Beilstein J. Org. Chem.2024,20, 1029–1036, doi:10.3762/bjoc.20.91
is able to stop the acute phase of the pandemic. However, antiviraltherapy for COVID-19 is indispensable in case of vaccine failure, virus mutation or suppressed immunity of some patients [2].
SARS-CoV-2 is part of the Coronaviridae family, a group of enveloped +ssRNA viruses. The genome can
directly act as a viral messenger RNA and encodes essential enzymes for replication [3]. Inhibiting these nonstructural proteins that are part of the replication complex has already shown great success in antiviraltherapy [4][5][6][7].
The viral RNA-dependent RNA polymerase (RdRp) is encoded in all RNA
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Graphical Abstract
Figure 1:
Structure of HeE1-2Tyr (1) and of the derivatives synthesized in this work.
Beilstein J. Org. Chem.2021,17, 1360–1373, doi:10.3762/bjoc.17.95
degradation of antiviral RNA molecules. The present work demonstrates that VLPs (virus-like particles) allow efficient delivery of dsRNAi as antiviraltherapy in shrimp. In particular, VLPs derived from a virus that infects plants, such as cowpea chlorotic mottle virus (CCMV), in which the capsid protein (CP
applied to pathogen control in shrimp and also other organisms, widening the application window in nanomedicine.
Keywords: antiviraltherapy; CCMV; oral administration; P. vannamei; plant VLPs; RNAi; VP28; white spot syndrome virus; Introduction
The white spot syndrome virus (WSSV) is recognized as one
with the antiviraltherapy was evaluated through the survival and mean lethal time (LT50) [52]. A Log-Rank (Mantel–Cox) test was used to analyze the Kaplan–Meier survival curves generated with the GraphPad Prism version 5.01 software (San Diego California USA). In all cases, a value of p < 0.05 was
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Graphical Abstract
Figure 1:
Analysis of the VLP-dsRNAvp28 assembly by electrophoresis mobility shift assay (EMSA) in a 1% nativ...