Emerging Strategies to Combat β-Lactamase Producing ESKAPE Pathogens

Since the discovery of penicillin by Alexander Fleming in 1929 as a therapeutic agent against staphylococci, β-lactam antibiotics (BLAs) remained the most successful antibiotic classes against the majority of bacterial strains, reaching a percentage of 65% of all medical prescriptions. Unfortunately...

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Main Authors: Corneliu Ovidiu Vrancianu, Irina Gheorghe, Elena-Georgiana Dobre, Ilda Czobor Barbu, Roxana Elena Cristian, Marcela Popa, Sang Hee Lee, Carmen Limban, Ilinca Margareta Vlad, Mariana Carmen Chifiriuc
Format: Article
Language:English
Published: MDPI AG 2020-11-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/21/22/8527
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spelling doaj-888af3d4b24547fc92e52cc657ae365a2020-11-25T04:06:59ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672020-11-01218527852710.3390/ijms21228527Emerging Strategies to Combat β-Lactamase Producing ESKAPE PathogensCorneliu Ovidiu Vrancianu0Irina Gheorghe1Elena-Georgiana Dobre2Ilda Czobor Barbu3Roxana Elena Cristian4Marcela Popa5Sang Hee Lee6Carmen Limban7Ilinca Margareta Vlad8Mariana Carmen Chifiriuc9Microbiology Immunology Department and The Research Institute of the University of Bucharest, Faculty of Biology, University of Bucharest, 020956 Bucharest, RomaniaMicrobiology Immunology Department and The Research Institute of the University of Bucharest, Faculty of Biology, University of Bucharest, 020956 Bucharest, RomaniaMicrobiology Immunology Department and The Research Institute of the University of Bucharest, Faculty of Biology, University of Bucharest, 020956 Bucharest, RomaniaMicrobiology Immunology Department and The Research Institute of the University of Bucharest, Faculty of Biology, University of Bucharest, 020956 Bucharest, RomaniaDepartment of Biochemistry and Molecular Biology, Faculty of Biology, University of Bucharest, 020956 Bucharest, RomaniaMicrobiology Immunology Department and The Research Institute of the University of Bucharest, Faculty of Biology, University of Bucharest, 020956 Bucharest, RomaniaDepartment of Biological Sciences, Myongji University, 03674 Myongjiro, Yongin 449-728, Gyeonggido, KoreaDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, “Carol Davila” University of Medicine and Pharmacy, Traian Vuia no.6, 020956 Bucharest, RomaniaDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, “Carol Davila” University of Medicine and Pharmacy, Traian Vuia no.6, 020956 Bucharest, RomaniaMicrobiology Immunology Department and The Research Institute of the University of Bucharest, Faculty of Biology, University of Bucharest, 020956 Bucharest, RomaniaSince the discovery of penicillin by Alexander Fleming in 1929 as a therapeutic agent against staphylococci, β-lactam antibiotics (BLAs) remained the most successful antibiotic classes against the majority of bacterial strains, reaching a percentage of 65% of all medical prescriptions. Unfortunately, the emergence and diversification of β-lactamases pose indefinite health issues, limiting the clinical effectiveness of all current BLAs. One solution is to develop β-lactamase inhibitors (BLIs) capable of restoring the activity of β-lactam drugs. In this review, we will briefly present the older and new BLAs classes, their mechanisms of action, and an update of the BLIs capable of restoring the activity of β-lactam drugs against ESKAPE (<i>Enterococcus </i>spp.<i>, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, </i>and<i> Enterobacter </i>spp.) pathogens. Subsequently, we will discuss several promising alternative approaches such as bacteriophages, antimicrobial peptides, nanoparticles, CRISPR (clustered regularly interspaced short palindromic repeats) cas technology, or vaccination developed to limit antimicrobial resistance in this endless fight against Gram-negative pathogens.https://www.mdpi.com/1422-0067/21/22/8527ESKAPEinhibitorsβ-lactamaseantimicrobial resistancevaccination
collection DOAJ
language English
format Article
sources DOAJ
author Corneliu Ovidiu Vrancianu
Irina Gheorghe
Elena-Georgiana Dobre
Ilda Czobor Barbu
Roxana Elena Cristian
Marcela Popa
Sang Hee Lee
Carmen Limban
Ilinca Margareta Vlad
Mariana Carmen Chifiriuc
spellingShingle Corneliu Ovidiu Vrancianu
Irina Gheorghe
Elena-Georgiana Dobre
Ilda Czobor Barbu
Roxana Elena Cristian
Marcela Popa
Sang Hee Lee
Carmen Limban
Ilinca Margareta Vlad
Mariana Carmen Chifiriuc
Emerging Strategies to Combat β-Lactamase Producing ESKAPE Pathogens
International Journal of Molecular Sciences
ESKAPE
inhibitors
β-lactamase
antimicrobial resistance
vaccination
author_facet Corneliu Ovidiu Vrancianu
Irina Gheorghe
Elena-Georgiana Dobre
Ilda Czobor Barbu
Roxana Elena Cristian
Marcela Popa
Sang Hee Lee
Carmen Limban
Ilinca Margareta Vlad
Mariana Carmen Chifiriuc
author_sort Corneliu Ovidiu Vrancianu
title Emerging Strategies to Combat β-Lactamase Producing ESKAPE Pathogens
title_short Emerging Strategies to Combat β-Lactamase Producing ESKAPE Pathogens
title_full Emerging Strategies to Combat β-Lactamase Producing ESKAPE Pathogens
title_fullStr Emerging Strategies to Combat β-Lactamase Producing ESKAPE Pathogens
title_full_unstemmed Emerging Strategies to Combat β-Lactamase Producing ESKAPE Pathogens
title_sort emerging strategies to combat β-lactamase producing eskape pathogens
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1661-6596
1422-0067
publishDate 2020-11-01
description Since the discovery of penicillin by Alexander Fleming in 1929 as a therapeutic agent against staphylococci, β-lactam antibiotics (BLAs) remained the most successful antibiotic classes against the majority of bacterial strains, reaching a percentage of 65% of all medical prescriptions. Unfortunately, the emergence and diversification of β-lactamases pose indefinite health issues, limiting the clinical effectiveness of all current BLAs. One solution is to develop β-lactamase inhibitors (BLIs) capable of restoring the activity of β-lactam drugs. In this review, we will briefly present the older and new BLAs classes, their mechanisms of action, and an update of the BLIs capable of restoring the activity of β-lactam drugs against ESKAPE (<i>Enterococcus </i>spp.<i>, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, </i>and<i> Enterobacter </i>spp.) pathogens. Subsequently, we will discuss several promising alternative approaches such as bacteriophages, antimicrobial peptides, nanoparticles, CRISPR (clustered regularly interspaced short palindromic repeats) cas technology, or vaccination developed to limit antimicrobial resistance in this endless fight against Gram-negative pathogens.
topic ESKAPE
inhibitors
β-lactamase
antimicrobial resistance
vaccination
url https://www.mdpi.com/1422-0067/21/22/8527
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