New UMD Biologist Studies How Organisms Steal Each Other’s DNA

Micrograph set against a dark background, showing a transparent oval snail egg shell enclosing a developing snail embryo in its center.Darkfield micrograph featuring multiple vibrant green, spherical Volvox colonies floating against a black background, several containing bright, glowing daughter colonies within their hollow structures.Darkfield micrograph featuring a tick glowing in warm orange-red tones against a black backdrop, detailing its oval body and eight jointed, spiky legs spread outward.Micrograph showing three spherical, starburst-like clusters of colonial rotifers against a deep black background, with individual organisms radiating outward from central points.Micrograph of a translucent damselfly nymph against a stark white background, showing its broad head, dark compound eyes, long legs, and elongated segmented body extending toward the upper left corner.Micrograph of a spiral, coiled foraminiferan shell on a white background, composed of distinct, granular chambers divided by dark, defined suture lines.Light micrograph showing a round, translucent heliozoan with fine, radiating axopodia extending outward, engulfing green cylindrical diatoms within its central body.Darkfield micrograph of a bright green, single-celled endosymbiont-bearing Hydra viridissima against a solid black background, showing its tubular body curved with extended, delicate tentacles radiating from its head.Composite collage against a white background showing an assortment of microscopic protists, green algae, and golden diatoms, including a branched colony, star-shaped desmids, and single-celled ciliates.Micrograph against a dark background featuring the translucent golden body and tentacles of a Hydra, positioned near a small, swimming water flea (Daphnia).Microscopic view of Hydrodictyon (water net alga), depicting a dense, interconnected mesh network of tubular green cells forming a geometric lattice.Micrograph of a translucent crab zoea (larva) against a white background, showing two large, dark compound eyes, a compact carapace, and spindly jointed legs spreading outward.Darkfield micrograph featuring a star-shaped, bright green Micrasterias desmid alga with intricately lobed edges, glowing vividly against a black backdrop.Brightfield micrograph of a single, circular green Micrasterias desmid alga against a plain white background, showing symmetrical, finely serrated edges divided across a central axis.Brightfield micrograph showing a green Micrasterias desmid alga on a plain white background, featuring deeply branched, star-like projections radiating symmetrically from two central halves.Darkfield micrograph revealing a dense colony of peritrich ciliates glowing bright blue-white against a black background, anchored by delicate, branching stalks.Composite collage on a plain white background featuring various microscopic diatoms in shapes ranging from circular and triangular to needle-like and ribbon-like chains, mostly in golden-brown hues.Micrograph displaying a network of branching red alga filaments with distinct cell walls glowing faintly against a pitch-black background.Light micrograph of a fan-shaped Rhipidodendron colony against a bright white background, composed of golden-brown, tube-like stalks clustered in a tree-like arrangement.Light micrograph showing two circular, brownish Arcella shells side-by-side on a light background, detailing their central doughnut-like openings and subtle surface texturing.Brightfield micrograph featuring the star-shaped, brownish shell of an Arcella testate amoeba, centered on a stark white background with sharp radial spines around its edge and a central aperture.Darkfield micrograph displaying two glowing yellow-green Coleochaete disk-shaped algal colonies against a stark black background, connected by a long, slender filament.Light micrograph of an oval, dying Nassula ciliate filled with green and yellow spherical granules, with cytoplasmic material spilling out from the lower right edge against a white background.Light micrograph of green, feathery Batrachospermum (red alga) whorls on a dark background, bisected vertically by a segmented algal filament.

Assistant Professor Julia Van Etten researches how organisms acquire genes from other species through a process called horizontal gene transfer. 

Julia Van Etten didn’t expect to make one of her biggest discoveries while on vacation. The assistant professor of biology who joined the University of Maryland this summer was in the Outer Banks, North Carolina, with her family when she passed a roadside marsh, grabbed a water sample and brought it back to her rental house. 

A woman standing on a wooden pier near a large body of water during sunset, smiling while holding a white conical plankton net in one hand and black cord in the other under a bright, cloudy sky.
Biology Assistant Professor Julia Van Etten samples microorganisms for Couch Microscopy. Photo courtesy of Julia Van Etten

There, Van Etten pulled out the hobby-grade $300 microscope and $198 camera she packed—necessary equipment for her art and science communication project, Couch Microscopy, where she photographs and video records overlooked microorganisms people encounter in their everyday lives. Among other species, she’s visualized swimming pink protistsroving marine worms and triangular phytoplankton called diatoms. Her Instagram account, which she started before graduate school, now has more than 30,000 followers. 

“I don't think that you have to go to the ends of the Earth or to exotic locations to find cool life. I get the most joy out of finding interesting-looking things and interesting-behaving organisms in very ordinary locations,” Van Etten said. And for her, sampling that Outer Banks marsh was nothing out of the ordinary. 

Van Etten often dips her net into ponds, puddles and other quotidian bodies of water. But when she got back to her room and looked at this sample under the microscope, she saw two cells she’d never seen before. 

She realized they belonged to a rare group of amoebas called Paulinella. Although each cell was only about 15 microns in length, they looked distinct enough that she realized they were two different, undescribed species—and they could be the key to advancing her research program. At UMD, she studies how organisms acquire new DNA and organelles through so-called “horizontal processes,” in which they steal traits from other organisms in the community rather than inherit them from their parents.

“I believe horizontal processes are some of the most fundamental genomic processes that have shaped evolution, ecology, life on Earth and the biodiversity that we see today,” Van Etten said. 

Horizontal gene transfer: how organisms steal DNA

The process by which an organism takes DNA from another species and embeds it into its genome is called horizontal gene transfer (HGT). This can happen in several ways—for example, when a cell picks up stray fragments of DNA from the environment, eats another organism or is infected by a virus. 

It had long been known that bacteria and archaea transfer DNA through HGT, but it wasn’t until modern genome sequencing efforts that scientists broadly accepted that HGT plays an important role in the evolution of more complex organisms like plants, animals, fungi and protists. These organisms, called eukaryotes, have their DNA bound in a membrane, so there’s a barrier for foreign genetic material to embed itself into the genome. 

During Van Etten’s Ph.D. research at Rutgers University, she studied HGT in a group of single-celled red algae called Cyanidiophyceae. The species she worked on live in the hot springs of Yellowstone National Park. Despite their name, Cyanidiophyceae grow in bright green mats because they lost the ability to produce the pigment that gives their relatives a warm red color. It’s in part because of HGTs that these red algae can thrive in Yellowstone’s scorching temperatures, acidity and heavy metal concentrations.

Scanning electron micrograph (SEM) showing a high-magnification, greyscale view of an elongated, oval-shaped Paulinella marae test (shell), constructed from overlapping, armor-like silica scales with a textured surface against a solid black background.
Scanning electron micrograph of Paulinella marae—a species discovered by Julia Van Etten. Credit: Julia Van Etten

Van Etten’s research validated that certain species of Cyanidiophyceae acquired genes from neighboring bacteria that help them detoxify metals like arsenic. She also showed that HGT is happening in the community in real time. Today, the organisms in the ecosystem each perform different tasks that contribute to neutralizing the environment of heavy metals. In a sense, Van Etten says, DNA can be a public good, transferred between these organisms for collective survival. 

Over the past few years, Van Etten scaled up this research as a National Science Foundation Postdoctoral Research Fellow in Biology at the Woods Hole Oceanographic Institution, where she studies HGT in the Narrow River in Rhode Island. This six-mile-long river has a gradient of oxygen levels, where the top is loaded with oxygen and the bottom layer has none. Van Etten studies how DNA is transferred within and between layers. 

It’s not just organisms in niche, specific habitats that have benefited from HGT, either. Studies show that the process could have played a critical role in the evolution of the first plants and animals, allowing them to acquire new traits that aided in their success in new and changing environments. Much like how the even earlier acquisition of bacteria that became mitochondria and chloroplasts led to the origin of eukaryotes and algae respectively, these events paved the way for the most complex life we see today.

Van Etten hopes to probe how new organelles evolve by studying the two species of Paulinella that she discovered on vacation. These amoebas recently evolved an organelle that allows them to photosynthesize, similar to a chloroplast. HGT appears to have helped integrate the new organelle into its host’s biology, and since this resembles what happened when mitochondria and chloroplasts first evolved billions of years ago, studying Paulinella could be scientists’ best chance to gain firsthand knowledge of some of the most consequential events in evolution. 

Paulinella: a model for primary endosymbiosis

A hundred million years ago, an ancestor of Paulinella ate a cyanobacterium and turned it into a new photosynthetic organelle called a chromatophore. This process, called primary endosymbiosis, is similar to how mitochondria and chloroplasts evolved in two separate events about 2 billion years ago. It’s a horizontal process, similar to HGT, but at a larger and more permanent scale. Those three instances, plus a fourth event involved in the evolution of a new organelle discovered in a marine alga in 2024, are the only times that scientists know primary endosymbiosis happened, Van Etten said. 

Scanning electron micrograph (SEM) showing a high-magnification, greyscale view of a rounded, spherical Paulinella murrayi test featuring patterned, scale-like rows with small pitted details, resting against organic matter on a dark background.
Scanning electron micrograph of Paulinella murrayi—a species discovered by Julia Van Etten. Credit: Julia Van Etten

Van Etten and her colleagues have long wanted to study Paulinella to understand how primary endosymbiosis happened and how it shaped early eukaryote evolution. The issue was that few scientists knew where to collect Paulinella or how to sustain them in the lab. That’s where Van Etten’s vacation discovery comes in. 

In a paper published September 4 in the Journal of Phycology, Van Etten described the two new species she discovered, named Paulinella marae and Paulinella murrayi, after family members who were with her and encouraged her to sample from the location where she first collected the species. She is starting lab cultures of the two species at UMD. If she’s successful, she’ll move on to cutting-edge genomic and transcriptomic studies to understand how the new organelle evolved—including the role that HGT played. 

Van Etten is also engaging other hobby microscopists and natural historians who have spotted Paulinella around the world, creating a new consortium that she hopes will have the collective knowledge to sample and describe countless new species. Eventually, she wants to understand how the ability to photosynthesize changed Paulinella genomes and ecological roles across their evolutionary tree.

This two-pronged approach, combining cutting-edge lab techniques with old-school naturalism, is at the heart of Van Etten’s research program. Her work has greatly benefited from the hours she’s spent staring at local microorganisms through her microscope. 

“The best way to learn about nature is to be in it,” she said, noting that she learned more during her first few weeks sampling for Couch Microscopy than she had in her 22 years of life before starting the account. 

Based on her large Instagram following, Van Etten suspects this sort of backyard naturalism attracts an audience for science communication, too. 

“I think people really like the concept that they could walk by a puddle, and there’s all this life in it that they can’t see,” she said. 

So, she’ll train her students to think like backyard natural historians. She wants to equip her lab with an arsenal of hobby-grade microscopes her trainees can use to explore. If they’re interested, she’ll even help them develop their own science communication platforms.

“It’s good for the soul to just go out in nature and see what happens,” Van Etten said. “The closer you are to your system, the better you understand it, and the more creative you’ll get with your questions and insights—and that leads to more success in science.”