Schmühl Carina, Beckstette Michael, Heroven Ann Kathrin, Bunk Boyke, Spröer Cathrin, McNally Alan, Overmann Jörg, Dersch Petra
Department of Molecular Infection Biology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Leibniz Institute DSMZ-German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany.
mSystems. 2019 Apr 23;4(2). doi: 10.1128/mSystems.00239-18. eCollection 2019 Mar-Apr.
Yersinia 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 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. 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.
小肠结肠炎耶尔森菌是一种人畜共患病原体,也是人类细菌性胃肠道感染的重要病因。大规模群体基因组分析揭示了该细菌物种的遗传和表型多样性,但对于转录组组织、小RNA(sRNA)库和转录输出的差异了解甚少。在此,我们首次对代表高致病性2型菌系(血清型O:8)和中度致病性3型菌系(血清型O:3)的小肠结肠炎耶尔森菌菌株在四种与感染相关的条件下进行了比较高分辨率转录组分析。我们的转录组测序(RNA-seq)方法揭示了1299个和1076个转录起始位点,并鉴定出可能导致不同菌系间差异调控的菌株特异性sRNA。比较转录组学进一步揭示了主要的基因表达差异,特别是在温度响应调节子方面。两种菌株之间多个与毒力相关的基因受到差异调控,支持了具有某些生态位适应性特征的菌系在生态上的分离。肠毒素基因的强烈上调与细胞侵袭因子InvA的组成型高表达相结合,进一步表明近期爆发的O:3菌株的毒性有所增加。总体而言,我们的报告为2型和3型菌系的特定转录组组织提供了新的见解,并揭示了导致不同菌系之间存在显著表型差异的基因表达差异。小肠结肠炎耶尔森菌是一种主要引起腹泻的病原体,与多种肠道相关疾病有关。该物种的成员已进化为具有基因型变异的不同菌系。我们首次对小肠结肠炎耶尔森菌的转录图谱进行了表征,并通过比较两种不同致病菌系在四种不同毒力相关条件下的RNA库、启动子使用情况和表达谱,追踪了基因组变异的后果。我们的分析揭示了密切相关菌株在转录输出方面的主要差异,表明存在一种生态分离,其中一种更适应环境生活方式,另一种更适应主要与哺乳动物相关的生活方式。此外,还鉴定出了多种致病适应性改变,包括耐酸性基因、定植因子和毒素的改变,这些改变影响毒力和宿主特异性。这表明比较转录组学是发现密切相关基因组在功能输出上影响生态位适应和毒力的差异的极佳方法,这些差异无法直接从DNA序列中推断出来。