TY - JOUR
T1 - Imaging Pseudomonas aeruginosa Biofilm Extracellular Polymer Scaffolds with Amphiphilic Carbon Dots
AU - Ritenberg, Margarita
AU - Nandi, Sukhendu
AU - Kolusheva, Sofiya
AU - Dandela, Rambabu
AU - Meijler, Michael M.
AU - Jelinek, Raz
N1 - Publisher Copyright:
© 2016 American Chemical Society.
PY - 2016/5/20
Y1 - 2016/5/20
N2 - Biofilm formation is a critical facet of pathogenesis and resilience of human, animal, and plant bacteria. Extracellular polymeric substances (EPS) constitute the physical scaffolding for bacterial biofilms and thus play central roles in their development and virulence. We show that newly synthesized amphiphilic fluorescent carbon dots (C-dots) readily bind to the EPS scaffold of Pseudomonas aeruginosa, a major biofilm-forming pathogen, resulting in unprecedented microscopic visualization of the EPS structural features. Fluorescence microscopy analysis utilizing the C-dots reveals that the P. aeruginosa EPS matrix exhibits a remarkable dendritic morphology. The experiments further illuminate the growth kinetics of the EPS and the effect of external factors such as temperature. We also show that the amphiphilic C-dot platform enabled screening of substances disrupting biofilm development, specifically quorum sensing inhibitors.
AB - Biofilm formation is a critical facet of pathogenesis and resilience of human, animal, and plant bacteria. Extracellular polymeric substances (EPS) constitute the physical scaffolding for bacterial biofilms and thus play central roles in their development and virulence. We show that newly synthesized amphiphilic fluorescent carbon dots (C-dots) readily bind to the EPS scaffold of Pseudomonas aeruginosa, a major biofilm-forming pathogen, resulting in unprecedented microscopic visualization of the EPS structural features. Fluorescence microscopy analysis utilizing the C-dots reveals that the P. aeruginosa EPS matrix exhibits a remarkable dendritic morphology. The experiments further illuminate the growth kinetics of the EPS and the effect of external factors such as temperature. We also show that the amphiphilic C-dot platform enabled screening of substances disrupting biofilm development, specifically quorum sensing inhibitors.
UR - http://www.scopus.com/inward/record.url?scp=84971268069&partnerID=8YFLogxK
U2 - 10.1021/acschembio.5b01000
DO - 10.1021/acschembio.5b01000
M3 - Article
AN - SCOPUS:84971268069
SN - 1554-8929
VL - 11
SP - 1265
EP - 1270
JO - ACS Chemical Biology
JF - ACS Chemical Biology
IS - 5
ER -