4.4 Article

Insights into a rapid screening method for anti-cucumber mosaic virus compounds

Journal

JOURNAL OF VIROLOGICAL METHODS
Volume 301, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.jviromet.2021.114402

Keywords

Cucumber mosaic virus; Anti-CMV compounds; Model and method; Binding affinities

Funding

  1. National Key Research and Development Program of China [2017YFD0200503-3]
  2. National Natural Science Foundation of China [31960546]
  3. Program of Introducing Talents of Discipline to Universities of China (111 Program) [D20023]
  4. Frontiers Science Center for Asymmetric Synthesis and Medicinal Molecules, Department of Education, Guizhou Province [(2020)004]

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In this study, a rapid screening model for anti-CMV compounds was established using labeled CMV particles and commercial compounds. The results showed that both commercial compounds and synthesized compounds had inhibition effects on CMV, which is significant for the development of anti-CMV drugs.
Cucumber mosaic virus (CMV) is a detrimental plant virus in agricultural production. Traditionally, the half-leaf method using Nicotiana glutinosa has been used for screening agrochemicals to control CMV. However, this forms a time-consuming experimental bottleneck. In this study, we constructed a rapid screening model for anti-CMV compounds using CMV. In short, purified CMV particles were labeled through amine reactions and then subjected to binding studies with commercial compounds. The relative gene expression levels were then confirmed. Additionally, the rapid screening model results were verified using synthesized compounds. The commercial compounds ningnanmycin, ribavirin, and moroxydine hydrochloride bound to CMV with dissociation constants of 0.012, 2.870, and 0.069 mu M, respectively, and they significantly inhibited expression of the gene for the CMV coat protein in CMV-infected tobacco leaves. This rapid screening model was assessed using our synthetic compounds N12, N16, and N18 through binding, which were shown to have dissociation constants 0.008, 0.025, and 70.800 mu M, respectively, as well as via gene expression studies. Thus, a rapid method for screening anti-CMV commercial compounds and our synthetic compounds was constructed and confirmed.

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