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A Reference Broth Microdilution Method for Dalbavancin In Vitro Susceptibility Testing of Bacteria that Grow Aerobically
Published on: September 9, 2015
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Quality control MIC ranges used for telavancin with application of a revised CLSI reference broth microdilution
James E Ross1, Rodrigo E Mendes2, Ronald N Jones2
1JMI Laboratories, North Liberty, Iowa, USA jim-ross@jmilabs.com.
Journal of Clinical Microbiology
|June 13, 2014
Summary
The revised telavancin broth microdilution method yields lower MIC results. New quality control ranges were established for Staphylococcus aureus, Enterococcus faecalis, and Streptococcus pneumoniae testing.
Area of Science:
- Microbiology
- Clinical Pharmacy
- Infectious Diseases
Background:
- The broth microdilution method is standard for determining antimicrobial susceptibility.
- Telavancin is a lipoglycopeptide antibiotic used to treat serious Gram-positive bacterial infections.
- A revised telavancin broth microdilution method has been developed, potentially impacting Minimum Inhibitory Concentration (MIC) results.
Purpose of the Study:
- To reestablish quality control (QC) ranges for telavancin using the revised broth microdilution method.
- To ensure accurate and reliable susceptibility testing for key bacterial pathogens.
Main Methods:
- The study involved performing broth microdilution susceptibility testing with telavancin.
- Standardized bacterial strains, including Staphylococcus aureus ATCC 29213, Enterococcus faecalis ATCC 29212, and Streptococcus pneumoniae ATCC 49619, were used.
- MIC values were determined and analyzed to establish new QC ranges.
Main Results:
- The revised method produced lower MIC results compared to the previous method.
- Updated MIC ranges for quality control were determined: Staphylococcus aureus ATCC 29213 (0.03 to 0.12 μg/ml), Enterococcus faecalis ATCC 29212 (0.03 to 0.12 μg/ml), and Streptococcus pneumoniae ATCC 49619 (0.004 to 0.015 μg/ml).
Conclusions:
- The established QC ranges are crucial for validating the revised telavancin susceptibility testing method.
- These updated ranges will support consistent and accurate clinical laboratory testing of telavancin efficacy.

