Literature DB >> 27655246

Probiotic Enterococcus faecalis Symbioflor® down regulates virulence genes of EHEC in vitro and decrease pathogenicity in a Caenorhabditis elegans model.

Klaus Neuhaus1, Marina C Lamparter2,3, Benjamin Zölch1, Richard Landstorfer1, Svenja Simon4, Britta Spanier5, Matthias A Ehrmann2, Rudi F Vogel6.   

Abstract

Enterohemorrhagic E. coli O157:H7 (EHEC) shorten the lifespan of Caenorhabditis elegans compared to avirulent bacteria. Co-feeding EHEC with Enterococcus faecalis Symbioflor® significantly increased the worms' lifespan. The transcriptome of EHEC grown in vitro with or without Symbioflor® was analyzed using RNA-seq. The analysis revealed downregulation of several virulence-associated genes in the presence of Symbioflor®, including virulence key genes (e.g., LEE, flagellum, quorum-sensing). The downregulation of the LEE genes was corroborated by lux-transposon mutants. Upregulated genes included acid response genes, due to a decrease in pH exerted by Symbioflor®. Further genes indicate cellular stress in EHEC (e.g. prophage/mobile elements involved in excision, cell lysis, and cell division inhibition). Thus, the observed protection of C. elegans during an EHEC infection by the probiotic Symbioflor® is suggested to be caused by triggering concomitant transcriptomic changes. To verify the biological relevance of this modulation, exemplary genes found to be influenced by Symbioflor® were knocked out (fliD, espB, Z3136, Z3917, and L7052). The lifespan of nematodes changed when using knock-outs as food source and the effect could be complemented in trans. In summary, Symbioflor® appears to be a protective probiotic in the nematode model.

Entities:  

Keywords:  Caenorhabditis elegans; EHEC; Enterococcus faecalis Symbioflor®; Transcriptome; Virulence; lux transposons

Mesh:

Substances:

Year:  2016        PMID: 27655246     DOI: 10.1007/s00203-016-1291-8

Source DB:  PubMed          Journal:  Arch Microbiol        ISSN: 0302-8933            Impact factor:   2.552


  8 in total

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2.  Exploiting CRISPR-Cas to manipulate Enterococcus faecalis populations.

Authors:  Karthik Hullahalli; Marinelle Rodrigues; Kelli L Palmer
Journal:  Elife       Date:  2017-06-23       Impact factor: 8.140

Review 3.  Model systems for the study of Enterococcal colonization and infection.

Authors:  H M Sharon Goh; M H Adeline Yong; Kelvin Kian Long Chong; Kimberly A Kline
Journal:  Virulence       Date:  2017-05-04       Impact factor: 5.882

4.  Complex Bacterial Consortia Reprogram the Colitogenic Activity of Enterococcus faecalis in a Gnotobiotic Mouse Model of Chronic, Immune-Mediated Colitis.

Authors:  Isabella Lengfelder; Irina G Sava; Jonathan J Hansen; Karin Kleigrewe; Jeremy Herzog; Klaus Neuhaus; Thomas Hofmann; R Balfour Sartor; Dirk Haller
Journal:  Front Immunol       Date:  2019-06-20       Impact factor: 7.561

5.  In Vitro and in Vivo Selection of Potentially Probiotic Lactobacilli From Nocellara del Belice Table Olives.

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Journal:  Front Microbiol       Date:  2018-03-28       Impact factor: 5.640

6.  In vivo screening platform for shiga toxin-producing Escherichia coli (STEC) using Caenorhabditis elegans as a model.

Authors:  Su-Bin Hwang; Jung-Gu Choi; Shuai Wei; Byung-Jae Park; Ramachandran Chelliah; Deog-Hwan Oh
Journal:  PLoS One       Date:  2018-02-28       Impact factor: 3.240

Review 7.  Caenorhabditis Elegans and Probiotics Interactions from a Prolongevity Perspective.

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Journal:  Int J Mol Sci       Date:  2019-10-10       Impact factor: 5.923

8.  Pediococcus acidilactici P25 Protected Caenorhabditis elegans against Enterotoxigenic Escherichia coli K88 Infection and Transcriptomic Analysis of Its Potential Mechanisms.

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Journal:  Biomed Res Int       Date:  2020-03-30       Impact factor: 3.411

  8 in total

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