Viruses evolve differently in space microgravity

Scientists have discovered that bacteria-infecting viruses sent to the International Space Station evolve in unexpected ways compared to Earth conditions. In microgravity, these viruses and their bacterial hosts undergo distinct genetic changes, potentially improving treatments for drug-resistant infections. The findings, from a study aboard the ISS, highlight how space alters microbial interactions.

Researchers exposed Escherichia coli bacteria to T7 phages—viruses that infect bacteria—both on Earth and in the microgravity environment of the International Space Station. The experiment, led by Phil Huss from the University of Wisconsin-Madison, revealed that while infections occurred in space after an initial delay, the evolutionary paths diverged significantly from terrestrial samples.

Whole-genome sequencing of the space samples showed that T7 phages developed mutations enhancing their infectivity and ability to bind to bacterial receptors. Meanwhile, the E. coli bacteria in microgravity acquired genetic alterations that bolstered defenses against the phages and improved survival in weightless conditions. These differences were further explored using deep mutational scanning on the T7 receptor binding protein, a critical component for infection.

Earth-based follow-up tests linked these microgravity-induced changes to greater effectiveness against E. coli strains responsible for human urinary tract infections, which typically resist T7 phages. The study, published on January 13 in PLOS Biology, suggests that space-based research could uncover novel microbial adaptations with applications for space travel and health on Earth.

As the authors noted, "Space fundamentally changes how phages and bacteria interact: infection is slowed, and both organisms evolve along a different trajectory than they do on Earth. By studying those space-driven adaptations, we identified new biological insights that allowed us to engineer phages with far superior activity against drug-resistant pathogens back on Earth."

This work underscores the value of the ISS for advancing phage therapy, a promising alternative to antibiotics amid rising antimicrobial resistance.

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Illustration of UC San Diego researchers' CRISPR pPro-MobV system spreading through bacterial biofilms to disable antibiotic resistance genes in a lab setting.
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UC San Diego researchers describe a gene-drive-like CRISPR system designed to reduce antibiotic resistance in bacteria

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Researchers at the University of California San Diego report they have developed a second-generation CRISPR-based “Pro-Active Genetics” system, called pPro-MobV, that is designed to spread between bacteria and disable antibiotic-resistance genes, including inside hard-to-treat biofilms.

Researchers have demonstrated that the extremophile bacterium Deinococcus radiodurans can endure extreme pressures mimicking an asteroid impact on Mars. In lab experiments, the microbe withstood forces up to 3 GPa, with 60% survival rate. The findings suggest microorganisms could potentially be ejected into space and survive.

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Researchers at Caltech have discovered how viruses infect bacteria by disabling a key protein called MurJ, essential for cell wall construction. This mechanism, revealed through high-resolution imaging, suggests a new approach to combating antibiotic-resistant superbugs. The findings highlight convergent evolution in unrelated viruses blocking MurJ similarly.

Researchers at Shandong University have modified the probiotic bacterium Escherichia coli Nissle 1917 to produce the anticancer drug Romidepsin directly in tumors. In mouse models of breast cancer, the engineered bacteria accumulated in tumors and released the drug. The findings were published on March 17 in PLOS Biology.

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Researchers at Edith Cowan University have discovered that varying training intensities can alter the gut bacteria composition in athletes. The study highlights how intense workouts influence microbial balance, while periods of rest lead to dietary shifts and slower digestion. These findings suggest potential links between gut health and athletic performance.

Scientists have produced the first living synthetic bacterial cells by transplanting a synthetic genome into bacteria whose own genomes were destroyed. The team at the J. Craig Venter Institute calls these revived cells 'zombie cells'. The method addresses challenges in synthetic biology by ensuring control over the new genome.

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