Regenerating worms have genetic control over their algal partners

Bo Wang, assistant professor of bioengineering in the Schools of Engineering and of Medicine at Stanford, has started to find some answers. His lab, in conjunction with the University of San Francisco, studies Convolutriloba longifissura, a species of acoel that hosts the symbiotic algae Tetraselmis. According to new research, published in Nature Communications, the researchers found that, when C. longifissura regenerates, a genetic factor that takes part in the acoel regeneration also controls how the algae inside of them reacts.

"We don't know yet how these species talk to each other or what the messengers are. But this shows their gene networks are connected," said Wang, who is a senior author of the paper.

Splitting worms

Because holobiont is a relatively new concept, scientists still aren't sure what the nature of some relationships are. The odd name "acoel" is Greek for "no cavity," as the worms have no separation between their inner and outer organs (called a coelom). In these animals, all their organs share the same space. Some acoels also have symbiotic algae sharing the space of the animals' organs, and photosynthesizing inside the animals' body. This relationship provides a safe zone for the algae and extra energy from photosynthesis to the acoel.

"There was no guarantee that there was communication because the algae are not within the acoel's cells, they're floating around them," says James Sikes, a researcher at the University of San Francisco and co-senior author of the paper. Sikes has been working with acoels for about 20 years, and their symbiotic relationship differentiates them from other animals that regenerate, like planarian flatworms and axolotls.

When these acoels reproduce asexually, they first bisect themselves. The head region grows a tail and becomes a new acoel. The tail, however, acts like the mythological Hydra and grows two new heads, which, then, split into two separate animals.

Animal regeneration requires communication across many different cell types, but in this case, it may also involve another organism entirely. Researchers were curious about how the algal colonies inside reacted to this process -- in particular, whether they continued to photosynthesize as normal, and if not, what was controlling that? This was especially puzzling as the team found that photosynthesis wasn't required for acoels to regenerate -- they could do it in the dark. But there has to be conversation between the species for their long-term survival.

"Testing if photosynthesis was affected was an adventure. None of us knew what we were doing," says Dania Nanes Sarfati, lead author of the paper, who was a doctoral student in Wang's lab and Stanford Bio-X Bowes Fellow. "One of the most exciting things was that we could actually measure algal photosynthesis happening inside the animal."

In addition, through sequencing, the team was able to differentiate the genes of the two species and figure out which pathways were responding to injury. These measurements helped them realize that the algae inside were undergoing a major reconstruction of their photosynthetic machinery during the regeneration -- but the process by which it was being controlled was shocking.

The role of runt

When the results came back, Wang said the unpredictable happened. During regeneration, both the acoel's regrowth and the algal photosynthesis appeared to be controlled by a common transcription factor in acoels called runt.

In the early stage, right after injury, runt is activated, kicking off the regeneration process. Meanwhile, algal photosynthesis drops off, but there is an upregulation in algal genes associated with photosynthesis -- likely to compensate for the loss in photosynthesis due to the split. However, when the researchers knocked down runt, it halted both regeneration and the algal responses.

What's special about runt is that it's highly conserved, meaning the same factor is responsible for regeneration in many different organisms, including non-symbiotic acoels. But now it's clear that instead of just controlling the acoel's regenerative process, it also controls the communication with another species.

How holobionts communicate

Understanding how partners in symbiotic relationships communicate at the molecular level opens up many new questions for this field of research. "Are there rules of symbiosis? Do they exist?" said Nanes Sarfati. "This research sparks these kinds of questions, which we can link to other organisms."

Wang believes it introduces more ways of investigating how symbiotic species interact and couple with each other to form holobionts. Some of these interactions could be potentially driven by chemicals, proteins, or environmental factors. But more concerningly, these interactions are now becoming vulnerable points under the challenge of climate change, causing symbiotic partners to separate. Sikes highlighted that he, Wang, and Nanes Sarfati all began from the animal side of the symbiotic relationship but realized that algae respond to host injury as well, potentially sparking similar questions in other systems.

"We often assume we know a lot, but we're humbled when we look at different species," Wang said. "They can do things in completely unexpected ways, which highlights the need to study more organisms and is becoming possible with technology."

This research was funded by a Bio-X Bowes Fellowship, a Stanford Interdisciplinary Graduate Fellowship, the Beckman Young Investigator Program, the Carnegie Institution for Science, and the National Institutes of Health.