Discussion The molecular mechanisms

involved in the initial interactions between Brucella and epithelial cells have not been well characterized. Previous studies have used HeLa cells as a model for studying adhesion and internalization of Brucella spp. in non-professional phagocytic cells [9, 10]. These studies found that brucellae bind to cellular receptors containing sialic acid residues and induce their own uptake by a local rearrangement of the host cell cytoskeleton around the invading organisms. The ability of the bacteria to adhere to and penetrate eukaryotic cells is a well orchestrated process that requires several factors/gene selleck chemicals products in order to be successful [28]. To date, only a few Brucella gene products involved in non-phagocytic cell invasion have been identified [11, 13, 14]. This study was Ro 61-8048 concentration performed with the goal of better understanding

initial molecular interactions between Brucella and its host through the molecular analysis PSI-7977 of growth phase-specific gene regulation. Our initial experiment indicated that cultures of B. melitensis at late-log growth phase in cell culture medium were more invasive to non-phagocytic cells than cultures at mid-log and stationary growth phases. Similar results have been observed for other invasive pathogens, such as Salmonella spp. or Yersinia enterocolitica [29, 30]. Even with the high MOI used (1,000:1), B. melitensis were internalized in lower numbers by epithelioid-like

HeLa cells at 30 min p.i. than reported in another study [14]. The difference in invasion may have been influenced by the F12K cell culture medium used to growth the agent. B. melitensis reach stationary phase at Rolziracetam a lower OD (A600 nm) in F12K cell culture medium than in rich bacterial culture medium (Tryptic soy broth; TSB) or another cell culture medium (complete RPMI1640 medium supplemented with 10% HI-FBS) (0.72 vs. 1.6 vs. 0.95, respectively; data not shown). These results suggest that F12K medium apparently contains suboptimal nutrients for Brucella development. Even though, we grew B. melitensis in F12K medium and immediately added the bacteria to HeLa cells with the goal of reducing bacterial pre-infection manipulations (centrifugation, washes and transfer to fresh new media), which had probably modified the original transcriptome of the cultures, since bacterial gene expression changes quickly in response to environmental modification [31]. The relationship between growth phase and invasiveness is dependent upon the expression of bacterial virulence factors at different growth-phase.