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. 2000 Aug;38(8):3092-5.
doi: 10.1128/JCM.38.8.3092-3095.2000.

Simple and reliable multiplex PCR assay for surveillance isolates of vancomycin-resistant enterococci

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Simple and reliable multiplex PCR assay for surveillance isolates of vancomycin-resistant enterococci

R Kariyama et al. J Clin Microbiol. 2000 Aug.

Abstract

Conditions have been optimized for the use of a multiplex PCR for the detection of vancomycin-resistant enterococci in nosocomial surveillance specimens. Seven primer sets targeting the genes vanA, vanB, vanC1, vanC2/C3 Enterococcus faecalis-specific, Enterococcus faecium-specific, and rrs (16S rRNA) were used in one reaction tube. The PCR method developed in the present study is simple and reliable for the rapid characterization of vancomycin-resistant enterococci.

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FIG. 1
FIG. 1
Agarose gel electrophoresis of amplified vanA, vanB, vanC1, vanC2, E. faecalis-specific, E. faecium-specific, and rrs genes by the optimized multiplex PCR assay containing seven primer sets. Lanes: M, 100-bp DNA ladder (New England Biolabs); 1, an E. faecalis vanA isolate; 2, an E. faecalis vanB isolate; 3, an E. faecium vanA isolate; 4, an E. faecium vanB isolate; 5, an E. gallinarum vanC1 isolate; 6, an E. casseliflavus vanC2 isolate; 7, a Pediococcus isolate; 8, a Leuconostoc isolate.

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