Comparison between Listeria sensu stricto and Listeria sensu lato strains identifies novel determinants involved in infection

The human pathogen L . monocytogenes and the animal pathogen L. ivanovii , together with four other species isolated from symptom-free animals, form the “ Listeria sensu stricto ” clade. The members of the second clade, “ Listeria sensu lato ”, are believed to be solely environmental bacteria withou...

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Published inScientific reports Vol. 7; no. 1; pp. 17821 - 14
Main Authors Schardt, Jakob, Jones, Grant, Müller-Herbst, Stefanie, Schauer, Kristina, D’Orazio, Sarah E. F., Fuchs, Thilo M.
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 19.12.2017
Nature Publishing Group
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Summary:The human pathogen L . monocytogenes and the animal pathogen L. ivanovii , together with four other species isolated from symptom-free animals, form the “ Listeria sensu stricto ” clade. The members of the second clade, “ Listeria sensu lato ”, are believed to be solely environmental bacteria without the ability to colonize mammalian hosts. To identify novel determinants that contribute to infection by L. monocytogenes , the causative agent of the foodborne disease listeriosis, we performed a genome comparison of the two clades and found 151 candidate genes that are conserved in the Listeria sensu stricto species. Two factors were investigated further in vitro and in vivo . A mutant lacking an ATP-binding cassette transporter exhibited defective adhesion and invasion of human Caco-2 cells. Using a mouse model of foodborne L. monocytogenes infection, a reduced number of the mutant strain compared to the parental strain was observed in the small intestine and the liver. Another mutant with a defective 1,2-propanediol degradation pathway showed reduced persistence in the stool of infected mice, suggesting a role of 1,2-propanediol as a carbon and energy source of listeriae during infection. These findings reveal the relevance of novel factors for the colonization process of L. monocytogenes .
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ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-017-17570-0