A multi-institution team co-led by a Cornell researcher has identified the genetic mechanisms that enable the production of a deadly toxin called Victorin – the causal agent for Victoria blight of oats, a disease that wiped out oat crops in the U.S. in the 1940s.
The study, “Victorin, the Host-Selective Cyclic Peptide Toxin from the Oat Pathogen Cochliobolus victoriae, is Ribosomally Encoded,” was published Sept. 15 in the journal Proceedings of the National Academy of Sciences.
Victoria blight is caused by the fungus Cochliobolus victoriae, which produces the Victorin toxin, but until now no one has uncovered the genes and mechanisms involved.
“The oat varieties favored by farmers in the 1940s were resistant to Crown Rust disease, but scientists later discovered this was the very trait that made those oat varieties susceptible to Victoria blight because the Victorin toxin was targeting that specific plant protein,” said co-senior author Gillian Turgeon, professor and chair of the Plant Pathology and Plant-Microbe Biology Section of the School of Integrative Plant Science, in the College of Agriculture and Life Sciences (CALS). “Unearthing the molecules involved in this fungus-plant interaction is fundamental to our understanding of how plants respond to attack by diverse microbes.”
Most fungal toxins are synthesized by large, multi-functional enzymes, and the small peptides created by these enzymes include both toxins and medicines, such as the antibiotic penicillin. But Turgeon and co-author Heng Chooi, a researcher at the University of Western Australia, discovered the Victorin toxin is actually synthesized directly in the ribosome, which is an organelle in cells that makes most proteins. These small molecules produced in ribosomes are known as ribosomally synthesized and post-translationally modified peptides, or RiPPs.
This alternate mechanism for producing small peptides like Victorin – coupled with the fact that fungal genomes likely contain many RiPP-associated genes – could lead to the discovery of additional small molecules, including both new toxins and beneficial compounds.
Further, first author Simon Kessler, a doctoral student at the University of Western Australia, confirmed the enzymatic function of several Victorin genes, including a novel enzyme that converts the Victorin peptide to its active form. Surprisingly, the research team found that the Victorin genes encoding these enzymes are scattered across repetitive regions in the pathogen genome – a stark contrast to genes for most known small molecules which are typically found in compact clusters on the fungal chromosomes.
The finding could help researchers better understand the evolutionary origins of molecules like the Victorin peptides, what determines the virulence of emerging crop diseases and how to better prevent them in the future.
Turgeon notes that Victorin peptides have also been shown to interact with targets in plant cells called thioredoxins, which are also found in humans, and have potential as a site for cancer therapies.
“The discovery that these genes are not found in closely related fungi gives us insight into how virulence factors are acquired and transmitted,” Turgeon said. “Our findings from this study vastly expand the potential for small molecule discovery in fungal organisms, which will increase our repertoire of knowledge about both their beneficial and harmful activities.”
Co-authors include Xianghui Zhang, Zeran Lin and Adriana Rightmyer in Cornell CALS’ School of Integrative Plant Science; Megan C. McDonald and Peter Solomon at the Australian National University; and Cameron Gilchrist at the University of Western Australia.
Funding for this work was provided by the Australian Research Council, the China Scholarship Council, the Australian National University Grains Research and Development Corporation, the New South Wales Department of Primary Industries, and the Joint Genome Institute.
Jana Wiegand, content manager in CALS’ Office of Marketing and Communications, contributed to this story.