Sunday, May 31, 2026

 

Stopping ticks in their tracks


UT researchers discover protein that may block disease transmission


University of Tennessee Institute of Agriculture

UT College of Veterinary Medicine Professor professor Hameeda Sultana 

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Research led by University of Tennessee College of Veterinary Medicine Professor Hameeda Sultana and alumni postdoctoral fellow Waqas Ahmed has identified a tick protein that could help block disease transmission before it fully happens.

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Credit: Photo by S. Bridges, courtesy the University of Tennessee.






Few creatures inspire as much universal dislike as ticks. Though small, these parasites have an enormous impact on human and animal health. Each year, ticks spread viruses and bacteria that infect people, livestock, wildlife and pets around the world. Scientists at the University of Tennessee College of Veterinary Medicine are working to better understand how ticks transmit these diseases—and how to stop them.

In a new study published in The EMBO Journal, researchers identified a tick protein that could help block disease transmission before it fully happens. The EMBO Journal, published by the European Molecular Biology Organization, is one of the world’s leading journals in molecular biology.

The research was led by professor Hameeda Sultana and alumni postdoctoral fellow Waqas Ahmed, and contributors included former graduate students Wenshuo Zhou and Kehinde Fasae, current graduate student Md Bayzid, and faculty collaborators professor Girish Neelakanta and former UT clinical assistant professor Denae LoBato. Supported by funding from the National Institutes of Health, the work highlights the UT Institute of Agriculture’s role in advancing research on vector-borne diseases.

Between 2018 and 2020, Sultana’s laboratory was the first to identify exosomes derived from tick saliva and salivary glands and from tick and mosquito cells. In this groundbreaking work, the UT research team discovered that ticks produce an exosomal glycine-rich protein that plays a vital role in helping ticks feed and transmit viruses. “Exosomes are tiny bubble-like vesicles with messages in them,” explains Sultana. “They are tiny membrane-bound particles that transport proteins and other biological signals between cells and tissues. “When a tick bites its host, the interaction is more complex than it may appear. Tick saliva contains exosomes filled with a sophisticated cocktail of molecules, allowing them to feed undetected while avoiding triggering the host’s immune defenses. These vesicles carry a variety of tick proteins that may help pathogens move between ticks and hosts. “They contain several arthropod proteins that could facilitate tick feeding, pathogen acquisition from infected hosts to naïve ticks, and transmission of pathogens from infected ticks to naïve hosts,” Sultana says.

When the researchers used genetic tools to silence the gene responsible for this protein, the effects were dramatic. Ticks lacking the protein struggled to feed effectively and showed reduced body weight after feeding. Even more importantly, virus levels were significantly lower. The findings build on years of work exploring how ticks use microscopic vesicles to interact with their hosts.

This protein could be used in a vaccine approach. Faculty collaborator Girish Neelakanta says discoveries like this highlight how understanding tick biology can reveal new opportunities to prevent disease transmission. “Ticks transmit several pathogens,” Neelakanta explains. “Studies like this provide evidence about tick molecules that play an important role not only in tick biology but also in the interactions with pathogens.”

Researchers believe exosomes could become an important target for disease prevention strategies. “Since the identification of exosomes from ticks from my laboratory, several studies—including our own—have emphasized the importance of these vesicles in tick feeding and interactions with pathogens,” Sultana says. “This is an exciting area of research that could open several avenues for the development of arthropod exosome-based strategies to target vector-borne diseases.”

According to Neelakanta, targeting these molecules may offer a new way to interrupt the transmission cycle. “Targeting this type of protein might be an ideal approach to affect transmission of several pathogens from ticks.” This type of approach is known as a transmission-blocking vaccine. Rather than targeting the virus itself, the vaccine targets a molecule in the tick, preventing the tick from successfully feeding or transmitting pathogens. By interrupting this process early, scientists hope to stop infections before they ever reach the host.

As tick-borne diseases continue to increase worldwide, the need for new prevention strategies is becoming more urgent. Current control methods rely on avoiding tick bites or reducing tick populations. However, researchers are increasingly investigating ways to interfere with the biological mechanisms that ticks rely on to feed and transmit disease.

The discovery of this exosomal protein adds to a growing body of research exploring how parasites communicate with their hosts at the microscopic level. Scientists are still in the early stages of understanding the role exosomes and other extracellular vesicles play in these complex interactions.

Findings like these demonstrate how fundamental molecular biology research can lead to practical advances in both animal and human health. By uncovering the hidden mechanisms ticks use to spread disease, scientists are opening the door to innovative new strategies for prevention.

Sometimes the best way to stop a parasite is to understand it at its smallest scale. In this case, the key to combatting ticks may lie within microscopic packages only billionths of a meter wide. One day, these tiny messengers could help prevent the spread of vector-borne diseases.

One of 33 veterinary colleges in the United States, the UT College of Veterinary Medicine educates students in the art and science of veterinary medicine and related biomedical sciences, promotes scientific research and enhances human and animal well-being.

The University of Tennessee Institute of Agriculture is comprised of the Herbert College of Agriculture, UT College of Veterinary Medicine, UT AgResearch and UT Extension. Through its land-grant mission of teaching, research and outreach, the Institute touches lives and provides Real. Life. Solutions. to Tennesseans and beyond. utia.tennessee.edu.

 

 

Wall lizards in Ohio reproduced their way out of a genetic bottleneck


Study suggests ecology mostly explains Cincinnati invasion success



Ohio State University





COLUMBUS, Ohio – Non-native wall lizards living in Cincinnati, Ohio, have thrived against the odds thanks to an ability to expand their population more quickly than any inbreeding-amplified harmful genes could weaken their chances for survival, new research suggests.

An estimated 10 of these European common wall lizards arrived in southwest Ohio in the 1950s, brought home by a boy who smuggled them in his luggage after a vacation in northern Italy. Now, hundreds of thousands – and maybe even millions – of them scamper through urban parks and neighborhoods across Cincinnati. They’re called “Lazarus lizards” in a nod to the boy’s family, founders of the Lazarus retail chain.

Researchers sequenced genomes from four different populations of the lizards, looking for genetic clues to explain how this tiny army could complete such a successful invasion. And though the analysis showed evidence of some loss of genetic variation and a dip in population size, the findings led the team to propose that rapid population growth was a major key to their survival, along with the likelihood that living conditions in Ohio resembled what they were used to back home.

“They just grew so fast. If you think you have a bottleneck, but it doesn’t last very long, then you don’t have a bottleneck,” said senior study author H. Lisle Gibbs, professor emeritus of evolution, ecology and organismal biology at The Ohio State University. “The hypothesis that we argue is they just grew their way out of their potential genetic problem.

“In some ways, we’re disproving the importance of genetic factors to the system, because it doesn’t really explain a lot about the tremendous success of these lizards in Cincinnati,” he said.

The study was published recently in the journal Molecular Ecology.

Genomes from four sets of samples were sequenced and analyzed for the study: a group collected in 2009 from the source location in northern Italy; samples from two Cincinnati populations collected in 2007 and 2022; and samples from a population that existed briefly in 2021 in Columbus, Ohio, which served as a surrogate for the original lizards introduced to Cincinnati in 1951 – in that it was a recent introduction likely founded by just a few individuals.

Results showed that the lizards experienced reduced genetic variation after their arrival in Cincinnati, but the loss didn’t seem to have an effect on population health.

Based on what was seen in the Columbus population – lots of inbreeding, evidence of homozygosity that would increase the risk for harmful gene variants that could lower survival, and a big drop in numbers followed by rapid growth – the researchers concluded a similar scenario played out in Cincinnati decades ago.

“But all of the inbreeding with one another didn’t seem to matter. They were able to get over that hump and grow like crazy,” Gibbs said.

Eric Gangloff, associate professor of biological sciences at Ohio Wesleyan University and a co-author of the study, has been studying European common wall lizard ecology since 2017 in France and Ohio. The lizards are a great example of a species that can do well in nature despite the damaging effects human activity can have on biodiversity, he said.

“By and large, it seems like they were plopped into an environment that was very conducive to their spread and not that different from what they experienced in Europe originally,” Gangloff said. “Milan and Cincinnati are very different. But from a lizard’s point of view, they have a very similar climate and very similar structural habitat. And in their case in Cincinnati, they just didn’t have any other competitors. And they were able to take off.”

There were a few genomic differences between the Italian source lizards and the Cincinnati populations that hinted at adaptation to the new environment, including genes related to neural function – suggesting behavioral flexibility – and a pathway involving learning and memory that, in humans, helps lessen the effects of lead toxicity.

This second finding is of interest because European common wall lizards have astronomically high levels of lead in their blood, but show no signs of suffering from lead poisoning. Gangloff’s lab is exploring this unusual characteristic.

“It is an interesting part of the story that of all the regions of the genome, we happened to find one that suggests they’re responding to levels of lead in the environment,” he said.

For these lizards, urban living may be a requirement rather than an environment they settle for.

“There are so many of them that you’d think they would just spill into the countryside, but they don’t. So something is constraining them to urban areas,” Gibbs said. “The world is full of invasive species, and we still don’t really understand why one group does really well and another doesn’t. This gives us a hint about that.

“But it’s also a story about urban adaptation. We recognize that urban environments exert a lot of selective influences on species, and this is another example of that.”

This work was funded by the U.S. National Science Foundation and Ohio State, and was performed using resources provided by the Ohio Supercomputer Center.

First author Emily Bode led this research while studying as an undergraduate at Ohio Wesleyan and a graduate student at Ohio State. Additional co-authors were Andrew Mason and Peri Bolton of Ohio State and Ken Petren of the University of Cincinnati.

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Ancient oceans began suffocating millions of years before Triassic mass extinction




Virginia Tech

Members of a field team examine an outcrop of rock layers in Grotto Creek in Alaska's Wrangell–St. Elias National Park in 2019. 

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Members of a field team examine an outcrop of rock layers in Grotto Creek in Alaska's Wrangell–St. Elias National Park in 2019.

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Credit: Photo courtesy of Ben Gill.





One of the most devastating extinctions in Earth’s history is best known for what didn’t die — dinosaurs.

But the end-Triassic extinction 201 million years ago wiped out roughly 60 percent of Earth’s species, and scientists are still piecing together how it unfolded.

New evidence from Virginia Tech geologists shows that the volcanic eruptions that ripped apart the land and acidified the oceans also stripped the oxygen out of their waters.

And, in an unexpected finding, the research team discovered that oxygen starvation began nearly 8 million years before the mass extinction.

Their study was published May 26 in Nature Communications Earth & Environment.

Hot planet, cold case

Scientists have long linked the end-Triassic extinction to massive volcanic eruptions that warmed the planet and set off cascading environmental changes.

In a warmer climate, rocks break down faster and release nutrients that increase ocean acidity. Warmer seawater also holds less oxygen, creating dead zones.

More acid and less oxygen is “kind of like a one-two punch,” said geochemist Ben Gill. “It wouldn't have been a very happy place to be.”

Until now, evidence for widespread marine deoxygenation came from a limited geographic area, leaving questions about when and where it began. Plus, there was something of a mystery associated with recent studies suggesting that environmental deterioration might have started a lot earlier than previously believed.

“It's a 200-million-year-old cold case,” said Kayla McCabe, a former geosciences graduate student and first author of the study.

Consulting the ancient ocean

To answer those questions, the Virginia Tech team members turned to the rock record.

In 2017, 2019, and 2022, they traveled to Grotto Creek in Alaska’s Wrangell–St. Elias National Park, a remote site accessible only by small aircraft.

There, they compared sedimentary rock layers deposited before, during, and after the extinction.

The rock layers preserve a record of past ocean conditions, like pages in a book. Flipping back through time revealed that oxygen levels in shallow oceans began to decline about 8 million years before the end-Triassic mass extinction.

That early loss of oxygen likely stressed marine ecosystems long before the main extinction event.

It got worse later. Geochemical analyses show that oxygen loss intensified during the extinction itself and became a major driver of species loss.

But what caused the apocalyptic opening act?

“There's evidence of another volcanic province that roughly lines up with this time interval,” Gill said. “But we're in the very beginning of trying to understand what happened.”

Scientists may not yet know the cause, but they know how it played out. Which means we have a rough guide for the future, as our oceans are again undergoing acidification and deoxygenation — including in the Chesapeake Bay

“Earth has run this experiment in the past. We have evidence that the climate gets warmer, and then all these other knock-on effects come afterwards,” Gill said. “It gives us some sense of what we can expect to happen.”

Study collaborators included:

  • Selva M. Marroquín, former graduate student, now faculty at University of Wisconsin-Madison
  • Rachel E. B. Reid, research assistant professor, Department of Geoscience, Global Change Center

This research was supported with funding from:

  • National Science Foundation
  • National Geographic Society
  • Alaska Geological Society
  • Virginia Tech Department of Geosciences
  • Virginia Tech College of Science Dean’s Discovery Fund

Original study DOI 10.1038/s43247-026-03362-w

 

Turning microalgae waste into high-performance membranes for cleaner municipal wastewater



Biochar Editorial Office, Shenyang Agricultural University

Amine-functionalized biochar/cellulose acetate hybrid membranes for sustainable municipal wastewater treatment 

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Amine-functionalized biochar/cellulose acetate hybrid membranes for sustainable municipal wastewater treatment

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Credit: Yazan Abuhasheesh, Mahendra Kumar, Farah Abuhatab, Pau Loke Show, Fawzi Banat & Shadi W. Hasan





A new study published in Biochar reports a sustainable membrane technology that converts microalgae-derived biochar into an advanced material for municipal wastewater treatment, offering a promising route to cleaner water and waste valorization.

Municipal wastewater contains a complex mixture of organic matter, nutrients, salts, and microorganisms. Among these pollutants, natural organic matter is particularly challenging because it can clog filtration membranes, reduce treatment efficiency, and contribute to the formation of unwanted by-products during disinfection. Membrane technologies are widely used in water treatment, but fouling remains one of their biggest barriers to long-term, cost-effective operation.

To address this challenge, researchers developed amine-functionalized biochar/cellulose acetate hybrid membranes using biochar derived from microalgae biomass. The biochar was chemically modified with amine groups through a one-step mussel-inspired polymerization and Schiff-base reaction. The resulting amine-functionalized biochar was then blended into cellulose acetate, a biodegradable polymer, to create hybrid ultrafiltration membranes.

Our goal was to design a membrane that not only performs well, but also fits within a more sustainable materials cycle,” said corresponding author Shadi W. Hasan. “By transforming microalgae biomass into a functional biochar filler, we can improve wastewater filtration while adding value to biological waste streams.

The team found that adding amine-functionalized biochar improved several key membrane properties. The hybrid membranes became more hydrophilic, more porous, and more negatively charged, all of which helped reduce foulant adhesion and improve water transport. Structural and chemical analyses confirmed that the functionalized biochar was successfully produced and incorporated within the cellulose acetate matrix.

Among the tested membranes, the one containing 4 wt.% amine-functionalized biochar showed the strongest overall performance. In municipal wastewater filtration, this membrane achieved a water flux of 169.1 L m⁻² h⁻¹ and 64.1% removal of natural organic matter, outperforming the pristine cellulose acetate membrane, which reached only 81.8 L m⁻² h⁻¹ and 31.1% removal.

The modified membrane also demonstrated complete bacterial removal during testing. In addition, it partially removed other common wastewater contaminants, including chemical oxygen demand, sulfate, phosphate, nitrate, ammonium, and magnesium. These results suggest that the membrane could provide broader benefits beyond organic matter control.

Membrane fouling resistance was another important outcome. After municipal wastewater filtration and simple cleaning with deionized water, the best-performing membrane showed a flux recovery ratio of 82.7%, indicating strong antifouling behavior without the need for harsh chemical cleaning.

Fouling is a major limitation for membrane-based wastewater treatment,” Hasan said. “The improved recovery and stable filtration performance suggest that biochar-based hybrid membranes can help make water treatment systems more durable and easier to operate.

The study also highlights the value of testing membranes with real municipal wastewater, rather than relying only on synthetic laboratory solutions. By demonstrating performance under more practical conditions, the work provides a stronger foundation for future scale-up and application.

The researchers conclude that microalgae-derived amine-functionalized biochar is a promising sustainable filler for next-generation hybrid membranes. The approach links biomass waste conversion with advanced water treatment, showing how renewable carbon materials could help build more efficient and environmentally friendly wastewater technologies.

 

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Journal Reference: Abuhasheesh, Y., Kumar, M., Abuhatab, F. et al. Amine-functionalized biochar/cellulose acetate hybrid membranes for sustainable municipal wastewater treatment. Biochar 8, 68 (2026).   

https://doi.org/10.1007/s42773-026-00582-3   

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About Biochar

Biochar (e-ISSN: 2524-7867) is the first journal dedicated exclusively to biochar research, spanning agronomy, environmental science, and materials science. It publishes original studies on biochar production, processing, and applications—such as bioenergy, environmental remediation, soil enhancement, climate mitigation, water treatment, and sustainability analysis. The journal serves as an innovative and professional platform for global researchers to share advances in this rapidly expanding field. 

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University of Toronto researchers aim to improve access to high-quality research and biomanufacturing tools in resource-limited settings



Keith Pardee and international collaborators show freeze-dried reagents and low-cost hardware can reliably support research and diagnostics in remote locations around the world




University of Toronto - Leslie Dan Faculty of Pharmacy

Researchers develop accessible biotech platform for labs worldwide 

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Using synthetic biology and cell-free systems, Associate Professor Keith Pardee and his team have developed a protocol to produce research-quality bioreagents without the use of traditional lab infrastructure

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Credit: Steve Southon




Researchers at the University of Toronto’s Leslie Dan Faculty of Pharmacy, working with collaborators around the world, have demonstrated the effectiveness of a suite of low-cost, portable biotechnology tools designed to improve access to laboratory research and diagnostics in resource-limited settings.

Published today in Science Advances, the study highlights how decentralized biomanufacturing tools and freeze-dried reagents can help researchers produce high-value biological materials locally — reducing reliance on fragile international supply chains and expanding access to life sciences innovation globally.

The research was led by Keith Pardee, associate professor at the Leslie Dan Faculty of Pharmacy, alongside collaborators including Camila González in Bogotá, Colombia, Fernán Federici in Santiago, Chile, and Lindomar Pena in Recife, Brazil.

“For labs in low- and middle-income countries, access to high-quality supplies and equipment is a chronic problem,” says Pardee. “Shipping can take a long time, it’s expensive, and products often require a cold chain to retain their effectiveness. This research is in response to those challenges to develop tools that are more accessible for labs in lower-resource settings and improve research equity.”

The team’s work focuses on synthetic biology and cell-free systems — technologies that isolate and freeze-dry the molecular machinery needed to produce proteins commonly used in life sciences research. Because the reagents are freeze-dried, they can be shipped and stored without refrigeration, then reactivated simply by adding water.

Researchers paired these systems with low-cost, adaptable hardware, including a 3D-printed hand-powered centrifuge developed by postdoctoral fellow Mohammad Simchi. Together, the technologies enabled teams to produce a range of research proteins and diagnostic tools in diverse settings, from conventional laboratories to remote field locations.

Using the platform, researchers successfully produced growth factors used in life sciences research and therapeutics, as well as a SARS-CoV-2 vaccine candidate tested in mice and diagnostic tools targeting several clinically relevant pathogens.

“Our work shows that it is possible to produce high-value bioreagents on site, essentially anywhere,” says Severino Jefferson Ribeiro da Silva, postdoctoral fellow in Pardee’s lab and first author of the study. “Through this work, we demonstrated our tools across diverse international settings while maintaining performance comparable to commercial products.”

A key component of the project involved testing the systems in a variety of environments across Canada and internationally. Da Silva travelled to the Algonquin Highlands to evaluate diagnostic tools for tick-borne pathogens and tuberculosis, while graduate student Quinn Matthews travelled to the Yukon where he produced and purified proteins using the portable system on a mountain outside Whitehorse.

Collaborators in Chile, Brazil, Colombia and India also tested the systems, helping ensure the technologies addressed the practical realities faced by researchers in different regions. The project involved extensive international collaboration, including regular meetings, student exchanges and knowledge sharing among participating teams.

Da Silva says the research team experienced firsthand many of the logistical challenges their collaborators routinely face, including lengthy customs delays and damaged shipments containing critical reagents.

“Those experiences highlighted how dependent many researchers and labs still are on fragile international supply chains. If a shipment is delayed, an entire project can stop,” says da Silva. “This work makes it possible to reduce that dependency by enabling local production of key proteins directly at the point of need.”

The researchers say the long-term goal is to help research labs in remote and underserved regions gain access to high-quality diagnostics, research reagents and biomanufacturing capabilities produced closer to home, strengthening resilience against future supply chain disruptions while empowering their research capacity and address local healthcare needs.

“This work is really about access and scientific empowerment,” says da Silva. “Many labs worldwide have the expertise and ideas to conduct life sciences and applied science research, but they face major challenges accessing key bioreagents and essential materials. Decentralized biomanufacturing could help reduce those barriers and make research and diagnostics more accessible globally.”

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Media Contact

Steve Southon
Interim Director, Communications
Leslie Dan Faculty of Pharmacy
University of Toronto
steve.southon@utoronto.ca
905 220 4963