January 14, 2026
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ISS microgravity experiments reshape virus–bacteria evolution, hint at new tools against drug‑resistant superbugs

University of Wisconsin–Madison scientists report that experiments on the International Space Station show bacteriophages and E. coli evolve along markedly different genetic paths in microgravity than on Earth, changes that could be exploited to fight drug‑resistant infections. In paired tests, E. coli infected with phage T7 were incubated on Earth and aboard the ISS; after an initial slowdown, the phage successfully infected space‑grown bacteria, but sequencing revealed distinct mutations in both virus and host under near‑weightless conditions. Lead researchers Dr. Phil Huss and biochemist Srivatsan Raman say microgravity drove mutations in poorly understood regions of the phage genome rarely seen in ground experiments, while space‑grown E. coli acquired changes that appear to boost resistance and survival. Using deep mutational scanning on Earth, the team found that some microgravity‑linked mutations in T7’s receptor‑binding protein made the virus more effective at infecting E. coli strains normally resistant to T7, suggesting space‑shaped phages might be engineered as more potent antibacterial tools. The work underscores that microgravity is a fundamentally different evolutionary environment and bolsters a broader push to use space‑based research to understand and counter antimicrobial resistance, which public‑health agencies warn could kill millions globally in coming decades.

Public Health & Antimicrobial Resistance Space Station & Microgravity Research

📌 Key Facts

  • Researchers infected E. coli with bacteriophage T7 in parallel experiments on Earth and aboard the International Space Station’s microgravity environment.
  • Genetic analysis showed that both the phage and the bacteria accumulated different mutations in space than on Earth, including in phage genome regions that rarely mutate in standard lab conditions.
  • Deep mutational scanning linked some space‑associated mutations in the phage’s receptor‑binding protein to increased effectiveness against E. coli strains that are normally resistant to T7 infection.

📊 Relevant Data

In the United States, more than 2.8 million antimicrobial-resistant infections occur each year, resulting in approximately 48,000 deaths.

About Antimicrobial Resistance — Centers for Disease Control and Prevention (CDC)

Black, Hispanic, and lower-income individuals are at higher risk for community-acquired antibiotic-resistant infections such as methicillin-resistant Staphylococcus aureus (MRSA) and drug-resistant Streptococcus pneumoniae.

Antibiotic resistance: a call to action to prevent the next epidemic of inequality — PMC (PubMed Central)

There is a higher risk for extended-spectrum beta-lactamase (ESBL)-producing E. coli urinary tract infections among people of Middle Eastern descent compared to Caucasian persons in the United States.

Race, ethnicity, and risk for colonization and infection with key bacterial pathogens: a scoping review — PMC (PubMed Central)

Non-Latino White patients are more likely to receive antibiotics for viral illnesses in pediatric emergency departments, with 4.3% of non-Latino White patients receiving antibiotics compared to 2.6% of Latino patients and 1.9% of non-Latino Black patients.

Racial and ethnic differences seen in antibiotics prescribed for viral illnesses in pediatric EDs — Children's National Hospital

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