Version 2 2021-11-23, 17:04Version 2 2021-11-23, 17:04
Version 1 2021-11-22, 19:07Version 1 2021-11-22, 19:07
journal contribution
posted on 2021-11-23, 17:04authored byMartin Müller, Birgit Urban, Gopala Krishna Mannala, Volker Alt
Herein,
polyelectrolyte (PEL)-based coatings including peripherally
bound bacteriophages (PHAG) at model substrates are reported to showcase
their applicability on surgically relevant implants with respect to
surface protection against bacterial proliferation and biofilm formation.
The established layer-by-layer concept based on the consecutive adsorption
of oppositely charged PEL was applied to generate polyelectrolyte
multilayer (PEM) coatings with either a cationic or anionic excess
surface charge. PHAG were bound at the outermost layer of such PEM
coatings utilizing electrostatic interaction forces. Branched poly(ethyleneimine)
(PEI) and poly(acrylic acid) (PAA) as cationic and anionic PEL, respectively,
and theEscherichia coli T4 bacteriophage
(T4 PHAG) and the Staphylococcus aureus bacteriophage (S.a. PHAG) were used. At first, PEM of PEI/PAA were
consecutively adsorbed from solutions at germanium model substrates
with z = 4 and 5 adsorption steps providing PAA-terminated
PEM-4 and PEI-terminated PEM-5, which were characterized by surface-sensitive
in situ attenuated total reflection Fourier transform infrared spectroscopy.
Second, both T4 and S.a. PHAG were bound to these PEM showing a higher
bound amount at cationic PEM-5 compared to anionic PEM-4. Electrostatic
interaction forces between anionic capsid proteins and respective
PEM are suggested. Furthermore, scanning force microscopy revealed
typical overall size (200–250 nm) and shape (head/tail) features
of the bound PHAG and supported qualitatively the preference for cationic
PEM-5 by number. Finally, PEM-4 and PEM-5 were deposited at standard
agar plates, S.a. PHAG were bound to those PEM, and plaque assay was
performed to check antibacterial properties. Thereby, coatings of
PHAG/PEM-5 showed a higher antibacterial activity and PHAG/PEM-4 a
lower one, which was evidenced by plaque formation testing. Conclusively,
PHAG/PEM coatings are promising for the reduction of implant-associated
infections at surgical implants and thus may replace or complement
established coatings based on low molecular synthetic antibiotics.