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TitleRole of daptomycin in the induction and persistence of the viable but non-culturable state of Staphylococcus Aureus biofilms
AbstractWe have recently demonstrated that antibiotic pressure can induce the viable but non-culturable (VBNC) state in Staphylococcus aureus biofilms. Since dormant bacterial cells can undermine anti-infective therapy, a greater understanding of the role of antibiotics of last resort, including daptomycin, is crucial. Methicillin-resistant S. aureus 10850 biofilms were maintained on non-nutrient (NN) agar in the presence or absence of the MIC of daptomycin until loss of culturability. Viable cells were monitored by epifluorescence microscopy and flow cytometry for 150 days. All biofilms reached non-culturability at 40 days and showed a similar amount of viable cells; however, in biofilms exposed to daptomycin, their number remained unchanged throughout the experiment, whereas in those maintained on NN agar alone, no viable cells were detected after 150 days. Gene expression assays showed that after achievement of non-culturability, 16S rDNA and mecA were expressed by all biofilms, whereas glt expression was found only in daptomycin-exposedbiofilms. Our findings suggest that low daptomycin concentrations, such as those that are likely to obtain within biofilms, can influence the viability and gene expression of non-culturable S. aureus cells. Resuscitation experiments are needed to establish the VBNC state of daptomycin-exposed biofilms.
SourcePathogens 3, pp. 759–768
KeywordsStaphylococcus aureus biofilm; VBNC; daptomycin
JournalPathogens
EditorMolecular Diversity Preservation International, Basel,
Year2014
TypeArticolo in rivista
DOI10.3390/pathogens3030759
AuthorsPasquaroli S.; Citterio B.; di Cesare A.D.; Amiri M.; Manti A.; Vuotto C.; Biavasco F.
Text420953 2014 10.3390/pathogens3030759 Scopus 2 s2.0 85006581427 Staphylococcus aureus biofilm; VBNC; daptomycin Role of daptomycin in the induction and persistence of the viable but non culturable state of Staphylococcus Aureus biofilms Pasquaroli S.; Citterio B.; di Cesare A.D.; Amiri M.; Manti A.; Vuotto C.; Biavasco F. Department of Life and Environmental Sciences, Polytechnic University of Marche, Ancona, 60131, , Italy; Department of Biomolecular Sciences, Sect. Toxicological, Hygiene, and Environmental Sciences, University of Urbino Carlo Bo, Urbino, 61029, , Italy; Department of Earth, Life and Environmental Sciences, University of Urbino Carlo Bo, Urbino, 61029, , Italy; Microbial Biofilm Laboratory, IRCCS Fondazione Santa Lucia, Rome, 00179, , Italy We have recently demonstrated that antibiotic pressure can induce the viable but non culturable VBNC state in Staphylococcus aureus biofilms. Since dormant bacterial cells can undermine anti infective therapy, a greater understanding of the role of antibiotics of last resort, including daptomycin, is crucial. Methicillin resistant S. aureus 10850 biofilms were maintained on non nutrient NN agar in the presence or absence of the MIC of daptomycin until loss of culturability. Viable cells were monitored by epifluorescence microscopy and flow cytometry for 150 days. All biofilms reached non culturability at 40 days and showed a similar amount of viable cells; however, in biofilms exposed to daptomycin, their number remained unchanged throughout the experiment, whereas in those maintained on NN agar alone, no viable cells were detected after 150 days. Gene expression assays showed that after achievement of non culturability, 16S rDNA and mecA were expressed by all biofilms, whereas glt expression was found only in daptomycin exposedbiofilms. Our findings suggest that low daptomycin concentrations, such as those that are likely to obtain within biofilms, can influence the viability and gene expression of non culturable S. aureus cells. Resuscitation experiments are needed to establish the VBNC state of daptomycin exposed biofilms. 3 Published version http //www.scopus.com/record/display.url eid=2 s2.0 85006581427 origin=inward Articolo in rivista Molecular Diversity Preservation International 2076 0817 Pathogens Pathogens andrea.dicesare DI CESARE ANDREA