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Amplicon Sequencing using the Long-Read Sequencing Technologies
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Linezolid surveillance program results for 2008 (LEADER Program for 2008).

David J Farrell1, Rodrigo E Mendes, James E Ross

  • 1JMI Laboratories, North Liberty, IA 52317, USA. david-farrell@jmilabs.com

Diagnostic Microbiology and Infectious Disease
|November 17, 2009
PubMed
Summary

The LEADER Program found linezolid remains highly effective against common bacteria in US hospitals. Surveillance in 2008 showed sustained potency, with only 0.36% of strains exhibiting resistance, indicating continued low rates of linezolid nonsusceptibility.

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Published on: August 30, 2018

Area of Science:

  • Antimicrobial resistance surveillance
  • Clinical microbiology
  • Infectious disease epidemiology

Background:

  • The Linezolid Emerging Resistance (LEADER) Program monitors linezolid resistance in US medical centers.
  • This report details findings from the 5th year of surveillance in 2008.

Purpose of the Study:

  • To assess the potency and spectrum of linezolid against key bacterial pathogens.
  • To monitor trends in linezolid nonsusceptibility and identify emerging resistance mechanisms.

Main Methods:

  • Data collected from 57 US medical centers in 2008.
  • Testing of 6113 bacterial isolates including Staphylococcus aureus, coagulase-negative staphylococci (CoNS), enterococci, and streptococci.
  • Reference broth microdilution and D-test methods were employed.

Main Results:

  • Linezolid demonstrated high potency with MIC(90) values ranging from 1-2 µg/mL.
  • Overall linezolid nonsusceptibility was low at 0.36%, a decrease from previous years.
  • Identified resistance mechanisms included target mutations and the mobile cfr element, with no evidence of widespread dissemination of cfr in 2008.

Conclusions:

  • Linezolid maintains excellent activity against a broad range of bacteria in US healthcare settings.
  • Nonsusceptible strain isolation rates remained stable, with no significant increase in plasmid-mediated resistance.
  • The LEADER Program effectively tracks oxazolidinone resistance phenotypes and genotypes, highlighting sustained linezolid potency.