Monday, May 11, 2026

 

Invisible smart bug fights gum disease




KeAi Communications Co., Ltd.

How the engineered HEpM remodel the periodontal microenvironment. 

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How the engineered HEpM remodel the periodontal microenvironment.

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Credit: Lili Chen





Periodontitis—a chronic inflammatory disease that damages the gums and bones supporting teeth—affects nearly half of adults worldwide. Current treatments often fail because they cannot simultaneously eliminate stubborn bacterial biofilms and calm the runaway inflammation that follows.

Now, researchers have engineered a living bacterium that does both, in the right order.

In a study published in Dental Research, a team of researchers from China and Australi started with Escherichia coli Nissle 1917 (EcN), a harmless probiotic, and gave it three clever upgrades. First, they loaded it with nanoparticles containing metronidazole, an antibiotic that only becomes active in the oxygen‑free environment of a diseased gum pocket. Second, they equipped the bacterium with a hemoglobin from a bacterium that loves oxygen (Vitreoscilla). This "invisible cloak" protects the probiotic from its own antibiotic. Finally, they added a heat-sensitive genetic switch that turns on an antioxidant enzyme (superoxide dismutase) only when triggered by a mild warm stimulus.

"We wanted a therapy that respects the natural course of the disease—first clean up the harmful microbes, then resolve the inflammation," says senior and co-corresponding author Lili Chen. "Our design allows us to remotely activate the anti‑inflammatory phase precisely when the first job is done."

In a rat model of periodontitis, the two‑stage treatment dramatically reduced the key pathogens P. gingivalis and F. nucleatum and restored a healthy-like oral microbiome. After heat activation, the engineered bacteria lowered oxidative stress and promoted repair of the periodontal ligament and alveolar bone. Single-cell sequencing revealed that fibroblasts became the central hub of tissue‑regenerating signals.

"What if something goes wrong? To that end, we built in a fail‑safe: the same hemoglobin that acts as an 'invisible cloak' also serves as a natural sonosensitizer," shares Chen. "Additionally, we introduced a short, low‑energy ultrasound pulse (1 W/cm², 5 min), which safely lyses the engineered bacteria with no trace left behind."

"This is the first time a living bacterium has been programmed to execute a temporal, two‑step therapeutic program inside the body," says co-corresponding author Yuzhou Wu. "The platform could be adapted for other inflammatory diseases where microbial imbalance and oxidative stress play a role."

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Contact the author: Lili Chen, Department of Stomatology, Union Hospital, Tongji Medical College, Hubei Province Key Laboratory of Oral and Maxillofacial Development and Regeneration, School of Stomatology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, P. R. China. E-mail: chenlili1030@hust.edu.cn.

The publisher KeAi was established by Elsevier and China Science Publishing & Media Ltd to unfold quality research globally. In 2013, our focus shifted to open access publishing. We now proudly publish more than 200 world-class, open access, English language journals, spanning all scientific disciplines. Many of these are titles we publish in partnership with prestigious societies and academic institutions, such as the National Natural Science Foundation of China (NSFC).

 

Metformin’s real power may be in the gut


Type 2 diabetes drug slows mitochondrial energy production in gut cells, forcing gut to metabolize excess sugar




Northwestern University

Navdeep Chandel 

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Corresponding author Navdeep Chandel in his lab in Chicago.

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Credit: Kristin Samuelson, Northwestern University





  • Supplement berberine — ‘nature’s Ozempic’ — appears to engage the same pathway as metformin in the gut 
  • Pre-clinical study’s findings help explain several gut-related clinical effects of people who take metformin
  • An effective strategy for controlling blood sugar could be modulating mitochondrial metabolism in the gut 

CHICAGO --- For decades, physicians and scientists thought metformin, the leading Type 2 diabetes medication taken by millions worldwide, mainly targets the liver to suppress glucose production. But a new Northwestern University study in mice has found this “wonder drug” instead focuses primarily on the gut, acting to prevent glucose levels rising in the blood by driving glucose utilization inside cells lining the intestine. 

The body relies on glucose as a fast and versatile fuel, but too much glucose can lead to insulin resistance and ultimately damage blood vessels and organs. The study found metformin slows mitochondrial energy production in gut cells, forcing the intestine to metabolize extra sugar. 

“Metformin essentially helps the intestine suck the glucose out of the bloodstream, which further highlights that the gut plays a major role in regulating blood sugar levels,” said corresponding author Navdeep Chandel, professor of biochemistry and molecular genetics at Northwestern University Feinberg School of Medicine. 

The study will be published May 8 in Nature Metabolism

The study builds off findings from previous work in Chandel’s lab, which found metformin lowers blood sugar by blocking a specific part of the cell’s energy-making machinery called mitochondrial complex I, a key enzyme in cellular respiration. The new study furthers that work by pinpointing the specific tissue targeted by metformin. The findings suggest directing drugs or supplements to the gut could be an effective strategy for controlling blood sugar, Chandel said.  

Chandel also is the David W. Cugell, MD, Professor of Medicine (Pulmonology and Critical Care), Biochemistry and Molecular Genetics and an investigator with the Chan Zuckerberg Initiative. The study’s first author is Zach Sebo, a postdoctoral fellow in the Chandel lab who will soon start his own research group at the University of Kansas School of Medicine.

“Our study suggests that revisiting assumptions about metformin’s mechanism may offer a more detailed understanding of how it works,” Sebo said.

Parallels with berberine, ‘nature’s Ozempic’ 

The findings also reveal unexpected parallels with berberine, a popular plant-derived, over-the-counter supplement often used to control blood sugar. Berberine has recently gained attention on social media as “nature’s Ozempic,” though experts caution that evidence is still limited, and it should not be used as a substitute for approved medications. The study found berberine appears to engage the same pathway as metformin in the intestine. 

“Metformin has decades of clinical evidence behind it, whereas supplements like berberine are far less rigorously tested,” Chandel said. “If you're going to use berberine, you may as well use the real deal.”

Gut-related clinical observations from metformin users explained

Lastly, the findings help explain the following clinical observations of people who take metformin. According to Chandel, people on metformin:

  • Tend to have lower blood sugar after meals. Metformin turns the gut into a “sponge” that soaks up extra sugar.
  • Have lower levels of circulating citrulline, which is made only by mitochondria in small‑intestine cells. If metformin inhibits mitochondria, citrulline production drops. 
  • Have increased levels of GDF15, a hormone linked to reduced appetite and weight loss. The gut senses energy stress and sends out GDF15, which tells the brain to eat less and adjust metabolism.

“People have always wondered how one drug can do 10 things,” Chandel said. “Well, it can do that if the drug is hitting a big node in a cell, and hitting mitochondria in a cell is a big node. So, if you can get into those cells and inhibit mitochondria, it's going to have huge effects.”

More about how the study worked

The study used a mouse model, genetically engineered to express a yeast enzyme (NDI1) that mimics mitochondrial complex I but is resistant to inhibition by metformin. By expressing NDI1 specifically in intestinal cells, those gut cells resist metformin’s effects. In these mice, the drug’s ability to lower blood glucose was significantly reduced, demonstrating that inhibition of mitochondrial complex I in the gut is a key driver of its therapeutic action.

Other Northwestern study authors include Ram Chakrabarty, Rogan Grant, Karis D’Alessandro, Alec Koss, Jenna Blum, Shawn Davidson and Colleen Reczek.

 

X-shaped sleepers improve load transfer under impact on railway tracks




KeAi Communications Co., Ltd.
HOW THE X-SHAPED SLEEPER COMPARES WITH CONVENTIONAL I-SHAPED SLEEPERS IN LOAD TRANSFER AND STRESS DISTRIBUTION. 

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HOW THE X-SHAPED SLEEPER COMPARES WITH CONVENTIONAL I-SHAPED SLEEPERS IN LOAD TRANSFER AND STRESS DISTRIBUTION.

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Credit: Cheng Chen





Researchers at Wuhan University of Technology have discovered that an X-shaped railway sleeper can change how impact loads travel through ballasted track—reducing peak sleeper acceleration by 23% and average ballast contact forces by 40% compared to conventional I-shaped sleepers.

Ballasted track accounts for the vast majority of railway lines worldwide, with wheel-rail impact representing one of its primary threats. Track irregularities caused by rail and wheel wear, uneven settlement, or joint defects cause wheels to momentarily lose contact with the rails before striking back at high velocity, generating impact forces that can reach three to four times the static wheel load.

"Under impact loading, conventional I-shaped sleepers create sparse but highly concentrated force chains beneath the sleeper, focusing stress on a small number of ballast particles and accelerating ballast degradation," explains the study's first author, Cheng Chen, an associate professor in geotechnical engineering. "Our proposed X-shaped sleeper, with its distinctive bidirectional V-shaped configuration, significantly increases the contact area with the ballast. However, the mechanical behavior and load transfer mechanisms at the X-shaped sleeper-ballast interface under impact loading remained unclear—this is precisely the key question our study set out to address."

The research team found that, unlike the sparse, high-intensity force chains formed beneath conventional I-shaped sleepers, the unique geometry of the X-shaped sleeper breaks down impact loads into a dense, uniform network of force chains.

"This spatially diffused load transfer mechanism effectively reduces stress concentrations, enhances interlocking between ballast particles, and allows impact energy to be dissipated across a broader area—significantly improving the overall stability and impact resistance of the trackbed," shares Chen. "Under impact loading, conventional I-shaped sleepers tend to generate localized high-intensity force chains that accelerate ballast breakage."

The X-shaped sleeper, by contrast, reconstitutes the force chain network, achieving a fundamental shift from concentrated load-bearing to spatial diffusion. "We hope our research inspires further exploration to enhance trackbed stability, ultimately delivering safer and more comfortable railway journeys for the public," adds Chen.

The team's findings are published in the KeAi journal Journal of Railway Science and Technology.

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Contact the author: Cheng Chen, School of Civil Engineering and Architecture, Wuhan University of Technology, Wuhan, Hubei, China. chengchen87@whut.edu.cn

The publisher KeAi was established by Elsevier and China Science Publishing & Media Ltd to unfold quality research globally. In 2013, our focus shifted to open access publishing. We now proudly publish more than 200 world-class, open access, English language journals, spanning all scientific disciplines. Many of these are titles we publish in partnership with prestigious societies and academic institutions, such as the National Natural Science Foundation of China (NSFC).

 

Study finds multiple PFAS, the man-made ‘forever chemicals’, in 98.5% of people tested in US study


Across more than 10,500 samples examined, 98.8% had at least one PFAS in their blood




Taylor & Francis Group






Man-made 'forever chemicals' have been detected in 98.8% of blood tests, in a new study which examined more than 10,500 samples.

The findings are the latest indication to suggest that nearly every single person in the US is living with PFAS (per- and polyfluoroalkyl substances) – and usually multiple – in their system.

The results, published in the peer-reviewed Journal of Occupational and Environmental Hygiene, show that most individuals (98.5%) were, in fact, carrying multiple types of these environmentally persistent chemicals in their blood.

The paper demonstrates one of the largest-ever sample sizes determining PFAS levels in blood.

PFAS are a group of approximately 10,000, so-called, forever chemicals – as they do not degrade easily and build-up in the environment and human body. Used for decades, they can be found in thousands of day-to-day items ranging from clothes and cooking utensils to electronics and medical equipment. They live in our food, water and homes.

The dangers of all PFAS are not fully known; however, previous studies have linked some of them to serious complications, including cancer, infertility, high cholesterol, and weakened immunity.

One of the PFAS most commonly detected in this new study (in 97.9% of samples) was perfluorohexane sulfonic acid (linear PFOA), which is already recognised as being linked to adverse health conditions – including potential impacts on the immune system, liver, and thyroid – prompting action, internationally, for its restriction.

Commenting on the results, lead author, Dr Laura Labay, Principal Toxicologist at NMS Labs – the leading independent provider of professional laboratory testing services in the USA – says it is hoped their new dataset can offer future interventions.

“This large dataset provides a real-world snapshot of how multiple PFAS commonly occur together in people. By identifying these shared exposure patterns, the study offers a greater understanding of what widespread, combined PFAS exposure may mean for human health. We hope these findings will help inform future risk-assessment efforts, guide research on harmful PFAS mixtures, and ultimately support clearer clinical and public-health guidance.”

The data in this report were derived from 10,566 serum and plasma samples, of which a PFAS co-positivity assessment was performed by the NMS Labs team. Most samples (10,478) were tested for 13 different PFAS, whilst 88 samples were tested for 18 PFAS. 58 unique chemical combinations were found when testing for 13 PFAS and 16 different combinations were found when testing for 18 PFAS.

Overall, they found 98.8% of samples contained at least one PFAS. Only 19 samples (0.18%) contained a single PFAS, at the lower limit of the reporting threshold (0.1 ng/mL).

Across both testing panels, the most common combination included five PFAS, including historically used PFOS and PFOA as well as their replacement chemicals, frequently found in consumer products such as nonstick cookware, stain-resistant fabrics, and firefighting foam. This combination was detected in 2,754 samples, or 26.1% of those tested.

“These findings reinforce that PFAS exposure rarely occurs as isolated compounds,” Dr Labay adds.

“Instead, individuals typically carry body burdens comprising five or more PFAS with differing bioaccumulation properties and half-lives. The high prevalence and consistency of specific PFAS combinations highlight the importance of mixture-based interpretation in biomonitoring, particularly given PFAS’ potential to affect multiple biological systems in the body.”

The authors detail that limitations of the paper include that not all PFAS potentially present in the samples may have been considered, which may have led to underestimation.

 

On air travel and digital currencies


Baker McKenzie Award Honors Two Outstanding Dissertations in Business Law




Goethe University Frankfurt

Alexander Heger 

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Alexander Heger was honored for his work on European competition law in the aviation sector.

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Credit: Philipp Allenbrand





FRANKFURT. This year’s Baker McKenzie Award has been awarded to Dr. Alexander Heger and Dr. Felix-Julius Konow in recognition of their exceptional doctoral research. Since 1988, the international law firm Baker McKenzie has presented the €6,000 award to honor outstanding dissertations and habilitations completed at Goethe University Frankfurt’s Faculty of Law. Eligible works must have received the highest distinction, summa cum laude. The award ceremony will take place on May 8, 2026, during the faculty’s doctoral graduation celebration at the Casino Building on Westend Campus. The prize will be presented by Dr. Florian Thamm, partner at Baker McKenzie.

Dr. Alexander Heger is being recognized for his dissertation, “European Competition Law and Air Transport – A Suitable Legal Framework?”. The study examines how the air transport sector operates within a market economy, how competitive conditions are shaped, and which legal principles can support a sustainable and competitive aviation sector in the European Union over the long term. Dissertation supervisor Prof. Rainer Hofmann praised the work as an outstanding analysis of a legally and factually complex field, noting that its quality is comparable to that of a habilitation. At the heart of the dissertation is the argument that the EU’s concept of the entrepreneurial state offers an appropriate framework for promoting a competitive and sustainable air transport system.

Dr. Felix-Julius Konow will receive the award for his dissertation, “Regulating Stablecoins – The Regulatory Treatment of E-Money Tokens under the Markets in Crypto-Assets Regulation in the Context of the Regulation of Bank Money, E-Money, and Money Market Funds.” In his research, Konow examines the economic function and legal structure of stablecoins – digital currencies linked to the value of traditional currencies. He analyzes potential risks to financial stability and public trust, while also exploring regulatory mechanisms to address them. Dissertation advisor Prof. Katja Langenbucher described the work as a major contribution to the legal classification and regulation of stablecoins and praised its interdisciplinary scope. In particular, she highlighted how the dissertation engages with macroeconomic questions relating to monetary policy, deposit insurance, reserve requirements, and competing monetary theories, integrating these perspectives into a coherent legal framework.

“Baker McKenzie is committed to supporting outstanding young legal scholars, and the Baker McKenzie Award is an important part of that commitment,” says Dr. Florian Thamm, who represents Baker McKenzie on the selection committee of Goethe University’s research council. The firm also supports aspiring legal professionals through additional initiatives such as the Scholarship for Equal Opportunity, which assists law students facing cultural, financial, or family-related barriers to entering legal studies.

 

Pregnant women’s mental images are directly linked to vaccine hesitancy and uptake





University of Plymouth






When pregnant women think about vaccinations, many experience vivid mental images – such as a sick baby in hospital – that have a direct link to their opinion of the vaccine and whether they ultimately have it, new research has shown.

The international study is the first known work to investigate the prevalence of vaccination-related mental imagery and to link it to both vaccine hesitancy and vaccination behaviour during pregnancy.

It was carried out with more than 400 pregnant women in Perth, Western Australia, who completed a brief survey while they were waiting for appointments in a maternity hospital.

The women were asked for their perceptions of risks relating to whooping cough, influenza, and COVID-19, and whether they experienced any mental images relating to the diseases or the vaccinations for these diseases.

Verified vaccine uptake data was subsequently obtained through official immunisation records at the end of participants’ pregnancy to examine whether and when each vaccine was received, if at all.

The findings, published in the journal Social Science & Medicine, showed that mental images were common and – depending on whether that mental image was a positive or negative one, and about the impacts of diseases or the vaccine itself – could be used in some cases to predict if and when the women ultimately became vaccinated during pregnancy.

Dr Julie Ji is the study's lead author, a Lecturer at the University of Plymouth's  School of Psychology and Centre for the Psychology of Health and Wellbeing, and Adjunct Research Fellow at the University of Western Australia School of Psychological Science. She explained that pregnancy is a sensitive period when health decisions carry extra emotional and psychological weight:

"Our results suggest that vivid emotional mental scenes that pop to mind when someone is thinking about vaccination are not just incidental, they may be meaningfully linked to how people feel about vaccines, and in some cases, whether and when they get vaccinated," she said.

The study’s key findings included that women who reported negative mental images about vaccines – such as worrying scenarios of harm or side effects – also tended to report greater hesitancy towards the whooping cough and influenza vaccines, particularly if they had not yet been vaccinated.

This pattern was observed even after taking into account women’s general attitudes towards receiving government-recommended vaccines during pregnancy, suggesting mental images capture a unique aspect of how vaccine decisions are psychologically experienced, rather than simply reflecting general maternal vaccination attitudes.

When the researchers looked at what women actually did, a different pattern emerged. Those who reported positive mental images about vaccines, such as imagining antibodies being passed through the umbilical cord, were more likely to receive the whooping cough vaccine, and to get it earlier in their pregnancies.

This highlights the potential importance of positive mental imagery in vaccine decision-making and behaviour, such as being able to imagine how vaccines offer protection for oneself and one’s baby. Again, these effects were not simply a reflection of general maternal vaccination attitudes or disease-specific hesitancy levels.

By the end of their pregnancy, participants were most likely to receive the whooping cough vaccine (82.1% vaccinated), with lower uptake for influenza (60.1%) and very low uptake for COVID-19 (7.2%). At a time when hesitancy and suboptimal vaccine uptake pose significant threats to public health, the study highlights the importance of examining modifiable psychological factors involved in maternal vaccination decision-making.

The study builds on extensive work on the cognitive, emotional, and motivational impacts of mental imagery by leading mental imagery researchers at the University of Plymouth.

Dr Ji added: "A lot of research, including that done here in Plymouth, shows that mental imagery makes memories and future thoughts feel real. These images can powerfully influence our emotions and beliefs, and motivate helpful or unhelpful behaviours. Because mental imagery is something we know how to work with from mental health research, understanding its role in vaccine decision making during vulnerable periods like pregnancy is an important step towards developing new ways to support both individual and public health."

The study was conducted by an interdisciplinary team of researchers spanning psychology, midwifery, paediatrics and infectious diseases, and social science, across institutions in Australia and the UK. It was funded by the Telethon Channel 7 Western Australia Child Research Fund, supporting work focused on improving health outcomes for children and families.

This unique collaboration brought together expertise in mental health and cognitive science with clinical knowledge of pregnancy care and vaccination, as well as population‑level insights into vaccine policy and uptake.

The authors say this interdisciplinary approach was critical to examining vaccine decision‑making during pregnancy using real‑world behavioural data, and they are now exploring how mental imagery can be harnessed to support informed decision-making during pregnancy.