Antiviral Activity of Double Stranded RNA and Virus-like Particles from Penicillium stoloniferum
THE antiviral activity of a culture filtrate from Penicillium stoloniferum was first described in 1952 1 . Landmarks in the evaluation of this material, termed ‘ Statolon ’, came with its initial chemical characterization as a polysaccharide 2 and the discovery that its mode of action was by the ind...
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Veröffentlicht in: | Nature (London) 1970-08, Vol.227 (5257), p.504-505 |
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Sprache: | eng |
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Zusammenfassung: | THE antiviral activity of a culture filtrate from
Penicillium stoloniferum
was first described in 1952
1
. Landmarks in the evaluation of this material, termed ‘
Statolon
’, came with its initial chemical characterization as a polysaccharide
2
and the discovery that its mode of action was by the induction of interferon
3
. Later it became apparent that a ribonucleic acid component accompanying the polysaccharide had interferon stimulating ability (personal communication from Professor Sir Ernst Chain). It has subsequently been shown that the antiviral activity resided in virus-like particles present in the mould
4
and in the double-stranded ribonucleic acid (ds-RNA) of these virus-like particles
5,6
. During our screening programme for antiviral substances from microorganisms, antiviral activity of a
Stemphylium
culture was discovered
*
which was attributed to the presence of virus-like particles. Coincidental with this, workers at the Merck Institute showed that the antiviral activity of helenine (also an antiviral agent produced by a mould) was attributable to ds-RNA, and that other ds-RNAs (poly I.poly C and the replicative form of MS2 phage) possessed similar antiviral activity
7
. Recently, there have been further publications (for example, refs. 8–10) in which the toxicity of poly I.poly C has been examined. It will be interesting to see if the naturally produced ds-RNA is less toxic than poly I.poly C, as might be postulated because of the unnatural base composition in the latter material. |
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ISSN: | 0028-0836 1476-4687 |
DOI: | 10.1038/227504a0 |