Accumulating clinical data suggest the main causes of death by COVID-19 include respiratory failure and the onset of sepsis.1 Importantly, sepsis has been observed in nearly all deceased patients.2,3,4,5 It remains elusive how SARS-CoV-2 infection results in viral sepsis in humans. Toll-like receptor 4 (TLR4) mediates anti-gram-negative bacterial immune responses by recognizing lipopolysaccharide (LPS) from bacteria.6 We recently found that SARS-CoV-2 infection provoked an anti-bacterial like response at the very early stage of infection via TLR4. However, the identity of the original trigger initiating these abnormal immune responses during SARS-CoV-2 infection is unknown.
Previous in silico studies predicted cell surface TLRs, especially TLR4, are most likely to be involved in recognizing molecular patterns, probably spike protein, from SARS-CoV-2 to induce inflammatory responses.7,8 Consistently, we found that the induction of IL1B by SARS-CoV-2 was completely blocked by TLR4-specific inhibitor Resatorvid (Fig. 1a). Combined with our recent data that TLR4 signaling was activated by SARS-CoV-2, we hypothesized that spike protein could activate TLR4 pathway. A recent study has reported that trimeric SARS-CoV-2 spike proteins are high quality antigens.9 To this end, we purified the trimeric spike protein (1–1208 aa) (Fig. 1b; Supplementary information, Fig. S1a), as this form of spike protein presents on the surface of viral particle, which most likely interacts with the proteins on the cell surface. Results of the surface plasmon resonance (SPR) assay showed that SARS-CoV-2 spike trimer directly bound to TLR4 with an affinity of ~300 nM (Fig. 1b), comparable to many virus-receptor interactions.
We then treated THP-1 cells, a cell line of human monocytes, with purified spike protein. IL1B was robustly induced by spike protein in a dose-dependent manner (Fig. 1c), which was comparable to LPS (Supplementary information, Fig. S1b). IL6 was also induced by spike protein (Supplementary information, Fig. S1c). As IL1B induction was much more robust than that of IL6, we chose IL1B production as a marker of immune activation. Moreover, the pseudovirus expressing spike protein can also induce IL1B production (Fig. 1d). Neutrophils also express TLR4 on their cell surface and play an important role in the development of sepsis. We utilized all-trans retinoic acid (ATRA) to treat HL-60 cell (a promyelocytic leukemia cell line), which directed those cells to differentiate into neutrophils. Spike proteins significantly induced IL1B production in HL-60 cells after ATRA treatment (Fig. 1e; Supplementary information, Fig. S1d).
We treated THP-1 cells with the N-terminal domain (NTD) or the receptor-binding domain (RBD) of spike protein. Only the trimeric protein could induce IL1B and IL6 (Fig. 1f; Supplementary information, Fig. S1e). To examine if this activation was mediated by TLR4, we treated cells with Resatorvid. Resatorvid greatly blocked induction of IL1B by spike protein and LPS (Fig. 1g). Moreover, spike protein was also able to induce IL1B production in murine macrophage cell line (Raw 264.7) in a TLR4- and MyD88-dependent manner (Fig. 1h). Consistently, spike protein induced production of IL1B in the primary bone marrow-derived macrophages (BMDM) and peritoneal macrophages from wild-type but not TLR4-deficient mice (Fig. 1i). The NF-κB inhibitor (JSH-23) was able to suppress IL1B induced by spike protein (Supplementary information, Fig. S1f), suggesting that NF-κB was involved in this immune response. Trypsin digestion almost completely abolished the activation of IL1B by spike protein ruling out the possibility that the protein was contaminated by LPS (Fig. 1j; Supplementary information, Fig. S1g). Collectively, SARS-CoV-2 spike protein is capable of interacting with and activating TLR4.
To determine if other coronaviruses could activate TLR4 signaling, we treated THP-1 cells with murine coronavirus MHV-A59. As expected, MHV-A59 significantly induced IL1B (Fig. 1k), which was blocked by Resatorvid (Supplementary information, Fig. S1h). Theoretically, there is no MHV-A59 receptor (murine Ceacam1) expression in THP-1 cells, so MHV-A59 was not able to infect and enter this type of human monocytes. To confirm this, we washed those cells following the treatment with virus. After washing with PBS, the viral load was significantly decreased, so was the induction of IL1B (Fig. 1l; Supplementary information, Fig. S1i). These data suggested that MHV-A59 could trigger TLR4 signaling probably via spike–TLR4 interaction. Moreover, we treated macrophages with the spike protein trimer of SARS-CoV or infected these cells with human coronavirus 229E (HCoV-229E; Fig. 1m, n). Both treatments can induce production of IL1B, which was suppressed by Resatorvid. Together, different coronaviruses were able to activate TLR4 via their spike proteins.
MD2 and CD14 are the coreceptors of TLR4 for sensing LPS. We suppressed MD2 with its specific inhibitor (T5342126) and blocked CD14 with anti-CD14 antibody (Supplementary information, Fig. S1j, k).10,11 Both treatments significantly suppressed IL1B induction by spike protein suggesting that MD2 and CD14 were involved in TLR4 activation. TRIF is another adaptor protein downstream of TLR4. We treated macrophages from TRIF-deficient mice with spike protein. Consistent with reported studies,12,13 TRIF was dispensable for transcription activation of IL1B by LPS (Supplementary information, Fig. S1l). Deficiency of TRIF also did not affect induction of IL1B by spike protein (Supplementary information, Fig. S1l). However, TRIF was required for IFNB induction by LPS or spike protein (Supplementary information, Fig. S1m). To address if other TLRs are activated by spike protein, we treated macrophages from TLR2- or TLR3-deficient mice with SARS-CoV and SARS-CoV-2 spike protein. Deficiency of TLR2 or TLR3 did not affect induction of IL1B by spike protein (Fig. 1o). In addition to IL1B, the transcriptomic analysis showed that spike protein of SARS-CoV-2 was able to induce a number of immune-related genes, including interleukins, chemokines and IFN-stimulated genes (ISGs) (Fig. 1p, q; Supplementary information, Fig. S1s).
Spike protein also interacts with host proteins ACE2 and TMPRSS2. We treated macrophages from ACE2-deficient or human ACE2-transgenic mice with spike protein. Deficiency of ACE2 or overexpression of human ACE2 did not affect the induction of IL1B (Supplementary information, Fig. S1n, o). Treatment with ACE2 inhibitor (MLN-4760) or soluble ACE2 was not able to inhibit the induction of IL1B by LPS or spike protein (Supplementary information, Fig. S1p, q). Moreover, TMPRSS2-specific inhibitor (Bromhexine hydrochloride) did not alter the induction of IL1B by spike protein (Supplementary information, Fig. S1r). Thus, activation of TLR4 by spike protein was not regulated by ACE2 and TMPRSS2 or virus entry.
The induction of IL1B by trimeric spike proteins from SARS-CoV-2 or SARS-CoV was comparable to LPS treatment. Moreover, IL1B was induced by SARS-CoV-2, HCoV-229E and MHV-A59 via TLR4. These observations indicated at least some coronaviruses might share common/conserved abilities to interact with and activate TLR4 or TLR4-related signalings. Multiple sequence alignments of spike proteins from these coronaviruses reveal the higher conservation for S2, rather than RBD or NTD (Supplementary information, Fig. S1t), but this does not indicate TLR4 binding to S2. Structural analysis by molecular docking suggests that TLR4 more likely targets a conformational concave constructed by RBD and NTD (Supplementary information, Fig. S1u). Therefore, the detailed molecular basis of the interaction between spike trimer with TLR4 and the activation of TLR4 or TLR4-related signaling by coronaviruses still remains open questions for future studies.
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This work was supported by the National Key R&D Program of China (2016YFA0500300, 2020YFA0707500 and 2020YFA0707800), the Strategic Priority Research Program (XDB29010000 and XDB08020200) and the National Natural Science Foundation of China (31570891; 31872736). X.W. was supported by Ten Thousand Talent Program and the NSFS Innovative Research Group (81921005). L.Z. was supported by the Youth Innovation Promotion Association at the Chinese Academy of Sciences (2019098). H.Y. was supported by National Natural Science Foundation of China (21825702) and the Beijing Outstanding Young Scientist Program (BJJWZYJH01201910003013). We thank Prof. Zhihua Liu (Tsinghua University) and Prof. Liyun Shi (Nanjing University of Chinese Medicine) for their TLR-deficient mice.
The authors declare no competing interests.
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Zhao, Y., Kuang, M., Li, J. et al. SARS-CoV-2 spike protein interacts with and activates TLR41. Cell Res 31, 818–820 (2021). https://doi.org/10.1038/s41422-021-00495-9
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