Bacteria and the viruses that infect them—known as phages—coexist in soils, oceans and living organisms. Scientists have long thought this coexistence reflects a microscopic version of an evolutionary arms race: As parasites and hosts continually adapt to one another, both evolve ways to survive. But a joint study by researchers at the University of Maryland and the University of Exeter shows different pathways to coexistence.
Bacteria and the viruses that infect them—known as phages—coexist in soils, oceans and living organisms. Scientists have long thought this coexistence reflects a microscopic version of an evolutionary arms race: As parasites and hosts continually adapt to one another, both evolve ways to survive. But a joint study by researchers at the University of Maryland and the University of Exeter shows different pathways to coexistence.
Whenever a cell divides, it has to split its chromosomes perfectly between two daughter cells, and even a single mistake can be disastrous. Now, researchers from Japan have found that one of the key structures that makes this possible takes a surprising shape: a hollow sphere.
Certain viruses attack bacteria and can sometimes clear antibiotic-resistant infections. Researchers said they had tailored a virus to attack one patient’s illness.
In hot weather, trees “sweat” to cool down by releasing water from their leaves or needles and then replacing it with water from the soil. But during long periods of high temperatures, trees may release more water than they can replace. To strengthen forests against heat stress and other environmental hazards, scientists have suggested adding fungi to the soil.
Soil fungi living on tree roots are called ectomycorrhizal fungi. They help trees absorb water by expanding their root networks, and trees help the fungi by providing them with sugars for energy. This beneficial partnership is known as symbiosis. Scientists at Fujian Agriculture and Forestry University in China tested whether symbiosis with ectomycorrhizal fungi could help the pine trees Pinus massoniana survive warmer temperatures.
For their experiment, the researchers grew pine seedlings with and without ectomycorrhizal fungi in a greenhouse under different temperature conditions. First, they grew fungi called Cenococcum geophilum for 45 days on a gel-like substance called agar. At the same time, they grew the pine seedlings for 30 days, then transferred them into pots with natural soil.
After 15 days in the pots, the researchers spread the gel-like agar containing the fungi over small 1 x 1 centimeter (cm) areas of the pine root tips to introduce the fungi to the seedlings, a process called inoculation. They assumed that the fungal network would expand from the starting area to colonize new root tips as the seedlings grew. The team’s inoculations included 6 different C. geophilum strains and 1 fungi-free control. To simulate heat stress, the researchers replicated each of the 7 inoculations at 25°C (77°F) and 35°C (95°F). They repeated each inoculation condition in 3 pots with 3 seedlings, for a total of 126 seedlings.
After 60 days, the researchers harvested the pine seedlings and used a microscope to count how many of their root tips had fungi. They divided the number of root tips with fungi by the total number of root tips to calculate a colonization rate. They considered seedlings with a colonization rate of 80% or higher to have successfully formed a symbiotic relationship with the fungi. Then, the researchers analyzed seedlings with an 80% colonization rate to investigate their symbiotic partnerships.
The team observed that pine seedlings grown under heat stress at 35°C were 24% to 59% smaller than those grown at 25°C, and their needles were yellow instead of a healthy green. However, the seedlings that formed a symbiotic relationship with the ectomycorrhizal fungi were greener and 80% heavier than the control seedlings.
Investigating the trees further, the team measured 3 chemical compounds related to plant stress, including malondialdehyde (MDA), proline, and nitric oxide. Plants release MDA when damaged, so high MDA levels mean a plant is struggling. In contrast, plants release proline and nitric oxide to repair cells or hold water, so high amounts of these compounds mean a plant is healing.
To measure MDA and proline levels in the pine needles, the researchers mixed them with different acids that change color depending on the sample’s MDA or proline content. To measure nitric oxide, the researchers mixed the needles with a protein that converts the compound into a chemical that changes color. They found that inoculated seedlings at 35°C had about 30% to 40% less MDA, 15% to 30% more proline, and 150% more nitric oxide in their roots than the control seedlings.
Finally, the researchers measured changes in gene activity in the inoculated pine seedlings. They identified active genes by analyzing RNA molecules from the pine seedling roots with a process called RNA sequencing or transcriptomics. They found that inoculating the seedlings with ectomycorrhizal fungi activated more genes related to root strength, water retention, cell defense, and general plant protection than were activated in the control seedlings.
By combining chemical analyses with growth measurements, the team concluded that a symbiotic partnership with the ectomycorrhizal fungi helped the pine seedlings survive heat stress. They demonstrated that through prolonged heat, inoculated seedlings maintained greener needles and lower levels of stress chemicals. They suggested that ectomycorrhizal fungi could be an ecological tool to help trees stay hydrated in a warming world. They recommended that future researchers conduct field trials with inoculated trees to translate these findings into forest management strategies.
Probiotics are part of a rapidly expanding field of research. They are live microorganisms that, when administered in adequate amounts, may confer health benefits[1]. Among the most extensively studied probiotics, some species of Lactobacillus and Bifidobacterium have been associated with the maintenance of gut microbiota balance and with several physiological functions[2]. Producing these microorganisms usually requires nutrient-rich culture media. But what if such bacteria could be obtained from a food by-product nowadays regarded as waste? This question formed the starting point of a study carried out by Esneki Dairy Centre – Leartiker to assess the potential of cheese whey as a substrate for producing microbial biomass enriched in microorganisms with probiotic potential.
The challenge of cheese whey
Cheesemaking inevitably generates substantial amounts of whey: a yellowish liquid released from the curd that still carries lactose, soluble proteins, minerals and other valuable compounds. In fact, whey can represent around 85% of the original milk volume used in cheese production[3].
Despite this nutritional richness, whey remains a difficult stream to manage for many artisanal dairies. This is particularly true in the Basque Country, where many cheesemaking farms are small, family-run businesses located in rural areas[4]. Its highly perishable nature means that whey must be preserved or processed soon after production, making storage, collection and transport especially challenging when volumes are small and geographically dispersed.
Moreover, uncontrolled whey discharge results in a high organic load that can affect aquatic ecosystems. Paradoxically, the same nutrients that make cheese whey a potential pollutant are also what give it considerable biotechnological value.
A natural culture medium
From a microbiological standpoint, cheese whey is not merely a residual stream, but a naturally nutrient-rich matrix[5]. Its lactose content, together with soluble proteins, minerals and other available compounds, provides a favourable environment for the growth of lactic acid bacteria, widely used microorganisms in fermented foods and increasingly explored for their probiotic potential.
The working hypothesis was simple: by steering whey fermentation under controlled conditions, it could be possible to recover a biomass enriched in microorganisms of interest, while at the same time increasing the stability and value of the by-product itself.
To explore this possibility, several fermentation strategies were tested using whey generated during the production of blue cheese from pasteurised cow’s milk. The study compared three different approaches:
Fermentation of previously pasteurised whey (Protocol 1).
Fermentation of whey after a deproteinisation step (Protocol 2).
Direct fermentation of raw whey, without any prior treatment (Protocol 3).
Two different blends of commercial microorganisms, inspired by the naturally diverse microbial communities found in kefir, were also evaluated. These included; Choozit Kefir DV LYO 1000L (Danisco) (starter culture A) and Ferlac Kefir Type C (Abiasa) (starter culture B). Additionally, unfermented whey (that is, whey to which no starter cultures were added and which was not subjected to fermentation) from each protocol was analysed as a control sample. Controlled fermentation processes were carried out under monitored conditions. Throughout the fermentation, key parameters were monitored, including temperature (25 ± 1 °C), incubation time (16 ± 1 h for starter culture A and 21 ± 1 h for starter culture B) and pH evolution, with fermentation being considered complete once the pH fell below 4,6. These measurements allowed the identification of the conditions that most effectively supported the growth and enrichment of the target microbial populations.
Exploring the microbiome through metagenomics
However, assessing the success of a fermentation process requires more than simply determining how many microorganisms grow. It is also essential to identify which species are present and how the microbial community changes over time.
Traditional culture-based microbiological methods remain fundamental tools for quantifying and isolating viable microorganisms. Yet they have important limitations when complex microbial communities need to be characterised, as they only detect microorganisms able to grow under the selected culture conditions. As a result, part of the microbial diversity present in the sample may remain undetected. To obtain a more comprehensive view of the microbial community, the study incorporated high-throughput amplicon sequencing, an approach that enables the direct analysis of DNA present in a sample and the identification of microorganisms regardless of their ability to grow under laboratory conditions.
Bacterial communities were characterised by amplifying the V4 region of the 16S rRNA gene, one of the most widely used markers in bacterial diversity studies. Fungal and yeast communities were analysed through the ITS region — the Internal Transcribed Spacer — which is considered the standard marker for fungal diversity studies.
Sequencing was performed using Illumina technology, generating approximately 100,000 reads per sample for bacteria and around 40,000 reads for fungi and yeasts. These sequences were then compared against specialised databases to determine the identity of the microorganisms present and estimate their relative abundance.
Before interpreting the results, sequencing depth was assessed using rarefaction curves. These curves showed a clear trend towards saturation, indicating that most of the microbial diversity present in the samples had been adequately captured.
Which protocol worked best?
High-throughput amplicon sequencing revealed clear differences among the fermentation strategies tested.
Fermentations carried out using raw whey (Protocol 3) maintained a more diverse bacterial community than those in which the whey had first been subjected to thermal treatment (Protocol 1 and Protocol 2), as can be seen in Figure 1, as can be seen in Figure 1, the number of observed microbial taxa increases with sequencing depth. This suggests that the partial preservation of the native microbiota originating from the cheesemaking process may play an important role in shaping the fermentation outcome.
Figure 1. Rarefaction curve illustrating the observed bacterial species richness as the number of sequences increases.
In contrast, the diversity of moulds and yeasts decreased. This trend may be related to the origin of the whey, which was obtained from blue cheese production, where specific mould (Penicillium roquefoti) species are deliberately enriched during manufacture. The competitive advantage of these dominant fungi appears to favour the development of a more specialised microbial community, reducing the abundance and diversity of other microbial populations present in the whey (Figure 2).
Figure 2: Rarefaction curve showing the number of observed mould and yeast species as a function of sequencing depth
Principal coordinates analysis (PCoA) based on Jaccard distances (Figure 3) showed a clear separation among the different fermentation protocols, indicating that each strategy gave rise to distinct microbial communities. In parallel, the relative abundance of profiles (Figure 4) made it possible to visualise how particular species increased or decreased depending on the conditions applied.
Figure 3. PCoA based on Jaccard distances, used to assess similarities among samples. Bacterial profiles based on 16S data are shown on the left, and fungal/yeast profiles based on ITS data on the right.
Figure 4. Relative microbial diversity observed across the different fermentation protocols.
Amplicon sequencing also enabled the identification of the dominant microorganisms during the process. In most samples, Lactococcus lactis was particularly abundant. This result was expected, as this bacterium was included in the commercial starts cultures used and is widely employed in dairy fermentations. However, some fermentation conditions, particularly those involving starter culture B, also favoured the development of species such as Lacticaseibacillus rhamnosus and Bifidobacterium animalis, wich were also present in the commercial starter culture. These microorganisms are frequently associated with probiotic applications[6],[7],[8].
To identify the most suitable protocol for producing a fermented whey enriched in microorganisms with probiotic potential, both microbial abundance (including aerobic mesophilic bacteria, yeasts and moulds) and the diversity of the resulting microbial communities were evaluated. The highest microbial counts were obtained in whey samples produced using Protocol 3, which was based on raw whey, and fermented with starter culture B. (Average counts of 8.2 log CFU/mL were obtained with starter culture A, and average counts of 8.5 log CFU/mL with starter culture B).
Furthermore, as mentioned previously, the highest levels of microbial diversity were observed in the samples produced using Protocol 3, where fermentation was carried out directly on raw whey without prior heat treatment.
Overall, the results pointed to the most effective strategy also being the simplest from a technological perspective: the direct fermentation of raw whey, without prior thermal treatment using starter culture B. This approach maintained high microbial diversity while reducing energy requirements and simplifying the overall process.
An opportunity for the circular economy
Beyond the microbiological results, the broader relevance of this work lies in showing that the role of whey within the cheesemaking chain can be reconsidered.
Rather than being treated as a waste stream associated with management costs, whey can be viewed as a raw material capable of supporting valuable biotechnological processes. Controlled fermentation not only helps stabilise whey but also makes it possible to harness the nutrients it still contains to generate added-value microbial biomass.
Such strategies are closely aligned with the principles of the circular bioeconomy, in which by-products are no longer seen as the end of a production chain, but as the starting point for another. In a context where sustainability and efficient resource use are increasingly important, initiatives of this kind show how microbiology and omics technologies can help turn an environmental challenge into an opportunity for innovation.
The PRO2O project (grant agreement No. 00003-BIO2022-48) was funded through the 2022 Bioeconomy Innovation Projects funding programme of the Basque Government’s Department of Economic Development, Sustainability and Environment.
References
[1] Guarner F, Requena T, Marcos A. Consensus statements from the Workshop “Probiotics and Health: Scientific evidence”. Nutr Hosp. 2010 Sep-Oct;25(5):700-4. PMID: 21336423.
[2] Martin, A. J. M., Serebrinsky-Duek, K., Riquelme, E., Saa, P., & Garrido, D. (2023). Microbial interactions and the homeostasis of the gut microbiome: the role of Bifidobacterium. Microbiome Research Reports, 2. https://doi.org/10.20517/mrr.2023.10
[5] Figueroa Pires, A., garcía Marnotes, N., Díaz Rubio, O., Cobos García, A., Dias Pereira, C. (2021). Dairy by-products: A review on the valorization of whey and second cheese whey. Foods, 10: 1067
[6]Neethu, M., Bunt, C., Hussain, M., 2015. Comparison of Microbiological and Probiotic Characteristics of Lactobacilli Isolates from Daity FOod Products and Animal Rumen Contens Microorganims 3, 198-212.
[7] Rama, G.R., Kuhn, D., Beux, S., aciel, M.J., Volken de Souz, C.F., 2019. Potential apllications of dairy why for the production of lactic acid bacteira cultures. Int Dairy J.
[8] Rodriguez-Palacios, 1., Staemplfli, H.R., Duffield, T., Weese, J.S., 009. Isolation of bovine intestinal Lactobacillus plantarum and Pediococcus acidilactici with inhibitory activity against Escherichia coli O157 and F5. J. Appl. Mcrobiol. 106, 393-401
The BRTA is a consortium that remains a step ahead of future socio-economic challenges worldwide and in the Basque Autonomous Community; it addresses them through research and technological development, thus projecting itself internationally. The BRTA centres collaborate to generate knowledge and transfer it to Basque society and industry so as to make them more innovative and competitive. The BRTA is an alliance of 17 R&D centres and cooperative research centres with the support of the Basque Government, the SPRI and the Chartered Provincial Councils of Araba, Bizkaia and Gipuzkoa.
Since the 1976 Viking missions, when NASA first successfully placed uncrewed landers on Mars, scientists who study life in the universe, known as astrobiologists, have been gathering evidence to determine whether microorganisms ever lived on the red planet. It has been a challenging determination to make. Until a Mars sample return mission occurs, all necessary analyses must take place on Mars, using instruments designed as much to withstand the stresses of space travel as to collect data, which limits how thoroughly scientists can study Martian rocks. As a result, the search for evidence of microbial life on Mars is inherently incremental.
Recently, scientists added another piece of exciting, yet inconclusive, evidence to their search. In the summer of 2024, the Mars 2020 Perseverance Rover science team was searching for signs of ancient microbial life in a 3,700-million-year-old lake bed on Mars, known as Jezero Crater. In the process, they detected complex, carbon-containing organic molecules in mudstones within a river channel that once brought water to the now-dry lake bed.
Widely dispersed organic molecules associated with minerals that can support microbial life are exactly what astrobiologists would expect to see if microorganisms once lived in Jezero Crater. However, organic molecules can also form through geological processes, like when gases and minerals react at high temperatures and pressures at deep-sea vents on Earth. Therefore, astrobiologists must carefully assess organic molecules to determine their origin.
In July of 2026, more than 60 Perseverance science team members took a first step towards determining whether ancient microorganisms could have made the organic molecules found in Jezero Crater. They compared the organic molecule detections in Martian mudstones to similar detections of organic molecules in samples of known origin, including fossilized Earth life, meteorites, and minerals.
NASA scientists detected the organic molecules in Jezero Crater with a rover instrument called Scanning Habitable Environments with Raman and Luminescence for Organics and Chemicals (SHERLOC). SHERLOC uses a 248.6 nanometer (nm) wavelength laser to excite molecules in unknown materials. When molecules are excited, they absorb and scatter the laser light, causing characteristic shifts in the wavelength of the scattered light.
Instruments like this, known as Raman spectrometers, detect the shifted light and display the detections as lines called spectra, which scientists use to identify the unknown molecules. The Raman spectra from the 4 mudstones in Jezero crater showed shifts of about 1600 nm, which is characteristic of complex carbon molecules. These shifts appear as bands in the spectra that are often called G-bands.
Raman spectrometers are common laboratory instruments, but most use lasers with wavelengths of 485 nm or higher, so the spectra they produce can be slightly different from SHERLOC spectra even when the laser excites the same kind of molecule. To get around this issue, the scientists compared the Mars spectra with spectra of complex carbon molecules from fossilized Earth microorganisms, coal, graphite, meteorites, and synthetic samples collected by Raman instruments using the same wavelength laser that SHERLOC uses. They found that the spectra collected on Mars overlap with at least one example from every sample type except graphite.
These results don’t rule out the possibility that organic molecules in Jezero Crater were produced by ancient microbial life, but they can’t tell us exactly how they formed either. That determination will have to wait until the samples are brought to Earth so they can be studied with laboratory instruments.
The Perseverance team has made a small but critical contribution towards determining whether microbial life ever inhabited our closest planetary neighbor, Mars. Their efforts exemplify how the science of astrobiology and the search for possible extraterrestrial life slowly and carefully move forward. If we keep at it, humans may one day have a definitive answer to one of our most consequential questions: Are we alone?
Electric vehicles (EVs) use high-powered rechargeable batteries to store electrical energy that powers their motors. Most EV batteries use a specific mixture of metals to hold the battery’s charge, called nanoscale lithiated nickel manganese cobalt oxides,aka NMC materials. NMC materials can store a large amount of energy, making them ideal for batteries, but the metals themselves can be toxic in soil and water if the batteries are not properly recycled.
NMC batteries leave behind a specific combination of toxic metals, so researchers can study how bacteria respond to this waste when it enters the environment. By understanding how bacteria adapt to toxic metals, scientists hope to predict how new technologies like EV batteries will affect the environment.
In 2019, a team of researchers from the University of Minnesota reported that a common soil bacterium called Shewanella oneidensis can rapidly evolve resistance to NMC materials, but they didn’t know how. True beneficial gene evolution usually develops over thousands of generations, but Shewanella oneidensis adapted much more quickly. The team recently conducted a follow-up study to determine the genetic mechanisms behind this bacterium’s unique metal resistance.
They started by analyzing the complete DNA sequences of 33 Shewanella colonies that were resistant to either pure NMC waste or individual metals like nickel and cobalt, using a process called whole-genome sequencing. They expected to find DNA mutations in genes that control how bacteria take up and expel toxic metals that would give the resistant Shewanella an advantage in surviving NMC metal toxicity. However, they didn’t find any DNA mutations in metal-related genes. Instead, they found that a specific DNA region was duplicated 10 to 15 times in all 33 NMC-resistant or metal-resistant colonies. This result suggested to the researchers that a temporary adaptation, not true gene evolution, was responsible for the bacteria’s metal resistance.
The researchers wanted to know more about the duplicated DNA region in metal-resistant Shewanella, so they focused on 2 gene duplication mechanisms that might serve as temporary adaptations in Shewanella. The first mechanism directly duplicates DNA regions to create extra copies of a gene, via a process called gene duplication amplification. The second mechanism moves DNA segments, called mobile genetic elements, into different DNA sections to create extra copies of a gene.
To test whether either of these mechanisms was causing the gene duplication in Shewanella, the team grew the bacteria in different liquid media containing only cobalt, only nickel, or cobalt and nickel together. The researchers used a technique that measures the exact amount of DNA in a given sequence, called quantitative polymerase chain reaction (qPCR), to calculate how many duplicated DNA regions were in each genome sequence. They found that neither cobalt nor nickel alone triggered DNA duplication. But the bacteria grown in the media with cobalt and nickel together had 8 additional copies of the DNA region. This suggested that something about the combination of nickel and cobalt triggered gene duplication.
To determine whether this gene duplication only occurred with nickel and cobalt, the team substituted copper and zinc for nickel in the growth media. They exposed Shewanella cells to different combinations of these metals using a grid pattern in a 96-well plate, a technique called a checkerboard assay. Then they repeated the qPCR process to measure the duplicated DNA region. They found that no other combinations of metals triggered gene duplication, suggesting that nickel and cobalt are especially toxic together, and that the gene duplication responds to this combined toxicity.
Finally, the researchers identified the function of the duplicated DNA region. They found that one of the genes within the region turned on a special protein that pushes metal ions and other toxins out of the cell, called an efflux pump protein. The team hypothesized that this efflux pump protein was responsible for removing cobalt and nickel from the bacteria’s cells. To test this theory, they grew modified Shewanella cells without the efflux pump gene in media containing cobalt, nickel, or cobalt and nickel together. They found that the modified bacteria grew well in the nickel-only treatment, but didn’t grow in the cobalt-only or combined treatments, which indicated that the efflux pump protein is necessary for Shewanella to resist cobalt toxicity.
Based on their experiments, the team concluded that nickel and cobalt together trigger a gene duplication event in Shewanella oneidensis. This gene duplication event increases the number of efflux proteins in Shewanella that can expel cobalt and underlies its unique NMC resistance. They suggested that future researchers study temporary adaptations similar to gene duplication in bacteria to track how they respond to electronic waste and other new technologies.
Biofilms are complex microbial communities that adhere to a surface and encase themselves in a viscous matrix they produce. This structure protects bacteria from antibiotics and the immune system far more effectively than if they lived in a free-floating state, making biofilms one of the most common causes of hard-to-treat chronic infections—such as respiratory infections in people with cystic fibrosis and chronic obstructive pulmonary disease (COPD), chronic wounds, or infections associated with catheters and prosthetic devices. Added to this is the global rise in antibiotic resistance, which makes it increasingly urgent to have tools capable of predicting which treatment will work in each case.
The ocean's aphotic zone—the dark, high-pressure region below the surface, where sunlight cannot reach—is home to a vast wealth of microbial life. Yet scientists know relatively little about the genetic makeup, growth and function of many of these enigmatic organisms.
The ocean's aphotic zone—the dark, high-pressure region below the surface, where sunlight cannot reach—is home to a vast wealth of microbial life. Yet scientists know relatively little about the genetic makeup, growth and function of many of these enigmatic organisms.
Researchers at Queen Mary University of London are closer to understanding tendinopathy, a common condition that can cause persistent pain and impaired movement in people and many animals.
The mammalian gut microbiome teems with a delicate balance of bacteria and the viruses that keep them in check, called bacteriophages, or phages. Each bacterial species usually has its own set of phage partners.
The mammalian gut microbiome teems with a delicate balance of bacteria and the viruses that keep them in check, called bacteriophages, or phages. Each bacterial species usually has its own set of phage partners.
Billions of people still suffer from hunger and food insecurity worldwide. Meanwhile, microbial contamination causes a third of global food waste annually, resulting in major economic losses and illnesses. Although antibiotics and pesticides help control contamination, their excessive use can promote bacterial resistance or leave toxic residues.
One alternative uses materials that generate highly reactive forms of oxygen when exposed to light, called photocatalysts, to prolong food freshness. These molecules kill bacteria by damaging their cell components in a process called photodynamic inactivation or PDI. However, current PDI systems rely on energy-intensive lasers and long exposure times because the bacteria’s protective cell membranes block reactive oxygen molecules. As a result, the systems don’t kill bacteria effectively and risk overheating food, affecting its freshness and nutritional value.
Scientists at Zhejiang University in China thought that it would be possible to achieve a PDI system using accessible, free sunlight with the right photocatalyst. Moreover, they also wanted to integrate this photocatalyst into food packaging to combat microbes during storage.
To make the photocatalyst, the researchers mixed water with a glue-like plant fiber that provides structural support, called pectin, and a chemical from plant seeds that supplies phosphorus, called phytic acid. Then they heated the mixture in a sealed reactor at 220ºC (428ºF) for 5 hours to form tiny structures composed of a carbon core surrounded by a phosphorus-rich shell called phosphorus-modified carbonized polymer dots or PCDs.
To incorporate the PCDs into film packaging, the researchers dissolved equal amounts of a plant fiber from konjac, called glucomannan,and another plant-derived molecule, called carboxymethylcellulose, in warm water to form a network of entangled molecular chains. Then, they added 1.5 milligrams of PCD per milliliter to this mixture, which linked the chains together like molecular fasteners. Finally, they added a moisture-binding chemical called glycerin to prevent brittleness. The researchers cast this mixture onto separate Petri dishes and dried them, forming thin, plastic-like PCD films.
To test the films, the researchers placed Escherichia coli bacteria between 2 sterilized film sheets and exposed the samples to either darkness or simulated sunlight for 20 minutes. They then transferred the microbes onto agar plates and incubated them for 15 hours, allowing surviving bacteria to form visible colonies. They compared the number of bacterial colonies with those of untreated samples to calculate the percentage of bacteria the films eliminated in each environment.
Tests under darkness showed that the films eliminated about 60% of the bacteria. The researchers attributed this result to the positive electrical charge of PCDs, which attracts the bacteria’s negatively charged cell surfaces. The electrical attraction stresses their cell membranes, interfering with essential life processes. This result suggested that the films use a separate charge-based antibacterial mechanism apart from PDI, which requires light to work.
Under simulated sunlight, the films eliminated nearly 100% of the bacteria. The researchers identified 2 principal mechanisms causing this. First, the PCDs acted as tiny heaters that generated localized heat, which stretched holes in the bacterial membranes, allowing contents to leak out of their cells through a process called photoporation. Second, the PCDs generated reactive oxygen molecules that could then penetrate the bacteria. Once inside the cells, these molecules irreversibly damage the bacteria’s internal components and genetic material through PDI.
The researchers also investigated whether PCD films could serve as food packaging by using them to wrap fresh strawberries. Compared with conventional nonbiodegradable polyethylene packaging where visible rotting occurred, the PCD films kept the strawberries fresh for more than 4 days by suppressing bacterial growth and regulating moisture levels. When the team tested whether the films were toxic, they found that the films are safe for humans and compatible for food applications. They also buried the films in soil for 24 days and found that they degraded by 78%, demonstrating biodegradability suitable for packaging fresh foods.
The team concluded that PCD films could be a biodegradable food packaging that combines plant-based materials with multiple antibacterial strategies. The films retained antibacterial activity in darkness and became more effective under sunlight through the combined effects of photoporation and PDI. These findings demonstrated that by combining multiple mechanisms into a single material, researchers can create multifunctional food packaging that remains effective across different storage conditions.
New findings raise questions about the role of microbes living in the lungs. More than 35 trillion bacteria live throughout the human body, forming microbiomes in the gut, mouth, lungs, skin, and urogenital tract. Researchers increasingly recognize that these microbial communities are connected to both health and disease, but much about what individual microbes do [...]
Even highly antibiotic-resistant bacteria become more vulnerable when their cell wall transport system is disrupted, according to a new study from Umeå University. The discovery reveals a previously overlooked weakness that could help researchers develop new strategies to combat antibiotic resistance.
Even highly antibiotic-resistant bacteria become more vulnerable when their cell wall transport system is disrupted, according to a new study from Umeå University. The discovery reveals a previously overlooked weakness that could help researchers develop new strategies to combat antibiotic resistance.
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