Ötzi’s Frozen Remains: Discovering Metabolically Active Microorganisms in Ancient Ice

Ötzi’s Preservation Conditions

South Tyrol Archaeological Museum/Eurac Research/Marion Lafogler

Recent research suggests that some microorganisms in the 5,300-year-old remains of Ötzi the Iceman may be metabolically active, despite his long-term ice preservation.

Ötzi’s mummified remains were discovered in 1991, as they melted from a glacier in the Alps near the Austria-Italy border. He is estimated to have lived between 3350 and 3120 BC. Over the last 35 years, studies of his remains revealed significant insights, including his probable dark complexion and baldness, and the fact that he had numerous tattoos. An arrow wound in his shoulder indicates he was murdered.

Ötzi is currently housed at the South Tyrol Archaeological Museum in Bolzano, Italy, under conditions that replicate those of his original icy environment: -6°C (21°F) with 99% relative humidity.

Researchers, including Frank Meixner from the Eulac Institute Mummy Research Institute, analyzed skin swabs, tissue fragments, and thawed water samples from Ötzi, collected in 1992, 2010, and 2019. They compared these to soil and ice samples from the discovery site in the 1990s.

Both ancient and modern microorganisms have been identified in Ötzi, with some possibly remaining metabolically active. “We can differentiate between Ötzi’s endogenous gut bacteria and those that entered his body from the environment after death,” Meixner explains.

Metagenomic analysis of internal tissues conducted by the research team has revealed specialized bacteria that thrive in mammalian intestines without oxygen, such as Treponema and Kineotrix. The extent of DNA damage in these bacteria suggests they were living in Ötzi’s body during his lifetime.

The diverse range of microbes found in Ötzi’s gut may reflect the varied diets of Chalcolithic humans, contrasting with those of modern Western societies, according to Meixner.

Additionally, the samples contained bacteria from the Pseudomonas genus, commonly found in soil and water. The DNA damage observed indicates these bacteria likely belong to an ancient microbial community at the discovery site.

The research team identified cold-tolerant or psychrophilic yeasts in Ötzi’s external samples: Phenoripheria, Graciojima, Gofojima, and Murakia.

Analysis indicated that these yeasts are also ancient microorganisms. Notably, the presence of Graciojima increased from 2010 to 2019, suggesting it may be metabolically active or capable of reproduction under current storage conditions.

Reconstructed Image of Ötzi

South Tyrol Archaeological Museum/Augustin Ochsenreiter

“This is compelling evidence that Graciojima has colonized the mummy post-mortem,” states Nikolai Oskolkov, although he’d like additional data points to ensure results are not influenced by experimental conditions.

The increasing prevalence of yeast is intriguing, as noted by Damra Kaptan from the University of Stavanger, Norway. “Determining if it’s active will require us to check for RNA produced from the yeast DNA,” she elaborates. “It’s possible the yeast was dormant or partially activated during thawing.”

Some yeasts possess enzymes capable of breaking down proteins and collagen, which could potentially harm the mummies; however, researchers found no evidence of such damage.

The research team also identified microorganisms containing genes that can degrade the toxic compound phenol. Professor Meixner suggests this may be linked to treatments applied to the mummy in the 1990s aimed at controlling mold growth. “When Ötzi was discovered, there was already active mold, and he was treated with phenol,” he explains. “This could have strengthened the microbiome.”

Overall, the study indicates that Ötzi is not merely a biological time capsule, but rather a complex ecosystem formed from the inheritance of his gut microbes, the glacial environment, and over 30 years of preservation. “Given these microbes have been associated with the mummy from the start, should we consider them as part of his biological makeup?” questions Meixner.

He recommends ongoing genomic monitoring, including checks for activity signs like RNA and metabolites, to determine if the microbial community is awakening and affecting Ötzi’s tissue. If this occurs, scientists may need to reassess storage conditions to mitigate microbial activity.

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Source: www.newscientist.com

Wax moth caterpillars can metabolically digest plastic and convert it into body fat.

Plastic polymers are everywhere in our daily lives, and their durability makes them suitable for numerous uses, yet effective disposal remains a significant issue. Recent discoveries of various plastiboa insects reveal their extraordinary capability to consume and swiftly decompose petroplastics. Specifically focusing on caterpillars of the Great Wax Moth (Galleria Mellonella)—commonly known as wax worms—and low-density polyethylene, researchers have explored the extent of plastic consumption, the roles of insects and their microbiota in biodegradation, and the impact of plastic ingestion on larvae health.

Polyethylene decomposition using wax worms. Left: Plastic bag after 12 hours of exposure to approximately 100 wax worms. Right: Enlarge the area shown in the image on the left. Image credit: Bomb et al doi: 10.1016/j.cub.2017.02.060.

Plastic is essential in contemporary life, but its disposal is extremely challenging due to its resistance to biodegradation.

In 2017, researchers illustrated that larger wax moth caterpillars can effectively break down polyethylene plastics.

Polyethylene is the most widely produced plastic globally, with an annual production exceeding 100 million tons.

This plastic’s chemical properties make it resistant to decomposition, often taking decades or even centuries to fully break down.

“Around 2,000 wax worms can degrade an entire polyethylene bag within just 24 hours, and we believe that supplementing this process with nutrients like sugar could significantly decrease the required number of worms,” said Dr. Brian Catthorne, a biologist at Brandon University.

“However, understanding the biological mechanisms and fitness implications linked to plastic biodegradation is crucial for harnessing wax worms for large-scale plastic remediation.”

Utilizing diverse methods combining animal physiology, materials science, molecular biology, and genomics, Dr. Catthorne and colleagues examined wax worms, their bacterial microbiome, and the potential for extensive plastic biodegradation, including the effects of wax worms on their health and survival.

“This scenario is akin to consuming steaks. When over-saturated, excess fat is stored in adipose tissue as lipid reserves instead of being used as energy,” Dr. Catthorne explained.

“Waxworms have a proclivity for polyethylene, yet this study indicates that such a diet can lead to rapid mortality.”

“They cannot survive for more than a few days on plastic-exclusive diets and undergo substantial mass loss.”

“Nonetheless, we are optimistic about devising a co-supply strategy that not only restores fitness to a natural level.”

Researchers have pinpointed two ways in which wax worms could aid in tackling the ongoing plastic pollution dilemma.

“Firstly, as part of a circular economy, we can efficiently process large quantities of rear wax worms derived from the supplemented polyethylene diet,” Dr. Catthorne noted.

“Secondly, we could explore redesigning the plastic biodegradation pathways outside of these insects.”

“A further advantage is that mass-producing wax worms yields a significant surplus of insect biomass, offering additional economic prospects for aquaculture.”

“Our preliminary findings suggest they could be incorporated into a nutrient-rich diet for commercially available food fish.”

The author presented these survey results today at the Society for Experimental Biology Annual Conference in Antwerp, Belgium.

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Brian J. Catthorne et al. Plastic biodegradation by insects. SEB 2025 Summary #A17.4

Source: www.sci.news