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D-Ala-d-Ser VanN-type transferable vancomycin resistance in Enterococcus faecium.


ABSTRACT: Enterococcus faecium UCN71, isolated from a blood culture, was resistant to low levels of vancomycin (MIC, 16 μg/ml) but susceptible to teicoplanin (MIC, 0.5 μg/ml). No amplification was observed with primers specific for the previously described glycopeptide resistance ligase genes, but a PCR product corresponding to a gene called vanN was obtained using degenerate primers and was sequenced. The deduced VanN protein was related (65% identity) to the d-alanine:d-serine VanL ligase. The organization of the vanN gene cluster, determined using degenerate primers and by thermal asymmetric interlaced (TAIL)-PCR, was similar to that of the vanC operons. A single promoter upstream from the resistance operon was identified by rapid amplification of cDNA ends (RACE)-PCR. The presence of peptidoglycan precursors ending in d-serine and d,d-peptidase activities in the absence of vancomycin indicated constitutive expression of the resistance operon. VanN-type resistance was transferable by conjugation to E. faecium. This is the first report of transferable d-Ala-d-Ser-type resistance in E. faecium.

SUBMITTER: Lebreton F 

PROVIDER: S-EPMC3187002 | biostudies-literature | 2011 Oct

REPOSITORIES: biostudies-literature

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D-Ala-d-Ser VanN-type transferable vancomycin resistance in Enterococcus faecium.

Lebreton François F   Depardieu Florence F   Bourdon Nancy N   Fines-Guyon Marguerite M   Berger Pierre P   Camiade Sabine S   Leclercq Roland R   Courvalin Patrice P   Cattoir Vincent V  

Antimicrobial agents and chemotherapy 20110801 10


Enterococcus faecium UCN71, isolated from a blood culture, was resistant to low levels of vancomycin (MIC, 16 μg/ml) but susceptible to teicoplanin (MIC, 0.5 μg/ml). No amplification was observed with primers specific for the previously described glycopeptide resistance ligase genes, but a PCR product corresponding to a gene called vanN was obtained using degenerate primers and was sequenced. The deduced VanN protein was related (65% identity) to the d-alanine:d-serine VanL ligase. The organizat  ...[more]

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