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      Biofilm morphology and antibiotic susceptibility of methicillin-resistant Staphylococcus aureus (MRSA) on poly-D,L-lactide- co-poly(ethylene glycol) (PDLLA-PEG) coated titanium

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          Abstract

          Biodegradable polymeric coatings are being explored as a preventive strategy for orthopaedic device-related infection. In this study, titanium surfaces (Ti) were coated with poly-D,L-lactide (PDLLA, (P)), polyethylene-glycol poly-D,L-lactide (PEGylated-PDLLA, (PP20)), or multi-layered PEGylated-PDLLA (M), with or without 1 % silver sulfadiazine. The aim was to evaluate their cytocompatibility, resistance to Staphylococcus aureus biofilm formation, and their potential to enhance the susceptibility of any biofilm formed to antibiotics. Using automated high-content screening confocal microscopy, biofilm formation of a clinical methicillin-resistant Staphylococcus aureus (MRSA) isolate expressing GFP was quantified, along with isogenic mutants that were unable to form polysaccharidic or proteinaceous biofilm matrices. The results showed that PEGylated-PDLLA coatings exhibited significant antibiofilm properties, with M showing the highest effect. This inhibitory effect was stronger in S. aureus biofilms with a matrix composed of proteins compared to those with an exopolysaccharide (PIA) biofilm matrix. Our data suggest that the antibiofilm effect may have been due to (i) inhibition of the initial attachment through microbial surface components recognising adhesive matrix molecules (MSCRAMMs), since PEG reduces protein surface adsorption via surface hydration layer and steric repulsion; and (ii) mechanical disaggregation and dispersal of microcolonies due to the bioresorbable/degradable nature of the polymers, which undergo hydration and hydrolysis over time. The disruption of biofilm morphology by the PDLLA-PEG co-polymers increased S. aureus susceptibility to antibiotics like rifampicin and fusidic acid. Adding 1 % AgSD provided additional early bactericidal effects on both biofilm and planktonic S. aureus. Additionally, the coatings were cytocompatible with immune cells, indicating their potential to enhance bacterial clearance and reduce bacterial colonisation of titanium-based orthopaedic biomaterials.

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          Highlights

          • PEGylated-PDLLA coatings had antibiofilm effect against multiresistant S. aureus and were cytocompatible.

          • These coatings may inhibit bacterial surface adhesins and mechanically disaggregate biofilms, increasing S. aureus susceptibility to antibiotics.

          • Incorporation of silver into the coatings provided additional bactericidal effects.

          • PEGylated-PDLLA coatings can potencially enhance the infection resistance of titanium.

          • HCS-confocal microscopy provides unbiased automated 3D-image analysis of S. aureus biofilms on biomaterials.

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          Animal models of necrotizing enterocolitis: review of the literature and state of the art

          Abstract Necrotizing enterocolitis (NEC) remains the leading cause of gastrointestinal surgical emergency in preterm neonates. Over the last five decades, a variety of experimental models have been developed to study the pathophysiology of this disease and to test the effectiveness of novel therapeutic strategies. Experimental NEC is mainly modeled in neonatal rats, mice and piglets. In this review, we focus on these experimental models and discuss the major advantages and disadvantages of each. We also briefly discuss other models that are not as widely used but have contributed to our current knowledge of NEC.
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            Biofilms: an emergent form of bacterial life.

            Bacterial biofilms are formed by communities that are embedded in a self-produced matrix of extracellular polymeric substances (EPS). Importantly, bacteria in biofilms exhibit a set of 'emergent properties' that differ substantially from free-living bacterial cells. In this Review, we consider the fundamental role of the biofilm matrix in establishing the emergent properties of biofilms, describing how the characteristic features of biofilms - such as social cooperation, resource capture and enhanced survival of exposure to antimicrobials - all rely on the structural and functional properties of the matrix. Finally, we highlight the value of an ecological perspective in the study of the emergent properties of biofilms, which enables an appreciation of the ecological success of biofilms as habitat formers and, more generally, as a bacterial lifestyle.
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              Implant infections: adhesion, biofilm formation and immune evasion

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                Author and article information

                Contributors
                Journal
                Biofilm
                Biofilm
                Biofilm
                Elsevier
                2590-2075
                05 October 2024
                December 2024
                05 October 2024
                : 8
                : 100228
                Affiliations
                [a ]Department of Biomaterials, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden
                [b ]Centre for Antibiotic Resistance Research in Gothenburg (CARe), Gothenburg, Sweden
                [c ]Ashland Specialties Ireland Ltd., Mullingar, Ireland
                [d ]School of Biomolecular and Biomedical Science, University College Dublin, Dublin, Ireland
                [e ]Cell Screening Laboratory, UCD School of Biology & Environmental Science, University College Dublin, Dublin, Ireland
                [f ]Microbial Pathogenesis Laboratory. Navarrabiomed-Complejo Hospitalario de Navarra (CHN)-Universidad Pública de Navarra (UPNA), IDISNA, Pamplona, Navarra, Spain
                Author notes
                [* ]Corresponding author. Department of Biomaterials, Institute of Clinial Sciences, Sahlgrenska Academy, University of Gothenburg, P.O. Box 412, 405 30 Gothenburg, Sweden. margarita.trobos@ 123456biomaterials.gu.se
                [** ]Corresponding author. UCD School of Biomolecular and Biomedical Science, Room C140, Health Science Centre, Belfield, Dublin, Ireland. tadhg.ocroinin@ 123456ucd.ie
                [1]

                Equal contribution.

                [2]

                Joint last authors.

                Article
                S2590-2075(24)00053-4 100228
                10.1016/j.bioflm.2024.100228
                11740804
                39830519
                a491f76d-745e-4436-b7f6-03cee2eebcb8
                © 2024 The Authors

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 9 July 2024
                : 27 September 2024
                : 3 October 2024
                Categories
                Article

                poly-d,l-lactide (pdlla),polyethylene-glycol (peg),biofilm,methicillin-resistant staphylococcus aureus (mrsa),antibiotics

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