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671. Impact of Dose-Administration Strategies of the Antistaphylococcal Lysin Exebacase, (CF-301), in Addition to Daptomycin (DAP) in an Experimental Infective Endocarditis (IE) Model due to Methicillin-Resistant Staphylococcus aureus (MRSA)

BACKGROUND: MRSA infections, especially involving the endovascular system (e.g., IE), are associated with unacceptably high morbidity and mortality rates. The use of bacteriophage-derived lysin, which acts as direct lytic agents, represents a novel adjunctive approach against virulent Gram-positive...

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Autores principales: Xiong, Yan, Abdelhady, Wessam, Li, Liang, Schuch, Raymond, Cassino, Cara, Lehoux, Dario, Bayer, Arnold
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6811205/
http://dx.doi.org/10.1093/ofid/ofz360.739
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author Xiong, Yan
Abdelhady, Wessam
Li, Liang
Schuch, Raymond
Cassino, Cara
Lehoux, Dario
Bayer, Arnold
author_facet Xiong, Yan
Abdelhady, Wessam
Li, Liang
Schuch, Raymond
Cassino, Cara
Lehoux, Dario
Bayer, Arnold
author_sort Xiong, Yan
collection PubMed
description BACKGROUND: MRSA infections, especially involving the endovascular system (e.g., IE), are associated with unacceptably high morbidity and mortality rates. The use of bacteriophage-derived lysin, which acts as direct lytic agents, represents a novel adjunctive approach against virulent Gram-positive bacteria, such as MRSA. The current study examined the efficacy of DAP alone or DAP plus CF-301administered on a single day using various dosing regimens, in a rabbit model of MRSA IE. METHODS: Aortic valve IE due to MRSA strain MW2 was induced by the IV administration of ~1 × 10(5)–2 × 10(5) cfu in aortic-catheterized rabbits. At 24-hour post-infection, animals were randomized into one of the 13 groups: (1) vehicle controls given once daily (QD); 2–13) DAP alone (at 4 mg/kg iv QD × 4d; this dose yields significant but modest clearance of MRSA in experimental IE); DAP + CF-301 (given as an IV dose on the first day of DAP treatment only by 5–10 min slow bolus at (mg/kg): 0.70 QD, 0.35 Q12h, 0.23 Q8h, 0.35 QD, 0.175 Q12h, 0.117 Q8h, 0.09 QD, 0.045 Q12h, 0.03 Q8h, 0.06 QD, 0.03 Q12h or 0.03 QD. At 24 hours after the last DAP dose, three target organs were quantitatively cultured (cardiac vegetations; kidneys and spleen). Data for each organ were calculated as mean log(10) cfu/g of tissue (±SD). RESULTS: Treatment with DAP alone caused ~2–3 log(10) cfu/g reduction in MRSA densities in all three target tissues vs. vehicle controls. All CF-301 doses given in addition to DAP, even at the lowest CF-301 dose (0.03 mg/kg), significantly reduced MRSA densities further in all target tissues vs. DAP alone (~3 log(10) cfu/g) and vehicle control groups (~6 log(10) cfu/g). In general, DAP plus CF-301 given as a single dose trended toward better microbiologic efficacy than CF-301 given at Q12h or Q8h, although this difference was not statistically significant. CONCLUSION: These results demonstrate that CF-301, given at multiple dose strategies and at different dose regimens, in addition to sublethal DAP, had significant efficacy in further decreasing MRSA densities in relevant target tissues in the IE model (vs. DAP alone and untreated controls). DAP plus a single dose of CF-301 trended to better efficacy than when it was administered in fractionated dose-strategies. DISCLOSURES: All authors: No reported disclosures.
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spelling pubmed-68112052019-10-29 671. Impact of Dose-Administration Strategies of the Antistaphylococcal Lysin Exebacase, (CF-301), in Addition to Daptomycin (DAP) in an Experimental Infective Endocarditis (IE) Model due to Methicillin-Resistant Staphylococcus aureus (MRSA) Xiong, Yan Abdelhady, Wessam Li, Liang Schuch, Raymond Cassino, Cara Lehoux, Dario Bayer, Arnold Open Forum Infect Dis Abstracts BACKGROUND: MRSA infections, especially involving the endovascular system (e.g., IE), are associated with unacceptably high morbidity and mortality rates. The use of bacteriophage-derived lysin, which acts as direct lytic agents, represents a novel adjunctive approach against virulent Gram-positive bacteria, such as MRSA. The current study examined the efficacy of DAP alone or DAP plus CF-301administered on a single day using various dosing regimens, in a rabbit model of MRSA IE. METHODS: Aortic valve IE due to MRSA strain MW2 was induced by the IV administration of ~1 × 10(5)–2 × 10(5) cfu in aortic-catheterized rabbits. At 24-hour post-infection, animals were randomized into one of the 13 groups: (1) vehicle controls given once daily (QD); 2–13) DAP alone (at 4 mg/kg iv QD × 4d; this dose yields significant but modest clearance of MRSA in experimental IE); DAP + CF-301 (given as an IV dose on the first day of DAP treatment only by 5–10 min slow bolus at (mg/kg): 0.70 QD, 0.35 Q12h, 0.23 Q8h, 0.35 QD, 0.175 Q12h, 0.117 Q8h, 0.09 QD, 0.045 Q12h, 0.03 Q8h, 0.06 QD, 0.03 Q12h or 0.03 QD. At 24 hours after the last DAP dose, three target organs were quantitatively cultured (cardiac vegetations; kidneys and spleen). Data for each organ were calculated as mean log(10) cfu/g of tissue (±SD). RESULTS: Treatment with DAP alone caused ~2–3 log(10) cfu/g reduction in MRSA densities in all three target tissues vs. vehicle controls. All CF-301 doses given in addition to DAP, even at the lowest CF-301 dose (0.03 mg/kg), significantly reduced MRSA densities further in all target tissues vs. DAP alone (~3 log(10) cfu/g) and vehicle control groups (~6 log(10) cfu/g). In general, DAP plus CF-301 given as a single dose trended toward better microbiologic efficacy than CF-301 given at Q12h or Q8h, although this difference was not statistically significant. CONCLUSION: These results demonstrate that CF-301, given at multiple dose strategies and at different dose regimens, in addition to sublethal DAP, had significant efficacy in further decreasing MRSA densities in relevant target tissues in the IE model (vs. DAP alone and untreated controls). DAP plus a single dose of CF-301 trended to better efficacy than when it was administered in fractionated dose-strategies. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2019-10-23 /pmc/articles/PMC6811205/ http://dx.doi.org/10.1093/ofid/ofz360.739 Text en © The Author(s) 2019. 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 Abstracts
Xiong, Yan
Abdelhady, Wessam
Li, Liang
Schuch, Raymond
Cassino, Cara
Lehoux, Dario
Bayer, Arnold
671. Impact of Dose-Administration Strategies of the Antistaphylococcal Lysin Exebacase, (CF-301), in Addition to Daptomycin (DAP) in an Experimental Infective Endocarditis (IE) Model due to Methicillin-Resistant Staphylococcus aureus (MRSA)
title 671. Impact of Dose-Administration Strategies of the Antistaphylococcal Lysin Exebacase, (CF-301), in Addition to Daptomycin (DAP) in an Experimental Infective Endocarditis (IE) Model due to Methicillin-Resistant Staphylococcus aureus (MRSA)
title_full 671. Impact of Dose-Administration Strategies of the Antistaphylococcal Lysin Exebacase, (CF-301), in Addition to Daptomycin (DAP) in an Experimental Infective Endocarditis (IE) Model due to Methicillin-Resistant Staphylococcus aureus (MRSA)
title_fullStr 671. Impact of Dose-Administration Strategies of the Antistaphylococcal Lysin Exebacase, (CF-301), in Addition to Daptomycin (DAP) in an Experimental Infective Endocarditis (IE) Model due to Methicillin-Resistant Staphylococcus aureus (MRSA)
title_full_unstemmed 671. Impact of Dose-Administration Strategies of the Antistaphylococcal Lysin Exebacase, (CF-301), in Addition to Daptomycin (DAP) in an Experimental Infective Endocarditis (IE) Model due to Methicillin-Resistant Staphylococcus aureus (MRSA)
title_short 671. Impact of Dose-Administration Strategies of the Antistaphylococcal Lysin Exebacase, (CF-301), in Addition to Daptomycin (DAP) in an Experimental Infective Endocarditis (IE) Model due to Methicillin-Resistant Staphylococcus aureus (MRSA)
title_sort 671. impact of dose-administration strategies of the antistaphylococcal lysin exebacase, (cf-301), in addition to daptomycin (dap) in an experimental infective endocarditis (ie) model due to methicillin-resistant staphylococcus aureus (mrsa)
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6811205/
http://dx.doi.org/10.1093/ofid/ofz360.739
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