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High-level aminoglycoside resistant enterococci isolated from swine.
C R Jackson1, P J Fedorka-Cray, J B Barrett
1United States Department of Agriculture, Agricultural Research Service, Antimicrobial Resistance Research Unit, USA. cjackson@saa.ars.usda.gov
Epidemiology and Infection
|April 9, 2005
Summary
High-level aminoglycoside resistance is prevalent in swine enterococci. Many resistant isolates harbored unknown resistance genes, suggesting novel antimicrobial resistance mechanisms in these bacteria.
Area of Science:
- Veterinary Microbiology
- Antimicrobial Resistance
- Molecular Biology
Background:
- Enterococci are significant pathogens in both human and animal health.
- Aminoglycoside resistance in enterococci poses a therapeutic challenge.
- Swine can serve as reservoirs for antimicrobial-resistant bacteria.
Purpose of the Study:
- To investigate the prevalence of high-level aminoglycoside resistance (HLAR) in swine enterococci.
- To identify known aminoglycoside resistance genes in resistant isolates.
- To explore the presence of potentially novel resistance mechanisms.
Main Methods:
- Bacterial isolates: Enterococci collected from swine between 1999-2000.
- Antimicrobial susceptibility testing: Minimum Inhibitory Concentrations (MICs) for gentamicin, kanamycin, and streptomycin.
- Molecular detection: Polymerase Chain Reaction (PCR) for eight known aminoglycoside resistance genes.
Main Results:
- 42% of swine enterococci exhibited HLAR to gentamicin, kanamycin, or streptomycin.
- The most frequent genes detected were ant(6)-Ia and aac(6')-Ii, primarily in Enterococcus faecium.
- A significant proportion (24%) of HLAR isolates and 26% of pan-resistant isolates were negative for all tested genes.
Conclusions:
- Swine enterococci harbor diverse aminoglycoside resistance mechanisms.
- The presence of gene-negative resistant isolates suggests the existence of unidentified aminoglycoside resistance genes.
- Further research is needed to characterize novel resistance determinants in swine-associated enterococci.