Negative pressures in full-scale distribution system: field investigation, modelling, estimation of intrusion volumes and risk for public health

International audienceVarious investigations encompassing microbial characterization of external sources of contamination (soil and trenchwater surrounding water mains, flooded air-valve vaults), field pressure monitoring, and hydraulic and transient analyses were conducted in the same distribution system where two epidemiological studies showing an increase in gastrointestinal illness for people drinking tap water were conducted in the 1990's. Interesting results include the detection of microorganisms indicators of fecal contamination in all external sources investigated but at a higher frequency in the water from flooded air-valve vaults, and the recording of 18 negative pressure events in the distribution system during a 17-month monitoring period. Transient analysis of this large and complex distribution system was challenging and highlighted the need to consider field pressure data in the process

icsB: a Shigella flexneri virulence gene necessary for the lysis of protrusions during intercellular spread

Shigella flexneri causes bacillary dysentery by invading epithelial cells of the colonic mucosa. We have characterized the icsB gene which is located on the virulence plasmid pWR100. After inactivation of icsB, the mutant strain remained invasive, but formed abnormally small plaques on HeLa cell monolayers, colonized only the peripheral cells of Caco-2 islets, and was unable to provoke a keratoconjunctivitis in guinea-pigs. Examination of infected HeLa cells showed that the icsB mutant was able to lyse the phagocytic vacuole and to form protrusions at the surface of infected cells, but, unlike the wild type, remained trapped in protrusions surrounded by two membranes. These results indicate that IcsB is involved in the lysis of the protrusions, a step necessary for intercellular spread.Journal ArticleResearch Support, Non-U.S. Gov'tFLWNAinfo:eu-repo/semantics/publishe

Dynamic interactions between the rna chaperone hfq, small regulatory rnas and mrnas in live bacterial cells

RNA-binding proteins play myriad roles in regulating RNAs and RNA-mediated functions. In bacteria, the RNA chaperone Hfq is an important post-transcriptional gene regulator. Using live-cell super-resolution imaging, we can distinguish Hfq binding to different sizes of cellular RNAs. We demonstrate that under normal growth conditions, Hfq exhibits widespread mRNA-binding activity, with the distal face of Hfq contributing mostly to the mRNA binding in vivo. In addition, sRNAs can either co-occupy Hfq with the mRNA as a ternary complex, or displace the mRNA from Hfq in a binding face-dependent manner, suggesting mechanisms through which sRNAs rapidly access Hfq to induce sRNA-mediated gene regulation. Finally, our data suggest that binding of Hfq to certain mRNAs through its distal face can recruit RNase E to promote turnover of these mRNAs in an sRNA-independent manner, and such regulatory function of Hfq can be decoyed by sRNA competitors that bind strongly at the distal face