to persistently silence the innate immune response unlike Delta. Both Alpha and Delta have evolved to resist IFN treatment while they are still susceptible to RLR activation, further highlighting the importance of RLR-mediated, IFN-independent mechanisms in restricting SARS-CoV-2. Our studies reveal that SARS-CoV-2 Delta has integrated multiple mechanisms to silence host innate immune response and evade IFN response. Deltas silent replication and sustained suppression of host innate immune response, possibly resulting in delayed or reduced intervention by the adaptive immune response, could potentially contribute to the severe symptoms and poor recovery index associated with it.
Matching journals
The top 3 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Retinoic Acid Inducible Gene-I like Receptors Activate Snail and Slug to Limit RNA Viral Infections 96%
- Human nasal and lung tissues infected ex vivo with SARS-CoV-2 provide insights into differential tissue-specific and virus-specific innate immune responses in the upper and lower respiratory tract 96%
- Human long noncoding RNA, VILMIR, is induced by major respiratory viral infections and modulates the host interferon response 96%
Similar papers in this journal
- Cell-to-cell variation in defective virus expression and effects on host responses during influenza virus infection 96%
- Comparison of SARS-CoV-2 variants of concern in primary human nasal cultures demonstrates Delta as most cytopathic and Omicron as fastest replicating 95%
- N6-methyladenosine (m6A) and reader protein YTHDF2 enhance innate immune response by mediating DUSP1 mRNA degradation and activating mitogen-activated protein kinases during bacterial and viral infections 95%
Similar papers in this journal
- Metabolic reprogramming tips vaccinia virus infection outcomes by stabilizing interferon-g induced IRF1 96%
- Viral interference between severe acute respiratory syndrome coronavirus 2 and influenza A viruses 95%
- CD169-mediated restrictive SARS-CoV-2 infection of macrophages induces pro-inflammatory responses 95%
Similar papers in this journal
Similar papers in this journal
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.