scholarly journals Molecular characterization of the Enterococcus faecalis cytolysin activator.

1991 ◽  
Vol 59 (4) ◽  
pp. 1239-1246 ◽  
Author(s):  
R A Segarra ◽  
M C Booth ◽  
D A Morales ◽  
M M Huycke ◽  
M S Gilmore
2019 ◽  
Vol 98 (11) ◽  
pp. 5892-5899 ◽  
Author(s):  
Yeong Bin Kim ◽  
Kwang Won Seo ◽  
Jong Bo Shim ◽  
Se hyun Son ◽  
Eun Bi Noh ◽  
...  

2019 ◽  
Vol 98 (2) ◽  
pp. 977-983 ◽  
Author(s):  
Yeong Bin Kim ◽  
Kwang Won Seo ◽  
Hye Young Jeon ◽  
Suk-Kyung Lim ◽  
Haan Woo Sung ◽  
...  

2010 ◽  
Vol 2010 ◽  
pp. 1-8 ◽  
Author(s):  
M. Biendo ◽  
C. Adjidé ◽  
S. Castelain ◽  
M. Belmekki ◽  
F. Rousseau ◽  
...  

We studied 138 glycopeptide-resistant enterococci (GRE) strains, consisting of 131 glycopeptide-resistantEnterococcus faecium(GREfm) and 7 glycopeptide-resistantEnterococcus faecalis(GREfs). The GREfm strains were resistant to penicillin, ampicillin, vancomycin, and teicoplanin, while the GREfs strains were only resistant to vancomycin and teicoplanin. Thevan Agene was the only glycopeptide determinant present in all GRE isolates investigated. Genes coding for Hyl and Hyl+ Esp were detected in 39 (29.8%) and 92 (70.2%) of the 131 GREfm isolates, respectively. Three of the 7 GREfs were positive forgelE+asa 1genes, 3 forgel Egene, and 1 forasa 1gene. The genetic relationship between the 138 GRE was analyzed by pulsed-field gel electrophoresis (PFGE) and multilocus sequence typing (MLST). GREfm isolates were clustered in a single genogroup (pulsotype A), and GREfs were clustered in six genogroups (pulsotypes B-G). Among the isolates investigated by MLST, only 18 PCR products were sequenced (12E. faeciumand 6E. faecalis), and 9 sequence types (STs) were identified.


2019 ◽  
Vol 39 (6) ◽  
Author(s):  
Tengfei Xie ◽  
Gang Wu ◽  
Xujun He ◽  
Zengzhe Lai ◽  
Huatong Zhang ◽  
...  

2002 ◽  
Vol 46 (6) ◽  
pp. 1977-1979 ◽  
Author(s):  
D. A. Boyd ◽  
T. Cabral ◽  
P. Van Caeseele ◽  
J. Wylie ◽  
M. R. Mulvey

ABSTRACT The vanE operon was characterized from Enterococcus faecalis N00-410 (MIC of vancomycin = 24 μg/ml). The organization of the vanE operon was identical to that of the vanC1 operon from Enterococcus gallinarum, with protein identities ranging from 46 to 63%. An open reading frame located downstream of the vanE operon showed significant homology to a number of integrase genes, all of which are located downstream of the chromosomal GMP synthase gene guaA.


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