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In vitro activity of newer antimicrobials against penicillin non-susceptible strains of Streptococcus pneumoniae

Background: Since the first isolation of Streptococcus pneumoniae with low penicillin susceptibility in the 1960s, resistant strains have spread over the globe, causing substantial problems in the treatment of pneumococcal infections. However, in Germany, rates of non-susceptibility are still below...

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Autores principales: Hipp, Marlene, Burckhardt, Irene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6612959/
https://www.ncbi.nlm.nih.gov/pubmed/31308709
http://dx.doi.org/10.2147/IDR.S202789
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author Hipp, Marlene
Burckhardt, Irene
author_facet Hipp, Marlene
Burckhardt, Irene
author_sort Hipp, Marlene
collection PubMed
description Background: Since the first isolation of Streptococcus pneumoniae with low penicillin susceptibility in the 1960s, resistant strains have spread over the globe, causing substantial problems in the treatment of pneumococcal infections. However, in Germany, rates of non-susceptibility are still below 5%. Methods: Since 2009 clinical pneumococcal strains have been collected at the Center for Infectious Diseases, Heidelberg University Hospital, Germany. In this study, 56 of these strains were chosen due to their decreased penicillin susceptibility (minimal inhibitory concentration (MIC)≥0.12 µg/mL). Sixteen of these strains even showed an MIC of ≥2 µg/mL. We examined the in vitro activity of newer antimicrobials known to be active against Gram-positive bacteria. For this purpose MICs of ceftaroline, ceftobiprole, dalbavancin, delafloxacin, eravacycline, tedizolid, and telavancin were determined and evaluated. Results: All of the 7 antimicrobial agents inhibited pneumococcal growth at concentrations of 0.5 µg/mL or lower. Currently, clinical breakpoints are only available for two substances, ceftaroline and ceftobiprole. According to these breakpoints, all MICs were below the susceptibility breakpoint; however, there was a correlation between high penicillin MICs (≥2 µg/mL) and MICs near the ceftaroline and ceftobiprole susceptibility breakpoint. The other agents showed very promising effects against all tested strains with the lowest MIC90 of 0.002 µg/mL for telavancin. Conclusion: Consequently, this study demonstrates the promising in vitro activity of newer antimicrobials against penicillin non-susceptible strains of S. pneumoniae.
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spelling pubmed-66129592019-07-15 In vitro activity of newer antimicrobials against penicillin non-susceptible strains of Streptococcus pneumoniae Hipp, Marlene Burckhardt, Irene Infect Drug Resist Original Research Background: Since the first isolation of Streptococcus pneumoniae with low penicillin susceptibility in the 1960s, resistant strains have spread over the globe, causing substantial problems in the treatment of pneumococcal infections. However, in Germany, rates of non-susceptibility are still below 5%. Methods: Since 2009 clinical pneumococcal strains have been collected at the Center for Infectious Diseases, Heidelberg University Hospital, Germany. In this study, 56 of these strains were chosen due to their decreased penicillin susceptibility (minimal inhibitory concentration (MIC)≥0.12 µg/mL). Sixteen of these strains even showed an MIC of ≥2 µg/mL. We examined the in vitro activity of newer antimicrobials known to be active against Gram-positive bacteria. For this purpose MICs of ceftaroline, ceftobiprole, dalbavancin, delafloxacin, eravacycline, tedizolid, and telavancin were determined and evaluated. Results: All of the 7 antimicrobial agents inhibited pneumococcal growth at concentrations of 0.5 µg/mL or lower. Currently, clinical breakpoints are only available for two substances, ceftaroline and ceftobiprole. According to these breakpoints, all MICs were below the susceptibility breakpoint; however, there was a correlation between high penicillin MICs (≥2 µg/mL) and MICs near the ceftaroline and ceftobiprole susceptibility breakpoint. The other agents showed very promising effects against all tested strains with the lowest MIC90 of 0.002 µg/mL for telavancin. Conclusion: Consequently, this study demonstrates the promising in vitro activity of newer antimicrobials against penicillin non-susceptible strains of S. pneumoniae. Dove 2019-07-01 /pmc/articles/PMC6612959/ /pubmed/31308709 http://dx.doi.org/10.2147/IDR.S202789 Text en © 2019 Hipp and Burckhardt. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Hipp, Marlene
Burckhardt, Irene
In vitro activity of newer antimicrobials against penicillin non-susceptible strains of Streptococcus pneumoniae
title In vitro activity of newer antimicrobials against penicillin non-susceptible strains of Streptococcus pneumoniae
title_full In vitro activity of newer antimicrobials against penicillin non-susceptible strains of Streptococcus pneumoniae
title_fullStr In vitro activity of newer antimicrobials against penicillin non-susceptible strains of Streptococcus pneumoniae
title_full_unstemmed In vitro activity of newer antimicrobials against penicillin non-susceptible strains of Streptococcus pneumoniae
title_short In vitro activity of newer antimicrobials against penicillin non-susceptible strains of Streptococcus pneumoniae
title_sort in vitro activity of newer antimicrobials against penicillin non-susceptible strains of streptococcus pneumoniae
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6612959/
https://www.ncbi.nlm.nih.gov/pubmed/31308709
http://dx.doi.org/10.2147/IDR.S202789
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