Summary: Researchers investigate the evolutionary development of psilocybin in some mushrooms. They conclude mushrooms may have evolved to be hallucinogenic to lower the odds of being eaten by insects.
Source: Ohio State University.
Psychedelic mushrooms likely developed their “magical” properties to trip up fungi-munching insects, suggests new research.
The work helps explain a biological mystery and could open scientific doors to studies of novel treatments for neurological disease, said lead researcher Jason Slot, an assistant professor of fungal evolutionary genomics at The Ohio State University.
Mushrooms that contain the brain-altering compound psilocybin vary widely in terms of their biological lineage and, on the surface, don’t appear to have a whole lot in common, he said.
From an evolutionary biology perspective, that is intriguing and points to a phenomenon in which genetic material hops from one species to another – a process called horizontal gene transfer, Slot said. When it happens in nature, it’s typically in response to stressors or opportunities in the environment.
He and his co-authors examined three species of psychedelic mushrooms – and related fungi that don’t cause hallucinations – and found a cluster of five genes that seem to explain what the psychedelic mushrooms have in common.
“But our main question is, ‘How did it evolve?'” Slot said. “What is the role of psilocybin in nature?”
Slot and his co-authors found an evolutionary clue to why the mushrooms gained the ability to send human users into a state of altered consciousness. The genes responsible for making psilocybin appear to have been exchanged in an environment with a lot of fungus-eating insects, namely animal manure.
Psilocybin allows fungi to interfere with a neurotransmitter in humans and also insects, which are probably their bigger foe. In flies, suppression of this neurotransmitter is known to decrease appetite.
“We speculate that mushrooms evolved to be hallucinogenic because it lowered the chances of the fungi getting eaten by insects,” Slot said. The study appears online in the journal Evolution Letters.
“The psilocybin probably doesn’t just poison predators or taste bad. These mushrooms are altering the insects’ ‘mind’ – if they have minds – to meet their own needs.”
And the reason that unrelated species have the same genetic protection probably comes down to the fact that they commonly grow in the same insect-rich mediums: animal feces and rotten wood.
This work could guide medical science by pointing researchers in the direction of other molecules that could be used to treat disorders of the brain, Slot said.
Psilocybin has been studied for the treatment of a variety of mental disorders, including treatment-resistant depression, addiction and end-of-life anxiety. A handful of researchers in the U.S. are looking at potential treatment applications, and much of the work is happening abroad. Strict drug laws have delayed those types of studies for decades, Slot said.
About this neuroscience research article
Other Ohio State researchers who worked on the study were Hannah Reynolds, Vinod Vijayakumar and Emile Gluck-Thaler. Hailee Korotkin and Patrick Matheny of the University of Tennessee also were on the research team.
[cbtabs][cbtab title=”MLA”]Ohio State University “Why Are Some Mushrooms “Magic”?.” NeuroscienceNews. NeuroscienceNews, 27 February 2018. <https://neurosciencenews.com/psilocybin-mushrooms-evolution-8571/>.[/cbtab][cbtab title=”APA”]Ohio State University (2018, February 27). Why Are Some Mushrooms “Magic”?. NeuroscienceNews. Retrieved February 27, 2018 from https://neurosciencenews.com/psilocybin-mushrooms-evolution-8571/[/cbtab][cbtab title=”Chicago”]Ohio State University “Why Are Some Mushrooms “Magic”?.” https://neurosciencenews.com/psilocybin-mushrooms-evolution-8571/ (accessed February 27, 2018).[/cbtab][/cbtabs]
Horizontal gene cluster transfer increased hallucinogenic mushroom diversity
Secondary metabolites are a heterogeneous class of chemicals that often mediate interactions between species. The tryptophan-derived secondary metabolite, psilocin, is a serotonin receptor agonist that induces altered states of consciousness. A phylogenetically disjunct group of mushroom-forming fungi in the Agaricales produce the psilocin prodrug, psilocybin. Spotty phylogenetic distributions of fungal compounds are sometimes explained by horizontal transfer of metabolic gene clusters among unrelated fungi with overlapping niches. We report the discovery of a psilocybin gene cluster in three hallucinogenic mushroom genomes, and evidence for its horizontal transfer between fungal lineages. Patterns of gene distribution and transmission suggest that synthesis of psilocybin may have provided a fitness advantage in the dung and late wood-decay fungal niches, which may serve as reservoirs of fungal indole-based metabolites that alter behavior of mycophagous and wood-eating invertebrates. These hallucinogenic mushroom genomes will serve as models in neurochemical ecology, advancing the (bio)prospecting and synthetic biology of novel neuropharmaceuticals.