Thursday, January 29, 2026

 

A tiny fish is helping clinicians avoid unnecessary multi-million-dollar treatment for babies suspected of having spinal muscular atrophy




Griffith University

A tiny fish is helping clinicians avoid unnecessary multi-million-dollar treatment for babies suspected of having spinal muscular atrophy 

image: 

A tiny fish is helping clinicians avoid unnecessary multi-million-dollar treatment for babies suspected of having spinal muscular atrophy
view more 

Credit: Griffith University




The tiny zebrafish is helping researchers rapidly determine whether a newborn’s genetic mutation is likely to cause spinal muscular atrophy (SMA), one of the leading causes of infant mortality worldwide.

The world-first research, led by Dr Jean Giacomotto from Griffith University’s Institute for Biomedicine and Glycomics, has featured on the front cover of EMBO Molecular Medicine this month (January).

Dr Giacomotto said: “SMA is a genetic disorder which causes progressive loss of motor neurons, leading to muscle weakness and loss of basic motor functions.”

“Without treatment, SMA is typically fatal, and while highly effective therapies now exist, they can exceed US$2 million per child per year and must be initiated before symptoms appear such as when a baby is able to sit but lacks sufficient neck strength to hold their head steady.

“If treatment starts after the emergence of these symptoms, the child will have already experienced irreversible degenerative damage, leading to life-long problems and possibly death within the first years of life.

“When a baby carries a mutation which has never been seen before, known as a ‘variant of uncertain significance or VUS’, clinicians face an impossible dilemma – start treatment immediately, risk unnecessary intervention, or wait and risk irreversible nerve damage.”

To solve this, Dr Giacomotto and his team developed a rapid zebrafish-based functional assay which could determine the pathogenicity of a novel SMN1 mutation within days, potentially informing urgent clinical decisions worldwide.

“Within a clinically meaningful timeframe, we were able to functionally test each baby’s exact mutation and show it was not harmful,” Dr Giacomotto said.

“This research provides the clearest demonstration to date that zebrafish can play a decisive role in clinical variant interpretation, particularly in newborns flagged through expanding genomic screening programs.

“With genomic sequencing rising worldwide, clinicians are encountering more and more uncertain variants.

“This tiny fish offers a fast and affordable way to help resolve these cases and reduce distress for families.”

The research titled ‘Clinical relevance of zebrafish for gene variants testing: Proof-of principle with SMN1/SMA’ has been published and featured as front cover in EMBO Molecular Medicine.

 

Fungus unlocks hidden phosphorus from massive industrial waste




Biochar Editorial Office, Shenyang Agricultural University
Bioextraction of residual phosphorus from phosphogypsum by phosphate-solubilizing fungus Aspergillus niger 

image: 

Bioextraction of residual phosphorus from phosphogypsum by phosphate-solubilizing fungus Aspergillus niger

view more 

Credit: Zhenyu Chao, Haoxuan Li, Jiakai Ji, Xin Sun, Yuhang Sun, Meiyu Xu, Ying Wang, Da Tian, Haoming Chen, Dan Yu & Zhen Li





A common soil fungus may offer a sustainable solution to one of the world’s largest industrial waste problems while helping recover a critical nutrient for agriculture.

Researchers have shown that Aspergillus niger, a naturally occurring phosphate solubilizing fungus, can extract large amounts of residual phosphorus from phosphogypsum, a byproduct of phosphoric acid production that is generated in enormous quantities worldwide. The study demonstrates that more than 40 percent of the phosphorus locked inside this waste material can be recovered through a biological process, offering a promising alternative to energy intensive chemical treatments.

Phosphogypsum is produced during the manufacture of phosphate fertilizers and is typically stored in large stacks that pose long term environmental risks. Globally, about 300 million tons are generated each year, while billions of tons have already accumulated. Although phosphogypsum contains roughly 1 percent phosphorus, most of it exists in insoluble forms that are difficult to reuse.

“Phosphogypsum has long been viewed as a liability, but it actually contains a valuable nutrient that is increasingly scarce,” said Zhen Li, the corresponding author of the study. “Our work shows that microorganisms can help transform this waste into a potential resource.”

In laboratory experiments, the research team incubated phosphogypsum with Aspergillus niger under controlled conditions. Over time, the fungus released organic acids, especially oxalic acid, which reacted with calcium in the waste material. This process reduced the tendency of calcium to bind phosphorus, allowing more phosphorus to dissolve into solution.

After 15 days of incubation, the bioextraction efficiency exceeded 40 percent, compared with only about 10 percent phosphorus release in systems without the fungus. Advanced imaging techniques revealed that much of the released phosphorus was absorbed directly into fungal cells, confirming active biological uptake rather than simple chemical dissolution.

“Our results show that the fungus is not just dissolving phosphorus, but actively using it for growth,” said Li. “This biological demand helps drive the extraction process forward.”

The study also found that sulfate from phosphogypsum contributed to the synthesis of sulfur containing amino acids inside the fungal cells, further supporting microbial growth and sustained phosphorus release. Computer simulations confirmed that oxalic acid played a key role by binding calcium and preventing the reformation of insoluble phosphate minerals.

Phosphorus is an essential element for food production, yet global phosphate rock reserves are finite and increasingly costly to mine. At the same time, conventional phosphate fertilizers often suffer from low use efficiency and can contribute to water pollution.

“Recovering phosphorus from industrial waste aligns well with the goals of sustainable agriculture and circular resource use,” Li said. “This approach could reduce environmental risks while supplementing existing phosphorus supplies.”

While the experiments were conducted at the laboratory scale, the researchers believe the findings provide a strong foundation for future development. With further optimization, fungal bioextraction could be integrated into waste management systems or used to produce phosphorus enriched materials for agricultural applications.

The study highlights the untapped potential of microorganisms in addressing global environmental challenges. By harnessing natural biological processes, scientists are finding new ways to recover valuable resources from materials once considered useless waste.

The research was published online on January 19, 2026, in Environmental and Biogeochemical Processes, and involved collaboration among scientists specializing in environmental science, microbiology, and geochemistry.

 

=== 

Journal reference: Chao Z, Li H, Ji J, Sun X, Sun Y, et al. 2026. Bioextraction of residual phosphorus from phosphogypsum by phosphate-solubilizing fungus Aspergillus nigerEnvironmental and Biogeochemical Processes 2: e002 doi: 10.48130/ebp-0025-001  

https://www.maxapress.com/article/doi/10.48130/ebp-0025-0018  

=== 

About the Journal:

Environmental and Biogeochemical Processes (e-ISSN 3070-1708) is a multidisciplinary platform for communicating advances in fundamental and applied research on the interactions and processes involving the cycling of elements and compounds between the biological, geological, and chemical components of the environment. 

Follow us on FacebookX, and Bluesky

 

Reducing drug deaths from novel psychoactive substances relies on foreign legislation, but here’s how it can be tackled closer to home




Guest editorial by Ric Treble and Caroline Copeland, authors of a new Frontiers in Pharmacology article on drug legislation



Frontiers




by Ric Treble and Caroline Copeland

The illicit drug trade is international, and different countries have developed different strategies intended to minimize its negative effects, most commonly through controls on, or prohibition of, specified substances. But which approaches to banning substances are actually most effective in reducing harm? 

The advent of NPS, and the range of subsequent legislative controls introduced by different countries, has created a natural experiment. Using data from the UK’s National Programme on Substance Abuse Mortality (NPSUM), our study examines how different national and international control strategies have translated into real-world outcomes within England, Wales, and Northern Ireland by examining NPS deaths.

Internationally, there has been a high degree of consistency in drug control. The United Nations (UN) annually reviews and updates the lists of substances (and precursors) named in its drugs conventions, based on recommendations from the World Health Organization’s expert committee. All signatory nations of the conventions are then required to incorporate these controls into their national laws. However, this process of problem identification, data compilation, formulation of recommendations, and achieving international consensus followed by national legislation, is inevitably slow. In contrast, the appearance and spread of NPS within drug markets can be incredibly rapid, so there can be significant delays between local identification of issues arising from novel substances and the international introduction of new controls.

Beyond international laws

In response, some nations have therefore chosen to act sooner, introducing their own national controls in response to local concerns, in advance of, or in addition to, those required by the UN. This means that there is an international patchwork of legislation regarding emerging drug threats, with different substances being controlled in different countries at different times. Whilst challenging for policymakers, this variation provides a valuable opportunity to assess the impact of the application of different nations’ controls on particular substances.

In the UK, there have been very few examples of the illicit synthesis of NPS and the vast majority of such substances are imported instead, often facilitated by internet trading and ‘fast parcel’ delivery services. To address the rapid appearance of NPS, the UK’s Misuse of Drugs Act (1971) has been supplemented by other measures, such as the introduction of Temporary Class Drugs Orders (2011) and the much broader Psychoactive Substances Act (2016). These measures effectively prevented open sale of NPS via ‘head shops’ and UK-based websites. However, NPS remained accessible to both individuals and distributors via internet trading and traditional drug distribution networks. 

The power of foreign legislation

Over the period studied, the major sources of NPS in the UK were chemical supply companies based in China. In response to both local and international concerns, China introduced a series of national controls over and above those required by UN scheduling, initially on specifically named substances and, more recently, on whole families of NPS by means of ‘generic’ controls. 

When we compared trends in NPS detections within the NPSUM’s mortality data with the timing of the UN’s international control requirements and the UK’s and China’s national legislations respectively, a clear pattern emerged: controls implemented in the producing countries were associated with larger reductions in NPS detections in deaths than controls introduced solely within the consuming country.

Action at home

National legislation within consumer countries is, of course, still essential. It enables national law-enforcement activity, including restricting the import and trafficking supply chain and the implementation of possession offences. However, national legislation and enforcement alone cannot eliminate drug use or its associated harms. For this reason, they must be complemented by wide-ranging harm-reduction strategies. However, legislative controls can also drive unintended consequences. Targeted bans on specific substances often stimulate the development of novel NPS, including the production of new, as yet uncontrolled, variants of substances controlled by name. This pattern has been particularly evident in the case of synthetic cannabinoids, where successive generations of legislation-avoiding substances have continued to appear, prompting the development of ever broader generic controls.

However, even generic controls have limits. Where entire families of drugs are prohibited, new drug families which produce similar effects may emerge instead. This dynamic is currently being seen in the case of highly potent synthetic opioids, a particularly concerning cause of drug-related deaths. Broad controls on fentanyl and their pre-cursors have been followed by the appearance of nitazenes and, as controls on nitazenes are being introduced, a new group of potent opioids, the orphines, has begun to appear. These cycles of control and innovation are therefore likely to continue.

Early legislative action by consumer countries remains necessary to limit the distribution and harms of newly emerging NPS. The findings of our study also demonstrate the particular effectiveness of prompt action to restrict production within source countries to prevent international distribution. If, as a result of Chinese legislative actions, production of NPS for the illicit drug trade becomes more geographically diverse, action to identify new sources of production and to encourage and support supplier nations to restrict production as soon as practicable will be required. This will present particular challenges if the substances being produced and exported are not perceived to present a threat within the producing country.

However, supply-side interventions alone cannot provide a lasting solution: as long as there is sustained demand for psychoactive substances, there will be strong incentives for suppliers to adapt, innovate, and profit. Reducing drug harms will therefore require not only responsive legislation and international co-operation, but also investment in education, prevention, and treatment to address the drivers of demand.