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Potent inhibition of respiratory syncytial virus by polyoxometalates of several structural classes
- Source :
- Antiviral Research. 34:27-37
- Publication Year :
- 1997
- Publisher :
- Elsevier BV, 1997.
-
Abstract
- A series of polyoxometalates (POM) were synthesized and evaluated for anti-respiratory syncytial virus (RSV) activity. POM containing zirconium, tungsten, silicon, platinum, niobium or germanium of a variety of structural types have been evaluated. Sixteen of the compounds had very striking anti-RSV activity against a clinical isolate, Utah 89, with median effective concentration (EC50) valuesor = 3 microM and selective indices80 as determined by viral cytopathic inhibition effect, neutral red uptake and virus yield reduction assays. The EC50 values for all three assays correlated very well (Pearson correlation coefficients0.90). POM containing sodium cations were totally inactive. Germanium-, niobium-, tin- and zirconium-containing compounds were found to be highly potent and selective. The antiviral activity was not cell line-dependent. The median cytotoxic concentration (IC50) values were generally greater than 100 microM. The compounds were also comparably active against a known laboratory RSV strain, A2, as well as other RSV strains. To detect any virus strain-specific inhibitory activity, seven POM were tested against other RSV strains; all were nearly equally inhibitory to the human virus strains, suggesting no strain specificity. Timing studies suggested that these compounds were most inhibitory during virus adsorption and penetration, although RSV was still significantly inhibited when the compound was added 3 h post-infection; which is considered well into the eclipse period. These data suggest that these potent, non-toxic compounds should be further studied as potential chemotherapeutic agents for treating RSV infections.
- Subjects :
- Neutral red
Paramyxoviridae
Cell Survival
viruses
Virus Replication
Antiviral Agents
Virus
Cell Line
Microbiology
chemistry.chemical_compound
Cytopathogenic Effect, Viral
Virology
Tumor Cells, Cultured
Animals
Humans
Cytotoxicity
IC50
EC50
Pharmacology
biology
biology.organism_classification
In vitro
Respiratory Syncytial Viruses
chemistry
Cell culture
Cattle
Subjects
Details
- ISSN :
- 01663542
- Volume :
- 34
- Database :
- OpenAIRE
- Journal :
- Antiviral Research
- Accession number :
- edsair.doi.dedup.....284561b5d46dcb100fbb51cd3e508505
- Full Text :
- https://doi.org/10.1016/s0166-3542(96)01019-4