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Therapeutic Methods and Therapies TCIM
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1.
Nutrients ; 12(10)2020 Oct 07.
Article in English | MEDLINE | ID: mdl-33036498

ABSTRACT

Lactic acid bacteria (LAB) "fermentates" confer a beneficial effect on intestinal function. However, the ability of new fermentations to improve LAB broth activity in preventing pathogen-induced intestinal inflammation and barrier dysfunction has not yet been studied. The objective of this study was to determine if broths of LAB fermented with Eruca sativa or Barbarea verna seed extracts prevent gut barrier dysfunction and interleukin-8 (CXCL8) release in vitro in human intestinal Caco-2 cells infected with enterohemorrhagic Escherichia coli (EHEC) O157:H7. LAB broths were assayed for their effects on EHEC growth and on Caco-2 viability; thereafter, their biological properties were analysed in a co-culture system consisting of EHEC and Caco-2 cells. Caco-2 cells infected with EHEC significantly increased CXCL8 release, and decreased Trans-Epithelial Electrical Resistance (TEER), a barrier-integrity marker. Notably, when Caco-2 cells were treated with LAB broth enriched with E. sativa seed extract and thereafter infected, both CXCL8 expression and epithelial dysfunction reduced compared to in untreated cells. These results underline the beneficial effect of broths from LAB fermented with E. sativa seed extracts in gut barrier and inflammation after EHEC infection and reveal that these LAB broths can be used as functional bioactive compounds to regulate intestinal function.


Subject(s)
Brassicaceae/chemistry , Escherichia coli O157/drug effects , Escherichia coli O157/growth & development , Fermentation , Gastroenteritis/prevention & control , Intestinal Mucosa/metabolism , Intestinal Mucosa/microbiology , Lactobacillus acidophilus , Plant Extracts/pharmacology , Probiotics/pharmacology , Seeds/chemistry , Anti-Bacterial Agents , Barbarea/chemistry , Caco-2 Cells , Cell Survival/drug effects , Coculture Techniques , Drug Resistance, Bacterial , Electric Impedance , Escherichia coli Infections , Escherichia coli O157/pathogenicity , Gastroenteritis/microbiology , Humans , Interleukin-8/metabolism , Intestinal Mucosa/physiology , Phytotherapy , Plant Extracts/isolation & purification
2.
Emerg Infect Dis ; 22(9): 1604-12, 2016 09.
Article in English | MEDLINE | ID: mdl-27533474

ABSTRACT

We describe the epidemiology, clinical features, and molecular characterization of enterohemorrhagic Escherichia coli (EHEC) infections caused by the singular hybrid pathotype O80:H2, and we examine the influence of antibiotics on Shiga toxin production. In France, during 2005-2014, a total of 54 patients were infected with EHEC O80:H2; 91% had hemolytic uremic syndrome. Two patients had invasive infections, and 2 died. All strains carried stx2 (variants stx2a, 2c, or 2d); the rare intimin gene (eae-ξ); and at least 4 genes characteristic of pS88, a plasmid associated with extraintestinal virulence. Similar strains were found in Spain. All isolates belonged to the same clonal group. At subinhibitory concentrations, azithromycin decreased Shiga toxin production significantly, ciprofloxacin increased it substantially, and ceftriaxone had no major effect. Antibiotic combinations that included azithromycin also were tested. EHEC O80:H2, which can induce hemolytic uremic syndrome complicated by bacteremia, is emerging in France. However, azithromycin might effectively combat these infections.


Subject(s)
Enterohemorrhagic Escherichia coli/classification , Enterohemorrhagic Escherichia coli/genetics , Hemolytic-Uremic Syndrome/epidemiology , Hemolytic-Uremic Syndrome/microbiology , Adolescent , Adult , Anti-Bacterial Agents/pharmacology , Child , Child, Preschool , Disease Outbreaks , Drug Resistance, Bacterial , Enterohemorrhagic Escherichia coli/metabolism , Enterohemorrhagic Escherichia coli/pathogenicity , Female , Follow-Up Studies , France/epidemiology , Genotype , Geography, Medical , Hemolytic-Uremic Syndrome/diagnosis , Hemolytic-Uremic Syndrome/drug therapy , Humans , Incidence , Infant , Male , Microbial Sensitivity Tests , Multilocus Sequence Typing , Serogroup , Serotyping , Shiga Toxin/biosynthesis , Shiga Toxin/genetics , Virulence , Virulence Factors/genetics , Young Adult
3.
Toxins (Basel) ; 8(1)2016 Jan 05.
Article in English | MEDLINE | ID: mdl-26742075

ABSTRACT

Enterohemorrhagic Escherichia coli (EHEC) are foodborne pathogens responsible for the development of bloody diarrhea and renal failure in humans. Many environmental factors have been shown to regulate the production of Shiga toxin 2 (Stx2), the main virulence factor of EHEC. Among them, soluble factors produced by human gut microbiota and in particular, by the predominant species Bacteroides thetaiotaomicron (B. thetaiotaomicron), inhibit Stx2 gene expression. In this study, we investigated the molecular mechanisms underlying the B. thetaiotaomicron-dependent inhibition of Stx2 production by EHEC. We determined that Stx2-regulating molecules are resistant to heat treatment but do not correspond to propionate and acetate, two short-chain fatty acids produced by B. thetaiotaomicron. Moreover, screening of a B. thetaiotaomicron mutant library identified seven mutants that do not inhibit Stx2 synthesis by EHEC. One mutant has impaired production of BtuB, an outer membrane receptor for vitamin B12. Together with restoration of Stx2 level after vitamin B12 supplementation, these data highlight vitamin B12 as a molecule produced by gut microbiota that modulates production of a key virulence factor of EHEC and consequently may affect the outcome of an infection.


Subject(s)
Bacteroides/drug effects , Enterohemorrhagic Escherichia coli/metabolism , Shiga Toxin 2/biosynthesis , Vitamin B 12/pharmacology , Bacteroides/genetics , Bacteroides/metabolism , Gastrointestinal Microbiome/drug effects , Gastrointestinal Microbiome/physiology , Mutation
4.
J Dairy Sci ; 96(12): 7467-77, 2013.
Article in English | MEDLINE | ID: mdl-24140320

ABSTRACT

A potential probiotic strain, Lactobacillus kefiranofaciens M1, was previously isolated from kefir grains, which are used to manufacture the traditional fermented drink kefir. The aim of this study was to investigate the effects of Lb. kefiranofaciens M1 on enterohemorrhagic Escherichia coli (EHEC) infection, using mice and intestinal cell models. BALB/c mice were daily administrated with either phosphate buffered saline or Lb. kefiranofaciens M1 at 2×10(8) cfu/mouse per day intragastrically for 7 d. Intragastric challenges with EHEC (2×10(9) cfu/mouse) were conducted on d 0, 4, and 7 after treatment. Administration of Lb. kefiranofaciens M1 was able to prevent EHEC infection-induced symptoms, intestinal damage, renal damage, bacterial translocation, and Shiga toxin penetration. Furthermore, the mucosal EHEC-specific IgA responses were increased after Lb. kefiranofaciens M1 administration in the EHEC-infected mouse system. Additionally, in vitro, Lb. kefiranofaciens M1 was shown to have a protective effect on Caco-2 intestinal epithelial cells and Caco-2 intestinal epithelial cell monolayers; the bacteria limited EHEC-induced cell death and reduced the loss of epithelial integrity. These findings support the potential of Lb. kefiranofaciens M1 treatment as an approach to preventing EHEC infection and its effects.


Subject(s)
Enterohemorrhagic Escherichia coli/physiology , Escherichia coli Infections/prevention & control , Lactobacillus/physiology , Microbial Interactions/physiology , Probiotics/pharmacology , Animals , Caco-2 Cells , Cultured Milk Products/microbiology , Drug Evaluation, Preclinical , Escherichia coli Infections/metabolism , Escherichia coli Infections/pathology , Humans , Intestinal Mucosa/metabolism , Lactobacillus/isolation & purification , Mice , Mice, Inbred BALB C
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