05). In terms of cultivable cells it was observed that no cultivable H. pylori were ever recovered from any of the mono or dual-species biofilms at any time point, with the exception of cells recovered from 1 day-old biofilms grown in the presence of M. chelonae or Sphingomonas
sp. (6.67 × 101 and 1.83 × 102 CFU cm-2, respectively). Discussion Auto and co-aggregation of L. pneumophila and H. pylori with drinking water bacteria In a previous study several bacterial strains were GANT61 order isolated from heterotrophic biofilms formed on uPVC coupons in a two-stage chemostat system . For the present work, the selection of the bacteria used was based on the prevalence of these isolated strains in biofilms, i.e., the strains that were always present BIX 1294 cost in biofilm samples when detected by culture were used rather than those only found intermittently. In the aggregation studies it was observed that there was no auto-aggregation of any of the bacteria tested in this study, as demonstrated previously for Brevundimonas vesicularis, Acidovorax delafieldii and V. paradoxus [34, 38]. No co-aggregation of L. pneumophila or H. pylori was observed
with any of the bacteria isolated from drinking water biofilms, demonstrating that while all learn more of the bacteria used in this study have the ability to form biofilms they are attaching to the uPVC surfaces without aggregating in the planktonic phase with the other microorganisms . L. pneumophila in biofilms The L. pneumophila cells from the inocula
prepared for the biofilm experiments were quantified for total, PNA-positive and cultivable cells. Results showed that cultivable and Oxaprozin PNA numbers were similar but were only 50% of the numbers obtained by SYTO 9 staining. It is still controversial whether PNA probes detect dead cells or if they just produce a detectable signal with viable cells. PNA probes have been used to detect pathogens in mixed biofilms but it has not been well established if this technique can also detect non-viable cells [23, 29, 39]. However the similarity in the cultivable and PNA-positive numbers, and the difference between PNA-labelled and total cells (stained by SYTO 9), strongly indicates that the PNA probe fails to detect dead cells. PNA probes bind specifically to rRNA molecules emitting a signal that can be visualized under microscopy. The intensity of that signal is related to the rRNA content, i.e., the higher the rRNA content the brighter the signal is . A very low content of rRNA would result in insufficient brightness and cells would not be visualized. After cellular death the content of rRNA decreases significantly and therefore some authors have suggested that the emission of a bright signal is a good indication of cell viability [39, 41, 42].