| Literature DB >> 27655246 |
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
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Year: 2016 PMID: 27655246 DOI: 10.1007/s00203-016-1291-8
Source DB: PubMed Journal: Arch Microbiol ISSN: 0302-8933 Impact factor: 2.552