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Comparative Study
. 2001 Sep;45(9):2594-7.
doi: 10.1128/AAC.45.9.2594-2597.2001.

Role of penicillin-binding protein 5 in expression of ampicillin resistance and peptidoglycan structure in Enterococcus faecium

Affiliations
Comparative Study

Role of penicillin-binding protein 5 in expression of ampicillin resistance and peptidoglycan structure in Enterococcus faecium

F Sifaoui et al. Antimicrob Agents Chemother. 2001 Sep.

Abstract

The contribution of penicillin-binding protein 5 (PBP 5) to intrinsic and acquired beta-lactam resistance was investigated by constructing isogenic strains of Enterococcus faecium producing different PBP 5. The pbp5 genes from three E. faecium clinical isolates (BM4107, D344, and H80721) were cloned into the shuttle vector pAT392 and introduced into E. faecium D344S, a spontaneous derivative of E. faecium D344 highly susceptible to ampicillin due to deletion of pbp5 (MIC, 0.03 microg/ml). Immunodetection of PBP5 indicated that cloning of the pbp5 genes into pAT392 resulted in moderate overproduction of PBP 5 in comparison to wild-type strains. This difference may be attributed to a difference in gene copy number. Expression of the pbp5 genes from BM4107 (MIC, 2 microg/ml), D344 (MIC, 24 microg/ml), and H80721 (MIC, 512 microg/ml) in D344S conferred relatively low levels of resistance to ampicillin (MICs, 6, 12, and 20 microg/ml, respectively). A methionine-to-alanine substitution was introduced at position 485 of the BM4107 PBP 5 by site-directed mutagenesis. In contrast to previous hypotheses based on comparison of nonisogenic strains, this substitution resulted in only a 2.5-fold increase in the ampicillin MIC. The reversed-phase high-performance liquid chromatography muropeptide profiles of D344 and D344S were similar, indicating that deletion of pbp5 was not associated with a detectable defect in cell wall synthesis. These results indicate that pbp5 is a nonessential gene responsible for intrinsic resistance to moderate levels of ampicillin and by itself cannot confer high-level resistance.

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Figures

FIG. 1
FIG. 1
Western blot detection of PBP 5 in membrane fractions from various E. faecium strains. Lanes: 1, derivative of D344S/pSF4(pbp5BM4107M485A) selected on ampicillin (MIC, 56 μg/ml); 2, D344S/pSF4(pbp5BM4107M485A); 3, derivative of D344S/pSF1(pb5pBM4107) (MIC, 12 μg/ml); 4, D344S/pSF1 (pb5pBM4107); 5, BM4107; 6, D344S; 7, derivative of D344S/pSF3(pbp5H80721) (MIC, 128 μg/ml); 8, D344S/pSF3(pbp5H80721); 9, H80721; 10, D344; 11, derivative of D344S/pSF2(pbp5D344) (MIC, 56 μg/ml); 12, D344S/pSF2(pbp5D344).

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