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. 1999 Oct;43(10):2395-9.
doi: 10.1128/AAC.43.10.2395.

Plasmid-mediated resistance to thrombin-induced platelet microbicidal protein in staphylococci: role of the qacA locus

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Plasmid-mediated resistance to thrombin-induced platelet microbicidal protein in staphylococci: role of the qacA locus

L I Kupferwasser et al. Antimicrob Agents Chemother. 1999 Oct.

Abstract

Thrombin-induced platelet microbicidal protein 1 (tPMP-1) is a small, cationic peptide released from rabbit platelets following thrombin stimulation. In vitro resistance to this peptide among strains of Staphylococcus aureus correlates with the survival advantage of such strains at sites of endothelial damage in humans as well as in experimental endovascular infections. The mechanisms involved in the phenotypic resistance of S. aureus to tPMP-1 are not fully delineated. The plasmid-encoded staphylococcal gene qacA mediates multidrug resistance to multiple organic cations via a proton motive force-dependent efflux pump. We studied whether the qacA gene might also confer resistance to cationic tPMP-1. Staphylococcal plasmids encoding qacA were found to confer resistance to tPMP-1 in an otherwise susceptible parental strain. Deletions which removed the region containing the qacA gene in the S. aureus multiresistance plasmid pSK1 abolished tPMP-1 resistance. Resistance to tPMP-1 in the qacA-bearing strains was inoculum independent but peptide concentration dependent, with the level of resistance decreasing at higher peptide concentrations for a given inoculum. There was no apparent cross-resistance in qacA-bearing strains to other endogenous cationic antimicrobial peptides which are structurally distinct from tPMP-1, including human neutrophil defensin 1, protamine, or the staphylococcal lantibiotics pep5 and nisin. These data demonstrate that the staphylococcal multidrug resistance gene qacA also mediates in vitro resistance to cationic tPMP-1.

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Figures

FIG. 1
FIG. 1
Maps of the S. aureus multiresistance plasmid pSK1 (23), its deletion derivatives pSK30 and pSK78, and the related S. epidermidis plasmid pSK105 (13) are aligned with respect to the qacA locus; in comparison to pSK1, pSK105 lacks Tn4003, and Tn4001 is located in a different position. The qacA-carrying S. epidermidis plasmids pSK107 and pSK638 are unrelated to the pSK1 family plasmids (13). Plasmid sizes are indicated on the right. The positions of the transposons are indicated above each map. White and black solid boxes denote copies of IS256 and IS257, respectively. The DNA segments deleted from pSK30 and pSK78 are denoted by broken lines, and the size of the deletion is shown below the line. Loci encoding the indicated functions are shown below the maps: aacA-aphD, resistance to the aminoglycosides, gentamicin, tobramycin, and kanamycin; dfrA, resistance to trimethoprim; qacA, multidrug resistance to antiseptics and disinfectants; and qacR, transcriptional regulation of qacA (the presence of qacR in pSK105, pSK107, and pSK638 is assumed but not proven at this time). Restriction sites: B, BglII; E, EcoRI; P, PvuII.

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References

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