Previous Article | Next Article ![]()
Journal of Clinical Microbiology, March 1999, p. 815-817, Vol. 37, No. 3
Microbiology Department, Clinical
Laboratories, Hennepin County Medical Center, Minneapolis, Minnesota
55415,1 and
Department of Laboratory
Medicine and Pathology, University of Minnesota Medical School,
Minneapolis, Minnesota 554552
Received 24 August 1998/Returned for modification 7 October
1998/Accepted 4 December 1998
Three different methodologies, reduction of litmus milk (LM) and
acidification of arabinose (ARA), acidification of
methyl-
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Comparison of Simple and Rapid Methods for
Identifying Enterococci Intrinsically Resistant to Vancomycin
-D-glucopyranoside (MGP), and rapid motility
(RM), for differentiating isolates of Enterococcus
casseliflavus and Enterococcus gallinarum
(intrinsically vancomycin-resistant enterococci [IVRE]) from
Enterococcus faecalis and Enterococcus faecium
were evaluated. All 33 isolates of E. faecalis tested
reduced LM within 4 h and were negative in all other tests, while
the 53 isolates of E. faecium were ARA positive only. In
contrast, 45 of 46 (98%) IVRE isolates examined (26 E. casseliflavus and 20 E. gallinarum isolates)
acidified MGP, 41 of 46 (89%) were LM and ARA positive, and 45 of 46 (98%) were RM positive. Acidification of MGP was therefore the single
most useful test for differentiating IVRE from vancomycin-resistant E. faecium and E. faecalis; however, a
combination of LM-ARA and RM testing enabled the correct designation of
organisms without the need for overnight incubation.
*
Corresponding author. Mailing address: Clinical
Laboratories, MC #812, Hennepin County Medical Center, 701 Park Ave.,
Minneapolis, MN 55415. Phone: (612) 347-3026. Fax: (612) 904-4229. E-mail: cartw006{at}tc.umn.edu.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»