TY - JOUR
T1 - Interplay between Immune and Bacterial Cells on a Biomimetic Nanostructured Surface
T2 - A “Race for the Surface” Study
AU - Bright, Richard
AU - Hayles, Andrew
AU - Wood, Jonathan
AU - Palms, Dennis
AU - Barker, Dan
AU - Vasilev, Krasimir
PY - 2023/9/18
Y1 - 2023/9/18
N2 - Biomaterial-associated infection is an ever-increasing risk with devasting consequences for patients. Considerable research has been undertaken to address this issue by imparting antibacterial properties to the surface of biomedical implants. One approach that generated much interest over recent years was the generation of bioinspired bactericidal nanostructures. In the present report, we have investigated the interplay between macrophages and bacteria on antibacterial nanostructured surfaces to determine the outcome of the so-called “race for the surface”. Our results showed that macrophages can indeed outcompete Staphylococcus aureus via multiple mechanisms. The early generation of reactive oxygen species by macrophages, downregulation of bacterial virulence gene expression, and the bactericidal nature of the nanostructured surface itself collectively acted to help the macrophage to win the race. This study highlights the potential of nanostructured surfaces to reduce infection rates and improve the long-term success of biomedical implants. This work can also serve as guidance to others to investigate in vitro host-bacteria interactions on other candidate antibacterial surfaces.
AB - Biomaterial-associated infection is an ever-increasing risk with devasting consequences for patients. Considerable research has been undertaken to address this issue by imparting antibacterial properties to the surface of biomedical implants. One approach that generated much interest over recent years was the generation of bioinspired bactericidal nanostructures. In the present report, we have investigated the interplay between macrophages and bacteria on antibacterial nanostructured surfaces to determine the outcome of the so-called “race for the surface”. Our results showed that macrophages can indeed outcompete Staphylococcus aureus via multiple mechanisms. The early generation of reactive oxygen species by macrophages, downregulation of bacterial virulence gene expression, and the bactericidal nature of the nanostructured surface itself collectively acted to help the macrophage to win the race. This study highlights the potential of nanostructured surfaces to reduce infection rates and improve the long-term success of biomedical implants. This work can also serve as guidance to others to investigate in vitro host-bacteria interactions on other candidate antibacterial surfaces.
KW - antibacterial
KW - biocompatible
KW - bioinspired
KW - competitive colonization
KW - gene expression
KW - macrophage
UR - http://www.scopus.com/inward/record.url?scp=85164927262&partnerID=8YFLogxK
UR - http://purl.org/au-research/grants/NHMRC/1194466
UR - http://purl.org/au-research/grants/ARC/DP180101254
U2 - 10.1021/acsabm.3c00351
DO - 10.1021/acsabm.3c00351
M3 - Article
AN - SCOPUS:85164927262
SN - 2576-6422
VL - 6
SP - 3472
EP - 3483
JO - ACS Applied Bio Materials
JF - ACS Applied Bio Materials
IS - 9
ER -