Physiological cost of antibiotic resistance: Insights from a ribosome variant in bacteria

Abstract

Antibiotic-resistant ribosome variants arise spontaneously in bacterial populations; however, their impact on the overall bacterial physiology remains unclear. We studied the naturally arising antibiotic-resistant L22* ribosome variant of Bacillus subtilis and identified a Mg²⁺-dependent physiological cost. Coculture competition experiments show that Mg²⁺ limitation hinders the growth of the L22* variant more than the wild type (WT), even under antibiotic pressure. This growth disadvantage of L22* cells is not due to lower ribosome abundance but rather due to reduced intracellular Mg²⁺ levels. Coarse-grained elastic-network modeling of ribosome conformational dynamics suggests that L22* ribosomes associate more tightly with Mg²⁺ when compared to WT. We combined the structural modeling and experimental measurements in a steady-state model to predict cellular adenosine 5′-triphosphate (ATP) levels, which also depend on Mg²⁺. Experiments confirmed a predicted ATP drop in L22* cells under Mg²⁺ limitation, while WT cells were less affected. Intracellular competition for a finite Mg²⁺ pool can thus suppress the establishment of an antibiotic-resistant ribosome variant.