In vitro antimicrobial activity of S-649266, a catechol-substituted siderophore cephalosporin, when tested against non-fermenting Gram-negative bacteria
S-649266 is a parenteral siderophore cephalosporin antibiotic with a catechol moiety on its side chain. The in vitro antimicrobial activity of S-649266 against non-fermenting Gram-negative bacteria was evaluated and compared with the activities of meropenem, levofloxacin, cefepime, ceftazidime and p...
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Published in: | Journal of antimicrobial chemotherapy Vol. 71; no. 3; pp. 670 - 677 |
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Abstract | S-649266 is a parenteral siderophore cephalosporin antibiotic with a catechol moiety on its side chain. The in vitro antimicrobial activity of S-649266 against non-fermenting Gram-negative bacteria was evaluated and compared with the activities of meropenem, levofloxacin, cefepime, ceftazidime and piperacillin/tazobactam.
MIC values of S-649266 were determined in Mueller-Hinton broth or Iso-Sensitest broth supplemented with apo-transferrin.
S-649266 showed potent in vitro activity against the non-fermenting Gram-negative bacteria Acinetobacter baumannii, Pseudomonas aeruginosa and Stenotrophomonas maltophilia, including MDR strains such as carbapenem-resistant A. baumannii and metallo-β-lactamase-producing P. aeruginosa. MIC90s of S-649266 for A. baumannii, P. aeruginosa and S. maltophilia were 2, 1 and 0.5 mg/L, respectively, whereas MIC90s of meropenem were >16 mg/L. S-649266 showed potent in vitro activities against A. baumannii producing carbapenemases such as OXA-type β-lactamases, and P. aeruginosa producing metallo-β-lactamases such as IMP type and VIM type. MIC90 values for these A. baumannii strains and P. aeruginosa strains were 8 and 4 mg/L, respectively.
S-649266 is a novel antibiotic with potent in vitro activity against a range of non-fermenting Gram-negative bacteria, including MDR strains. |
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AbstractList | S-649266 is a parenteral siderophore cephalosporin antibiotic with a catechol moiety on its side chain. The in vitro antimicrobial activity of S-649266 against non-fermenting Gram-negative bacteria was evaluated and compared with the activities of meropenem, levofloxacin, cefepime, ceftazidime and piperacillin/tazobactam.
MIC values of S-649266 were determined in Mueller-Hinton broth or Iso-Sensitest broth supplemented with apo-transferrin.
S-649266 showed potent in vitro activity against the non-fermenting Gram-negative bacteria Acinetobacter baumannii, Pseudomonas aeruginosa and Stenotrophomonas maltophilia, including MDR strains such as carbapenem-resistant A. baumannii and metallo-β-lactamase-producing P. aeruginosa. MIC90s of S-649266 for A. baumannii, P. aeruginosa and S. maltophilia were 2, 1 and 0.5 mg/L, respectively, whereas MIC90s of meropenem were >16 mg/L. S-649266 showed potent in vitro activities against A. baumannii producing carbapenemases such as OXA-type β-lactamases, and P. aeruginosa producing metallo-β-lactamases such as IMP type and VIM type. MIC90 values for these A. baumannii strains and P. aeruginosa strains were 8 and 4 mg/L, respectively.
S-649266 is a novel antibiotic with potent in vitro activity against a range of non-fermenting Gram-negative bacteria, including MDR strains. OBJECTIVESS-649266 is a parenteral siderophore cephalosporin antibiotic with a catechol moiety on its side chain. The in vitro antimicrobial activity of S-649266 against non-fermenting Gram-negative bacteria was evaluated and compared with the activities of meropenem, levofloxacin, cefepime, ceftazidime and piperacillin/tazobactam.METHODSMIC values of S-649266 were determined in Mueller-Hinton broth or Iso-Sensitest broth supplemented with apo-transferrin.RESULTSS-649266 showed potent in vitro activity against the non-fermenting Gram-negative bacteria Acinetobacter baumannii, Pseudomonas aeruginosa and Stenotrophomonas maltophilia, including MDR strains such as carbapenem-resistant A. baumannii and metallo-β-lactamase-producing P. aeruginosa. MIC90s of S-649266 for A. baumannii, P. aeruginosa and S. maltophilia were 2, 1 and 0.5 mg/L, respectively, whereas MIC90s of meropenem were >16 mg/L. S-649266 showed potent in vitro activities against A. baumannii producing carbapenemases such as OXA-type β-lactamases, and P. aeruginosa producing metallo-β-lactamases such as IMP type and VIM type. MIC90 values for these A. baumannii strains and P. aeruginosa strains were 8 and 4 mg/L, respectively.CONCLUSIONSS-649266 is a novel antibiotic with potent in vitro activity against a range of non-fermenting Gram-negative bacteria, including MDR strains. Objectives S-649266 is a parenteral siderophore cephalosporin antibiotic with a catechol moiety on its side chain. The in vitro antimicrobial activity of S-649266 against non-fermenting Gram-negative bacteria was evaluated and compared with the activities of meropenem, levofloxacin, cefepime, ceftazidime and piperacillin/tazobactam. Methods MIC values of S-649266 were determined in Mueller-Hinton broth or Iso-Sensitest broth supplemented with apo-transferrin. Results S-649266 showed potent in vitro activity against the non-fermenting Gram-negative bacteria Acinetobacter baumannii, Pseudomonas aeruginosa and Stenotrophomonas maltophilia, including MDR strains such as carbapenem-resistant A. baumannii and metallo- beta -lactamase-producing P. aeruginosa. MIC sub(90)s of S-649266 for A. baumannii, P. aeruginosa and S. maltophilia were 2, 1 and 0.5 mg/L, respectively, whereas MIC sub(90)s of meropenem were >16 mg/L. S-649266 showed potent in vitro activities against A. baumannii producing carbapenemases such as OXA-type beta -lactamases, and P. aeruginosa producing metallo- beta -lactamases such as IMP type and VIM type. MIC sub(90) values for these A. baumannii strains and P. aeruginosa strains were 8 and 4 mg/L, respectively. Conclusions S-649266 is a novel antibiotic with potent in vitro activity against a range of non-fermenting Gram-negative bacteria, including MDR strains. S-649266 is a parenteral siderophore cephalosporin antibiotic with a catechol moiety on its side chain. The in vitro antimicrobial activity of S-649266 against non-fermenting Gram-negative bacteria was evaluated and compared with the activities of meropenem, levofloxacin, cefepime, ceftazidime and piperacillin/tazobactam. MIC values of S-649266 were determined in Mueller-Hinton broth or Iso-Sensitest broth supplemented with apo-transferrin. S-649266 showed potent in vitro activity against the non-fermenting Gram-negative bacteria Acinetobacter baumannii, Pseudomonas aeruginosa and Stenotrophomonas maltophilia, including MDR strains such as carbapenem-resistant A. baumannii and metallo-β-lactamase-producing P. aeruginosa. MIC... of S-649266 for A. baumannii, P. aeruginosa and S. maltophilia were 2, 1 and 0.5 mg/L, respectively, whereas MIC... of meropenem were >16 mg/L. S-649266 showed potent in vitro activities against A. baumannii producing carbapenemases such as OXA-type β-lactamases, and P. aeruginosa producing metallo-β-lactamases such as IMP type and VIM type. MIC... values for these A. baumannii strains and P. aeruginosa strains were 8 and 4 mg/L, respectively. S-649266 is a novel antibiotic with potent in vitro activity against a range of non-fermenting Gram-negative bacteria, including MDR strains. (ProQuest: ... denotes formulae/symbols omitted.) |
Author | Kohira, Naoki Bouchillon, Samuel K Yamano, Yoshinori West, Joshua Rittenhouse, Stephen Tsuji, Masakatsu Sader, Helio S Jones, Ronald N Yoshizawa, Hidenori Ito, Akinobu Rhomberg, Paul R Nakamura, Rio |
Author_xml | – sequence: 1 givenname: Akinobu surname: Ito fullname: Ito, Akinobu email: akinobu.ito@shionogi.co.jp organization: Discovery Research Laboratory for Core Therapeutic Areas, Shionogi & Co., Ltd, Toyonaka, Osaka, Japan akinobu.ito@shionogi.co.jp – sequence: 2 givenname: Naoki surname: Kohira fullname: Kohira, Naoki organization: Discovery Research Laboratory for Core Therapeutic Areas, Shionogi & Co., Ltd, Toyonaka, Osaka, Japan – sequence: 3 givenname: Samuel K surname: Bouchillon fullname: Bouchillon, Samuel K organization: International Health Management Associates, Inc., Schaumberg, IL 60173, USA – sequence: 4 givenname: Joshua surname: West fullname: West, Joshua organization: GlaxoSmithKline, Collegeville, PA 19426, USA – sequence: 5 givenname: Stephen surname: Rittenhouse fullname: Rittenhouse, Stephen organization: GlaxoSmithKline, Collegeville, PA 19426, USA – sequence: 6 givenname: Helio S surname: Sader fullname: Sader, Helio S organization: JMI Laboratories, North Liberty, IA 52317, USA – sequence: 7 givenname: Paul R surname: Rhomberg fullname: Rhomberg, Paul R organization: JMI Laboratories, North Liberty, IA 52317, USA – sequence: 8 givenname: Ronald N surname: Jones fullname: Jones, Ronald N organization: JMI Laboratories, North Liberty, IA 52317, USA – sequence: 9 givenname: Hidenori surname: Yoshizawa fullname: Yoshizawa, Hidenori organization: Discovery Research Laboratory for Core Therapeutic Areas, Shionogi & Co., Ltd, Toyonaka, Osaka, Japan – sequence: 10 givenname: Rio surname: Nakamura fullname: Nakamura, Rio organization: Discovery Research Laboratory for Core Therapeutic Areas, Shionogi & Co., Ltd, Toyonaka, Osaka, Japan – sequence: 11 givenname: Masakatsu surname: Tsuji fullname: Tsuji, Masakatsu organization: Discovery Research Laboratory for Core Therapeutic Areas, Shionogi & Co., Ltd, Toyonaka, Osaka, Japan – sequence: 12 givenname: Yoshinori surname: Yamano fullname: Yamano, Yoshinori organization: Discovery Research Laboratory for Core Therapeutic Areas, Shionogi & Co., Ltd, Toyonaka, Osaka, Japan |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/26645269$$D View this record in MEDLINE/PubMed |
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ContentType | Journal Article |
Copyright | The Author 2015. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com. Copyright Oxford Publishing Limited(England) Mar 2016 |
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References_xml | – ident: 2016020508432041000_71.3.670.36 – ident: 2016020508432041000_71.3.670.16 doi: 10.1016/j.ijantimicag.2007.12.016 – ident: 2016020508432041000_71.3.670.24 doi: 10.1128/AAC.00248-09 – ident: 2016020508432041000_71.3.670.1 doi: 10.1016/j.jgar.2014.05.001 – ident: 2016020508432041000_71.3.670.40 – ident: 2016020508432041000_71.3.670.46 – ident: 2016020508432041000_71.3.670.25 doi: 10.1128/CMR.00019-11 – ident: 2016020508432041000_71.3.670.44 – ident: 2016020508432041000_71.3.670.19 doi: 10.1128/AAC.46.8.2696-2699.2002 – ident: 2016020508432041000_71.3.670.29 doi: 10.1093/clinids/10.4.765 – ident: 2016020508432041000_71.3.670.5 doi: 10.1093/jac/dkp428 – ident: 2016020508432041000_71.3.670.7 doi: 10.1111/j.1469-0691.2006.01456.x – ident: 2016020508432041000_71.3.670.35 doi: 10.1128/AAC.44.2.287-293.2000 – ident: 2016020508432041000_71.3.670.47 – ident: 2016020508432041000_71.3.670.28 doi: 10.1089/107662902760326904 – ident: 2016020508432041000_71.3.670.21 doi: 10.1128/CMR.18.2.306-325.2005 – ident: 2016020508432041000_71.3.670.4 doi: 10.1016/j.ijantimicag.2012.09.008 – ident: 2016020508432041000_71.3.670.33 doi: 10.1016/0167-4781(94)90011-6 – ident: 2016020508432041000_71.3.670.9 doi: 10.1111/j.1469-0691.2005.01320.x – volume: 45 start-page: 131 year: 1999 ident: 2016020508432041000_71.3.670.37 article-title: Absolute or relative measurement of carbohydrate-deficient transferrin in serum? Experiences with three immunological assays publication-title: Clin Chem doi: 10.1093/clinchem/45.1.131 contributor: fullname: Helander – ident: 2016020508432041000_71.3.670.13 doi: 10.1016/j.ijantimicag.2011.10.004 – ident: 2016020508432041000_71.3.670.42 doi: 10.1128/AAC.01345-12 – ident: 2016020508432041000_71.3.670.2 doi: 10.1016/j.ijantimicag.2013.10.011 – ident: 2016020508432041000_71.3.670.3 doi: 10.1111/j.1574-6976.2011.00268.x – ident: 2016020508432041000_71.3.670.10 doi: 10.1111/j.1574-6968.2006.00195.x – ident: 2016020508432041000_71.3.670.8 doi: 10.1093/jac/dki482 – ident: 2016020508432041000_71.3.670.14 doi: 10.3904/kjim.2012.27.2.128 – volume: 41 start-page: 1460 year: 1997 ident: 2016020508432041000_71.3.670.34 article-title: Sequence analysis and enzyme kinetics of the L2 serine β-lactamase from Stenotrophomonas maltophilia publication-title: Antimicrob Agents Chemother doi: 10.1128/AAC.41.7.1460 contributor: fullname: Walsh – ident: 2016020508432041000_71.3.670.30 doi: 10.1111/j.1469-0691.2004.00763.x – ident: 2016020508432041000_71.3.670.31 doi: 10.1086/514912 – volume: 41 start-page: 1140 year: 1997 ident: 2016020508432041000_71.3.670.23 article-title: Multiple antibiotic resistance in Stenotrophomonas maltophilia publication-title: Antimicrob Agents Chemother doi: 10.1128/AAC.41.5.1140 contributor: fullname: Alonso – ident: 2016020508432041000_71.3.670.43 doi: 10.1128/AAC.00629-13 – ident: 2016020508432041000_71.3.670.22 doi: 10.1099/00222615-35-4-208 – ident: 2016020508432041000_71.3.670.32 doi: 10.1128/AAC.38.3.624 – ident: 2016020508432041000_71.3.670.45 – ident: 2016020508432041000_71.3.670.15 doi: 10.1086/504477 – ident: 2016020508432041000_71.3.670.39 doi: 10.3109/10408419209114559 – ident: 2016020508432041000_71.3.670.18 doi: 10.1093/jac/47.3.247 – ident: 2016020508432041000_71.3.670.12 doi: 10.1128/AAC.00598-10 – ident: 2016020508432041000_71.3.670.6 doi: 10.1016/j.drup.2012.06.001 – ident: 2016020508432041000_71.3.670.20 doi: 10.1099/jmm.0.009142-0 – ident: 2016020508432041000_71.3.670.27 doi: 10.1016/j.ijantimicag.2009.09.015 – ident: 2016020508432041000_71.3.670.26 doi: 10.1093/jac/dkg148 – ident: 2016020508432041000_71.3.670.41 doi: 10.1128/AAC.02474-12 – ident: 2016020508432041000_71.3.670.38 – ident: 2016020508432041000_71.3.670.11 doi: 10.1128/AAC.01388-10 – ident: 2016020508432041000_71.3.670.17 doi: 10.1517/13543784.17.2.131 |
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Snippet | S-649266 is a parenteral siderophore cephalosporin antibiotic with a catechol moiety on its side chain. The in vitro antimicrobial activity of S-649266 against... OBJECTIVESS-649266 is a parenteral siderophore cephalosporin antibiotic with a catechol moiety on its side chain. The in vitro antimicrobial activity of... Objectives S-649266 is a parenteral siderophore cephalosporin antibiotic with a catechol moiety on its side chain. The in vitro antimicrobial activity of... |
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SubjectTerms | Acinetobacter baumannii Acinetobacter baumannii - drug effects Anti-Bacterial Agents - pharmacology Antibiotics Antimicrobial agents Bacteria Catechols - pharmacology Cephalosporins - pharmacology Drug resistance Gram-negative bacteria Gram-Negative Bacteria - drug effects Humans Microbial Sensitivity Tests Pseudomonas aeruginosa Pseudomonas aeruginosa - drug effects Siderophores - pharmacology Stenotrophomonas maltophilia Stenotrophomonas maltophilia - drug effects |
Title | In vitro antimicrobial activity of S-649266, a catechol-substituted siderophore cephalosporin, when tested against non-fermenting Gram-negative bacteria |
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