TY - JOUR
T1 - A Novel Approach of Antiviral Drugs Targeting Viral Genomes
AU - Hoang, Phuong Thi
AU - Luong, Quynh Xuan Thi
AU - Ayun, Ramadhani Qurrota
AU - Lee, Yongjun
AU - Vo, Thuy Thi Bich
AU - Kim, Taehyun
AU - Lee, Sukchan
N1 - Publisher Copyright:
© 2022 by the authors.
PY - 2022/8
Y1 - 2022/8
N2 - Outbreaks of viral diseases, which cause morbidity and mortality in animals and humans, are increasing annually worldwide. Vaccines, antiviral drugs, and antibody therapeutics are the most effective tools for combating viral infection. The ongoing coronavirus disease 2019 pandemic, in particular, raises an urgent need for the development of rapid and broad-spectrum therapeutics. Current antiviral drugs and antiviral antibodies, which are mostly specific at protein levels, have encountered difficulties because the rapid evolution of mutant viral strains resulted in drug resistance. Therefore, degrading viral genomes is considered a novel approach for developing antiviral drugs. The current article highlights all potent candidates that exhibit antiviral activity by digesting viral genomes such as RNases, RNA interference, interferon-stimulated genes 20, and CRISPR/Cas systems. Besides that, we introduce a potential single-chain variable fragment (scFv) that presents antiviral activity against various DNA and RNA viruses due to its unique nucleic acid hydrolyzing characteristic, promoting it as a promising candidate for broad-spectrum antiviral therapeutics.
AB - Outbreaks of viral diseases, which cause morbidity and mortality in animals and humans, are increasing annually worldwide. Vaccines, antiviral drugs, and antibody therapeutics are the most effective tools for combating viral infection. The ongoing coronavirus disease 2019 pandemic, in particular, raises an urgent need for the development of rapid and broad-spectrum therapeutics. Current antiviral drugs and antiviral antibodies, which are mostly specific at protein levels, have encountered difficulties because the rapid evolution of mutant viral strains resulted in drug resistance. Therefore, degrading viral genomes is considered a novel approach for developing antiviral drugs. The current article highlights all potent candidates that exhibit antiviral activity by digesting viral genomes such as RNases, RNA interference, interferon-stimulated genes 20, and CRISPR/Cas systems. Besides that, we introduce a potential single-chain variable fragment (scFv) that presents antiviral activity against various DNA and RNA viruses due to its unique nucleic acid hydrolyzing characteristic, promoting it as a promising candidate for broad-spectrum antiviral therapeutics.
KW - 3D8 scFv
KW - antiviral antibodies
KW - broad-spectrum antiviral drugs
KW - CRISPR/Cas
KW - ISGs
KW - RNAi
KW - viral disease
KW - viral genome degradation
UR - https://www.scopus.com/pages/publications/85137342847
U2 - 10.3390/microorganisms10081552
DO - 10.3390/microorganisms10081552
M3 - Review article
AN - SCOPUS:85137342847
SN - 2076-2607
VL - 10
JO - Microorganisms
JF - Microorganisms
IS - 8
M1 - 1552
ER -