Gene vanXYC encodes d,d -dipeptidase (VanX) and d,d-carboxypeptidase (VanY) activities in vancomycin-resistant Enterococcus gallinarum BM4174

1999 ◽  
Vol 34 (2) ◽  
pp. 341-349 ◽  
Author(s):  
Peter E. Reynolds ◽  
Cesar A. Arias ◽  
Patrice Courvalin
2008 ◽  
Vol 57 (2) ◽  
pp. 244-245 ◽  
Author(s):  
Vânia Lúcia Carreira Merquior ◽  
Felipe Piedade Gonçalves Neves ◽  
Rachel Leite Ribeiro ◽  
Rafael Silva Duarte ◽  
Elizabeth de Andrade Marques ◽  
...  

A case of a post-surgical patient who developed a fatal bloodstream infection caused by high-level vancomycin-resistant Enterococcus gallinarum is reported. The isolate was found to carry both the vanC1 and vanA genes. This is the first report of an invasive infection associated with a vanA E. gallinarum isolate in Brazil.


1994 ◽  
Vol 301 (1) ◽  
pp. 5-8 ◽  
Author(s):  
P E Reynolds ◽  
H A Snaith ◽  
A J Maguire ◽  
S Dutka-Malen ◽  
P Courvalin

Vancomycin resistance in enterococci is an increasing clinical problem, and several phenotypes have been identified. We demonstrate here that the resistance mechanism in the constitutively vancomycin-resistant Enterococcus gallinarum BM4174 involves an altered pathway of peptidoglycan synthesis and hydrolysis of the normal precursors in the vancomycin-sensitive pathway. A ligase encoded by the vanC gene catalyses synthesis of D-Ala-D-Ser and substitutes this dipeptide for D-Ala-D-Ala in peptidoglycan precursors. It is presumed that this substitution lowers the affinity of vancomycin for its target site. Destruction of D-Ala-D-Ala (D,D-peptidase activity) and of UDP-MurNAc-L-Ala-D-isoGlu-L-Lys-D-Ala-D-Ala by removal of the terminal D-Ala residue (D,D-carboxypeptidase activity) ensures that the normal vancomycin-sensitive pathway of peptidoglycan synthesis cannot function in the resistant strain.


1999 ◽  
Vol 31 (6) ◽  
pp. 1653-1664 ◽  
Author(s):  
Cesar A. Arias ◽  
Mercedes Martin-Martinez ◽  
Tom L. Blundell ◽  
Michel Arthur ◽  
Patrice Courvalin ◽  
...  

1998 ◽  
Vol 36 (8) ◽  
pp. 2333-2335 ◽  
Author(s):  
Christine Y. Turenne ◽  
Daryl J. Hoban ◽  
James A. Karlowsky ◽  
George G. Zhanel ◽  
Amin M. Kabani

The methyl-α-d-glucopyranoside (MDG) test has been shown to be superior to motility testing in differentiatingEnterococcus faecium from E. gallinarum. In the present study, 33 vancomycin-resistant enterococcus (VRE) isolates collected as part of a stool surveillance study were compared by using motility and MDG. Motility testing identified all 33 isolates asE. faecium, whereas MDG identified 11 of the 33 isolates as nonmotile E. gallinarum. The MDG results were confirmed by sequencing the 16S rDNA V6-to-V8 region. We conclude that the MDG test is a necessary component of routine VRE screening.


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.


Pathology ◽  
2001 ◽  
Vol 33 (2) ◽  
pp. 216-221
Author(s):  
Lynette L. E. Oon ◽  
Moi-Lin Ling ◽  
Yoke-Fong Chiew

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