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

被引:0
|
作者
Ciudad, Carlos J. [1 ,2 ]
Valiuska, Simonas [1 ,2 ]
Rojas, Jose Manuel [3 ]
Nogales-Altozano, Pablo [3 ]
Avino, Anna [4 ,5 ]
Eritja, Ramon [4 ,5 ]
Chillon, Miguel [6 ]
Sevilla, Noemi [3 ]
Noe, Veronique [1 ,2 ]
机构
[1] Univ Barcelona, Sch Pharm & Food Sci, Dept Biochem & Physiol, Barcelona, Spain
[2] Univ Barcelona, Inst Nanociencia & Nanotecnol IN2UB, Barcelona, Spain
[3] CSIC, Ctr Invest San Anim CISA, INIA, Madrid, Spain
[4] CSIC, Inst Adv Chem Catalonia, Barcelona, Spain
[5] Inst Salud Carlos III, Ctr Invest Biomed Red Bioingn Biomat & Nanomed, Madrid, Spain
[6] Univ Autonoma Barcelona, Inst Neurosci, Barcelona, Spain
关键词
GENE; DELIVERY; DESIGN;
D O I
10.1016/j.jbc.2024.107884
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页数:11
相关论文
共 50 条
  • [1] Polypurine Reverse Hoogsteen Hairpins as a Gene Silencing Tool for Cancer
    Ciudad, Carlos J.
    Rodriguez, Laura
    Villalobos, Xenia
    Felix, Alex J.
    Noe, Veronique
    CURRENT MEDICINAL CHEMISTRY, 2017, 24 (26) : 2809 - 2826
  • [2] Exon skipping by Polypurine Reverse Hoogsteen hairpins
    Noe, V.
    Ciudad, C. J.
    HUMAN GENE THERAPY, 2021, 32 (19-20) : A69 - A69
  • [3] RNA-PolyPurine Reverse Hoogsteen Hairpins as tool for gene silencing
    Aubets, E.
    Chillon, M.
    Ciudad, C. J.
    Noe, V.
    HUMAN GENE THERAPY, 2021, 32 (19-20) : A80 - A80
  • [4] Nucleic acids therapeutics using PolyPurine Reverse Hoogsteen hairpins
    Noe, Veronique
    Aubets, Eva
    Felix, Alex J.
    Ciudad, Carlos J.
    BIOCHEMICAL PHARMACOLOGY, 2021, 189
  • [5] Polypurine Reverse-Hoogsteen Hairpins as a Tool for Exon Skipping at the Genomic Level in Mammalian Cells
    Noe, Veronique
    Ciudad, Carlos J.
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (07)
  • [6] Repair of Single-Point Mutations by Polypurine Reverse Hoogsteen Hairpins
    Sole, Anna
    Villalobos, Xenia
    Ciudad, Carlos J.
    Noe, Veronique
    HUMAN GENE THERAPY METHODS, 2014, 25 (05) : 288 - 302
  • [7] PolyPurine Reverse Hoogsteen Hairpins Work as RNA Species for Gene Silencing
    Aubets, Eva
    Chillon, Miguel
    Ciudad, Carlos J.
    Noe, Veronique
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (18)
  • [8] Gene Correction of Point Mutations Using PolyPurine Reverse Hoogsteen Hairpins Technology
    Felix, Alex J.
    Sole, Anna
    Noe, Veronique
    Ciudad, Carlos J.
    FRONTIERS IN GENOME EDITING, 2020, 2
  • [9] Stability and Immunogenicity Properties of the Gene-Silencing Polypurine Reverse Hoogsteen Hairpins
    Villalobos, Xenia
    Rodriguez, Laura
    Prevot, Jeanne
    Oleaga, Carlota
    Ciudad, Carlos J.
    Noe, Veronique
    MOLECULAR PHARMACEUTICS, 2014, 11 (01) : 254 - 264
  • [10] Gene silencing polypurine reverse hoogsteen hairpins: in vivo effect, stability and immunogenicit
    Rodriguez, L.
    Villalobos, X.
    Oleaga, C.
    Prevot, J.
    Mencia, N.
    Ciudad, C. J.
    Noe, V.
    HUMAN GENE THERAPY, 2013, 24 (12) : A85 - A85