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Charette, S. J.

Publications and source records attributed to Charette, S. J..

2 recordsLinked to original sources

Quantitative measurements of shear stress-dependent adhesion and motion of Dictyostelium discoideum cells in a microfluidic device

Shear stress plays a crucial role in modulating cell adhesion and signaling. We present a microfluidic shear stress generator used to investigate the adhesion dynamics of Dictyostelium discoideum, an amoeba cell model organism with well-characterized adhesion properties. We applied shear stress and tracked cell adhesion, motility, and detachment using time-lapse videomicroscopy. In the precise shear conditions generated on-chip, our results show cell migration patterns influenced by shear stress, with cells displaying an adaptive response to shear forces as they alter their adhesion and motility behavior in reaction to shear stress. Additionally, we observed that DH1-10 wild-type D. discoideum cells exhibit stronger adhesion and resistance to shear-induced detachment compared to phg2 adhesion-defective mutant cells and also highlighted the influence of initial cell density on detachment behavior.

microbiology↗

Escherichia coli O157:H7 responds to phosphate starvation by modifying LPS involved in biofilm formation

In open environments such as water, enterohemorrhagic Escherichia coli O157:H7 responds to inorganic phosphate (Pi) starvation by inducing the Pho regulon controlled by PhoB. The phosphate-specific transport (Pst) system is the high-affinity Pi transporter. In the {Delta}pst mutant, PhoB is constitutively activated and regulates the expression of genes from the Pho regulon. In E. coli O157:H7, the {Delta}pst mutant, biofilm, and autoagglutination were increased. In the double-deletion mutant {Delta}pst {Delta}phoB, biofilm and autoagglutination were similar to the wild-type strain, suggesting that PhoB is involved. We investigated the relationship between PhoB activation and enhanced biofilm formation by screening a transposon mutant library derived from {Delta}pst mutant for decreased autoagglutination and biofilms mutants. Lipopolysaccharide (LPS) genes involved in the synthesis of the LPS core were identified. Transcriptomic studies indicate the influence of Pi-starvation and pst mutation on LPS biosynthetic gene expression. LPS analysis indicated that the O-antigen was deficient in the {Delta}pst mutant. Interestingly, waaH, encoding a glycosyltransferase associated with LPS modifications in E. coli K-12, was highly expressed in the {Delta}pst mutant of E. coli O157:H7. Deletion of waaH from the {Delta}pst mutant and from the wild-type strain grown in Pi-starvation conditions decreased the biofilm formation but without affecting LPS. Our findings suggest that LPS core is involved in the autoagglutination and biofilm phenotypes of the {Delta}pst mutant and that WaaH plays a role in biofilm in response to Pi-starvation. This study highlights the importance of Pi-starvation in biofilm formation of E. coli O157:H7, which may affect its transmission and persistence. IMPORTANCEEnterohemorrhagic Escherichia coli O157:H7 is a human pathogen responsible for bloody diarrhea and renal failures. In the environment, O157:H7 can survive for prolonged periods of time under nutrient-deprived conditions. Biofilms are thought to participate in this environmental lifestyle. Previous reports have shown that the availability of extracellular inorganic phosphate (Pi) affected bacterial biofilm formation; however, nothing was known about O157:H7 biofilm formation. Our results show that O157:H7 membrane undergoes modifications upon PhoB activation leading to increased biofilm formation. A mutation in the Pst system results in reduced amount of the smooth type LPS and that this could influence the biofilm composition. This demonstrates how the E. coli O157:H7 adapts to Pi starvation increasing its ability to occupy different ecological niches.

microbiology↗