A TLR-pathway kinase-inhibitor screen identifies PPM18 as a spontaneous stress-granule inducer with SG-independent potential antiviral activity

Stress granules (SG) are cytoplasmic membraneless compartments that regulate cellular stress responses and have been implicated in antiviral defense against Influenza A Virus (IAV). SG stabilization has been reported to be a viable strategy to develop antiviral drug. To expand the repertoire of SG-modulating compounds, we performed a targeted pharmacological screen focusing on inhibitors of toll-like receptor (TLR) signaling pathway, based on our previous work showing that TLR signaling can destabilize SGs. Using the synthetic dsRNA analog polyinosinic:polycytidylic acid (poly(I:C)) to induce SGs in A549 human lung cancer cell line, we screened a panel of TLR signaling pathway inhibitors for their effect on SG stability. We developed a robust image analysis pipeline for high-throughput analysis of SG alterations. The screen identified PPM18 as an inducer of SGs even in the absence of poly(I:C) transfection. Using knockout cell lines our data shows that PPM18 induced SG assembly was dependent on Protein Kinase R-like Endoplasmic Reticulum Kinase, partially on heme regulated inhibitor, and that SG formation is substantially reduced in G3BP1 -/- cells. PPM18 reduced the abundance of IAV RNA and viral ribonucleoproteins (vRNPs) in a dose-dependent manner, with a lowest effective concentration of 12.5 µM. Notably, this antiviral effect was independent of SG formation, as PPM18 robustly reduced IAV RNA and vRNP abundances in G3BP1 -/- cells. PPM18 also induced caspase-independent regulated cell death at 50 µM, as the pan-caspase inhibitor zVAD-fmk did not protect cells. Although the narrow therapeutic window of PPM18 limits its direct translational potential, our study identifies a tool compound for interrogating the relationship between SGs and antiviral activity. More broadly, our image-based screen provides a feasible approach for identifying SG-modulating compounds, although the finding that PPM18’s antiviral activity is SG-independent indicates that SG modulation alone may not be sufficient to predict antiviral efficacy.

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Journal
Scientific Reports
Published
2026-07-16
DOI
https://doi.org/10.1038/s41598-026-62049-6
Primary Topic
RNA Research and Splicing
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article
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article

A TLR-pathway kinase-inhibitor screen identifies PPM18 as a spontaneous stress-granule inducer with SG-independent potential antiviral activity

Parimal Samir, Xuping Xie, Prem Prasad Lamichhane, Aditi
Scientific Reports
RNA Research and Splicing
article

A TLR-pathway kinase-inhibitor screen identifies PPM18 as a spontaneous stress-granule inducer with SG-independent potential antiviral activity

Parimal Samir, Xuping Xie, Prem Prasad Lamichhane, Aditi
article en

Abstract

Stress granules (SG) are cytoplasmic membraneless compartments that regulate cellular stress responses and have been implicated in antiviral defense against Influenza A Virus (IAV). SG stabilization has been reported to be a viable strategy to develop antiviral drug. To expand the repertoire of SG-modulating compounds, we performed a targeted pharmacological screen focusing on inhibitors of toll-like receptor (TLR) signaling pathway, based on our previous work showing that TLR signaling can destabilize SGs. Using the synthetic dsRNA analog polyinosinic:polycytidylic acid (poly(I:C)) to induce SGs in A549 human lung cancer cell line, we screened a panel of TLR signaling pathway inhibitors for their effect on SG stability. We developed a robust image analysis pipeline for high-throughput analysis of SG alterations. The screen identified PPM18 as an inducer of SGs even in the absence of poly(I:C) transfection. Using knockout cell lines our data shows that PPM18 induced SG assembly was dependent on Protein Kinase R-like Endoplasmic Reticulum Kinase, partially on heme regulated inhibitor, and that SG formation is substantially reduced in G3BP1 -/- cells. PPM18 reduced the abundance of IAV RNA and viral ribonucleoproteins (vRNPs) in a dose-dependent manner, with a lowest effective concentration of 12.5 µM. Notably, this antiviral effect was independent of SG formation, as PPM18 robustly reduced IAV RNA and vRNP abundances in G3BP1 -/- cells. PPM18 also induced caspase-independent regulated cell death at 50 µM, as the pan-caspase inhibitor zVAD-fmk did not protect cells. Although the narrow therapeutic window of PPM18 limits its direct translational potential, our study identifies a tool compound for interrogating the relationship between SGs and antiviral activity. More broadly, our image-based screen provides a feasible approach for identifying SG-modulating compounds, although the finding that PPM18’s antiviral activity is SG-independent indicates that SG modulation alone may not be sufficient to predict antiviral efficacy.

Scientific Reports
The University of Texas Medical Branch at Galveston (US)
Good health and well-being
Openalex Percentile: Top 14%
RNA Research and Splicing
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