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Testing the Role of Multicopy Plasmids in the Evolution of Antibiotic Resistance
Published on: May 2, 2018
Co-occurrence of 3 different resistance plasmids in a multi-drug resistant Cronobacter sakazakii isolate causing
Lining Shi1, Quanhui Liang2, Zhe Zhan3
1a Institute of Medical Laboratory Sciences, Jinling Hospital, School of Medicine, Nanjing University , Nanjing , China.
Abstract:
Cronobacter sakazakii 505108 was isolated from a sputum specimen of a neonate with severe pneumonia. C. sakazakii 505108 co-harbors 3 resistance plasmids of the IncHI2, IncX3, and IncFIB incomparability groups, respectively. These 3 plasmids have acquired several accessory modules, which carry an extremely large number of resistance genes, especially including those involved in resistance to carbapenems, aminoglycoside, tetracyclines, and phenicols and sulphonamide/trimethoprim. These plasmid-borne antibiotic resistance genes were associated with insertion sequences, integrons, and transposons, indicating that the assembly and mobilization of the corresponding accessory modules with complex chimera structures are facilitated by transposition and/or homologous recombination. This is the first report of fully sequence plasmids in clinical Cronobacter, which provides a deeper insight into plasmid-mediated multi-drug resistance in Cronobacter from hospital settings.
Insights
This study details Cronobacter sakazakii harboring multiple resistance plasmids, carrying numerous antibiotic resistance genes including carbapenem resistance. This finding offers insights into multi-drug resistance in clinical settings.
Area of Science:
- Microbiology
- Genetics
- Infectious Diseases
Background:
- Cronobacter sakazakii is an opportunistic pathogen causing severe infections, particularly in neonates.
- Antibiotic resistance in bacteria poses a significant global health threat.
- Understanding the genetic basis of resistance is crucial for effective treatment strategies.
Observation:
- A clinical isolate of Cronobacter sakazakii (strain 505108) was recovered from a neonate with severe pneumonia.
- This isolate harbored three distinct resistance plasmids belonging to IncHI2, IncX3, and IncFIB incompatibility groups.
- These plasmids contained numerous antibiotic resistance genes, including those conferring resistance to carbapenems, aminoglycosides, tetracyclines, phenicols, and sulfonamides/trimethoprim.
Findings:
- The resistance plasmids exhibited complex accessory modules acquired through mobile genetic elements like insertion sequences, integrons, and transposons.
- The co-acquisition and mobilization of these resistance genes are likely facilitated by transposition and homologous recombination.
- This is the first comprehensive sequencing of plasmids from a clinical Cronobacter isolate, revealing extensive multi-drug resistance mechanisms.
Implications:
- The findings highlight the significant role of plasmids in disseminating multi-drug resistance within Cronobacter species in hospital environments.
- This provides critical insights into the evolution and spread of antibiotic resistance in a clinically relevant pathogen.
- Understanding these plasmid-mediated resistance mechanisms is essential for developing targeted therapies and infection control measures against Cronobacter infections.
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