Emerging Strategies to Combat ESKAPE Pathogens in the Era of Antimicrobial Resistance: A Review

The acronym ESKAPE includes six nosocomial pathogens that exhibit multidrug resistance and virulence: Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter spp. Persistent use of antibiotics has provoked the emergence of...

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Main Authors: Mansura S. Mulani, Ekta E. Kamble, Shital N. Kumkar, Madhumita S. Tawre, Karishma R. Pardesi
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-04-01
Series:Frontiers in Microbiology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fmicb.2019.00539/full
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spelling doaj-dda7409c418343a19adee35cc1b411f22020-11-24T23:41:42ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2019-04-011010.3389/fmicb.2019.00539403107Emerging Strategies to Combat ESKAPE Pathogens in the Era of Antimicrobial Resistance: A ReviewMansura S. MulaniEkta E. KambleShital N. KumkarMadhumita S. TawreKarishma R. PardesiThe acronym ESKAPE includes six nosocomial pathogens that exhibit multidrug resistance and virulence: Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter spp. Persistent use of antibiotics has provoked the emergence of multidrug resistant (MDR) and extensively drug resistant (XDR) bacteria, which render even the most effective drugs ineffective. Extended spectrum β-lactamase (ESBL) and carbapenemase producing Gram negative bacteria have emerged as an important therapeutic challenge. Development of novel therapeutics to treat drug resistant infections, especially those caused by ESKAPE pathogens is the need of the hour. Alternative therapies such as use of antibiotics in combination or with adjuvants, bacteriophages, antimicrobial peptides, nanoparticles, and photodynamic light therapy are widely reported. Many reviews published till date describe these therapies with respect to the various agents used, their dosage details and mechanism of action against MDR pathogens but very few have focused specifically on ESKAPE. The objective of this review is to describe the alternative therapies reported to treat ESKAPE infections, their advantages and limitations, potential application in vivo, and status in clinical trials. The review further highlights the importance of a combinatorial approach, wherein two or more therapies are used in combination in order to overcome their individual limitations, additional studies on which are warranted, before translating them into clinical practice. These advances could possibly give an alternate solution or extend the lifetime of current antimicrobials.https://www.frontiersin.org/article/10.3389/fmicb.2019.00539/fullESKAPEmultidrug resistancealternative therapycombination therapyphage therapyantimicrobial peptides
collection DOAJ
language English
format Article
sources DOAJ
author Mansura S. Mulani
Ekta E. Kamble
Shital N. Kumkar
Madhumita S. Tawre
Karishma R. Pardesi
spellingShingle Mansura S. Mulani
Ekta E. Kamble
Shital N. Kumkar
Madhumita S. Tawre
Karishma R. Pardesi
Emerging Strategies to Combat ESKAPE Pathogens in the Era of Antimicrobial Resistance: A Review
Frontiers in Microbiology
ESKAPE
multidrug resistance
alternative therapy
combination therapy
phage therapy
antimicrobial peptides
author_facet Mansura S. Mulani
Ekta E. Kamble
Shital N. Kumkar
Madhumita S. Tawre
Karishma R. Pardesi
author_sort Mansura S. Mulani
title Emerging Strategies to Combat ESKAPE Pathogens in the Era of Antimicrobial Resistance: A Review
title_short Emerging Strategies to Combat ESKAPE Pathogens in the Era of Antimicrobial Resistance: A Review
title_full Emerging Strategies to Combat ESKAPE Pathogens in the Era of Antimicrobial Resistance: A Review
title_fullStr Emerging Strategies to Combat ESKAPE Pathogens in the Era of Antimicrobial Resistance: A Review
title_full_unstemmed Emerging Strategies to Combat ESKAPE Pathogens in the Era of Antimicrobial Resistance: A Review
title_sort emerging strategies to combat eskape pathogens in the era of antimicrobial resistance: a review
publisher Frontiers Media S.A.
series Frontiers in Microbiology
issn 1664-302X
publishDate 2019-04-01
description The acronym ESKAPE includes six nosocomial pathogens that exhibit multidrug resistance and virulence: Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter spp. Persistent use of antibiotics has provoked the emergence of multidrug resistant (MDR) and extensively drug resistant (XDR) bacteria, which render even the most effective drugs ineffective. Extended spectrum β-lactamase (ESBL) and carbapenemase producing Gram negative bacteria have emerged as an important therapeutic challenge. Development of novel therapeutics to treat drug resistant infections, especially those caused by ESKAPE pathogens is the need of the hour. Alternative therapies such as use of antibiotics in combination or with adjuvants, bacteriophages, antimicrobial peptides, nanoparticles, and photodynamic light therapy are widely reported. Many reviews published till date describe these therapies with respect to the various agents used, their dosage details and mechanism of action against MDR pathogens but very few have focused specifically on ESKAPE. The objective of this review is to describe the alternative therapies reported to treat ESKAPE infections, their advantages and limitations, potential application in vivo, and status in clinical trials. The review further highlights the importance of a combinatorial approach, wherein two or more therapies are used in combination in order to overcome their individual limitations, additional studies on which are warranted, before translating them into clinical practice. These advances could possibly give an alternate solution or extend the lifetime of current antimicrobials.
topic ESKAPE
multidrug resistance
alternative therapy
combination therapy
phage therapy
antimicrobial peptides
url https://www.frontiersin.org/article/10.3389/fmicb.2019.00539/full
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