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Related Concept Videos

Biofilms01:29

Biofilms

297
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...
297

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Evaluation of Antimicrobial Activities of Nanoparticles and Nanostructured Surfaces In Vitro
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Targeting ESKAPE pathogens with ZnS and Au@ZnS Core-Shell nanoconjugates for improved biofilm control.

Shaikh Imran Ibrahim1, Ajith Manayil Parambil2,3, Neha Jha4

  • 1Central Laboratory of The Lishui Hospital of Wenzhou Medical University, The First Affiliated Hospital of Lishui University, Lishui People's Hospital, Lishui, 323000, Zhejiang, China.

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Novel gold-containing zinc sulfide nanoconjugates (Au@ZnS NC) show potent anti-biofilm activity against ESKAPE pathogens. These nanoconjugates effectively prevent biofilm formation on medical devices, offering a promising solution for antibiotic resistance.

Keywords:
AntibiofilmAu@ZnSDrug resistanceExo-polysaccharidesMedical implantsNanoconjugates

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Area of Science:

  • Nanotechnology
  • Materials Science
  • Infectious Diseases

Background:

  • Antibiotic-resistant infections and biofilm formation on medical implants are critical global health concerns.
  • ESKAPE pathogens, including Acinetobacter baumannii and Staphylococcus aureus, pose significant threats.
  • There is an urgent need for novel anti-biofilm strategies to combat these infections.

Purpose of the Study:

  • To synthesize and evaluate zinc sulfide quantum dots (ZnS QD) and Au@ZnS nanoconjugates (Au@ZnS NC).
  • To determine the antibacterial and anti-biofilm efficacy of these nanomaterials against a panel of ESKAPE pathogens.
  • To investigate the mechanism of action of Au@ZnS NC in inhibiting biofilm formation.

Main Methods:

  • Synthesis of ZnS QD and Au@ZnS NC.
  • Minimum Inhibitory Concentration (MIC) assays, tube dilution, and biofilm formation assays.
  • Cell permeability assays, reactive oxygen species analysis, and comet assays were used to elucidate the mechanism of action.

Main Results:

  • Au@ZnS NC demonstrated significant reduction in biofilm formation and extracellular polymeric substances (EPS) production.
  • Au@ZnS NC induced oxidative stress, destabilized bacterial cell structure, and caused DNA strand breakage.
  • Au@ZnS nanoconjugates inhibited biofilm formation within 24 hours across all tested strains, outperforming ZnS QD and showing minimal colonization on treated urinary catheters.

Conclusions:

  • Au@ZnS nanoconjugates exhibit potent antibacterial and anti-biofilm properties.
  • These nanoconjugates offer a promising therapeutic strategy for controlling infections associated with medical devices and implants.
  • The findings highlight the potential of Au@ZnS NC to address the challenge of biofilm-forming pathogens in healthcare settings.