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Clinical Significance of Antibiotic Resistance01:25

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Methicillin-resistant Staphylococcus aureus (MRSA) presents a critical public health threat, arising from its capacity to resist β-lactam antibiotics due to acquisition of the mecA gene within the staphylococcal cassette chromosome mec (SCCmec). This gene encodes penicillin-binding protein 2a (PBP2a), which impairs binding efficacy of methicillin and other β-lactams. MRSA has evolved into distinct clonal lineages impacting humans and animals alike, reinforcing its significance within...
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Staphylococcus aureus is a Gram-positive coccus that resides harmlessly on the skin and mucous membranes of healthy individuals. When the skin barrier is breached, it can shift from a commensal to an opportunistic pathogen. This transition is facilitated by surface adhesins, such as clumping factor B and S. aureus surface protein G (SasG), which bind to structural proteins, including loricrin and cytokeratin, in the damaged epidermis. Protein A, another key factor, binds the Fc region of...
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The skin and mucous membranes serve as the primary line of defense against pathogens by providing both physical and chemical protection. These barriers are essential in preventing the entry and establishment of microbes, thereby maintaining the integrity of the host.
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Evaluation of Antimicrobial Activities of Nanoparticles and Nanostructured Surfaces In Vitro
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Biogenic selenium nanoparticles inhibit Staphylococcus aureus adherence on different surfaces.

Praveen Sonkusre1, Swaranjit Singh Cameotra1

  • 1Institute of Microbial Technology, Sector 39 A, Chandigarh 160036, India.

Colloids and Surfaces. B, Biointerfaces
|November 23, 2015
PubMed
Summary

Selenium nanoparticles (SeNPs) derived from Bacillus licheniformis JS2 effectively prevent Staphylococcus aureus colonization and biofilm formation on medical device surfaces, reducing bacterial load by over 60%. This offers a promising strategy against nosocomial infections.

Keywords:
AdherenceBacillus licheniformis JS2Biofilm formationMicro-colonySelenium nanoparticlesStaphylococcus aureus

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Area of Science:

  • Biotechnology
  • Materials Science
  • Infectious Diseases

Background:

  • Nosocomial infections are a significant global health concern, often stemming from bacterial colonization and biofilm formation on medical devices.
  • Critically ill and immunocompromised patients are particularly vulnerable to these infections, which can also impair device functionality.

Purpose of the Study:

  • To investigate the efficacy of biogenic selenium nanoparticles (SeNPs) derived from Bacillus licheniformis JS2 as an antimicrobial coating for medical devices.
  • To evaluate the SeNPs' ability to inhibit bacterial adherence and biofilm formation by Staphylococcus aureus on various surfaces.

Main Methods:

  • Coating of polystyrene, glass, and catheter surfaces with Bacillus licheniformis JS2 derived SeNPs at a concentration of 0.5 mgSe/ml.
  • Incubation of coated surfaces with Staphylococcus aureus under different conditions (4 °C for 24h in PBS; 37 °C for 72h in nutrient-rich medium).
  • Quantification of bacterial load and microscopic analysis (confocal and electron microscopy) to assess bacterial adherence, micro-colony, and biofilm formation.

Main Results:

  • SeNP coating significantly inhibited Staphylococcus aureus adherence and micro-colony formation on polystyrene, glass, and catheter surfaces.
  • A reduction of over 60% in bacterial load was observed on glass and catheter surfaces coated with SeNPs.
  • Microscopic analysis confirmed the inhibition of biofilm and micro-colony formation on SeNP-coated surfaces.

Conclusions:

  • Biogenic SeNPs demonstrate potent antimicrobial properties against Staphylococcus aureus adherence and biofilm formation.
  • Coating medical devices with these non-toxic SeNPs presents a viable alternative strategy for preventing biofilm-related infections.
  • This approach holds potential for enhancing patient safety and improving medical device performance.