
When archaeologists opened King Tutankhamun’s tomb in 1920, a string of sudden deaths among the excavation team shocked the world. Newspapers quickly called it the “curse of the Pharaoh,” fueling tales of supernatural revenge. A similar wave of deaths struck excavators in 1970 at the tomb of Casimir IV in Poland. Mysterious at first, these tragedies seemed to confirm ancient warnings.
Yet modern science uncovered a surprising truth. Aspergillus flavus, a toxic crop fungus, was the real killer. Its spores, dormant for centuries in the tomb offerings, were released into the air during excavation. Inhaling them caused fatal lung infections, especially in people with weakened immune systems. The fungus that once inspired terror would soon become an unexpected ally.
Aspergillus flavus, long feared for producing harmful aflatoxins and yellow spores on grains, hid something remarkable. Scientists at the University of Pennsylvania identified a group of ribosomally synthesized and post-translationally modified peptides, or RiPPs, within the fungus. These were entirely distinct from the well-known toxins.
Qiuyue Nie, a postdoctoral fellow in chemical and biomolecular engineering, explains, “The synthesis of these compounds is complicated, but that's also what gives them this remarkable bioactivity.” The team purified four RiPPs with unique interlocking ring structures and named them Aspergillomycins.
Two of the four Aspergillomycins showed strong effects against leukaemia cells, even without further modification. They worked by blocking the formation of microtubules, structures essential for cancer cells to divide. As Sherry Gao, senior author of the study, describes, “Cancer cells divide uncontrollably. These compounds block microtubule formation, stopping cell division.”
This finding is especially exciting because Aspergillomycins showed minimal activity against breast, lung, or liver cancer cells, suggesting a unique affinity for leukaemia. Researchers believe similar RiPP-producing genes exist in other fungi as well, opening new avenues for discovering natural cancer-fighting compounds.
“Fungi gave us penicillin. These results show that many more medicines derived from natural products remain to be found,” says Gao. Indeed, what was once seen as a deadly curse now offers a glimmer of hope. With continued research and clinical trials, these fungal peptides could redefine cancer treatment in the years ahead.
From ancient tombs to tomorrow’s hospital wards, the journey of Aspergillus flavus is a testament to how science can transform our deepest fears into life-saving breakthroughs.
(Rh/Dr. Thansiya A K/MSM/SE)