CRISPR-Cas, a Revolution in the Treatment and Study of ESKAPE Infections: Pre-Clinical Studies

One of the biggest threats we face globally is the emergence of antimicrobial-resistant (AMR) bacteria, which runs in parallel with the lack in the development of new antimicrobials. Among these AMR bacteria pathogens belonging to the ESKAPE group can be highlighted (<i>Enterococcus</i>...

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Main Authors: Manuel González de Aledo, Mónica González-Bardanca, Lucía Blasco, Olga Pacios, Inés Bleriot, Laura Fernández-García, Melisa Fernández-Quejo, María López, Germán Bou, María Tomás
Format: Article
Language:English
Published: MDPI AG 2021-06-01
Series:Antibiotics
Subjects:
Online Access:https://www.mdpi.com/2079-6382/10/7/756
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author Manuel González de Aledo
Mónica González-Bardanca
Lucía Blasco
Olga Pacios
Inés Bleriot
Laura Fernández-García
Melisa Fernández-Quejo
María López
Germán Bou
María Tomás
author_facet Manuel González de Aledo
Mónica González-Bardanca
Lucía Blasco
Olga Pacios
Inés Bleriot
Laura Fernández-García
Melisa Fernández-Quejo
María López
Germán Bou
María Tomás
author_sort Manuel González de Aledo
collection DOAJ
description One of the biggest threats we face globally is the emergence of antimicrobial-resistant (AMR) bacteria, which runs in parallel with the lack in the development of new antimicrobials. Among these AMR bacteria pathogens belonging to the ESKAPE group can be highlighted (<i>Enterococcus</i> spp., <i>Staphylococcus aureus</i>, <i>Klebsiella pneumoniae</i>, <i>Acinetobacter baumannii</i>, <i>Pseudomonas aeruginosa</i> and <i>Enterobacter</i> spp.) due to their profile of drug resistance and virulence. Therefore, innovative lines of treatment must be developed for these bacteria. In this review, we summarize the different strategies for the treatment and study of molecular mechanisms of AMR in the ESKAPE pathogens based on the clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated (Cas) proteins’ technologies: loss of plasmid or cellular viability, random mutation or gene deletion as well directed mutations that lead to a gene’s loss of function.
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spelling doaj.art-0db6dd7665e0468e9cef6392769c5cd12023-11-22T01:12:45ZengMDPI AGAntibiotics2079-63822021-06-0110775610.3390/antibiotics10070756CRISPR-Cas, a Revolution in the Treatment and Study of ESKAPE Infections: Pre-Clinical StudiesManuel González de Aledo0Mónica González-Bardanca1Lucía Blasco2Olga Pacios3Inés Bleriot4Laura Fernández-García5Melisa Fernández-Quejo6María López7Germán Bou8María Tomás9Microbiology Department—A Coruña University Hospital (CHUAC), 15006 A Coruña, SpainMicrobiology Department—A Coruña University Hospital (CHUAC), 15006 A Coruña, SpainA Coruña Biomedical Research Institute (INIBIC), University of A Coruña (UDC), 15006 A Coruña, SpainA Coruña Biomedical Research Institute (INIBIC), University of A Coruña (UDC), 15006 A Coruña, SpainA Coruña Biomedical Research Institute (INIBIC), University of A Coruña (UDC), 15006 A Coruña, SpainA Coruña Biomedical Research Institute (INIBIC), University of A Coruña (UDC), 15006 A Coruña, SpainMicrobiology Department—A Coruña University Hospital (CHUAC), 15006 A Coruña, SpainA Coruña Biomedical Research Institute (INIBIC), University of A Coruña (UDC), 15006 A Coruña, SpainMicrobiology Department—A Coruña University Hospital (CHUAC), 15006 A Coruña, SpainMicrobiology Department—A Coruña University Hospital (CHUAC), 15006 A Coruña, SpainOne of the biggest threats we face globally is the emergence of antimicrobial-resistant (AMR) bacteria, which runs in parallel with the lack in the development of new antimicrobials. Among these AMR bacteria pathogens belonging to the ESKAPE group can be highlighted (<i>Enterococcus</i> spp., <i>Staphylococcus aureus</i>, <i>Klebsiella pneumoniae</i>, <i>Acinetobacter baumannii</i>, <i>Pseudomonas aeruginosa</i> and <i>Enterobacter</i> spp.) due to their profile of drug resistance and virulence. Therefore, innovative lines of treatment must be developed for these bacteria. In this review, we summarize the different strategies for the treatment and study of molecular mechanisms of AMR in the ESKAPE pathogens based on the clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated (Cas) proteins’ technologies: loss of plasmid or cellular viability, random mutation or gene deletion as well directed mutations that lead to a gene’s loss of function.https://www.mdpi.com/2079-6382/10/7/756CRISPR-CasESKAPE pathogenstreatment
spellingShingle Manuel González de Aledo
Mónica González-Bardanca
Lucía Blasco
Olga Pacios
Inés Bleriot
Laura Fernández-García
Melisa Fernández-Quejo
María López
Germán Bou
María Tomás
CRISPR-Cas, a Revolution in the Treatment and Study of ESKAPE Infections: Pre-Clinical Studies
Antibiotics
CRISPR-Cas
ESKAPE pathogens
treatment
title CRISPR-Cas, a Revolution in the Treatment and Study of ESKAPE Infections: Pre-Clinical Studies
title_full CRISPR-Cas, a Revolution in the Treatment and Study of ESKAPE Infections: Pre-Clinical Studies
title_fullStr CRISPR-Cas, a Revolution in the Treatment and Study of ESKAPE Infections: Pre-Clinical Studies
title_full_unstemmed CRISPR-Cas, a Revolution in the Treatment and Study of ESKAPE Infections: Pre-Clinical Studies
title_short CRISPR-Cas, a Revolution in the Treatment and Study of ESKAPE Infections: Pre-Clinical Studies
title_sort crispr cas a revolution in the treatment and study of eskape infections pre clinical studies
topic CRISPR-Cas
ESKAPE pathogens
treatment
url https://www.mdpi.com/2079-6382/10/7/756
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