Heterogeneity of SOS response expression in clinical isolates of Escherichia coli influences adaptation to antimicrobial stress

• Published in: Drug resistance updates Vol. 75; p. 101087
• Main Authors: Diaz-Diaz, Sara, Garcia-Montaner, Andrea, Vanni, Roberta, Murillo-Torres, Marina, Recacha, Esther, Pulido, Marina R., Romero-Muñoz, Maria, Docobo-Pérez, Fernando, Pascual, Alvaro, Rodriguez-Martinez, Jose Manuel
• Format: Journal Article
• Language: English
• Published: Scotland Elsevier Ltd 01.07.2024
• Subjects: Antimicrobial stress; Clinical isolates; Heterogeneity of gene expression; Quinolones; recA gene; SOS response; Clinical isolates; Antimicrobial stress; Heterogeneity of gene expression; SOS response; recA gene; Quinolones
• ISSN: 1368-7646; 1532-2084
• DOI: 10.1016/j.drup.2024.101087

In recent years, new evidence has shown that the SOS response plays an important role in the response to antimicrobials, with involvement in the generation of clinical resistance. Here we evaluate the impact of heterogeneous expression of the SOS response in clinical isolates of Escherichia coli on response to the fluoroquinolone, ciprofloxacin. In silico analysis of whole genome sequencing data showed remarkable sequence conservation of the SOS response regulators, RecA and LexA. Despite the genetic homogeneity, our results revealed a marked differential heterogeneity in SOS response activation, both at population and single-cell level, among clinical isolates of E. coli in the presence of subinhibitory concentrations of ciprofloxacin. Four main stages of SOS response activation were identified and correlated with cell filamentation. Interestingly, there was a correlation between clinical isolates with higher expression of the SOS response and further progression to resistance. This heterogeneity in response to DNA damage repair (mediated by the SOS response) and induced by antimicrobial agents could be a new factor with implications for bacterial evolution and survival contributing to the generation of antimicrobial resistance.