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Isolate and presumptively identify vancomycin-resistant enterococci (VRE) from surveillance cultures with Thermo Scientific™ Remel™ Bile Esculin Azide Agar with Vancomycin. Sodium azide and 1% oxgall are inhibitory to Gram-negative bacteria other than group D streptococci. Vancomycin (6µg/mL) is added to select for resistant strains of enterococci. Differentiation is facilitated by the hydrolysis of esculin in the presence of bile, resulting in the production of esculetin and dextrose. Ferric ammonium citrate supplies ferric ions which react with esculitin to form a black-brown complex.
Description | Bile Esculin Azide Agar w/Vancomycin |
Format | 12mm x 85mm Monoplate |
Product Type | Agar |
Quantity | 10/Pk. |
Unit Size | Each |
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Members of the genus Enterococcus are normal residents of the gastrointestinal and biliary tracts1,2. Enterococci have become significant agents of human disease, largely because of their evolving resistance to antimicrobial agents. VRE surveillance-screening has been found to facilitate earlier identification of colonized patients leading to more efficient containment of the organism. Timely identification of VRE is improved with the use of the primary isolation medium for surveillance cultures.
Sahm et al. demonstrated that Bile Esculin Azide Agar with 6µg/mL Vancomycin provides for rapid presumptive identification of VRE3.
Esculin in the medium allows for early recognition of presumptive enterococcal isolates, selective agents inhibit the growth of most commensal microbial flora, and vancomycin provides additional selectivity against vancomycin-sensitive and other Gram-positive organisms.
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Remel™ and Oxoid™ products are now part of the Thermo Scientific brand.
1. Winn, W.C. Jr., S.D. Allen, W.M. Janda, E.W. Koneman, G.W. Procop, P.C. Schreckenberger, and G.L. Woods. 2006. Koneman’s Colour Atlas and Textbook of Diagnostic Microbiology. 6th ed. Lippincott Williams and Wilkins, Philadelphia, PA.
2. Murry, P.R., E.J. Baron, J.H. Jorgesen, M.L. Landry, and M.A. Pfellaer. 2007. Manual of Clinical Microbiology. 9th ed. ASM Press, Washington, D.C>
3. Sahm, D.F., L. Mundy. 1997. J.Clin.Microbiol. 35: 2026-2023.