1998
DOI: 10.1007/s002849900318
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Identification of Clinically Important Species of Enterococcus Within 1 Day with Randomly Amplified Polymorphic DNA (RAPD)

Abstract: The use of randomly amplified polymorphic DNA (RAPD) for rapid, reliable, and easily interpreted identification of enterococci was evaluated. Nineteen type strains of Enterococcus, 12 reference strains, and 114 clinical isolates of Enterococcus were analyzed. Discrimination was obtained between most type strains, the exceptions being Ent. casseliflavus and Ent. flavescens, which had relatively similar RAPD-profiles. Ent. faecalis and Ent. faecium were readily separated, and Ent. gallinarum and Ent. durans coul… Show more

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Cited by 54 publications
(36 citation statements)
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“…faecium at WWTF-1 was 9:1, which is similar to other studies that have surveyed enterococci at meat processing operations (beef, pork and poultry) and from associated meat products. In most of those studies, E. faecalis was dominant followed by E. faecium [14,30,36,45,49,54,58]. In the current study, the species composition among sludge and house flies was comparable with E. faecalis being the most abundant species from both sources (Fig.…”
Section: Discussionmentioning
confidence: 50%
“…faecium at WWTF-1 was 9:1, which is similar to other studies that have surveyed enterococci at meat processing operations (beef, pork and poultry) and from associated meat products. In most of those studies, E. faecalis was dominant followed by E. faecium [14,30,36,45,49,54,58]. In the current study, the species composition among sludge and house flies was comparable with E. faecalis being the most abundant species from both sources (Fig.…”
Section: Discussionmentioning
confidence: 50%
“…Randomly amplified polymorphic DNA (RAPD) analysis (10,22) was used to group the isolates; temporal temperature gradient gel electrophoresis (TTGE), where the 16S ribosomal DNA (rDNA) molecule is used, was used for identification to the species level (29); and multiplex PCR, where another area of the rDNA, namely, the intergenic spacer region between the 16S and the 23S rDNAs, is used for the identification (27), was also used.…”
mentioning
confidence: 99%
“…The polymerase chain reaction (PCR) of the samples was run with a 9-mer primer (5?-ACGCGCCCT-3? ; Scandinavian Gene Synthesis, Kö ping, Sweden), as previously described (26). Agarose gel electrophoresis was run; the gels were stained with ethidium bromide and photographed under UV illumination.…”
Section: Randomly Amplified Polymorphic Dna (Rapd) Analysismentioning
confidence: 99%
“…paracasei group to the liver site (three isolates), to the portal blood (two isolates), to the arterial blood (three isolates), to the MLNs (three isolates), from one rat in L. gasseri group to the MLN site (one isolate), from three rats in Bifidobacterium 'urinalis' group to the liver site (10 isolates), to the portal blood (three isolates), to the MLN site (one isolate) and from one rat in B. infantis to the liver site (one isolate). Crude cell extracts were prepared (26). The polymerase chain reaction (PCR) of the samples was run with a 9-mer primer (5?-ACGCGCCCT-3?…”
Section: Randomly Amplified Polymorphic Dna (Rapd) Analysismentioning
confidence: 99%