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Genetically engineered phages and engineered phage-derived enzymes to destroy biofilms of antibiotics resistance bacteria. | LitMetric

AI Article Synopsis

  • Bacterial biofilms can be compared to strongholds in warfare, where bacteria can evade medical treatments, making them tough adversaries against antibiotics.
  • The success of treating infections caused by biofilms depends on the ability of medical professionals (defenders) to strengthen their strategies, while bacteria (assailants) can outsmart treatments with new tactics.
  • Engineered phages and phage-derived enzymes show promising potential to destroy and prevent biofilms more effectively than natural options, offering new hope in the fight against antibiotic-resistant infections.

Article Abstract

"An impregnable stronghold where one or more warrior clans can evade enemy attacks" may serve as a description of bacterial biofilm on a smaller level than human conflicts. Consider this hypothetical conflict: who would emerge victorious? The occupants of secure trenches or those carrying out relentless assault? Either faction has the potential for triumph; the defenders will prevail if they can fortify the trench with unwavering resolve, while the assailants will succeed if they can devise innovative means to breach the trench. Hence, bacterial biofilms pose a significant challenge and are formidable adversaries for medical professionals, often leading to the failure of antibiotic treatments in numerous hospital infections. Phage engineering has become the foundation for the targeted enhancement of various phage properties, facilitating the eradication of biofilms. Researchers across the globe have studied the impact of engineered phages and phage-derived enzymes on biofilms formed by difficult-to-treat bacteria. These novel biological agents have shown promising results in addressing biofilm-related challenges. The compilation of research findings highlights the impressive capabilities of engineered phages in combating antibiotic-resistant bacteria, superbugs, and challenging infections. Specifically, these engineered phages exhibit enhanced biofilm destruction, penetration, and prevention capabilities compared to their natural counterparts. Additionally, the engineered enzymes derived from phages demonstrate improved effectiveness in addressing bacterial biofilms. As a result, these novel solutions, which demonstrate high penetration, destruction, and inhibition of biofilms, can be regarded as a viable option for addressing infectious biofilms in the near future.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11336853PMC
http://dx.doi.org/10.1016/j.heliyon.2024.e35666DOI Listing

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