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In Vitro Activity of Cefiderocol against Clinical Gram-Negative Isolates Originating from Germany in 2016/17
Antimicrobial resistance poses a global threat to public health. Of great concern are Acinetobacter baumannii, Pseudomonas aeruginosa and Enterobacterales with resistance to carbapenems or third-generation cephalosporins. The aim of the present study was to investigate the in vitro activity of the n...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10215668/ https://www.ncbi.nlm.nih.gov/pubmed/37237767 http://dx.doi.org/10.3390/antibiotics12050864 |
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author | Wohlfarth, Esther Kresken, Michael Deuchert, Fabian Gatermann, Sören G. Pfeifer, Yvonne Pfennigwerth, Niels Seifert, Harald Higgins, Paul G. Werner, Guido |
author_facet | Wohlfarth, Esther Kresken, Michael Deuchert, Fabian Gatermann, Sören G. Pfeifer, Yvonne Pfennigwerth, Niels Seifert, Harald Higgins, Paul G. Werner, Guido |
author_sort | Wohlfarth, Esther |
collection | PubMed |
description | Antimicrobial resistance poses a global threat to public health. Of great concern are Acinetobacter baumannii, Pseudomonas aeruginosa and Enterobacterales with resistance to carbapenems or third-generation cephalosporins. The aim of the present study was to investigate the in vitro activity of the novel siderophore cephaloporin cefiderocol (CID) and four comparator β-lactam-β-lactamase-inhibitor combinations and to give insights into the genetic background of CID-resistant isolates. In total, 301 clinical Enterobacterales and non-fermenting bacterial isolates were selected for this study, including randomly chosen isolates (set I, n = 195) and challenge isolates (set II, n = 106; enriched with ESBL and carbapenemase producers, as well as colistin-resistant isolates). Isolates displayed CID MIC(50/90) values of 0.12/0.5 mg/L (set I) and 0.5/1 mg/L (set II). Overall, the CID activity was superior to the comparators against A. baumannii, Stenotrophomonas maltophilia and set II isolates of P. aeruginosa. There were eight CID-resistant isolates detected (MIC > 2 mg/L): A. baumannii (n = 1), E. cloacae complex (n = 5) and P. aeruginosa (n = 2). Sequencing analyses of these isolates detected the acquired β-lactamase (bla) genes bla(NDM-1,) bla(SHV-12) and naturally occurring bla(OXA-396), bla(ACT-)type and bla(CMH-3). In conclusion, CID revealed potent activity against clinically relevant organisms of multidrug-resistant Enterobacterales and non-fermenters. |
format | Online Article Text |
id | pubmed-10215668 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102156682023-05-27 In Vitro Activity of Cefiderocol against Clinical Gram-Negative Isolates Originating from Germany in 2016/17 Wohlfarth, Esther Kresken, Michael Deuchert, Fabian Gatermann, Sören G. Pfeifer, Yvonne Pfennigwerth, Niels Seifert, Harald Higgins, Paul G. Werner, Guido Antibiotics (Basel) Article Antimicrobial resistance poses a global threat to public health. Of great concern are Acinetobacter baumannii, Pseudomonas aeruginosa and Enterobacterales with resistance to carbapenems or third-generation cephalosporins. The aim of the present study was to investigate the in vitro activity of the novel siderophore cephaloporin cefiderocol (CID) and four comparator β-lactam-β-lactamase-inhibitor combinations and to give insights into the genetic background of CID-resistant isolates. In total, 301 clinical Enterobacterales and non-fermenting bacterial isolates were selected for this study, including randomly chosen isolates (set I, n = 195) and challenge isolates (set II, n = 106; enriched with ESBL and carbapenemase producers, as well as colistin-resistant isolates). Isolates displayed CID MIC(50/90) values of 0.12/0.5 mg/L (set I) and 0.5/1 mg/L (set II). Overall, the CID activity was superior to the comparators against A. baumannii, Stenotrophomonas maltophilia and set II isolates of P. aeruginosa. There were eight CID-resistant isolates detected (MIC > 2 mg/L): A. baumannii (n = 1), E. cloacae complex (n = 5) and P. aeruginosa (n = 2). Sequencing analyses of these isolates detected the acquired β-lactamase (bla) genes bla(NDM-1,) bla(SHV-12) and naturally occurring bla(OXA-396), bla(ACT-)type and bla(CMH-3). In conclusion, CID revealed potent activity against clinically relevant organisms of multidrug-resistant Enterobacterales and non-fermenters. MDPI 2023-05-06 /pmc/articles/PMC10215668/ /pubmed/37237767 http://dx.doi.org/10.3390/antibiotics12050864 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wohlfarth, Esther Kresken, Michael Deuchert, Fabian Gatermann, Sören G. Pfeifer, Yvonne Pfennigwerth, Niels Seifert, Harald Higgins, Paul G. Werner, Guido In Vitro Activity of Cefiderocol against Clinical Gram-Negative Isolates Originating from Germany in 2016/17 |
title | In Vitro Activity of Cefiderocol against Clinical Gram-Negative Isolates Originating from Germany in 2016/17 |
title_full | In Vitro Activity of Cefiderocol against Clinical Gram-Negative Isolates Originating from Germany in 2016/17 |
title_fullStr | In Vitro Activity of Cefiderocol against Clinical Gram-Negative Isolates Originating from Germany in 2016/17 |
title_full_unstemmed | In Vitro Activity of Cefiderocol against Clinical Gram-Negative Isolates Originating from Germany in 2016/17 |
title_short | In Vitro Activity of Cefiderocol against Clinical Gram-Negative Isolates Originating from Germany in 2016/17 |
title_sort | in vitro activity of cefiderocol against clinical gram-negative isolates originating from germany in 2016/17 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10215668/ https://www.ncbi.nlm.nih.gov/pubmed/37237767 http://dx.doi.org/10.3390/antibiotics12050864 |
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