Fructooligosacharides reduce Pseudomonas aeruginosa PAO1 pathogenicity through distinct mechanisms. 2014

Mercedes Ortega-González, and Fermín Sánchez de Medina, and Carlos Molina-Santiago, and Rocío López-Posadas, and Daniel Pacheco, and Tino Krell, and Olga Martínez-Augustin, and Daddaoua Abdelali
Department of Biochemistry and Molecular Biology II, Centre of networked Biomedical Research about Hepatic and Digestive Diseases, School of Pharmacy, University of Granada, Granada, Spain.

Pseudomonas aeruginosa is ubiquitously present in the environment and acts as an opportunistic pathogen on humans, animals and plants. We report here the effects of the prebiotic polysaccharide inulin and its hydrolysed form FOS on this bacterium. FOS was found to inhibit bacterial growth of strain PAO1, while inulin did not affect growth rate or yield in a significant manner. Inulin stimulated biofilm formation, whereas a dramatic reduction of the biofilm formation was observed in the presence of FOS. Similar opposing effects were observed for bacterial motility, where FOS inhibited the swarming and twitching behaviour whereas inulin caused its stimulation. In co-cultures with eukaryotic cells (macrophages) FOS and, to a lesser extent, inulin reduced the secretion of the inflammatory cytokines IL-6, IL-10 and TNF-α. Western blot experiments indicated that the effects mediated by FOS in macrophages are associated with a decreased activation of the NF-κB pathway. Since FOS and inulin stimulate pathway activation in the absence of bacteria, the FOS mediated effect is likely to be of indirect nature, such as via a reduction of bacterial virulence. Further, this modulatory effect is observed also with the highly virulent ptxS mutated strain. Co-culture experiments of P. aeruginosa with IEC18 eukaryotic cells showed that FOS reduces the concentration of the major virulence factor, exotoxin A, suggesting that this is a possible mechanism for the reduction of pathogenicity. The potential of these compounds as components of antibacterial and anti-inflammatory cocktails is discussed.

UI MeSH Term Description Entries
D007328 Insulin A 51-amino acid pancreatic hormone that plays a major role in the regulation of glucose metabolism, directly by suppressing endogenous glucose production (GLYCOGENOLYSIS; GLUCONEOGENESIS) and indirectly by suppressing GLUCAGON secretion and LIPOLYSIS. Native insulin is a globular protein comprised of a zinc-coordinated hexamer. Each insulin monomer containing two chains, A (21 residues) and B (30 residues), linked by two disulfide bonds. Insulin is used as a drug to control insulin-dependent diabetes mellitus (DIABETES MELLITUS, TYPE 1). Iletin,Insulin A Chain,Insulin B Chain,Insulin, Regular,Novolin,Sodium Insulin,Soluble Insulin,Chain, Insulin B,Insulin, Sodium,Insulin, Soluble,Regular Insulin
D008264 Macrophages The relatively long-lived phagocytic cell of mammalian tissues that are derived from blood MONOCYTES. Main types are PERITONEAL MACROPHAGES; ALVEOLAR MACROPHAGES; HISTIOCYTES; KUPFFER CELLS of the liver; and OSTEOCLASTS. They may further differentiate within chronic inflammatory lesions to EPITHELIOID CELLS or may fuse to form FOREIGN BODY GIANT CELLS or LANGHANS GIANT CELLS. (from The Dictionary of Cell Biology, Lackie and Dow, 3rd ed.) Bone Marrow-Derived Macrophages,Monocyte-Derived Macrophages,Macrophage,Macrophages, Monocyte-Derived,Bone Marrow Derived Macrophages,Bone Marrow-Derived Macrophage,Macrophage, Bone Marrow-Derived,Macrophage, Monocyte-Derived,Macrophages, Bone Marrow-Derived,Macrophages, Monocyte Derived,Monocyte Derived Macrophages,Monocyte-Derived Macrophage
D009154 Mutation Any detectable and heritable change in the genetic material that causes a change in the GENOTYPE and which is transmitted to daughter cells and to succeeding generations. Mutations
D009844 Oligosaccharides Carbohydrates consisting of between two (DISACCHARIDES) and ten MONOSACCHARIDES connected by either an alpha- or beta-glycosidic link. They are found throughout nature in both the free and bound form. Oligosaccharide
D011550 Pseudomonas aeruginosa A species of gram-negative, aerobic, rod-shaped bacteria commonly isolated from clinical specimens (wound, burn, and urinary tract infections). It is also found widely distributed in soil and water. P. aeruginosa is a major agent of nosocomial infection. Bacillus aeruginosus,Bacillus pyocyaneus,Bacterium aeruginosum,Bacterium pyocyaneum,Micrococcus pyocyaneus,Pseudomonas polycolor,Pseudomonas pyocyanea
D002460 Cell Line Established cell cultures that have the potential to propagate indefinitely. Cell Lines,Line, Cell,Lines, Cell
D002478 Cells, Cultured Cells propagated in vitro in special media conducive to their growth. Cultured cells are used to study developmental, morphologic, metabolic, physiologic, and genetic processes, among others. Cultured Cells,Cell, Cultured,Cultured Cell
D004268 DNA-Binding Proteins Proteins which bind to DNA. The family includes proteins which bind to both double- and single-stranded DNA and also includes specific DNA binding proteins in serum which can be used as markers for malignant diseases. DNA Helix Destabilizing Proteins,DNA-Binding Protein,Single-Stranded DNA Binding Proteins,DNA Binding Protein,DNA Single-Stranded Binding Protein,SS DNA BP,Single-Stranded DNA-Binding Protein,Binding Protein, DNA,DNA Binding Proteins,DNA Single Stranded Binding Protein,DNA-Binding Protein, Single-Stranded,Protein, DNA-Binding,Single Stranded DNA Binding Protein,Single Stranded DNA Binding Proteins
D004847 Epithelial Cells Cells that line the inner and outer surfaces of the body by forming cellular layers (EPITHELIUM) or masses. Epithelial cells lining the SKIN; the MOUTH; the NOSE; and the ANAL CANAL derive from ectoderm; those lining the RESPIRATORY SYSTEM and the DIGESTIVE SYSTEM derive from endoderm; others (CARDIOVASCULAR SYSTEM and LYMPHATIC SYSTEM) derive from mesoderm. Epithelial cells can be classified mainly by cell shape and function into squamous, glandular and transitional epithelial cells. Adenomatous Epithelial Cells,Columnar Glandular Epithelial Cells,Cuboidal Glandular Epithelial Cells,Glandular Epithelial Cells,Squamous Cells,Squamous Epithelial Cells,Transitional Epithelial Cells,Adenomatous Epithelial Cell,Cell, Adenomatous Epithelial,Cell, Epithelial,Cell, Glandular Epithelial,Cell, Squamous,Cell, Squamous Epithelial,Cell, Transitional Epithelial,Cells, Adenomatous Epithelial,Cells, Epithelial,Cells, Glandular Epithelial,Cells, Squamous,Cells, Squamous Epithelial,Cells, Transitional Epithelial,Epithelial Cell,Epithelial Cell, Adenomatous,Epithelial Cell, Glandular,Epithelial Cell, Squamous,Epithelial Cell, Transitional,Epithelial Cells, Adenomatous,Epithelial Cells, Glandular,Epithelial Cells, Squamous,Epithelial Cells, Transitional,Glandular Epithelial Cell,Squamous Cell,Squamous Epithelial Cell,Transitional Epithelial Cell
D005098 Exotoxins Toxins produced, especially by bacterial or fungal cells, and released into the culture medium or environment. Exotoxin

Related Publications

Mercedes Ortega-González, and Fermín Sánchez de Medina, and Carlos Molina-Santiago, and Rocío López-Posadas, and Daniel Pacheco, and Tino Krell, and Olga Martínez-Augustin, and Daddaoua Abdelali
October 2015, Journal of basic microbiology,
Mercedes Ortega-González, and Fermín Sánchez de Medina, and Carlos Molina-Santiago, and Rocío López-Posadas, and Daniel Pacheco, and Tino Krell, and Olga Martínez-Augustin, and Daddaoua Abdelali
January 2017, Frontiers in microbiology,
Mercedes Ortega-González, and Fermín Sánchez de Medina, and Carlos Molina-Santiago, and Rocío López-Posadas, and Daniel Pacheco, and Tino Krell, and Olga Martínez-Augustin, and Daddaoua Abdelali
December 2022, The Science of the total environment,
Mercedes Ortega-González, and Fermín Sánchez de Medina, and Carlos Molina-Santiago, and Rocío López-Posadas, and Daniel Pacheco, and Tino Krell, and Olga Martínez-Augustin, and Daddaoua Abdelali
November 2008, Applied and environmental microbiology,
Mercedes Ortega-González, and Fermín Sánchez de Medina, and Carlos Molina-Santiago, and Rocío López-Posadas, and Daniel Pacheco, and Tino Krell, and Olga Martínez-Augustin, and Daddaoua Abdelali
November 2018, Environmental microbiology,
Mercedes Ortega-González, and Fermín Sánchez de Medina, and Carlos Molina-Santiago, and Rocío López-Posadas, and Daniel Pacheco, and Tino Krell, and Olga Martínez-Augustin, and Daddaoua Abdelali
March 1988, Zhurnal mikrobiologii, epidemiologii i immunobiologii,
Mercedes Ortega-González, and Fermín Sánchez de Medina, and Carlos Molina-Santiago, and Rocío López-Posadas, and Daniel Pacheco, and Tino Krell, and Olga Martínez-Augustin, and Daddaoua Abdelali
September 2017, Indian journal of microbiology,
Mercedes Ortega-González, and Fermín Sánchez de Medina, and Carlos Molina-Santiago, and Rocío López-Posadas, and Daniel Pacheco, and Tino Krell, and Olga Martínez-Augustin, and Daddaoua Abdelali
December 2023, mSystems,
Mercedes Ortega-González, and Fermín Sánchez de Medina, and Carlos Molina-Santiago, and Rocío López-Posadas, and Daniel Pacheco, and Tino Krell, and Olga Martínez-Augustin, and Daddaoua Abdelali
June 2014, Drug development and industrial pharmacy,
Mercedes Ortega-González, and Fermín Sánchez de Medina, and Carlos Molina-Santiago, and Rocío López-Posadas, and Daniel Pacheco, and Tino Krell, and Olga Martínez-Augustin, and Daddaoua Abdelali
February 2010, Journal of bacteriology,
Copied contents to your clipboard!