Polypurine reverse hoogsteen hairpins as a therapeutic tool for SARS-CoV-2 infection

Although the COVID-19 pandemic was declared no longer a global emergency by the World Health Organization in May 2023, SARS-CoV-2 is still infecting people across the world. Many therapeutic oligonucleotides such as ASOs, siRNAs, or CRISPR-based systems emerged as promising antiviral strategies for the treatment of SARS-CoV-2. In this work, we explored the inhibitory potential on SARS-CoV-2 replication of Polypurine Reverse Hoogsteen Hairpins (PPRHs), CC1-PPRH, and CC3-PPRH, targeting specific polypyrimidine sequences within the replicase and Spike regions, respectively, and previously validated for COVID-19 diagnosis. Both PPRHs are bound to their target sequences in the viral genome with high affinity in the order of nM. In vitro, both PPRHs reduced viral replication by more than 92% when transfected into VERO-E6 cells 24 h prior to infection with SARS-CoV-2. In vivo intranasal administration of CC1-PPRH in K18-hACE2 mice expressing the human ACE receptor protected all the animals from SARS-CoV-2 infection. The properties of PPRHs position them as promising candidates for the development of novel therapeutics against SARS-CoV-2 and other viral infections.

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Publication Details

Journal
Journal of Biological Chemistry
Published
2024-10-11
DOI
https://doi.org/10.1016/j.jbc.2024.107884
Citations
6
Primary Topic
SARS-CoV-2 and COVID-19 Research
Type
article
Field-Weighted Citation Impact
2.33

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article

Polypurine reverse hoogsteen hairpins as a therapeutic tool for SARS-CoV-2 infection

José M. Rojas, Miguel Chillón, Noemı́ Sevilla, Ramón Eritja et al.
6 citations
Journal of Biological Chemistry
SARS-CoV-2 and COVID-19 Research
2.33
article

Polypurine reverse hoogsteen hairpins as a therapeutic tool for SARS-CoV-2 infection

José M. Rojas, Miguel Chillón, Noemı́ Sevilla, Ramón Eritja, Simonas Valiuska, Anna Aviñó, Carlos J. Ciudad, Pablo Nogales‐Altozano, Verónique Noé
article en
6 citations

Abstract

Although the COVID-19 pandemic was declared no longer a global emergency by the World Health Organization in May 2023, SARS-CoV-2 is still infecting people across the world. Many therapeutic oligonucleotides such as ASOs, siRNAs, or CRISPR-based systems emerged as promising antiviral strategies for the treatment of SARS-CoV-2. In this work, we explored the inhibitory potential on SARS-CoV-2 replication of Polypurine Reverse Hoogsteen Hairpins (PPRHs), CC1-PPRH, and CC3-PPRH, targeting specific polypyrimidine sequences within the replicase and Spike regions, respectively, and previously validated for COVID-19 diagnosis. Both PPRHs are bound to their target sequences in the viral genome with high affinity in the order of nM. In vitro, both PPRHs reduced viral replication by more than 92% when transfected into VERO-E6 cells 24 h prior to infection with SARS-CoV-2. In vivo intranasal administration of CC1-PPRH in K18-hACE2 mice expressing the human ACE receptor protected all the animals from SARS-CoV-2 infection. The properties of PPRHs position them as promising candidates for the development of novel therapeutics against SARS-CoV-2 and other viral infections.

Journal of Biological ChemistryVol. 300(11)
Universitat Autònoma de Barcelona (ES), Consejo Superior de Investigaciones Científicas (ES), Instituto de Salud Carlos III (ES), Biomedical Research Networking Center in Bioengineering, Biomaterials and Nanomedicine (ES), Institut de Nanociència i Nanotecnologia de la Universitat de Barcelona
Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria, Fundació la Marató de TV3, Comunidad de Madrid, Ministerio de Ciencia e Innovación, Universitat de Barcelona, Consejo Superior de Investigaciones Científicas
Openalex Percentile: Top 11%
SARS-CoV-2 and COVID-19 Research
2.33
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