Antivirals from other mushrooms have been identified previously: lentinan from Shiitake, Lentinula edodes, (Sarkar et al., 1993); PSP from Turkey Tail, Trametes versicolor, and ganaderiol-F, ganoderic acid-ß, lucidumol from Reishi, Ganoderma lucidum,) A number of unique antivirals from mushrooms have shown efficacy in inhibiting the replication of the human immunodeficiency virus. (Suzuki, 1989; Nanba, 1992; Kim et al., 1994; Collins & Ng, 1997; Ghoneum, 1998; Hattori, 1997). Other antivirals, not yet characterized, but having shown activity from hot water extracts from Chaga , Inonotus obliquus, (Kahlos et al. 1997) and Zhu Ling, Polyporus umbellatus (Yan, 1988).
The predominant mushrooms showing promise for their antiviral activities are polyporesthe so-called woody conks, thought to be the ancestors of most, if not all, gilled mushrooms. (Interestingly we know of no poisonous polypores whereas there are more than hundred poisonous gilled mushrooms, of which only a few are deadly.) Most all these antivirals are water soluble, relatively heat-stable, and most of the mushrooms mentioned and/or their mycelia can be cultured to commercially significant levels. The causal compounds are present both in the mycelium and in the fruiting bodies. The current literature points to mushrooms, particularly those in the Polyporaceae, as a rich frontier of new medicines. Many of these mushroom species are long-term residents of Old Growth Forests, playing an essential role in nutrient recycling by decomposing aged trees. In a time when new anti-viral medicines are critically needed, mushrooms stand out as an untapped resource and deserve intensive studies.
Supporting Bibliography
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