Abstract

The ability of bacteria to develop antibiotic resistance and colonize abiotic surfaces by forming biofilms is a major cause of medical implant-associated infections and results in prolonged hospitalization periods and patient mortality. Different approaches have been used for preventing biofilm-related infections in health care settings. Many of these methods have their own demerits that include chemical-based complications; emergent antibiotic-resistant strains, and so on. Silver nanoparticles (AgNPs) are renowned for their influential antimicrobial activity. We demonstrate the biofilm formation by extended spectrum β-lactamases-producing Escherichia coli and Klebsiella spp. by direct visualization applying tissue culture plate, tube, and Congo red agar methods. Double fluorescent staining for confocal laser scanning microscopy (CLSM) consisted of propidium iodide staining to detect bacterial cells and concanavalin A-fluorescein isothiocyanate staining to detect the exopolysaccharides matrix were used. Scanning electron microscopy observations clearly indicate that AgNPs reduced the surface coverage by E. coli and Klebsiella spp. thus prevent the biofilm formations. Double-staining technique using CLSM provides the visual evidence that AgNPs arrested the bacterial growth and prevent the exopolysaccharides formation. The AgNPs-coated surfaces effectively restricted biofilm formation of the tested bacteria. In our study, we could demonstrate the complete antibiofilm activity AgNPs at a concentration as low as 50 μg/ml. Our findings suggested that AgNPs can be exploited towards the development of potential antibacterial coatings for various biomedical and environmental applications. These formulations can be used for the treatment of drug-resistant bacterial infections caused by biofilms, at much lower nanosilver loading with higher efficiency.

Highlights

  • The widespread use of antibiotics both inside and outside of medicine is playing a significant role in the emergence of multi-drug-resistant bacteria

  • High-resolution transmission electron microscopy analysis revealed that the AgNPs were prominently spherical in morphology and monodisperse

  • All strains of E. coli (40) and K. pneumoniae (6) were tested for Extended spectrum b-lactamases (ESBLs) production

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Summary

Introduction

The widespread use of antibiotics both inside and outside of medicine is playing a significant role in the emergence of multi-drug-resistant bacteria. About 70 % of the bacteria that cause infections in hospitals are resistant to at least one of the drugs most commonly used for treatment. Some organisms are resistant to all approved antibiotics and they can only treat with experimental and potentially toxic drugs (Todar 2008). Extended spectrum b-lactamases (ESBLs)-producing microorganisms are very dynamic and. Appl Nanosci (2014) 4:859–868 constitutes an increasing problem due to their hydrolyzing activity against extended spectrum third generation cephalosporins such as cefotaxime, ceftriaxone, ceftazidime, and the monobactam aztreonam often employed in the treatment of hospital-acquired infections (Romero et al 2005; Dechen et al 2009). The majority of ESBL-producing strains are Enterobacteriaceae members such as Klebsiella pneumoniae, Klebsiella oxytoca, and Escherichia coli (Ami et al 2008)

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