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In vitro Activity of Cefiderocol against Globally Collected Carbapenem-Resistant Gram-Negative Bacteria Isolated from Urinary Track Source: SIDERO-CR-2014/2016

BACKGROUND: Cefiderocol (S-649266) is a novel siderophore cephalosporin active against a wide variety of Gram-negative bacteria, not only Enterobacteriaceae but also non-fermenting bacteria such as Pseudomonas aeruginosa and Acinetobacter spp., including carbapenem-resistant strains. This potent act...

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Autores principales: Tsuji, Masakatsu, Hackel, Meredith, Echols, Roger, Yamano, Yoshinori, Sahm, Dan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5631406/
http://dx.doi.org/10.1093/ofid/ofx163.895
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author Tsuji, Masakatsu
Hackel, Meredith
Echols, Roger
Yamano, Yoshinori
Sahm, Dan
author_facet Tsuji, Masakatsu
Hackel, Meredith
Echols, Roger
Yamano, Yoshinori
Sahm, Dan
author_sort Tsuji, Masakatsu
collection PubMed
description BACKGROUND: Cefiderocol (S-649266) is a novel siderophore cephalosporin active against a wide variety of Gram-negative bacteria, not only Enterobacteriaceae but also non-fermenting bacteria such as Pseudomonas aeruginosa and Acinetobacter spp., including carbapenem-resistant strains. This potent activity is due to its efficient penetration through the outer membrane via active iron transporter systems and its high stability to both serine- and metallo-carbapenemases.This study evaluated the in vitro activity of cefiderocol and comparator agents against carbapenem-resistant clinical isolates collected from urinary track source in 2014–2016 from global countries. METHODS /METHODS: Carbapenem-resistant Enterobacteriaceae (CRE) and multidrug-resistant (MDR) non-fermenters (defined as resistant to imipenem, ciprofloxacin and amikacin) were collected globally from 2014 to 2016 by IHMA Inc. A total of 226 Enterobacteriaceae, 44 Acinetobacter baumannii, 45 P. aeruginosa, 7 Stenotrophomonas maltophilia and 1 Burkholderia cepacia isolated from a urinary track source were tested. MICs were determined for cefiderocol, cefepime (FEP), ceftazidime-avibactam (CZA), ceftolozane-tazobactam (C/T), ciprofloxacin (CIP), colistin (CST), and meropenem (MEM) by broth microdilution and interpreted according to CLSI 2016 guidelines. As recommended by CLSI, cefiderocol was tested in iron-depleted cation-adjusted Mueller Hinton broth. Quality control testing was performed on each day of testing by using E. coli ATCC25922 and P. aeruginosa ATCC27853. RESULTS: MIC(90) of cefiderocol against carbapenem-resistant Enterobacteriaceae, MDR P. aeruginosa, MDR A. baumannii, and S. maltophilia were 4 µg/mL or less. However, MEM, C/T and CZA had MIC(90)s of >64µg/mL. Cefiderocol demonstrated potent in vitro activity against carbapenem-resistant Enterobacteriaceae, A. baumannii, and P. aeruginosa isolates collected from a UTI source. At 4 µg/mL or less, cefiderocol inhibited the growth of 95.8% of the isolates. CONCLUSION: These results strongly indicated that cefiderocol is a promising candidate for the treatment of the serious infections caused by cUTI isolated Gram-negative bacteria including carbapenem-resistant strains. DISCLOSURES: M. Tsuji, Shionogi & Co.: Employee, Salary; M. Hackel, IHMA: Employee, Salary; R. Echols, Shionogi & CO., LTD.: Consultant, Consulting fee; Y. Yamano, Shionogi & Co.: Employee, Salary
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spelling pubmed-56314062017-11-07 In vitro Activity of Cefiderocol against Globally Collected Carbapenem-Resistant Gram-Negative Bacteria Isolated from Urinary Track Source: SIDERO-CR-2014/2016 Tsuji, Masakatsu Hackel, Meredith Echols, Roger Yamano, Yoshinori Sahm, Dan Open Forum Infect Dis Abstracts BACKGROUND: Cefiderocol (S-649266) is a novel siderophore cephalosporin active against a wide variety of Gram-negative bacteria, not only Enterobacteriaceae but also non-fermenting bacteria such as Pseudomonas aeruginosa and Acinetobacter spp., including carbapenem-resistant strains. This potent activity is due to its efficient penetration through the outer membrane via active iron transporter systems and its high stability to both serine- and metallo-carbapenemases.This study evaluated the in vitro activity of cefiderocol and comparator agents against carbapenem-resistant clinical isolates collected from urinary track source in 2014–2016 from global countries. METHODS /METHODS: Carbapenem-resistant Enterobacteriaceae (CRE) and multidrug-resistant (MDR) non-fermenters (defined as resistant to imipenem, ciprofloxacin and amikacin) were collected globally from 2014 to 2016 by IHMA Inc. A total of 226 Enterobacteriaceae, 44 Acinetobacter baumannii, 45 P. aeruginosa, 7 Stenotrophomonas maltophilia and 1 Burkholderia cepacia isolated from a urinary track source were tested. MICs were determined for cefiderocol, cefepime (FEP), ceftazidime-avibactam (CZA), ceftolozane-tazobactam (C/T), ciprofloxacin (CIP), colistin (CST), and meropenem (MEM) by broth microdilution and interpreted according to CLSI 2016 guidelines. As recommended by CLSI, cefiderocol was tested in iron-depleted cation-adjusted Mueller Hinton broth. Quality control testing was performed on each day of testing by using E. coli ATCC25922 and P. aeruginosa ATCC27853. RESULTS: MIC(90) of cefiderocol against carbapenem-resistant Enterobacteriaceae, MDR P. aeruginosa, MDR A. baumannii, and S. maltophilia were 4 µg/mL or less. However, MEM, C/T and CZA had MIC(90)s of >64µg/mL. Cefiderocol demonstrated potent in vitro activity against carbapenem-resistant Enterobacteriaceae, A. baumannii, and P. aeruginosa isolates collected from a UTI source. At 4 µg/mL or less, cefiderocol inhibited the growth of 95.8% of the isolates. CONCLUSION: These results strongly indicated that cefiderocol is a promising candidate for the treatment of the serious infections caused by cUTI isolated Gram-negative bacteria including carbapenem-resistant strains. DISCLOSURES: M. Tsuji, Shionogi & Co.: Employee, Salary; M. Hackel, IHMA: Employee, Salary; R. Echols, Shionogi & CO., LTD.: Consultant, Consulting fee; Y. Yamano, Shionogi & Co.: Employee, Salary Oxford University Press 2017-10-04 /pmc/articles/PMC5631406/ http://dx.doi.org/10.1093/ofid/ofx163.895 Text en © The Author 2017. 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
Tsuji, Masakatsu
Hackel, Meredith
Echols, Roger
Yamano, Yoshinori
Sahm, Dan
In vitro Activity of Cefiderocol against Globally Collected Carbapenem-Resistant Gram-Negative Bacteria Isolated from Urinary Track Source: SIDERO-CR-2014/2016
title In vitro Activity of Cefiderocol against Globally Collected Carbapenem-Resistant Gram-Negative Bacteria Isolated from Urinary Track Source: SIDERO-CR-2014/2016
title_full In vitro Activity of Cefiderocol against Globally Collected Carbapenem-Resistant Gram-Negative Bacteria Isolated from Urinary Track Source: SIDERO-CR-2014/2016
title_fullStr In vitro Activity of Cefiderocol against Globally Collected Carbapenem-Resistant Gram-Negative Bacteria Isolated from Urinary Track Source: SIDERO-CR-2014/2016
title_full_unstemmed In vitro Activity of Cefiderocol against Globally Collected Carbapenem-Resistant Gram-Negative Bacteria Isolated from Urinary Track Source: SIDERO-CR-2014/2016
title_short In vitro Activity of Cefiderocol against Globally Collected Carbapenem-Resistant Gram-Negative Bacteria Isolated from Urinary Track Source: SIDERO-CR-2014/2016
title_sort in vitro activity of cefiderocol against globally collected carbapenem-resistant gram-negative bacteria isolated from urinary track source: sidero-cr-2014/2016
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5631406/
http://dx.doi.org/10.1093/ofid/ofx163.895
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