Bacteria are highly adaptable organisms capable of surviving challenging environmental conditions, including temperature changes, acidity, exposure to harmful substances, DNA damage, and nutrient shortages. This adaptability makes bacterial infections difficult to treat and contributes to the growing crisis of antibiotic resistance. Currently, antibiotic resistance causes 700,000 deaths annually, a number projected to rise to 10 million by 2050 without urgent intervention. The BARTAS project (Revealing the Bacterial Response to Temperature and Antibiotics Stress via Multiscale Imaging) investigated how bacteria respond to the combined stresses of heat and antibiotics at the single-cell level, using advanced imaging technologies to uncover new insights into their survival mechanisms.
When the body fights an infection, it often raises its temperature, causing a fever. This heat puts bacteria under stress, forcing them to adapt quickly to survive and grow. If they fail to adapt, the heat could disrupt essential functions such as maintaining cell walls, producing proteins, and preserving DNA. In addition to heat, antibiotics challenge bacteria by targeting critical survival mechanisms. However, the interaction between heat stress and antibiotic effectiveness remains poorly understood. BARTAS addressed this knowledge gap by combining microfluidic and microscopy techniques to explore bacterial survival mechanisms under these stresses.