Suppressing the CRISPR/Cas adaptive immune system in bacterial infections.
P GholizadehM AghazadehM AsgharzadehHossein Samadi KafilPublished in: European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology (2017)
Clustered regularly interspaced short palindromic repeats (CRISPR) coupled with CRISPR-associated (Cas) proteins (CRISPR/Cas) are the adaptive immune system of eubacteria and archaebacteria. This system provides protection of bacteria against invading foreign DNA, such as transposons, bacteriophages and plasmids. Three-stage processes in this system for immunity against foreign DNAs are defined as adaptation, expression and interference. Recent studies suggested a correlation between the interfering of the CRISPR/Cas locus, acquisition of antibiotic resistance and pathogenicity island. In this review article, we demonstrate and discuss the CRISPR/Cas system's roles in interference with acquisition of antibiotic resistance and pathogenicity island in some eubacteria. Totally, these systems function as the adaptive immune system of bacteria against invading foreign DNA, blocking the acquisition of antibiotic resistance and virulence factor, detecting serotypes, indirect effects of CRISPR self-targeting, associating with physiological functions, associating with infections in humans at the transmission stage, interfering with natural transformation, a tool for genome editing in genome engineering, monitoring foodborne pathogens etc. These results showed that the CRISPR/Cas system might prevent the emergence of virulence both in vitro and in vivo. Moreover, this system was shown to be a strong selective pressure for the acquisition of antibiotic resistance and virulence factor in bacterial pathogens.
Keyphrases
- crispr cas
- genome editing
- escherichia coli
- antimicrobial resistance
- biofilm formation
- pseudomonas aeruginosa
- staphylococcus aureus
- circulating tumor
- cell free
- single molecule
- poor prognosis
- gram negative
- dna methylation
- signaling pathway
- candida albicans
- gene expression
- genome wide
- drug delivery
- cancer therapy
- binding protein