Analyzing Possible Native Functions of the Quinolone Resistance Gene qnr in Vibrio vulnificus.
María Luisa Gil-MarquésGeorge A JacobyDavid C HooperPublished in: Antimicrobial agents and chemotherapy (2021)
The worldwide distribution of qnr genes found on plasmids and their presence on the chromosomes of aquatic bacteria, such as Vibrio vulnificus, one of the suspected sources, suggests an origin before the development of synthetic quinolones. However, their native function remains unknown. Previous work indicated that expression of qnrVv in V. vulnificus was induced by cold shock. To investigate its role further, we constructed single in-frame deletion mutants in qnrVv and cspA (the gene for cold shock protein) and a double mutant in qnrVv and cspA in V. vulnificus ATCC 17562 to evaluate the response to different environmental conditions and stresses and to exposure to various DNA-damaging agents. We found that qnrVv is involved in resistance to ciprofloxacin, levofloxacin, and mitomycin C and in the cold shock response in V. vulnificus Moreover, ΔqnrVv and ΔcspA mutants showed slower growth when they were treated with bile salts at 37°C and then shifted to 15°C (cold shock) without bile salts in the medium, with the effect being stronger in the double mutant. This transition may mimic what happens when V. vulnificus is ingested into the gastrointestinal tract and released in its natural environment. Cold shock and bile salts induced the expression of cspA and DNA gyrase and topoisomerase IV genes. However, no induction was found in the ΔqnrVv mutant, suggesting that the qnrVv gene is involved in the response to DNA damage and nucleic acid secondary structure.
Keyphrases
- nucleic acid
- genome wide
- genome wide identification
- wild type
- dna damage
- poor prognosis
- copy number
- circulating tumor
- genome wide analysis
- ionic liquid
- single molecule
- dna methylation
- risk assessment
- oxidative stress
- transcription factor
- cell free
- escherichia coli
- wastewater treatment
- dna repair
- high glucose
- small molecule
- long non coding rna
- diabetic rats
- protein protein
- multidrug resistant
- climate change
- drug induced
- circulating tumor cells
- newly diagnosed