International Journal of Antimicrobial Agents
Volume 36, Issue 4 , Pages 374-379, October 2010

Activity of telavancin and comparator antimicrobial agents tested against Staphylococcus spp. isolated from hospitalised patients in Europe (2007–2008)

  • Rodrigo E. Mendes

      Affiliations

    • JMI Laboratories, 345 Beaver Kreek Centre, Suite A, North Liberty, IA 52317, USA
    • Corresponding Author InformationCorresponding author. Tel.: +1 319 665 3370; fax: +1 319 655 3371.
  • ,
  • Helio S. Sader

      Affiliations

    • JMI Laboratories, 345 Beaver Kreek Centre, Suite A, North Liberty, IA 52317, USA
  • ,
  • Ronald N. Jones

      Affiliations

    • JMI Laboratories, 345 Beaver Kreek Centre, Suite A, North Liberty, IA 52317, USA
    • Tufts University School of Medicine, Boston, MA, USA

Received 2 March 2010; accepted 26 May 2010. published online 05 July 2010.

Abstract 

The activity of telavancin was evaluated against Staphylococcus spp. collected from European hospitals as part of an international surveillance study (2007–2008). A total of 7534 staphylococcal clinical isolates [5726 Staphylococcus aureus and 1808 coagulase-negative staphylococci (CoNS)] were included. Isolates were tested for susceptibility according to reference methods and minimum inhibitory concentration (MIC) values were interpreted based on Clinical and Laboratory Standards Institute (CLSI) 2010 and European Committee on Antimicrobial Susceptibility Testing (EUCAST) 2009 criteria. Telavancin breakpoints approved by the US Food and Drug Administration (FDA) were applied. Telavancin activity was evaluated against meticillin-resistant S. aureus (MRSA) displaying several antibiogram resistance patterns, including multidrug-resistant isolates. Telavancin was active against S. aureus [MIC50/90 values (MICs for 50% and 90% of the isolates, respectively)=0.12/0.25mg/L; 100.0% susceptible] and CoNS (MIC50/90=0.12/0.25mg/L), inhibiting all isolates at ≤0.5mg/L. Similar results were observed when S. aureus were stratified by year or country of origin (MIC50/90=0.12/0.25mg/L). When MRSA isolates were clustered according to 48 different resistance patterns, telavancin showed consistent MIC90 values (0.25mg/L) regardless of multidrug resistance. Amongst CoNS, telavancin was slightly more active against Staphylococcus capitis, Staphylococcus epidermidis, Staphylococcus hominis, Staphylococcus lugdunensis and Staphylococcus xylosus (MIC50=0.12mg/L) compared with Staphylococcus haemolyticus, Staphylococcus saprophyticus and Staphylococcus warneri (MIC50=0.25mg/L). Overall, telavancin exhibited MIC90 results two- to eight-fold lower than comparators (daptomycin, quinupristin/dalfopristin, vancomycin and linezolid). Based upon MIC90 values, telavancin demonstrated potent in vitro activity against a contemporary (2007–2008) collection of Staphylococcus spp. recovered from nearly 30 European medical centres.

Keywords: Telavancin, Lipoglycopeptide, Staphylococcus spp., Surveillance, Europe

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PII: S0924-8579(10)00235-9

doi:10.1016/j.ijantimicag.2010.05.016

International Journal of Antimicrobial Agents
Volume 36, Issue 4 , Pages 374-379, October 2010