4). Gingipain and hemagglutination activities were also restored in FLL350c (Figs 3 and 4), thus confirming a role for PG0162 in virulence regulation in P. gingivalis W83. It is noteworthy that although FLL354 had the lowest gingipain

activity, its hemolysin profile was similar to the wild-type strain. Taken together, this is consistent with previous observations suggesting that hemolysin and gingipain activities can be distinct from each other (Deshpande & Khan, 1999). Collectively, our study showed that ECF sigma factors PG0162 and PG1660 play an important role in the regulation Selleck MK-3475 of gingipain, hemolytic, and hemagglutination activities, and could likely modulate the virulence potential of P. gingivalis. Because the exterior surface structures and factors of the infectious bacteria are the first to come in contact

with the host and must respond and adapt to the host environment, our observations are consistent with the role of ECF sigma factors in the regulation of virulence-associated genes (reviewed in Brooks & Buchanan, 2008). The activity of ECF sigma factors is most often negatively regulated by direct interaction with cognate antisigma factors, which prevent their association with http://www.selleckchem.com/products/CP-690550.html the core RNA polymerase or facilitate holoenzyme dissociation (reviewed in Staron et al., 2009). While PG1660 appear to have a putative cognate antisigma factor PG1659 (http://www.oralgen.lanl.gov/, http://www.cbs.dtu.dk/services/TMHMM/), a similar putative component is missing for PG0162. It is noteworthy

that the regulation of PG0162 on virulence observed in this study is occurring at the post-transcriptional level. It is likely that PG0162 may be involved in a unique and complex regulatory mechanism, and this requires further evaluation. This work was supported by Loma Linda University and Public Health Grant DE13664 and DE019730 from NIDCR (to H.M.F.). ”
“A technique based on an inverted Petri dish system was developed for the growth and isolation of soil oxalotrophic bacteria able to disperse on fungal mycelia. The method is related to the ‘fungal highways’ dispersion theory in which mycelial fungal networks allow active movement of bacteria in soil. Quantification of this phenomenon showed that bacterial dispersal occurs preferentially STK38 in upper soil horizons. Eight bacteria and one fungal strain were isolated by this method. The oxalotrophic activity of the isolated bacteria was confirmed through calcium oxalate dissolution in solid selective medium. After separation of the bacteria–fungus couple, partial sequencing of the 16S and the ITS1 and ITS2 sequences of the ribosomal RNA genes were used for the identification of bacteria and the associated fungus. The isolated oxalotrophic bacteria included strains related to Stenotrophomonas, Achromobacter, Lysobacter, Pseudomonas, Agrobacterium, Cohnella, and Variovorax. The recovered fungus corresponded to Trichoderma sp.