Collateral Changes in Cell Physiology Associated with ADC-7 β-Lactamase Expression in Acinetobacter baumannii.
Jennifer M ColquhounMarjan FarokhyfarAlexander C AndersonChristopher R BethelRobert A BonomoAnthony J ClarkePhilip N RatherPublished in: Microbiology spectrum (2023)
The ADC (AmpC) β-lactamase is universally present in the Acinetobacter baumannii chromosome, suggesting it may have a yet-to-be-identified cellular function. Using peptidoglycan composition analysis, we show that overexpressing the ADC-7 β-lactamase in A. baumannii drives changes consistent with altered l,d-transpeptidase activity. Based on this, we tested whether cells overexpressing ADC-7 would exhibit new vulnerabilities. As proof of principle, a screen of transposon insertions revealed that an insertion in the distal 3' end of canB , encoding carbonic anhydrase, resulted in a significant loss of viability when the adc-7 gene was overexpressed. A canB deletion mutant exhibited a more pronounced loss of viability than the transposon insertion, and this became amplified when cells overexpressed ADC-7. Interestingly, overexpression of the OXA-23 or TEM-1 β-lactamases also led to a pronounced loss of viability in cells with reduced carbonic anhydrase activity. In addition, we demonstrate that reduced CanB activity led to increased sensitivity to peptidoglycan synthesis inhibitors and to the carbonic anhydrase inhibitor ethoxzolamide. Furthermore, this strain exhibited a synergistic interaction with the peptidoglycan inhibitor fosfomycin and ethoxzolamide. Our results highlight the impact of ADC-7 overexpression on cell physiology and reveal that the essential carbonic anhydrase CanB may represent a novel target for antimicrobial agents that would exhibit increased potency against β-lactamase-overexpressing A. baumannii. IMPORTANCE Acinetobacter baumannii has become resistant to all classes of antibiotics, with β-lactam resistance responsible for the majority of treatment failures. New classes of antimicrobials are needed to treat this high-priority pathogen. This study had uncovered a new genetic vulnerability in β-lactamase-expressing A. baumannii, where reduced carbonic anhydrase activity becomes lethal. Inhibitors of carbonic anhydrase could represent a new method for treating A. baumannii infections.
Keyphrases
- acinetobacter baumannii
- multidrug resistant
- gram negative
- drug resistant
- klebsiella pneumoniae
- diffusion weighted imaging
- escherichia coli
- diffusion weighted
- induced apoptosis
- pseudomonas aeruginosa
- cell cycle arrest
- single cell
- endoplasmic reticulum stress
- genome wide
- cell proliferation
- contrast enhanced
- transcription factor
- climate change
- gene expression
- magnetic resonance imaging
- copy number
- signaling pathway
- high throughput
- cell wall
- cell therapy
- candida albicans
- cystic fibrosis
- pi k akt
- cell death
- computed tomography
- bacillus subtilis
- drug delivery