An optimal method for generating stable vancomycin heteroresistance and intermediate susceptibility in methicillin-resistant Staphylococcus aureus blood isolates under in-vitro vancomycin pressure

Volume: 2 Number: 04 December 1, 2012
  • Riad Khatib
  • Jinson Jose
  • Leonard B Johnson
  • Kathleen Riederer
  • Stephen Shemes
EN TR

An optimal method for generating stable vancomycin heteroresistance and intermediate susceptibility in methicillin-resistant Staphylococcus aureus blood isolates under in-vitro vancomycin pressure

Abstract

Objectives: The relevance of vancomycin intermediately-susceptible (VISA) and hetero-resistant (hVISA) methicillin-resistant Staphylococcus aureus (MRSA) remains uncertain because of their low frequency. In vitro attempts to generate reduced susceptibility have been inconsistent. We describe a simple method for generating VISA/hVISA. Materials and methods: Twenty-four SCCmec type II and IV MRSA blood isolates plus USA100 and USA300 controls were cultured (107 CFU/ml) in BHI broth with 0, 2 and 3 mg/L vancomycin for 10 days followed by 10 days vancomycin-free-passage. We monitored vancomycin minimum inhibitory concentration (MIC; Etest) and population analysis profile-area under the curve (PAP-AUC) ratios of tested isolate/Mu3 during and after vancomycin pressure (VP). PAP-AUC ratios 1.3 were considered consistent with susceptible, hVISA and VISA, respectively. Results: VP at 2 mg/L (VP-2) increased MIC to 3 mg/L in 20 (83.3%) isolates and raised PAP-AUC ratio to hVISA (n=18; 75.0%) and VISA (six; 25.0%) ranges. VP-3 increased MIC to 3 and 4 mg/L in 19 (79.2%) and three (12.5%) isolates, respectively and raised PAP-AUC ratio to hVISA (n=3; 12.5%) and VISA (n=19; 79.2%) ranges. SCCmec IV isolates had lower pre-exposure PAP-AUC ratios (0.48&plusmn;0.14 vs. 0.69&plusmn;0.10; p<0.001) and lower MIC (1.6&plusmn;0.2 vs. 1.8&plusmn;0.2 mg/L; p=0.1) but MIC rise and hVISA/VISA emergence was comparable. MIC and PAP-AUC ratio rises were stable in 20/22 isolates during drug-free passages. Conclusions: VISA/hVISA readily emerges among MRSA SCCmec type II and IV isolates under VP. VP at the MIC level generates hVISA while pressure at slightly higher level results in the VISA phenotype.

Keywords

References

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Details

Primary Language

English

Subjects

Health Care Administration

Journal Section

-

Authors

Riad Khatib This is me

Jinson Jose This is me

Leonard B Johnson This is me

Kathleen Riederer This is me

Stephen Shemes This is me

Publication Date

December 1, 2012

Submission Date

January 12, 2015

Acceptance Date

-

Published in Issue

Year 2012 Volume: 2 Number: 04

APA
Khatib, R., Jose, J., Johnson, L. B., Riederer, K., & Shemes, S. (2012). An optimal method for generating stable vancomycin heteroresistance and intermediate susceptibility in methicillin-resistant Staphylococcus aureus blood isolates under in-vitro vancomycin pressure. Journal of Microbiology and Infectious Diseases, 2(04), 129-134. https://doi.org/10.5799/jmid.123125
AMA
1.Khatib R, Jose J, Johnson LB, Riederer K, Shemes S. An optimal method for generating stable vancomycin heteroresistance and intermediate susceptibility in methicillin-resistant Staphylococcus aureus blood isolates under in-vitro vancomycin pressure. J Microbil Infect Dis. 2012;2(04):129-134. doi:10.5799/jmid.123125
Chicago
Khatib, Riad, Jinson Jose, Leonard B Johnson, Kathleen Riederer, and Stephen Shemes. 2012. “An Optimal Method for Generating Stable Vancomycin Heteroresistance and Intermediate Susceptibility in Methicillin-Resistant Staphylococcus Aureus Blood Isolates under In-Vitro Vancomycin Pressure”. Journal of Microbiology and Infectious Diseases 2 (04): 129-34. https://doi.org/10.5799/jmid.123125.
EndNote
Khatib R, Jose J, Johnson LB, Riederer K, Shemes S (December 1, 2012) An optimal method for generating stable vancomycin heteroresistance and intermediate susceptibility in methicillin-resistant Staphylococcus aureus blood isolates under in-vitro vancomycin pressure. Journal of Microbiology and Infectious Diseases 2 04 129–134.
IEEE
[1]R. Khatib, J. Jose, L. B. Johnson, K. Riederer, and S. Shemes, “An optimal method for generating stable vancomycin heteroresistance and intermediate susceptibility in methicillin-resistant Staphylococcus aureus blood isolates under in-vitro vancomycin pressure”, J Microbil Infect Dis, vol. 2, no. 04, pp. 129–134, Dec. 2012, doi: 10.5799/jmid.123125.
ISNAD
Khatib, Riad - Jose, Jinson - Johnson, Leonard B - Riederer, Kathleen - Shemes, Stephen. “An Optimal Method for Generating Stable Vancomycin Heteroresistance and Intermediate Susceptibility in Methicillin-Resistant Staphylococcus Aureus Blood Isolates under In-Vitro Vancomycin Pressure”. Journal of Microbiology and Infectious Diseases 2/04 (December 1, 2012): 129-134. https://doi.org/10.5799/jmid.123125.
JAMA
1.Khatib R, Jose J, Johnson LB, Riederer K, Shemes S. An optimal method for generating stable vancomycin heteroresistance and intermediate susceptibility in methicillin-resistant Staphylococcus aureus blood isolates under in-vitro vancomycin pressure. J Microbil Infect Dis. 2012;2:129–134.
MLA
Khatib, Riad, et al. “An Optimal Method for Generating Stable Vancomycin Heteroresistance and Intermediate Susceptibility in Methicillin-Resistant Staphylococcus Aureus Blood Isolates under In-Vitro Vancomycin Pressure”. Journal of Microbiology and Infectious Diseases, vol. 2, no. 04, Dec. 2012, pp. 129-34, doi:10.5799/jmid.123125.
Vancouver
1.Riad Khatib, Jinson Jose, Leonard B Johnson, Kathleen Riederer, Stephen Shemes. An optimal method for generating stable vancomycin heteroresistance and intermediate susceptibility in methicillin-resistant Staphylococcus aureus blood isolates under in-vitro vancomycin pressure. J Microbil Infect Dis. 2012 Dec. 1;2(04):129-34. doi:10.5799/jmid.123125

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