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Liquid-Infused Structured Titanium Surfaces: Antiadhesive Mechanism to Repel Streptococcus oralis Biofilms

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autorschaft

  • Katharina Doll
  • Ines Yang
  • Elena Fadeeva
  • Nadine Kommerein
  • Boris N. Chichkov

Organisationseinheiten

Externe Organisationen

  • Medizinische Hochschule Hannover (MHH)

Details

OriginalspracheEnglisch
Seiten (von - bis)23026-23038
Seitenumfang13
FachzeitschriftACS Applied Materials and Interfaces
Jahrgang11
Ausgabenummer26
Frühes Online-Datum7 Juni 2019
PublikationsstatusVeröffentlicht - 3 Juli 2019

Abstract

To combat implant-associated infections, there is a need for novel materials which effectively inhibit bacterial biofilm formation. In the present study, the antiadhesive properties of titanium surface functionalization based on the "slippery liquid-infused porous surfaces" (SLIPS) principle were demonstrated and the underlying mechanism was analyzed. The immobilized liquid layer was stable over 13 days of continuous flow in an oral flow chamber system. With increasing flow rates, the surface exhibited a significant reduction in attached biofilm of both the oral initial colonizer Streptococcus oralis and an oral multispecies biofilm composed of S. oralis, Actinomyces naeslundii, Veillonella dispar, and Porphyromonas gingivalis. Using single cell force spectroscopy, reduced S. oralis adhesion forces on the lubricant layer could be measured. Gene expression patterns in biofilms on SLIPS, on control surfaces, and expression patterns of planktonic cultures were also compared. For this purpose, the genome of S. oralis strain ATCC 9811 was sequenced using PacBio Sequel technology. Even though biofilm cells showed clear changes in gene expression compared to planktonic cells, no differences could be detected between bacteria on SLIPS and on control surfaces. Therefore, it can be concluded that the ability of liquid-infused titanium to repel S. oralis biofilms is mainly due to weakened bacterial adhesion to the underlying liquid interface.

ASJC Scopus Sachgebiete

Zitieren

Liquid-Infused Structured Titanium Surfaces: Antiadhesive Mechanism to Repel Streptococcus oralis Biofilms. / Doll, Katharina; Yang, Ines; Fadeeva, Elena et al.
in: ACS Applied Materials and Interfaces, Jahrgang 11, Nr. 26, 03.07.2019, S. 23026-23038.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Doll, K, Yang, I, Fadeeva, E, Kommerein, N, Szafrański, SP, Bei Der Wieden, G, Greuling, A, Winkel, A, Chichkov, BN, Stumpp, NS & Stiesch, M 2019, 'Liquid-Infused Structured Titanium Surfaces: Antiadhesive Mechanism to Repel Streptococcus oralis Biofilms', ACS Applied Materials and Interfaces, Jg. 11, Nr. 26, S. 23026-23038. https://doi.org/10.1021/acsami.9b06817
Doll, K., Yang, I., Fadeeva, E., Kommerein, N., Szafrański, S. P., Bei Der Wieden, G., Greuling, A., Winkel, A., Chichkov, B. N., Stumpp, N. S., & Stiesch, M. (2019). Liquid-Infused Structured Titanium Surfaces: Antiadhesive Mechanism to Repel Streptococcus oralis Biofilms. ACS Applied Materials and Interfaces, 11(26), 23026-23038. https://doi.org/10.1021/acsami.9b06817
Doll K, Yang I, Fadeeva E, Kommerein N, Szafrański SP, Bei Der Wieden G et al. Liquid-Infused Structured Titanium Surfaces: Antiadhesive Mechanism to Repel Streptococcus oralis Biofilms. ACS Applied Materials and Interfaces. 2019 Jul 3;11(26):23026-23038. Epub 2019 Jun 7. doi: 10.1021/acsami.9b06817
Doll, Katharina ; Yang, Ines ; Fadeeva, Elena et al. / Liquid-Infused Structured Titanium Surfaces : Antiadhesive Mechanism to Repel Streptococcus oralis Biofilms. in: ACS Applied Materials and Interfaces. 2019 ; Jahrgang 11, Nr. 26. S. 23026-23038.
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title = "Liquid-Infused Structured Titanium Surfaces: Antiadhesive Mechanism to Repel Streptococcus oralis Biofilms",
abstract = "To combat implant-associated infections, there is a need for novel materials which effectively inhibit bacterial biofilm formation. In the present study, the antiadhesive properties of titanium surface functionalization based on the {"}slippery liquid-infused porous surfaces{"} (SLIPS) principle were demonstrated and the underlying mechanism was analyzed. The immobilized liquid layer was stable over 13 days of continuous flow in an oral flow chamber system. With increasing flow rates, the surface exhibited a significant reduction in attached biofilm of both the oral initial colonizer Streptococcus oralis and an oral multispecies biofilm composed of S. oralis, Actinomyces naeslundii, Veillonella dispar, and Porphyromonas gingivalis. Using single cell force spectroscopy, reduced S. oralis adhesion forces on the lubricant layer could be measured. Gene expression patterns in biofilms on SLIPS, on control surfaces, and expression patterns of planktonic cultures were also compared. For this purpose, the genome of S. oralis strain ATCC 9811 was sequenced using PacBio Sequel technology. Even though biofilm cells showed clear changes in gene expression compared to planktonic cells, no differences could be detected between bacteria on SLIPS and on control surfaces. Therefore, it can be concluded that the ability of liquid-infused titanium to repel S. oralis biofilms is mainly due to weakened bacterial adhesion to the underlying liquid interface.",
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author = "Katharina Doll and Ines Yang and Elena Fadeeva and Nadine Kommerein and Szafra{\'n}ski, {Szymon P.} and {Bei Der Wieden}, Gesa and Andreas Greuling and Andreas Winkel and Chichkov, {Boris N.} and Stumpp, {Nico S.} and Meike Stiesch",
note = "unding information: The authors would like to thank: Marcus Stollhans and Costenoble GmbH & Co. KG for kindly providing Krytox lubricant; Patrick Lang and Henrik Peisker from Nanosurf AG and Dario Ossola from Cytosurge AG for their substantial support with single bacterial cell force spectroscopy; Marly Dalton and Rainer Schreeb for genome sequencing; Agnes Nielsen, Michael Jarek, Sabin Bhuju and Susanne H{\"a}u{\ss}ler from the Helmholtz Center for Infection Research for cDNA synthesis and RNASeq; and Lara K{\"u} hnle, Kerstin Elbert and Ronja Hagemeier for excellent technical assistance.",
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Download

TY - JOUR

T1 - Liquid-Infused Structured Titanium Surfaces

T2 - Antiadhesive Mechanism to Repel Streptococcus oralis Biofilms

AU - Doll, Katharina

AU - Yang, Ines

AU - Fadeeva, Elena

AU - Kommerein, Nadine

AU - Szafrański, Szymon P.

AU - Bei Der Wieden, Gesa

AU - Greuling, Andreas

AU - Winkel, Andreas

AU - Chichkov, Boris N.

AU - Stumpp, Nico S.

AU - Stiesch, Meike

N1 - unding information: The authors would like to thank: Marcus Stollhans and Costenoble GmbH & Co. KG for kindly providing Krytox lubricant; Patrick Lang and Henrik Peisker from Nanosurf AG and Dario Ossola from Cytosurge AG for their substantial support with single bacterial cell force spectroscopy; Marly Dalton and Rainer Schreeb for genome sequencing; Agnes Nielsen, Michael Jarek, Sabin Bhuju and Susanne Häußler from the Helmholtz Center for Infection Research for cDNA synthesis and RNASeq; and Lara Kü hnle, Kerstin Elbert and Ronja Hagemeier for excellent technical assistance.

PY - 2019/7/3

Y1 - 2019/7/3

N2 - To combat implant-associated infections, there is a need for novel materials which effectively inhibit bacterial biofilm formation. In the present study, the antiadhesive properties of titanium surface functionalization based on the "slippery liquid-infused porous surfaces" (SLIPS) principle were demonstrated and the underlying mechanism was analyzed. The immobilized liquid layer was stable over 13 days of continuous flow in an oral flow chamber system. With increasing flow rates, the surface exhibited a significant reduction in attached biofilm of both the oral initial colonizer Streptococcus oralis and an oral multispecies biofilm composed of S. oralis, Actinomyces naeslundii, Veillonella dispar, and Porphyromonas gingivalis. Using single cell force spectroscopy, reduced S. oralis adhesion forces on the lubricant layer could be measured. Gene expression patterns in biofilms on SLIPS, on control surfaces, and expression patterns of planktonic cultures were also compared. For this purpose, the genome of S. oralis strain ATCC 9811 was sequenced using PacBio Sequel technology. Even though biofilm cells showed clear changes in gene expression compared to planktonic cells, no differences could be detected between bacteria on SLIPS and on control surfaces. Therefore, it can be concluded that the ability of liquid-infused titanium to repel S. oralis biofilms is mainly due to weakened bacterial adhesion to the underlying liquid interface.

AB - To combat implant-associated infections, there is a need for novel materials which effectively inhibit bacterial biofilm formation. In the present study, the antiadhesive properties of titanium surface functionalization based on the "slippery liquid-infused porous surfaces" (SLIPS) principle were demonstrated and the underlying mechanism was analyzed. The immobilized liquid layer was stable over 13 days of continuous flow in an oral flow chamber system. With increasing flow rates, the surface exhibited a significant reduction in attached biofilm of both the oral initial colonizer Streptococcus oralis and an oral multispecies biofilm composed of S. oralis, Actinomyces naeslundii, Veillonella dispar, and Porphyromonas gingivalis. Using single cell force spectroscopy, reduced S. oralis adhesion forces on the lubricant layer could be measured. Gene expression patterns in biofilms on SLIPS, on control surfaces, and expression patterns of planktonic cultures were also compared. For this purpose, the genome of S. oralis strain ATCC 9811 was sequenced using PacBio Sequel technology. Even though biofilm cells showed clear changes in gene expression compared to planktonic cells, no differences could be detected between bacteria on SLIPS and on control surfaces. Therefore, it can be concluded that the ability of liquid-infused titanium to repel S. oralis biofilms is mainly due to weakened bacterial adhesion to the underlying liquid interface.

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KW - FluidFM

KW - oral multispecies biofilm

KW - RNASeq

KW - Slippery liquid-infused porous surface

KW - Streptococcus oralis genome sequencing

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