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. 2006 Nov 25:6:168.
doi: 10.1186/1471-2334-6-168.

Antibacterial resistance and their genetic location in MRSA isolated in Kuwait hospitals, 1994-2004

Affiliations

Antibacterial resistance and their genetic location in MRSA isolated in Kuwait hospitals, 1994-2004

Edet E Udo et al. BMC Infect Dis. .

Abstract

Background: Methicillin-resistant Staphylococcus aureus (MRSA) continues to be a major cause of serious infections in hospitals and in the community worldwide. In this study, MRSA isolated from patients in Kuwait hospitals were analyzed for resistance trends and the genetic location of their resistance determinants.

Methods: Between April 1994 and December 2004, 5644 MRSA isolates obtained from different clinical samples were studied for resistance to antibacterial agents according to guidelines from the National Committee for Clinical Laboratory Standards and the British Society for Antimicrobial Chemotherapy. The genetic location of their resistance determinants was determined by curing and transfer experiments.

Results: They were resistant to aminoglycosides, erythromycin, tetracycline, trimethoprim, fusidic acid, ciprofloxacin, chloramphenicol, rifampicin, mupirocin, cadmium acetate, mercuric chloride, propamidine isethionate and ethidium bromide but susceptible to vancomycin, teicoplanin and linezolid. The proportion of the isolates resistant to erythromycin, ciprofloxacin and fusidic acid increased during the study period. In contrast, the proportion of isolates resistant to gentamicin, tetracycline, chloramphenicol and trimethoprim declined. High-level mupirocin resistance increased rapidly from 1996 to 1999 and then declined. They contained plasmids of 1.9, 2.8, 3.0, 4.4, 27 and 38 kilobases. Genetic studies revealed that they carried plasmid-borne resistance to high-level mupirocin resistance (38 kb), chloramphenicol (2.8-4.4 kb), erythromycin (2.8-3.0 kb) and cadmium acetate, mercuric chloride, propamidine isethionate and ethidium bromide (27 kb) and chromosomal location for methicillin, the aminoglycosides, tetracycline, fusidic acid, ciprofloxacin and trimethoprim resistance. Thus, the 27 kb plasmids had resistance phenotypes similar to plasmids reported in MRSA isolates in South East Asia.

Conclusion: The prevalence of resistance to erythromycin, ciprofloxacin, high-level mupirocin and fusidic acid increased whereas the proportion of isolates resistant to gentamicin, tetracycline, chloramphenicol and trimethoprim declined during the study period. They contained 27-kb plasmids encoding resistance to cadmium acetate, mercuric chloride, propamidine isethionate and ethidium bromide similar to plasmids isolated in MRSA from South East Asia. Molecular typing of these isolates will clarify their relationship to MRSA from South East Asia.

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Figures

Figure 1
Figure 1
Plasmid content of mupirocin-susceptible MRSA, Lanes 1–6, representatives of multiresistant MRSA carrying the 27 kb plasmid encoding resistance to cadmium acetate, mercuric chloride, propamidine isethionate and ethidium bromide and the 2.8–3.0 kb plasmids. Lane 7, a representative of non multiresistant MRSA. Lane 8, S. aureus strain WBG4483 containing plasmid molecular weight standards. Sizes are in kb.
Figure 2
Figure 2
Plasmid contents of high-level mupirocin-resistantisolates Lanes 1, 3, 4, 5, 6, 9, 10 contained the 38-kb mupirocin resistance plasmid and 4.4 kb chloramphenicol resistance plasmid in addition to the 27 kb plasmids. Sizes are in kb.

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