GVB contributed to overall study design, development of molecular

GVB contributed to overall study design, development of molecular methods and critical revision of the draft. NB contributed

to the overall study design, acquisition of clinical samples and data and drafting the manuscript. All authors read and approved the final manuscript.”
“Background Inorganic polyphosphate (polyP) is a chain of few or many hundreds of phosphate (Pi) residues linked by high-energy phosphoanhydride [1]. polyP has attracted considerable attention as a GRAS (generally recognized Stattic cost as safe) food additive by FDA with antimicrobial properties that can prevent spoilage of food [2,3]. polyP inhibits the growth of various gram-positive AZD1390 cost bacteria such as Staphylococcus aureus [4-8], Listeria monocytogenes [8,9], Sarcina lutea [7], Bacillus cereus [10], and mutans streptococci [11,12], and of fungi such as Aspergillus flavus [5]. The ability of polyP to chelate divalent cations is regarded as relevant

to the antibacterial effects, contributing to BLZ945 cell division inhibition and loss of cell-wall integrity [5,13,14]. On the other hand, large numbers of gram-negative bacteria including Escherichia coli and Salmonella enterica serovar Typhimurium are capable of growing in higher concentrations, even up to 10% of polyP [5,7,15]. Periodontal disease is caused by bacterial infection which is associated with gram-negative oral anaerobes. In our previous study [16], polyP (Nan+2PnO3n+1; n = the number of phosphorus atoms in the chain) with

RANTES different linear phosphorus (Pi) chain lengths (3 to 75) demonstrated to have antibacterial activity against Porphyromonas gingivalis, a black pigmented, gram-negative periodontopathogen. polyP also showed antibacterial activity against other black-pigmented, gram-negative oral anaerobes such as Prevotella intermedia and Porphyromonas endodontalis [17,18]. However, the antimicrobial mechanism of polyP against gram-negative bacteria has not yet been fully understood. In the past decade, global genome-wide studies of changes in expression patterns in response to existing and new antimicrobial agents have provided us with a deeper understanding of antimicrobial action [19]. In the present study, we performed the full-genome gene expression microarrays of P. gingivalis, and gene ontology (GO) and protein-protein interaction network analysis of the differentially expressed genes were also performed for elucidating the mechanism of antibacterial action of polyP. Results and discussion The complete list of the average gene expression values has been deposited in NCBI’s Gene Expression Omnibus (GEO) (http://​www.​ncbi.​nlm.​nih.​gov/​geo/​) and is accessible through GEO Series accession number GSE11471. Using filtering criteria of a 1.5 or greater fold-change in expression and significance P-values of <0.05, 706 out of 1,909 genes in P. gingivalis W83 were differentially expressed by polyP75 treatment.

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