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1573. Daptomycin Resistant Enterococcus faecium: Combination Therapy Screening

BACKGROUND: Enterococcus faecium infections are difficult to treat and there is a growing concern regarding the rising occurrence of daptomycin resistance. We have previously demonstrated that only daptomycin plus ampicillin combination was effective against DAP-R E. faecium R497. The efficacy and s...

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Autores principales: Kebriaei, Razieh, Stamper, Kyle, Lev, Katherine, Morrisette, Taylor, Arias, Cesar A, Rybak, Michael J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7778037/
http://dx.doi.org/10.1093/ofid/ofaa439.1753
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author Kebriaei, Razieh
Stamper, Kyle
Lev, Katherine
Morrisette, Taylor
Arias, Cesar A
Rybak, Michael J
author_facet Kebriaei, Razieh
Stamper, Kyle
Lev, Katherine
Morrisette, Taylor
Arias, Cesar A
Rybak, Michael J
author_sort Kebriaei, Razieh
collection PubMed
description BACKGROUND: Enterococcus faecium infections are difficult to treat and there is a growing concern regarding the rising occurrence of daptomycin resistance. We have previously demonstrated that only daptomycin plus ampicillin combination was effective against DAP-R E. faecium R497. The efficacy and systematic screening DAP plus β-lactams and DAP plus other combinations against daptomycin-resistant strains of E. faecium has not been investigated. Here, we evaluated 40 selected single, dual and triple combinations of antibacterial regimens against two clinical isolates of DAP-R E. faecium (R497 and R496 (with daptomycin MIC of 16 and 32 µg/ml, respectively). METHODS: E.faecium R497 and R496 were tested against an array of antibacterial agents including daptomycin, tigecycline, linezolid, ertapenem, ceftaroline and ceftriaxone using MIC susceptibility tests and 24h time-kill curves (TKC). All susceptibility tests and TKCs were performed in MHB broth containing 50 mg/L calcium. TKCs were performed at half MIC or free peak concentration of each antibacterial (whichever was lower). Synergy was defined as >2 log(10) CFU/ml decrease compared to the most potent antibacterial agent. RESULTS: Susceptibility tests demonstrated resistance to all listed β-lactams for both organisms. TKCs demonstrated that combination of daptomycin-ertapenem, daptomycin-ceftriaxone and daptomycin-ceftaroline was not effective against R497. However, addition of ceftriaxone or linezolid to either daptomycin-ertapenem or daptomycin-ceftaroline combinations resulted in synergy against this organism. Combinations of daptomycin-ertapenem and daptomycin-ceftaroline were synergistic against R496. Addition of linezolid, ceftriaxone or tigecycline to either daptomycin-ceftaroline or daptomycin-ertapenem combination did not increase killing activity against R496. CONCLUSION: Differential affinity of β-lactams to specific PBP isotypes seems to be a key parameter for the success of daptomycin- β-lactam combinations against multi-drug resistant E. faecium . The optimized use of double β-lactam therapy in addition to daptomycin can potentially lead to improved patient outcomes and preserving antibiotic therapy for serious enterococcus infections. DISCLOSURES: Cesar A. Arias, MD, MSc, PhD, FIDSA, Entasis Therapeutics (Scientific Research Study Investigator)MeMed (Scientific Research Study Investigator)Merck (Grant/Research Support) Michael J. Rybak, PharmD, MPH, PhD, Paratek (Grant/Research Support)
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spelling pubmed-77780372021-01-07 1573. Daptomycin Resistant Enterococcus faecium: Combination Therapy Screening Kebriaei, Razieh Stamper, Kyle Lev, Katherine Morrisette, Taylor Arias, Cesar A Rybak, Michael J Open Forum Infect Dis Poster Abstracts BACKGROUND: Enterococcus faecium infections are difficult to treat and there is a growing concern regarding the rising occurrence of daptomycin resistance. We have previously demonstrated that only daptomycin plus ampicillin combination was effective against DAP-R E. faecium R497. The efficacy and systematic screening DAP plus β-lactams and DAP plus other combinations against daptomycin-resistant strains of E. faecium has not been investigated. Here, we evaluated 40 selected single, dual and triple combinations of antibacterial regimens against two clinical isolates of DAP-R E. faecium (R497 and R496 (with daptomycin MIC of 16 and 32 µg/ml, respectively). METHODS: E.faecium R497 and R496 were tested against an array of antibacterial agents including daptomycin, tigecycline, linezolid, ertapenem, ceftaroline and ceftriaxone using MIC susceptibility tests and 24h time-kill curves (TKC). All susceptibility tests and TKCs were performed in MHB broth containing 50 mg/L calcium. TKCs were performed at half MIC or free peak concentration of each antibacterial (whichever was lower). Synergy was defined as >2 log(10) CFU/ml decrease compared to the most potent antibacterial agent. RESULTS: Susceptibility tests demonstrated resistance to all listed β-lactams for both organisms. TKCs demonstrated that combination of daptomycin-ertapenem, daptomycin-ceftriaxone and daptomycin-ceftaroline was not effective against R497. However, addition of ceftriaxone or linezolid to either daptomycin-ertapenem or daptomycin-ceftaroline combinations resulted in synergy against this organism. Combinations of daptomycin-ertapenem and daptomycin-ceftaroline were synergistic against R496. Addition of linezolid, ceftriaxone or tigecycline to either daptomycin-ceftaroline or daptomycin-ertapenem combination did not increase killing activity against R496. CONCLUSION: Differential affinity of β-lactams to specific PBP isotypes seems to be a key parameter for the success of daptomycin- β-lactam combinations against multi-drug resistant E. faecium . The optimized use of double β-lactam therapy in addition to daptomycin can potentially lead to improved patient outcomes and preserving antibiotic therapy for serious enterococcus infections. DISCLOSURES: Cesar A. Arias, MD, MSc, PhD, FIDSA, Entasis Therapeutics (Scientific Research Study Investigator)MeMed (Scientific Research Study Investigator)Merck (Grant/Research Support) Michael J. Rybak, PharmD, MPH, PhD, Paratek (Grant/Research Support) Oxford University Press 2020-12-31 /pmc/articles/PMC7778037/ http://dx.doi.org/10.1093/ofid/ofaa439.1753 Text en © The Author 2020. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Poster Abstracts
Kebriaei, Razieh
Stamper, Kyle
Lev, Katherine
Morrisette, Taylor
Arias, Cesar A
Rybak, Michael J
1573. Daptomycin Resistant Enterococcus faecium: Combination Therapy Screening
title 1573. Daptomycin Resistant Enterococcus faecium: Combination Therapy Screening
title_full 1573. Daptomycin Resistant Enterococcus faecium: Combination Therapy Screening
title_fullStr 1573. Daptomycin Resistant Enterococcus faecium: Combination Therapy Screening
title_full_unstemmed 1573. Daptomycin Resistant Enterococcus faecium: Combination Therapy Screening
title_short 1573. Daptomycin Resistant Enterococcus faecium: Combination Therapy Screening
title_sort 1573. daptomycin resistant enterococcus faecium: combination therapy screening
topic Poster Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7778037/
http://dx.doi.org/10.1093/ofid/ofaa439.1753
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