Daptomycin Resistance and Tolerance Due to Loss of Function in Staphylococcus aureus dsp1 and asp23

• Published in: Antimicrobial agents and chemotherapy Vol. 63; no. 1
• Main Authors: Barros, Elaine M, Martin, Melissa J, Selleck, Elizabeth M, Lebreton, François, Sampaio, Jorge Luiz M, Gilmore, Michael S
• Format: Journal Article
• Language: English
• Published: United States American Society for Microbiology 01.01.2019
• Subjects: Anti-Bacterial Agents; Anti-Bacterial Agents - pharmacology; Bacterial Proteins; Bacterial Proteins - genetics; Cell Membrane - drug effects; Daptomycin; Daptomycin - pharmacology; DNA Transposable Elements - genetics; Drug Resistance, Multiple, Bacterial - genetics; Mechanisms of Resistance; Microbial Sensitivity Tests; Staphylococcal Infections - drug therapy; Staphylococcus aureus; Staphylococcus aureus - drug effects; Staphylococcus aureus - genetics; Vancomycin - pharmacology; daptomycin; vancomycin; antibiotic resistance; Staphylococcus aureus
• ISSN: 0066-4804; 1098-6596
• DOI: 10.1128/AAC.01542-18

Lipopeptide daptomycin is a last-line cell-membrane-targeting antibiotic to treat multidrug-resistant Alarmingly, daptomycin-resistant isolates have emerged. The mechanisms underlying daptomycin resistance are diverse and share similarities with resistances to cationic antimicrobial peptides and other lipopeptides, but they remain to be fully elucidated. We selected mutants with increased resistance to daptomycin from a library of transposon insertions in sequent type 8 (ST8) HG003. Insertions conferring increased daptomycin resistance were localized to two genes, one coding for a hypothetical lipoprotein (SAOUHSC_00362, Dsp1), and the other for an alkaline shock protein (SAOUHSC_02441, Asp23). Markerless loss-of-function mutants were then generated for comparison. All transposon mutants and knockout strains exhibited increased daptomycin resistance compared to those of wild-type and complemented strains. Null and transposon insertion mutants also exhibited increased resistance to cationic antimicrobial peptides. Interestingly, the mutant also showed increased resistance to vancomycin, a cell-wall-targeting drug with a different mode of action. Null mutations in both and resulted in increased tolerance as reflected by reduced killing to both daptomycin and vancomycin, as well as an increased tolerance to surfactant (Triton X-100). Neither mutant exhibited increased resistance to lysostaphin, a cell-wall-targeting endopeptidase. These findings identified two genes core to the species that make previously uncharacterized contributions to antimicrobial resistance and tolerance in .