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CRISPR Interference (CRISPRi) Inhibition of luxS Gene Expression in : An Approach to Inhibit Biofilm. | LitMetric

CRISPR Interference (CRISPRi) Inhibition of luxS Gene Expression in : An Approach to Inhibit Biofilm.

Front Cell Infect Microbiol

Medical Microbiology and Molecular Biology Lab., Interdisciplinary Biotechnology Unit, Aligarh Muslim UniversityAligarh, India.

Published: January 2018

AI Article Synopsis

  • - Biofilm, a bacterial layer linked to roughly 80% of infections, notably affects medical devices and contributes to hospital-acquired infections.
  • - This study aimed to disrupt biofilm formation by targeting the luxS gene, which plays a key role in the quorum sensing process that initiates biofilm development.
  • - Researchers utilized the CRISPRi system to inhibit luxS expression, confirming its effectiveness through various assays, indicating that CRISPRi could be a promising method for preventing bacterial biofilm formation.

Article Abstract

Biofilm is a sessile bacterial accretion embedded in self-producing matrix. It is the root cause of about 80% microbial infections in human. Among them, biofilms are most prevalent in medical devices associated nosocomial infections. The objective of this study was to inhibit biofilm formation by targeting gene involved in quorum sensing, one of the main mechanisms of biofilm formation. Hence we have introduced the CRISPRi, first time to target luxS gene. luxS is a synthase, involved in the synthesis of Autoinducer-2(AI-2), which in turn guides the initial stage of biofilm formation. To implement CRISPRi system for luxS gene suppression, we have synthesized complementary sgRNA to target gene sequence and co-expressed with dCas9, a mutated form of an endonuclease. Suppression of luxS expression was confirmed through qRT-PCR. The effect of luxS gene on biofilm inhibition was studied through crystal violet assay, XTT reduction assay and scanning electron microscopy. We conclude that CRISPRi system could be a potential strategy to inhibit bacterial biofilm through mechanism base approach.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5445563PMC
http://dx.doi.org/10.3389/fcimb.2017.00214DOI Listing

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