The treatment of bone and joint infections is challenging due to the presence of bacterial biofilm and the increasing emergence of multiresistant strains. BAG-S53P4 is a bone substitute that is characterized by osteoconductive and antimicrobial properties. The aim of this study was to assess the effectiveness of BAG-S53P4 against biofilm produced in vitro by multiresistant bacterial strains. METHODS: Multiresistant Staphylococcus epidermidis, Acinetobacter baumannii and Klebsiella pneumoniae isolated from bone and joint infections were used in this study. Titanium discs covered by bacterial biofilm were incubated with BAG-S53P4 or inert glass as a control. The amount of biofilm on each titanium disc was evaluated after 48 h of incubation by means of confocal laser scanning microscopy. RESULTS: Significantly lower total biomass volumes were observed for all strains after treatment with BAG-S53P4 when compared with controls. Moreover, the percentage of dead cells was significantly higher in treated samples than in controls for all the tested strains. CONCLUSIONS: BAG-S53P4 is able to reduce the biofilm produced by multiresistant S. epidermidis, A. baumannii and K. pneumoniae on titanium substrates in vitro, probably by interfering with cell viability. Owing to its osteoconductive, antibacterial and antibiofilm properties, the use of BAG-S53P4 may be a successful strategy for the treatment of bone and prosthetic joint infections.

Antibiofilm agents against MDR bacterial strains : is bioactive glass BAG-S53P4 also effective? / M. Bortolin, E. De Vecchi, C.L. Romanò, M. Toscano, R. Mattina, L. Drago. - In: JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY. - ISSN 0305-7453. - 71:1(2016 Jan), pp. 123-127. [10.1093/jac/dkv327]

Antibiofilm agents against MDR bacterial strains : is bioactive glass BAG-S53P4 also effective?

M. Bortolin;E. De Vecchi;M. Toscano;R. Mattina;L. Drago
2016

Abstract

The treatment of bone and joint infections is challenging due to the presence of bacterial biofilm and the increasing emergence of multiresistant strains. BAG-S53P4 is a bone substitute that is characterized by osteoconductive and antimicrobial properties. The aim of this study was to assess the effectiveness of BAG-S53P4 against biofilm produced in vitro by multiresistant bacterial strains. METHODS: Multiresistant Staphylococcus epidermidis, Acinetobacter baumannii and Klebsiella pneumoniae isolated from bone and joint infections were used in this study. Titanium discs covered by bacterial biofilm were incubated with BAG-S53P4 or inert glass as a control. The amount of biofilm on each titanium disc was evaluated after 48 h of incubation by means of confocal laser scanning microscopy. RESULTS: Significantly lower total biomass volumes were observed for all strains after treatment with BAG-S53P4 when compared with controls. Moreover, the percentage of dead cells was significantly higher in treated samples than in controls for all the tested strains. CONCLUSIONS: BAG-S53P4 is able to reduce the biofilm produced by multiresistant S. epidermidis, A. baumannii and K. pneumoniae on titanium substrates in vitro, probably by interfering with cell viability. Owing to its osteoconductive, antibacterial and antibiofilm properties, the use of BAG-S53P4 may be a successful strategy for the treatment of bone and prosthetic joint infections.
No
English
Settore MED/07 - Microbiologia e Microbiologia Clinica
Articolo
Esperti anonimi
Pubblicazione scientifica
gen-2016
12-ott-2015
Oxford University Press
71
1
123
127
5
Pubblicato
Periodico con rilevanza internazionale
Aderisco
info:eu-repo/semantics/article
Antibiofilm agents against MDR bacterial strains : is bioactive glass BAG-S53P4 also effective? / M. Bortolin, E. De Vecchi, C.L. Romanò, M. Toscano, R. Mattina, L. Drago. - In: JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY. - ISSN 0305-7453. - 71:1(2016 Jan), pp. 123-127. [10.1093/jac/dkv327]
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Prodotti della ricerca::01 - Articolo su periodico
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262
Article (author)
no
M. Bortolin, E. De Vecchi, C.L. Romanò, M. Toscano, R. Mattina, L. Drago
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/342641
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