2022
DOI: 10.3390/ph15121498
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CRISPR-Cas System: A Tool to Eliminate Drug-Resistant Gram-Negative Bacteria

Abstract: Rapidly emerging drug-resistant superbugs, especially Gram-negative bacteria, pose a serious threat to healthcare systems all over the globe. Newer strategies are being developed to detect and overcome the arsenal of weapons that these bacteria possess. The development of antibiotics is time-consuming and may not provide full proof of action on evolving drug-resistant pathogens. The clustered regularly interspaced short palindromic repeats/CRISPR-associated protein (CRISPR/Cas) systems are promising in curbing… Show more

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Cited by 14 publications
(10 citation statements)
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“…9.9 | CRISPR-Cas in S. aureus: Precision gene editing CRISPR/Cas is a promising gene editing technology with huge potential and application in reversing the AMR among pathogenic bacteria [248]. The precise DNA editing ability of the short palindromic repeats that are clustered together at regular interspace, also known as the CRISPR system, produces the Cas9 enzyme that binds, alters, and cuts the DNA accurately, thereby shutting the activation of the gene or silencing of the gene.…”
Section: Naturally Occurring Antibiotics: Fighting Drug Resistancementioning
confidence: 99%
“…9.9 | CRISPR-Cas in S. aureus: Precision gene editing CRISPR/Cas is a promising gene editing technology with huge potential and application in reversing the AMR among pathogenic bacteria [248]. The precise DNA editing ability of the short palindromic repeats that are clustered together at regular interspace, also known as the CRISPR system, produces the Cas9 enzyme that binds, alters, and cuts the DNA accurately, thereby shutting the activation of the gene or silencing of the gene.…”
Section: Naturally Occurring Antibiotics: Fighting Drug Resistancementioning
confidence: 99%
“…180 Other studies indicate that a high number of target sites can still limit the evolution of resistant strains with chromosomal mutations. 181 In addition to the previous resistance response, it was found that the most common site of mutations was localized in the plasmid-encoded SpCas9 used to introduce the system into the target strain. Some studies described recombination and deletions that resulted in the inactivation of the CRISPR loci and the elimination of Cas genes and target sequences, to name a few.…”
Section: ■ Bacterial Mechanisms Of Resistancementioning
confidence: 99%
“…Some studies, however, showed no correlation between the number of target sites and killing efficiency by assessing 10 different gRNAs with 1 to 25 target sites in an E. coli genome and obtaining similar results . Other studies indicate that a high number of target sites can still limit the evolution of resistant strains with chromosomal mutations …”
Section: Bacterial Mechanisms Of Resistancementioning
confidence: 99%
“…Moreover, CRISPR-Cas systems can be employed to either target and remove the AMR pathogen or to eliminate the bacteria themselves, which harbor the drug-resistant genes. As the evolution of bacterial resistance cannot be prevented, various CRISPR-Cas system-usage strategies can be evaluated further because the system is practical and easily reprogrammable [260]. Retrieved and modified from [333,334].…”
Section: Recent Studies On the Application Of Crispr-cas System In Am...mentioning
confidence: 99%