Scientists have identified a new species of extinct parasitic fungus bursting from the backside of a 50 million-year-old ant, all perfectly preserved in amber.
In addition to the bulbous mushroom protruding from the ant's rectum, evidence of the freaky fungus can be seen throughout the body of its unlucky host. The ant likely died as a result of its fungal infection and was fortuitously fixed in tree resin (which fossilizes into amber) shortly afterward. It is the oldest example of a fungal parasite ever discovered in ants.
The researchers named the new species of fungi Allocordyceps baltica — Allocordyceps translates to "new genus" in Greek and baltica refers to the Baltic region where the amber was discovered.
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"These types of discoveries are extremely rare," George Poinar Jr., an entomologist at Oregon State University who helped pioneer the extraction of DNA from amber, told Live Science. "The amber resin contains chemicals that fixes cells and tissues and also destroys associated microbes that would normally decompose specimens."
Parasitic fungi are hard to find and study due to their short life cycles, Poinar said. "But we all bear some fungal growth on our bodies," he added.
Insects are a great host for these types of parasites because they are "readily available and supply a rich source of nutrients," Poinar said.
Carpenter ants of the genus Camponotus, like the one trapped in the amber, are common hosts of modern parasitic fungi of the genus Ophiocordyceps, which belong to the same order as A. baltica. "I was quite excited when I realized that these particular fungi extend back so far," Poinar said.
Although A. baltica are likely extinct today, its lineage could have evolved into modern-day Ophiocordyceps, Poinar said, although this has not yet been proved genetically.
Out the backdoor
The main difference between A. baltica and Ophiocordyceps is where their mushroom emerges from an ant. The mushroom, or ascomata, acts as the reproductive organ of the fungi, releasing spores into the environment. Ophiocordyceps fungi grow their ascomata around the neck and head of their host ants; the fungi hijack the host ants’ brain in a form of mind control, which the fungi use to force the ants to bite into plants where other carpenter ants lay their eggs. This enables the fungi to release their spores in areas with a high concentration of potential new hosts.
It is unclear why A. baltica grew its ascomata through the ant’s rectum instead, although Poinar suspects it may have allowed the fungus to keep its host alive for a longer period of time, meaning it had more time to distribute spores.
"The rectum is already open while the fungus would have to penetrate the head capsule to emerge through the head," Poinar said. "It would have allowed the ant to survive a few more days, since once the fungus enters the ant’s head the ant dies."
Nasty way to go
Although the reproductive ascomata emerges through the rectum of the fossilized ant, there is evidence that the fungus spread through that ant’s entire body. Stromata ― solid plates of the vegetative part of the fungus, known as mycelium ― can be seen protruding from the ant at the abdomen and the back of the neck; and the researchers also found sacs where the reproductive spores would have been produced in the abdomen and neck.
This would have "almost certainly" led to a slow and gruesome for the infected ant, Poinar said.
"As the hyphae [the branching filaments of mycelium] spread through the body, it would have been like a cancer," Poinar said, "but converting the tissues into fungal stages instead of cancer cells."
Originally published on Live Science.