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Nanoscale surface modification favors benign biofilm formation and impedes adherence by pathogens

Year: 2011

Journal: Nanomedicine: Nanotechnology, Biology and Medicine 2012, 8 (3) pp 261-270, 20121211

Authors: Barbara W. Trautner, MD, PhD, Analette I. Lopez, PhD, Amit Kumar, PhD, Danish M. Siddiq, MD, Kershena S. Liao, BAb, Yan Li, PhD, David J. Tweardy, MD, Chengzhi Cai, PhD

Organizations: Houston VA Health Services Research and Development Center of Excellence, Michael E. DeBakey Veterans Affairs Medical Center, Houston, Texas, USA; Section of Infectious Diseases, Department of Medicine, Baylor College of Medicine, Houston, Texas, USA; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas, USA; Department of Chemistry, University of Houston, Houston, Texas, USA; Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas, USA

We have found in vitro that a biofilm of benignEscherichia coli 83972 interferes with urinary catheter colonization by pathogens, and in human studies E. coli 83972–coated urinary catheters are associated with lower rates of catheter-associated urinary tract infections. We hypothesized that modifying surfaces to present mannose ligands for the type 1 fimbriae of E. coli would promote formation of dense E. coli 83972 biofilms, thereby interfering with surface colonization by Enterococcus faecalis, a common uropathogen. We covalently immobilized mannose on silicon substrates by attaching amino-terminated mannose derivative to carboxylic acid–terminated monolayers via amidation. Fluorescence microscopy showed that E. coli 83972 adherence to mannose-modified surfaces increased 4.4-fold compared to unmodified silicon surfaces. Pre-exposing mannose-modified surfaces to E. coli 83972 established a protective biofilm that reduced E. faecalisadherence by 83-fold. Mannose-fimbrial interactions were essential for the improved E. coli 83927 adherence and interference effects.