Relative inhibitory activities of newly developed diazabicyclooctanes, boronic acid derivatives, and penicillin-based sulfone β-lactamase inhibitors against broad-spectrum AmpC β-lactamases
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
Grantová podpora
Université de Fribourg (Universität Freiburg)
National Institute of Virology and Bacteriology (Programme EXCELES, ID Project No. LX22NPO5103) - funded by the European Union - Next Generation EU
PubMed
39365068
PubMed Central
PMC11539244
DOI
10.1128/aac.00775-24
Knihovny.cz E-zdroje
- Klíčová slova
- AmpC, avibactam, class C, durlobactam, enmetazobactam, nacubactam, relebactam, taniborbactam, vaborbactam, xeruborbactam, zidebactam, β-lactamase,
- MeSH
- Acinetobacter baumannii * účinky léků enzymologie MeSH
- antibakteriální látky * farmakologie chemie MeSH
- azabicyklické sloučeniny * farmakologie chemie MeSH
- bakteriální proteiny * antagonisté a inhibitory metabolismus MeSH
- beta-laktamasy * metabolismus MeSH
- bicyklické sloučeniny heterocyklické farmakologie chemie MeSH
- cyklooktany MeSH
- inhibitory beta-laktamasy * farmakologie chemie MeSH
- kyseliny boronové * farmakologie chemie MeSH
- laktamy MeSH
- mikrobiální testy citlivosti * MeSH
- peniciliny farmakologie chemie MeSH
- piperidiny MeSH
- sulfony farmakologie chemie MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- AmpC beta-lactamases MeSH Prohlížeč
- antibakteriální látky * MeSH
- avibactam MeSH Prohlížeč
- azabicyklické sloučeniny * MeSH
- bakteriální proteiny * MeSH
- beta-laktamasy * MeSH
- bicyklické sloučeniny heterocyklické MeSH
- cyklooktany MeSH
- durlobactam MeSH Prohlížeč
- inhibitory beta-laktamasy * MeSH
- kyseliny boronové * MeSH
- laktamy MeSH
- nacubactam MeSH Prohlížeč
- peniciliny MeSH
- piperidiny MeSH
- relebactam MeSH Prohlížeč
- sulfony MeSH
- vaborbactam MeSH Prohlížeč
- zidebactam MeSH Prohlížeč
The relative inhibitory activities of diazabicyclooctanes (avibactam, relebactam, zidebactam, nacubactam, durlobactam), boronic acid derivatives (vaborbactam, taniborbactam, xeruborbactam), and penicillin-based sulfone derivative enmetazobactam were evaluated against several intrinsic and acquired class C β-lactamases. By contrast to vaborbactam and enmetazobactam, taniborbactam, xeruborbactam, and all diazabicyclooctanes demonstrated effective activities against most AmpC enzymes. Notably, durlobactam exhibited the most pronounced inhibitory effect. Interstingly, the chromosomal AmpC of Acinetobacter baumannii was the least sensitive enzyme to the newly developed β-lactamase inhibitors.
Division of Intensive Care Unit University Hospitals of Geneva Geneva Switzerland
Swiss National Reference Center for Emerging Antibiotic Resistance Fribourg Switzerland
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