Sunday, April 19, 2026

 

Songbird brains can generate new neurons. Can we help human brains do the same?




New Boston University study shines fresh light on how songbird brains refresh themselves; it could one day open the door to new human therapies




Boston University






Despite its small size—it could sit in the palm of your hand—the zebra finch is a remarkable learner. A songbird native to Australia, it’s renowned for its ability to pick up new songs.

That talent has made it a favorite of scientists studying how animal brains imprint new skills, particularly vocal learning, or the capacity to perfect new sounds. And now researchers at Boston University have discovered another quirk to the zebra finch brain—one that could also have implications for understanding our own gray matter. 

In a study that looked at the bird’s brain in unprecedented detail, they uncovered new insights into a mechanism known as neurogenesis—the birth, migration, and maturation of neurons—that may help the brain learn, add new skills, and restore and repair itself.

Observing the finch brain using a high-powered microscope, the researchers watched as new neurons bullied their way through the brain en route to bolstering existing circuits and connections. They’d expected the neurons to gingerly step around established brain structures, including more mature brain cells, to better preserve them; instead, they saw them tunnel right through, squishing and shoving as they went.

According to the BU-led team, their findings could help explain human vulnerability to a range of brain disorders. They also noted that cell tunneling is used by some metastatic cancer cells. The findings were published in Current Biology.

“We found that in songbirds, new neurons in the adult brain behave like explorers forging a path through a dense jungle,” says Benjamin Scott, a BU College of Arts & Sciences assistant professor of psychological and brain sciences and the study’s corresponding author. That may help them learn new things or repair damage, but it could come with a cost to existing cells and memories—and that might be why neurogenesis is a skill humans don’t seem to have beyond the womb.

“This potentially disruptive behavior may help explain why humans and other mammals have limited capacity to regenerate brain tissue in adulthood,” says Scott, “leaving us more vulnerable to neurodegenerative disorders such as Alzheimer’s disease.”

Tunneling Neurons

When you’re born, your brain pretty much has all the neurons it’s ever going to have. Other organs—from your skin to your heart—might get frequent cell updates, but the brain is working on version 1.0.

That’s true for most mammals, but not fish, reptiles, and birds—their brains get a regular refresh.

“This raises two questions,” says Scott, who’s also affiliated with BU’s centers for neurophotonics, photonics, and systems neuroscience. “Why do other species have high rates of neurogenesis throughout life and why is it so restricted in humans? And is there something we can learn from their biology that we might be able to harness in future?”

Scott typically studies the neural circuits that control behavior in humans and other mammals, but chose the zebra finch to investigate neurogenesis because it has a reputation as a champion species—it’s really good at generating new neurons.

“We applied a new tool to study this process [neurogenesis] called electron microscopy-based connectomics—basically a really high-powered microscope—to image these cells at a very high resolution,” says Scott. “Our first hope was just to say, what does this look like at a detail we couldn’t see before?” Instead, they spotted the tunneling neurons.

If these new neurons are deforming brain tissue, says Scott, are they also disrupting memories along the way? And, if neurogenesis comes with a cost, how does that balance against the brain’s capacity for learning new things and repairing after injury?

Scott has two—as yet untested—hypotheses for what the findings might mean for the human brain. The first is that our brains evolved to limit neurogenesis after birth as a form of protection—a way of making sure determined neurons couldn’t barge through mature connections and damage memory storage.

“There is an alternative framing that is more optimistic,” he says. “Our discovery of tunneling shows how cells can move without glia scaffolds.” These are the structures that operate as highways for migrating neurons.

“Most glia scaffolds are lost in humans after birth, and this loss was thought to be an obstacle for neurogenesis in the adult brain,” says Scott. “However, our work shows that new neurons in the bird do not need this glia scaffold. This is exciting because it means that brain repair may not require specialized glia scaffolds.” That opens the door for scientists to explore potential stem-cell therapies that would spark neurogenesis in humans.

Next: Figuring Out the How and Why of Neurogenesis

In current studies, Scott and the team in his BU Laboratory of Comparative Cognition are digging into the biology driving neurogenesis to uncover which genes are regulating the process. Much of the work merges ideas and tools from biomedical engineering and neuroethology, the study of the mechanisms underpinning animal behavior.

“Right now, we’re using a technique called single-cell RNA sequencing to identify genes that are expressed by these new neurons as they migrate,” says Scott. “We want to know what other cells they’re talking to as they move and how they are speaking to these different cells.”

That’ll help them figure out whether neurons warn other cells they’re travelling through and how they know where to stop and integrate with a current circuit.

“We share a lot with our animal relatives on this planet,” says Scott. And, while the term “bird brain” might be an insult, by learning more about the biology of songbird brains, he says, we could learn some remarkable things about our own.

 

This research was funded with support from the BU Neurophotonics Center. The study also included researchers from the MRC Laboratory of Molecular Biology, United Kingdom, and the Max Planck Institute for Biological Intelligence, Germany.

 

 

Helping corals survive future heatwaves requires strong and strategic trait selection





Newcastle University

One year old pedigree tracked corals growing in an ocean nursery. 

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One year old pedigree tracked corals growing in an ocean nursery. 

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Credit: Dr Liam Lachs





Assisted evolution could help corals survive future heatwaves, but careful trait choice and strong repeated selection will be needed for it to be effective.

As global temperatures rise, marine heatwaves are becoming more frequent and severe, driving coral bleaching and mortality. While some coral populations are already showing signs of natural adaptation, researchers warn that these changes are unlikely to keep pace with future warming.

A new study published today (16 April) in Current Biology explores whether host assisted evolution, which aims to accelerate natural adaptation rates of corals, could help them survive future heatwaves and what it would take to achieve required tolerance gains.

The international research team, led by Newcastle University, have created a unique, pedigree-tracked coral population over the last eight years, allowing them to map family relationships and measure how multiple key traits—such as growth, reproduction and survival—are inherited.

By combining information on multiple traits for each coral, their family relationships and advanced statistical modelling, the scientists were able to estimate each coral’s genetic merit for heat tolerance and other traits, and the genetic links among traits, insights that go beyond what can be simply observed.

Dr James Guest, Reader in Coral Reef Ecology at Newcastle University and the principal investigator of the project supporting this study, said: “Developing and maintaining this pedigree-tracked coral population has driven a step change in our ability to identify which traits to select for to enhance tolerance under future climate stress. Being able to produce corals from parental colonies with known histories and well-characterised traits—and then observe how this genetic information influences offspring performance—has significantly advanced our understanding of how assisted evolution can be effectively implemented to conserve coral reefs.”

The results show that assisted evolution methods targeting the coral host—rather than its symbionts—will require choosing the right traits and repeatedly selecting corals over multiple generations to strengthen those traits.

Selection must directly target long-term heatwave survival, or traits that have a strong genetically based correlation to heatwave survival. To keep pace with climate change, efforts will need to implement very strong selection, choosing the top 1-5% most tolerant corals as broodstock. And this process will have to be repeated over multiple generations to achieve desired evolutionary benefits. Such intense selection introduces other challenges, including the maintenance of genetic diversity and practicality of scaling up selection efforts.

Study lead author, Dr Liam Lachs, a former Postdoctoral Research Associate at Newcastle University’s School of Natural and Environmental Sciences and current Research Fellow at University of Queensland, Australia, said: “Local adaptation involves more than just heat tolerance. Traits like growth, reproduction, calcification, tissue biomass, and symbiont flexibility all contribute to overall fitness. If improving heat tolerance came at the cost of these traits, it could undermine population viability. But encouragingly, we found no detectable negative genetic correlations among any traits; good news for assisted evolution interventions.”

Not a silver bullet

The researchers stress that assisted evolution is not a substitute for cutting greenhouse gas emissions, which remains essential to limit ocean warming.

However, as global mitigation efforts continue, targeted local interventions could play an important supporting role at certain scales. Strategic conservation approaches, including assisted evolution, may help key coral species adapt and persist in a rapidly changing climate.

Study lead author, Dr Adriana Humanes, a Research Associate at Newcastle University, said: “Our results show that increasing coral heat tolerance can, in principle, deliver meaningful gains for coral persistence. But success will depend on choosing the right traits and strong, sustained selection. While reducing greenhouse gas emissions is still the main priority to mitigate the warming corals face, other mitigation efforts such as assisted evolution will be crucial to help key species adapt and persist in our rapidly warming world.”

Reference 

https://doi.org/10.1016/j.cub.2026.03.055


 

 

Want to restore oyster reefs? Find a site where they don’t wash away or become buried under the sand!






Royal Netherlands Institute for Sea Research





Disappearing reefs

Oyster reefs were once abundant in the North Sea and other, so-called marginal seas at the edges of continental shelves. They hosted a significant biodiversity but have disappeared from 97 % of their original locations. Therefore, various restoration initiatives are undertaken, often with limited success.

Deep experiments

In an experimental setting at a depth of 32 m, in the Gemini wind park (85 km north of the Wadden islands), Zhiyuan and colleagues placed oysters on a rack 0,5 m above the seabed, where they were monitored for filtering activity. Also, oysters were placed on the seabed, to see if they were displaced or buried by currents or sediments. Lastly, they placed oysters in an experimental ‘mesocosm’, to monitor how they survived burial.

Keep on gaping

The experiments showed that oysters kept above the seabed survived well, even during storms, as shown by continuous ‘gaping’, showing filtering activity. But oysters on the soft seabed faced a different reality: stronger near-bed hydrodynamics could dislodge them, while rapid sediment accumulation could bury them beyond recovery. 

Practical implications

The results of these experiments have several practical implications, Zhiyuan says. “First, it is very important to look at potential short-term physical disturbance, when introducing new oysters to the seabed. Water quality is not the only thing to look at”, he warns. “Oysters may remain physiologically healthy, but still fail, because they are dislodged by strong near-bed hydrodynamics or buried by rapid sediment accretion before a reef can establish.” 

Find promising sites

To help select potentially successful sites for reintroduction, the paper describes thresholds at which the risks from hydrodynamic-induced loss and burial-caused mortality become critical. If burial seems likely, only oysters that are placed above the sediment may succeed, while placement in prefab reef structures is an option in areas where dislodgement is likely. “This helps move restoration planning away from trial and error and toward a more risk-informed strategy”, Zhiyuan says. “Our study suggests that the key is not only choosing the right place but also choosing the right method for that place.”

 

Engineered dual-bacterial sensors turn chemical signals into electricity



Rice researchers develop e-COSENS to detect analytes important to human and environmental health



Rice University

Prepping e-COSENs 

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A close-up of Siliang Li manipulating the e-COSENs setup. 

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Credit: Jared Jones/Rice University





Bacterial sensors usually rely on emitting light to transfer information about what they’re sensing, but that method isn’t practical in many settings. That’s why most information transmission is done via electricity. And while electricity-emitting bacteria exist, manipulating them into useful sensors has been quite challenging. Rice University professor Caroline Ajo-Franklin’s group, working in collaboration with researchers from Tufts University and Baylor College of Medicine, recently developed a flexible bioelectrical sensor system called electroactive co-culture sensing system (e-COSENS). The study was published in Nature Biotechnology

“Bioelectrical sensing is by no means a new concept,” said Ajo-Franklin, the Ralph and Dorothy Looney Professor of Biosciences and corresponding author on this paper. “But e-COSENS is the first system that allows us to easily engineer bioelectronic sensors in a modular manner, like assembling Legos, allowing us to potentially use them to monitor everything from human health to environmental contaminates.”

Bioelectrical sensing requires bacteria that produce electricity and are easy for researchers to manipulate to respond to different substances. Ideally, the bacteria would be able to live in a variety of different places so that the system could be used in environments ranging from rivers to milk.  

The challenge was finding bacteria that met all three conditions. E. coli, for example, is simple to engineer but doesn’t produce electricity. L. plantarum, a common food bacterium, produces electricity using a molecule called quinone but is incredibly difficult to engineer. 

“Instead of forcing a single bacterium to do everything, we split the job between two bacteria,” said Siliang Li, the first author on this study and postdoctoral fellow. “That division of labor is what makes e-COSENS so flexible and powerful.” 

The key to e-COSENS is quinone, the molecule L. plantarum uses to create electricity. L. plantarum cannot create its own quinone; it has to be provided by the environment. This means the quinone can be used as a signal, or trigger, to turn electricity on or off.

The researchers revealed that they could easily manipulate bacteria like E. coli, a bioengineering workhorse, to make quinone only in the presence of a specific substance called an analyte. Once E. coli released the quinone in the environment, L. plantarum would use it to send an electrical signal, which could be read by an electrode — in this case, a current meter. 

To test this system, the researchers designed systems to look for four different analytes in four different environments. They used E. coli to sense heavy metal ions in bayou water and inflammation markers in artificial saliva, and L. lactis, another quinone-producing bacterium, to sense antimicrobial peptides in human fecal-derived samples provided by Baylor and an antibiotic in milk from the grocery store. They placed each sample and bacterial systems into individual reactors connected to current meters. Within a few hours, all four current meters showed an electrical charge, revealing the bacteria were responding to the analytes — some in as few as 20 minutes. 

All four versions of the system were successful, but the large reactors they used wouldn’t easily translate from the lab to the outdoors. Luckily, their collaborators at Tufts had a solution: a compact electronic disk roughly the size of a quarter which can be paired with commercially available digital multimeters. 

“This simplified hardware dramatically lowers the barrier to using bioelectronic sensors outside the lab and opens possibilities for low-cost, field-ready diagnostics,” Li said. The researchers had also identified multiple other bacteria that could either send or receive a quinone signal, increasing the number of possible environments e-COSENS could be used in. 

“The strength of e-COSENS is the flexibility derived from sharing the work across multiple cells,” said Ajo-Franklin, director of the Rice Synthetic Biology Institute, which focuses on supporting interdisciplinary research. “In the same manner, the success of this research hinged on sharing expertise and work among my research group and our partners, Duolong Zhu and Robert Britton at Baylor and Kundan Saha and Sameer Sonkusale at Tufts.” 

This work was supported by the Cancer Prevention and Research Institute of Texas (RR190063) and the Army Research Office (W911NF-22-1-0239). Two of the authors filed a provisional patent entitled “Compositions and Methods of Bioelectronic Sensing” on Aug. 12, 2024 (No. 63/682,083), covering the design criteria of e-COSENS. A subsequent appendance was filed on June 23, 2025 (No. 63/828,835), covering the use of the MFC device with a multimeter for electrical signal detection, as well as a provisional patent entitled “Nanosheet Clay Cation Exchange Membrane for Microbial Fuel Cell” on March 4, 2025 (No. 63/766,456), covering the fabrication and application of the clay membrane.

Setting up e-COSENs 

Siliang Li adjusts the e-COSENs setup

Credit

Jared Jones/Rice University

 

 

Houston Methodist study finds blood pressure drug effective for treating antibiotic-resistant bacteria



Houston Methodist





Infections from antibiotic-resistant bacteria are difficult to treat and are responsible for over 2.8 million infections and more than 35,000 deaths in the U.S. each year. A new study in Nature Communications reports that a drug used to lower blood pressure could also be the basis of a promising new treatment for methicillin-resistant Staphylococcus aureus (MRSA).
 

“MRSA commonly causes infections in both hospitals and the community. It infects people in different ways and can survive even when antibiotics are used, which makes treatment extremely difficult,” said corresponding author Eleftherios Mylonakis, M.D., Ph.D., chair, Houston Methodist Charles W. Duncan Jr. Department of Medicine. “Scientists around the world are looking at various ways to provide treatment options outside of established antibiotics. The high cost of developing new drugs, and the time it takes to do so, led our team to explore the possibility of using existing medications, approved for other uses, to treat bacterial infections.”
 

Researchers were interested in determining if existing drugs can change the physical properties of bacterial membranes, which can weaken the bacteria and make the bacteria more susceptible to treatment. The blood pressure drug Candesartan cilexetil (CC), a common and inexpensive medication already used clinically, was identified as having this potential.

In the lab, Dr. Nagendran Tharmalingam, first author of the study, and a team of researchers and collaborators were able to prove that the drug effectively fights MRSA by disrupting its cell membrane and interfering with cell function. It not only killed MRSA bacteria at different growth stages, but also reduced the formation of biofilms, which are clusters of the bacteria that are more difficult to treat. By weakening the bacteria and stopping its growth, researchers showed that the drug has the potential to be a tool in the arsenal of treatment options for antibiotic-resistant infections.


Other collaborators on the study included Robert Wilson-Kovacs and Orlando Acevedo from the University of Miami; Suelen Scarpa de Mello and Michael Gilmore from Harvard Medical School and Massachusetts Eye and Ear Infirmary; Philip Rupert Baldwin and Steven Ludtke from Baylor College of Medicine; Harikrishna Sekar Jayanthan from Vanderbilt University; Kulandaisamy Arulsamy from Boston Children’s Hospital; Rajmohan Rajmuthiah,Fernanda Cristina Possamai Rossatto, Katherine Manz and Kurt Pennell from Brown University; Joseph DeGiorgis from Providence College and Frederick Ausubel from Harvard Medical School and Massachusetts General Hospital.
 

For more information about Houston Methodist, visit houstonmethodist.org