Literature DB >> 25733524

Escherichia coli EDL933 requires gluconeogenic nutrients to successfully colonize the intestines of streptomycin-treated mice precolonized with E. coli Nissle 1917.

Silvia A C Schinner1, Matthew E Mokszycki1, Jimmy Adediran1, Mary Leatham-Jensen1, Tyrrell Conway2, Paul S Cohen3.   

Abstract

Escherichia coli MG1655, a K-12 strain, uses glycolytic nutrients exclusively to colonize the intestines of streptomycin-treated mice when it is the only E. coli strain present or when it is confronted with E. coli EDL933, an O157:H7 strain. In contrast, E. coli EDL933 uses glycolytic nutrients exclusively when it is the only E. coli strain in the intestine but switches in part to gluconeogenic nutrients when it colonizes mice precolonized with E. coli MG1655 (R. L. Miranda et al., Infect Immun 72:1666-1676, 2004, http://dx.doi.org/10.1128/IAI.72.3.1666-1676.2004). Recently, J. W. Njoroge et al. (mBio 3:e00280-12, 2012, http://dx.doi.org/10.1128/mBio.00280-12) reported that E. coli 86-24, an O157:H7 strain, activates the expression of virulence genes under gluconeogenic conditions, suggesting that colonization of the intestine with a probiotic E. coli strain that outcompetes O157:H7 strains for gluconeogenic nutrients could render them nonpathogenic. Here we report that E. coli Nissle 1917, a probiotic strain, uses both glycolytic and gluconeogenic nutrients to colonize the mouse intestine between 1 and 5 days postfeeding, appears to stop using gluconeogenic nutrients thereafter in a large, long-term colonization niche, but continues to use them in a smaller niche to compete with invading E. coli EDL933. Evidence is also presented suggesting that invading E. coli EDL933 uses both glycolytic and gluconeogenic nutrients and needs the ability to perform gluconeogenesis in order to colonize mice precolonized with E. coli Nissle 1917. The data presented here therefore rule out the possibility that E. coli Nissle 1917 can starve the O157:H7 E. coli strain EDL933 of gluconeogenic nutrients, even though E. coli Nissle 1917 uses such nutrients to compete with E. coli EDL933 in the mouse intestine.
Copyright © 2015, American Society for Microbiology. All Rights Reserved.

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Year:  2015        PMID: 25733524      PMCID: PMC4399065          DOI: 10.1128/IAI.02943-14

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  38 in total

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Journal:  Science       Date:  1997-09-05       Impact factor: 47.728

2.  Genome sequence of enterohaemorrhagic Escherichia coli O157:H7.

Authors:  N T Perna; G Plunkett; V Burland; B Mau; J D Glasner; D J Rose; G F Mayhew; P S Evans; J Gregor; H A Kirkpatrick; G Pósfai; J Hackett; S Klink; A Boutin; Y Shao; L Miller; E J Grotbeck; N W Davis; A Lim; E T Dimalanta; K D Potamousis; J Apodaca; T S Anantharaman; J Lin; G Yen; D C Schwartz; R A Welch; F R Blattner
Journal:  Nature       Date:  2001-01-25       Impact factor: 49.962

3.  The streptomycin-treated mouse intestine selects Escherichia coli envZ missense mutants that interact with dense and diverse intestinal microbiota.

Authors:  Mary P Leatham-Jensen; Jakob Frimodt-Møller; Jimmy Adediran; Matthew E Mokszycki; Megan E Banner; Joyce E Caughron; Karen A Krogfelt; Tyrrell Conway; Paul S Cohen
Journal:  Infect Immun       Date:  2012-03-05       Impact factor: 3.441

4.  Re.: Oral administration of a certain strain of live Escherichia coli for intestinal disorders? (Infection 23 [1995] 51-54)

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5.  Analysis of the genome structure of the nonpathogenic probiotic Escherichia coli strain Nissle 1917.

Authors:  Lubomir Grozdanov; Carsten Raasch; Jürgen Schulze; Ulrich Sonnenborn; Gerhard Gottschalk; Jörg Hacker; Ulrich Dobrindt
Journal:  J Bacteriol       Date:  2004-08       Impact factor: 3.490

6.  Properties of Escherichia coli strains of serotype O6.

Authors:  G Blum; R Marre; J Hacker
Journal:  Infection       Date:  1995 Jul-Aug       Impact factor: 3.553

7.  An Escherichia coli Nissle 1917 missense mutant colonizes the streptomycin-treated mouse intestine better than the wild type but is not a better probiotic.

Authors:  Jimmy Adediran; Mary P Leatham-Jensen; Matthew E Mokszycki; Jakob Frimodt-Møller; Karen A Krogfelt; Krystyna Kazmierczak; Linda J Kenney; Tyrrell Conway; Paul S Cohen
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Authors:  Katharine M Ng; Jessica A Ferreyra; Steven K Higginbottom; Jonathan B Lynch; Purna C Kashyap; Smita Gopinath; Natasha Naidu; Biswa Choudhury; Bart C Weimer; Denise M Monack; Justin L Sonnenburg
Journal:  Nature       Date:  2013-09-01       Impact factor: 49.962

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Review 3.  Frenemies: Signaling and Nutritional Integration in Pathogen-Microbiota-Host Interactions.

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4.  Escherichia coli Nissle 1917 secondary metabolism: aryl polyene biosynthesis and phosphopantetheinyl transferase crosstalk.

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5.  A Simple In Vitro Gut Model for Studying the Interaction between Escherichia coli and the Intestinal Commensal Microbiota in Cecal Mucus.

Authors:  Matthew E Mokszycki; Mary Leatham-Jensen; Jon L Steffensen; Ying Zhang; Karen A Krogfelt; Matthew E Caldwell; Tyrrell Conway; Paul S Cohen
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8.  Distinct but Spatially Overlapping Intestinal Niches for Vancomycin-Resistant Enterococcus faecium and Carbapenem-Resistant Klebsiella pneumoniae.

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9.  Host-Derived Sialic Acids Are an Important Nutrient Source Required for Optimal Bacterial Fitness In Vivo.

Authors:  Nathan D McDonald; Jean-Bernard Lubin; Nityananda Chowdhury; E Fidelma Boyd
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10.  Phosphotyrosine-Mediated Regulation of Enterohemorrhagic Escherichia coli Virulence.

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Journal:  mBio       Date:  2018-02-27       Impact factor: 7.867

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