Comparative genomics of IncQ1 plasmids carrying bla GES variants from clinical and environmental sources in Brazil.
Danieli ConteDany MesaDamaris KrulLarissa BailCarmen Antônia Sanches ItoJussara Kasuko PalmeiroLibera Maria Dalla-CostaPublished in: Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases (2024)
IncQ-type plasmids have become important vectors in the dissemination of bla GES among different bacterial genera and species from different environments around the world, and studies estimating the occurrence of Guiana extended-spectrum (GES)-type β-lactamases are gaining prominence. We analyzed the genetic aspects of two IncQ1 plasmids harboring different bla GES variants from human and environmental sources. The bla GES variants were identified using polymerase chain reaction (PCR) in Aeromonas veronii isolated from hospital effluent and Klebsiella variicola isolated from a rectal swab of a patient admitted to the cardiovascular intensive care unit in a different hospital. Antimicrobial-susceptibility testing and transformation experiments were performed for phenotypic analysis. Whole-genome sequencing was performed using Illumina and Oxford Nanopore platforms. The comparative analysis of plasmids was performed using BLASTn, and the IncQ1 plasmids showed a high identity and similar size. A. veronii harbored bla GES-7 in a class 1 integron (In2061), recently described by our group, and K. variicola carried bla GES-5 in the known class 1 integron. Both integrons showed a fused gene cassette that encodes resistance to aminoglycosides and fluoroquinolones, with an IS6100 truncating the 3'-conserved segment. The fused genes are transcribed together, although the attC site is disrupted. These gene cassettes can no longer be mobilized. This study revealed a mobilome that may contribute to the dissemination of GES-type β-lactamases in Brazil. Class 1 integrons are hot spots for bacterial evolution, and their insertion into small IncQ-like plasmids displayed successful recombination, allowing the spread of bla GES variants in various environments. Therefore, they can become prevalent across clinically relevant pathogens.
Keyphrases
- klebsiella pneumoniae
- copy number
- escherichia coli
- multidrug resistant
- intensive care unit
- genome wide
- healthcare
- endothelial cells
- gram negative
- dna damage
- risk assessment
- oxidative stress
- single cell
- human health
- genome wide identification
- dna repair
- dna methylation
- single molecule
- peripheral blood
- wastewater treatment
- mechanical ventilation
- antibiotic resistance genes