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dc.contributor.authorSchmühl, Carina
dc.contributor.authorBeckstette, Michael
dc.contributor.authorHeroven, Ann Kathrin
dc.contributor.authorBunk, Boyke
dc.contributor.authorSpröer, Cathrin
dc.contributor.authorMcNally, Alan
dc.contributor.authorOvermann, Jörg
dc.contributor.authorDersch, Petra
dc.date.accessioned2019-06-13T14:55:12Z
dc.date.available2019-06-13T14:55:12Z
dc.identifier.citationmSystems. 2019 Apr 23;4(2). pii: mSystems00239-18. doi:10.1128/mSystems.00239-18. eCollection 2019 Mar-Apr.en_US
dc.identifier.issn2379-5077
dc.identifier.pmid31020044
dc.identifier.doi10.1128/mSystems.00239-18
dc.identifier.urihttp://hdl.handle.net/10033/621816
dc.description.abstractYersinia enterocolitica is a zoonotic pathogen and an important cause of bacterial gastrointestinal infections in humans. Large-scale population genomic analyses revealed genetic and phenotypic diversity of this bacterial species, but little is known about the differences in the transcriptome organization, small RNA (sRNA) repertoire, and transcriptional output. Here, we present the first comparative high-resolution transcriptome analysis of Y. enterocolitica strains representing highly pathogenic phylogroup 2 (serotype O:8) and moderately pathogenic phylogroup 3 (serotype O:3) grown under four infection-relevant conditions. Our transcriptome sequencing (RNA-seq) approach revealed 1,299 and 1,076 transcriptional start sites and identified strain-specific sRNAs that could contribute to differential regulation among the phylogroups. Comparative transcriptomics further uncovered major gene expression differences, in particular, in the temperature-responsive regulon. Multiple virulence-relevant genes are differentially regulated between the two strains, supporting an ecological separation of phylogroups with certain niche-adapted properties. Strong upregulation of the ystA enterotoxin gene in combination with constitutive high expression of cell invasion factor InvA further showed that the toxicity of recent outbreak O:3 strains has increased. Overall, our report provides new insights into the specific transcriptome organization of phylogroups 2 and 3 and reveals gene expression differences contributing to the substantial phenotypic differences that exist between the lineages. IMPORTANCE Yersinia enterocolitica is a major diarrheal pathogen and is associated with a large range of gut-associated diseases. Members of this species have evolved into different phylogroups with genotypic variations. We performed the first characterization of the Y. enterocolitica transcriptional landscape and tracked the consequences of the genomic variations between two different pathogenic phylogroups by comparing their RNA repertoire, promoter usage, and expression profiles under four different virulence-relevant conditions. Our analysis revealed major differences in the transcriptional outputs of the closely related strains, pointing to an ecological separation in which one is more adapted to an environmental lifestyle and the other to a mostly mammal-associated lifestyle. Moreover, a variety of pathoadaptive alterations, including alterations in acid resistance genes, colonization factors, and toxins, were identified which affect virulence and host specificity. This illustrates that comparative transcriptomics is an excellent approach to discover differences in the functional output from closely related genomes affecting niche adaptation and virulence, which cannot be directly inferred from DNA sequences.en_US
dc.language.isoenen_US
dc.publisherASMen_US
dc.rightsAttribution-NonCommercial-ShareAlike 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.subjectYersinia enterocoliticaen_US
dc.subjectYstA toxinen_US
dc.subjectcomparative transcriptomicsen_US
dc.subjectgrowth-phase controlen_US
dc.subjecttemperature regulationen_US
dc.titleComparative Transcriptomic Profiling of Yersinia enterocolitica O:3 and O:8 Reveals Major Expression Differences of Fitness- and Virulence-Relevant Genes Indicating Ecological Separation.en_US
dc.typeArticleen_US
dc.contributor.departmentHZI,Helmholtz-Zentrum für Infektionsforschung GmbH, Inhoffenstr. 7,38124 Braunschweig, Germany.en_US
dc.identifier.journalmSystemsen_US
refterms.dateFOA2019-06-13T14:55:12Z
dc.source.journaltitlemSystems


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