Biofilm control with natural and genetically-modified phages.

World J Microbiol Biotechnol

Department of Civil and Environmental Engineering, University of Utah, 110 S Central Campus Drive, Salt Lake City, 84112, UT, USA.

Published: April 2016

Bacteriophages, as the most dominant and diverse entities in the universe, have the potential to be one of the most promising therapeutic agents. The emergence of multidrug-resistant bacteria and the antibiotic crisis in the last few decades have resulted in a renewed interest in phage therapy. Furthermore, bacteriophages, with the capacity to rapidly infect and overcome bacterial resistance, have demonstrated a sustainable approach against bacterial pathogens-particularly in biofilm. Biofilm, as complex microbial communities located at interphases embedded in a matrix of bacterial extracellular polysaccharide substances (EPS), is involved in health issues such as infections associated with the use of biomaterials and chronic infections by multidrug resistant bacteria, as well as industrial issues such as biofilm formation on stainless steel surfaces in food industry and membrane biofouling in water and wastewater treatment processes. In this paper, the most recent studies on the potential of phage therapy using natural and genetically-modified lytic phages and their associated enzymes in fighting biofilm development in various fields including engineering, industry, and medical applications are reviewed. Phage-mediated prevention approaches as an indirect phage therapy strategy are also explored in this review. In addition, the limitations of these approaches and suggestions to overcome these constraints are discussed to enhance the efficiency of phage therapy process. Finally, future perspectives and directions for further research towards a better understanding of phage therapy to control biofilm are recommended.

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http://dx.doi.org/10.1007/s11274-016-2009-4DOI Listing

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  • Quorum sensing (QS) regulates various bacterial adaptations to environmental changes and may influence phage infections, but current knowledge about this interaction is incomplete.
  • A novel phage, BUCT640, was characterized as having a unique morphology and depended on Psl polysaccharides for adsorption, revealing how bacterial QS pathways affect phage sensitivity.
  • The study discovered that QS could inhibit phage adsorption by altering biofilm thickness, suggesting that disrupting QS could enhance phage therapy efficacy against drug-resistant bacterial infections.
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Article Synopsis
  • Acinetobacter baumannii, especially the carbapenem-resistant strains (CRAB), is a critical pathogen linked to antimicrobial resistance (AMR) and is prioritized by the WHO.
  • Phage therapy is being explored as a potential treatment for CRAB infections due to increasing resistance to conventional antibiotics.
  • A newly isolated lytic phage, vAbaIN10, exhibits effective lytic activity against CRAB in various conditions and shows promise in advancing treatment options for multidrug-resistant infections.
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