4.8 Article

Nanopillared Surfaces Disrupt Pseudomonas aeruginosa Mechanoresponsive Upstream Motility

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 11, Issue 11, Pages 10532-10539

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.8b22262

Keywords

antibacterial; antifouling; coating; nanopillared surfaces; Pseudomonas aeruginosa; mechanoresponsive; type IV pill; upstream motility

Funding

  1. NSF MRI [0521674]
  2. Office of Science, Office of Basic Energy Science, of the U.S. Department of Energy [DE-AC02-05CH11231]
  3. Department of Defense (DoD) Peer-Reviewed Medical Research Program (PRMRP) award [W81XWH-17-0355]
  4. National Institutes of Health (NIH) Career Transition award [K22AI112816]
  5. Directorate For Engineering [0521674] Funding Source: National Science Foundation
  6. Div Of Electrical, Commun & Cyber Sys [0521674] Funding Source: National Science Foundation

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Pseudomonas aeruginosa is an opportunistic, multidrug-resistant, human pathogen that forms biofilms in environments with fluid flow, such as the lungs of cystic fibrosis patients, industrial pipelines, and medical devices. P. aeruginosa twitches upstream on surfaces by the cyclic extension and retraction of its mechanoresponsive type IV pili motility appendages. The prevention of upstream motility, host invasion, and infectious biofilm formation in fluid flow systems remains an unmet challenge. Here, we describe the design and application of scalable nanopillared surface structures fabricated using nanoimprint lithography that reduce upstream motility and colonization by P. aeruginosa. We used flow channels to induce shear stress typically found in catheter tubes and microscopy analysis to investigate the impact of nanopillared surfaces with different packing fractions on upstream motility trajectory, displacement, velocity, and surface attachment. We found that densely packed, subcellular nanopillared surfaces, with pillar periodicities ranging from 200 to 600 nm and widths ranging from 70 to 215 nm, inhibit the mechanoresponsive upstream motility and surface attachment. This bacteria-nanostructured surface interface effect allows us to tailor surfaces with specific nanopillared geometries for disrupting cell motility and attachment in fluid flow systems.

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