Emerging resistance in Staphylococcus epidermidis during dalbavancin exposure: a case report and in vitro analysis of isolates from prosthetic joint infections

被引:10
作者
Al Janabi, Jasmina [1 ]
Tevell, Staffan [1 ,2 ,3 ]
Sieber, Raphael Niklaus [4 ]
Stegger, Marc [1 ,4 ]
Soderquist, Bo [1 ,5 ]
机构
[1] Orebro Univ, Fac Med & Hlth, Sch Med Sci, Orebro, Sweden
[2] Karlstad Hosp, Dept Infect Dis, Karlstad, Sweden
[3] Reg Varmland, Ctr Clin Res & Educ, Karlstad, Sweden
[4] Statens Serum Inst, Dept Bacteria Parasites & Fungi, Copenhagen, Denmark
[5] Orebro Univ, Fac Med & Hlth, Dept Lab Med, Orebro, Sweden
关键词
VANCOMYCIN-INTERMEDIATE; AUREUS; SUSCEPTIBILITY; DAPTOMYCIN; STRAINS;
D O I
10.1093/jac/dkac434
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background Dalbavancin, a semisynthetic lipoglycopeptide with exceptionally long half-life and Gram-positive spectrum, is an attractive option for infections requiring prolonged therapy, including prosthetic joint infections (PJIs). Objectives To investigate the prevalence of reduced susceptibility to dalbavancin in a strain collection of Staphylococcus epidermidis from PJIs, and to investigate genomic variation in isolates with reduced susceptibility selected during growth under dalbavancin exposure. Methods MIC determination was performed on S. epidermidis isolates from a strain collection (n = 64) and from one patient with emerging resistance during treatment (n = 4). These isolates were subsequently cultured on dalbavancin-containing agar and evaluated at 48 h; MIC determination was repeated if phenotypical heterogeneity was detected during growth. Population analysis profile (PAP-AUC) was performed in isolates where a >= 2-fold increase in MIC was detected, together with corresponding parental isolates (n = 21). Finally, WGS was performed. Results All strains grew at 48 h on agar containing 0.125 mg/L dalbavancin. PAP-AUC demonstrated significant differences between parental and derived strains in four of the eight analysed groups. An amino acid change in the walK gene coinciding with emergence of phenotypic resistance was detected in the patient isolates, whereas no alterations were found in this region in the in vitro derived strains. Conclusions Exposure to dalbavancin may lead to reduced susceptibility to dalbavancin through either selection of pre-existing subpopulations, epigenetic changes or spontaneous mutations during antibiotic exposure. Source control combined with adequate antibiotic concentrations may be important to prevent emerging reduced susceptibility during dalbavancin treatment.
引用
收藏
页码:669 / 677
页数:9
相关论文
共 45 条
  • [31] Roary: rapid large-scale prokaryote pan genome analysis
    Page, Andrew J.
    Cummins, Carla A.
    Hunt, Martin
    Wong, Vanessa K.
    Reuter, Sandra
    Holden, Matthew T. G.
    Fookes, Maria
    Falush, Daniel
    Keane, Jacqueline A.
    Parkhill, Julian
    [J]. BIOINFORMATICS, 2015, 31 (22) : 3691 - 3693
  • [32] Intracellular Staphylococcus aureus persisters upon antibiotic exposure
    Peyrusson, Frederic
    Varet, Hugo
    Tiep Khac Nguyen
    Legendre, Rachel
    Sismeiro, Odile
    Coppee, Jean-Yves
    Wolz, Christiane
    Tenson, Tanel
    Van Bambeke, Francoise
    [J]. NATURE COMMUNICATIONS, 2020, 11 (01)
  • [33] Evaluation of Vancomycin Susceptibility Testing for Methicillin-Resistant Staphylococcus aureus: Comparison of Etest and Three Automated Testing Methods
    Rybak, Michael J.
    Vidaillac, Celine
    Sader, Helio S.
    Rhomberg, Paul R.
    Salimnia, Hossein
    Briski, Lawrence E.
    Wanger, Audrey
    Jones, Ronald N.
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2013, 51 (07) : 2077 - 2081
  • [34] Antimicrobial activity of dalbavancin against clinical isolates of coagulase-negative staphylococci from the USA and Europe stratified by species
    Sader, Helio S.
    Carvalhaes, Cecilia G.
    Streit, Jennifer M.
    Arends, S. J. Ryan
    Mendes, Rodrigo E.
    [J]. JOURNAL OF GLOBAL ANTIMICROBIAL RESISTANCE, 2021, 24 : 48 - 52
  • [35] NASP: an accurate, rapid method for the identification of SNPs in WGS datasets that supports flexible input and output formats
    Sahl, Jason W.
    Lemmer, Darrin
    Travis, Jason
    Schupp, James M.
    Gillece, John D.
    Aziz, Maliha
    Driebe, Elizabeth M.
    Drees, Kevin P.
    Hicks, Nathan D.
    Williamson, Charles Hall Davis
    Hepp, Crystal M.
    Smith, David Earl
    Roe, Chandler
    Engelthaler, David M.
    Wagner, David M.
    Keim, Paul
    [J]. MICROBIAL GENOMICS, 2016, 2 (08): : e000074
  • [36] In vitro activity of tedizolid against staphylococci isolated from prosthetic joint infections
    Schmidt-Malan, Suzannah M.
    Quaintance, Kerryl E. Greenwood
    Karau, Melissa J.
    Patel, Robin
    [J]. DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2016, 85 (01) : 77 - 79
  • [37] Prokka: rapid prokaryotic genome annotation
    Seemann, Torsten
    [J]. BIOINFORMATICS, 2014, 30 (14) : 2068 - 2069
  • [38] Once-weekly dalbavancin versus standard-of-care antimicrobial regimens for treatment of skin and soft-tissue infections
    Seltzer, E
    Dorr, MB
    Goldstein, BP
    Perry, M
    Dowell, JA
    Henkel, T
    [J]. CLINICAL INFECTIOUS DISEASES, 2003, 37 (10) : 1298 - 1303
  • [39] Characterisation of a Staphylococcus aureus strain with progressive loss of susceptibility to vancomycin and daptomycin during therapy
    Tenover, Fred C.
    Sinner, Scott W.
    Segal, Robert E.
    Huang, Vanthida
    Alexandre, Shandline S.
    McGowan, John E., Jr.
    Weinstein, Melvin P.
    [J]. INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2009, 33 (06) : 564 - 568
  • [40] Heterogeneous glycopeptide intermediate Staphylococcus epidermidis isolated from prosthetic joint infections
    Tevell, S.
    Claesson, C.
    Hellmark, B.
    Soderquist, B.
    Nilsdotter-Augustinsson, A.
    [J]. EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2014, 33 (06) : 911 - 917