Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/67467

TitleThe protective effect of Staphylococcus epidermidis biofilm matrix against phage predation
Author(s)Melo, Luís Daniel Rodrigues
Pinto, Maria Graça Cerqueira
Oliveira, Fernando Eduardo Freitas
Vilas Boas, Diana
Almeida, Carina
Sillankorva, Sanna
Cerca, Nuno
Azeredo, Joana
Keywordsphage
biofilms
biofilm matrix
phage/host interactions
S. epidermidis
Issue date25-Sep-2020
PublisherMDPI AG
JournalViruses
CitationMelo, Luís D. R.; Pinto, Graça; Oliveira, Fernando E.; Vilas Boas, Diana; Almeida, Carina; Sillankorva, Sanna; Cerca, Nuno; Azeredo, Joana, The protective effect of Staphylococcus epidermidis biofilm matrix against phage predation. Viruses, 12(10), 1076, 2020
Abstract(s)Staphylococcus epidermidis is a major causative agent of nosocomial infections, mainly associated with the use of indwelling devices, on which this bacterium forms structures known as biofilms. Due to biofilms’ high tolerance to antibiotics, virulent bacteriophages were previously tested as novel therapeutic agents. However, several staphylococcal bacteriophages were shown to be inefficient against biofilms. In this study, the previously characterized S. epidermidis-specific Sepunavirus phiIBB-SEP1 (SEP1), which has a broad spectrum and high activity against planktonic cells, was evaluated concerning its efficacy against S. epidermidis biofilms. The in vitro biofilm killing assays demonstrated a reduced activity of the phage. To understand the underlying factors impairing SEP1 inefficacy against biofilms, this phage was tested against distinct planktonic and biofilm-derived bacterial populations. Interestingly, SEP1 was able to lyse planktonic cells in different physiological states, suggesting that the inefficacy for biofilm control resulted from the biofilm 3D structure and the protective effect of the matrix. To assess the impact of the biofilm architecture on phage predation, SEP1 was tested in disrupted biofilms resulting in a 2 orders-of-magnitude reduction in the number of viable cells after 6 h of infection. The interaction between SEP1 and the biofilm matrix was further assessed by the addition of matrix to phage particles. Results showed that the matrix did not inactivate phages nor affected phage adsorption. Moreover, confocal laser scanning microscopy data demonstrated that phage infected cells were less predominant in the biofilm regions where the matrix was more abundant. Our results provide compelling evidence indicating that the biofilm matrix can work as a barrier, allowing the bacteria to be hindered from phage infection.
TypeArticle
URIhttp://hdl.handle.net/1822/67467
DOI10.3390/v12101076
e-ISSN1999-4915
Publisher versionhttps://www.mdpi.com/1999-4915/12/10/1076
Peer-Reviewedyes
AccessOpen access
Appears in Collections:CEB - Publicações em Revistas/Séries Internacionais / Publications in International Journals/Series

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