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- W3126109965 abstract "Biofilm-forming bacteria may be 10-1000 times more resistant to antibiotics than planktonic bacteria and represent about 75% of bacterial infections in humans. Antibiofilm treatments are scarce, and no effective therapies have been reported so far. In this context, antibiofilm peptides (ABPs) represent an exciting class of agents with potent activity against biofilms both in vitro and in vivo. Moreover, murine models of bacterial biofilm infections have been used to evaluate the in vivo effectiveness of ABPs. Therefore, here we highlight the translational potential of ABPs and provide an overview of the different clinically relevant murine models to assess ABP efficacy, including wound, foreign body, chronic lung, and oral models of infection. We discuss key challenges to translate ABPs to the clinic and the pros and cons of the existing murine biofilm models for reliable assessment of the efficacy of ABPs." @default.
- W3126109965 created "2021-02-01" @default.
- W3126109965 creator A5008027681 @default.
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- W3126109965 creator A5071385373 @default.
- W3126109965 creator A5072853076 @default.
- W3126109965 creator A5080190091 @default.
- W3126109965 date "2021-01-27" @default.
- W3126109965 modified "2023-10-03" @default.
- W3126109965 title "Antibiofilm Peptides: Relevant Preclinical Animal Infection Models and Translational Potential" @default.
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