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Related Concept Videos

Biofilms01:29

Biofilms

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Biofilms are complex communities of microorganisms encased in a self-produced extracellular polysaccharide matrix attached to surfaces. These microbial consortia can include single or multiple species, providing enhanced survival benefits by forming organized, multilayered structures.The formation of biofilms occurs through four key stages: attachment, colonization, development, and dispersal.During attachment, free-swimming planktonic cells adhere to a surface, often facilitated by...
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In vitro Biofilm Formation in an 8-well Chamber Slide
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The Relationship Between NETosis and Biofilm Formation in Chronic Infections.

Wafa Aziz1, Hina Sultana2, Vinay Kumar1

  • 1Department of Medicine, Pennsylvania State University Hershey Medical Centre, Hershey, PA 17033, USA.

Biomolecules
|December 30, 2025
PubMed
Summary
This summary is machine-generated.

Neutrophil extracellular traps (NETs) can paradoxically aid chronic infections by stabilizing biofilms, despite their role in pathogen defense. Targeting this interplay offers new therapeutic avenues for persistent diseases.

Keywords:
NETosisbiofilmschronic infectionsimmune responseneutrophil extracellular traps (NETs)

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Area of Science:

  • Immunology
  • Microbiology
  • Pathogenesis

Background:

  • Chronic infections present significant challenges due to treatment resistance and biofilm formation.
  • Neutrophil extracellular traps (NETs), released via NETosis, are part of innate immunity but can paradoxically support biofilms.
  • The interplay between NETs and biofilms is crucial in persistent infections like cystic fibrosis and diabetic foot ulcers.

Purpose of the Study:

  • To explore the bidirectional interactions between NETosis and biofilm formation in chronic infections.
  • To elucidate the synergistic roles of NETs and biofilms in disease pathogenesis.
  • To evaluate emerging therapeutic strategies targeting this pathogenic interplay.

Main Methods:

  • Review of existing literature on NETosis mechanisms and biofilm dynamics.
  • Analysis of the intersection between NETosis and biofilm formation in specific chronic infections.
  • Critical evaluation of novel therapeutic interventions, including DNase treatments and PAD4 inhibitors.

Main Results:

  • NETs can immobilize microbes but their components (DNA, proteins) often enhance biofilm stability and immune evasion.
  • This synergy contributes to the persistence of recalcitrant infections in conditions like cystic fibrosis, diabetic foot ulcers, periodontitis, and implant-associated infections.
  • Emerging therapies aim to disrupt the NET-biofilm interaction.

Conclusions:

  • The interplay between NETosis and biofilms is a key factor in chronic infection persistence.
  • Targeting this synergy requires integrated immunomodulatory and anti-biofilm strategies.
  • Effective management of chronic infections necessitates novel therapeutic approaches addressing both NETs and biofilms.