Division of Infectious Diseases, Brigham & Women's Hospital, Boston, Massachusetts, United States of America.
Department of Microbiology, Harvard Medical School, Boston, Massachusetts, United States of America.
PLoS Pathog. 2021 Feb 2;17(2):e1009290. doi: 10.1371/journal.ppat.1009290. eCollection 2021 Feb.
Enterohemorrhagic Escherichia coli (EHEC) is a food-borne pathogen that causes diarrheal disease and the potentially lethal hemolytic uremic syndrome. We used an infant rabbit model of EHEC infection that recapitulates many aspects of human intestinal disease to comprehensively assess colonic transcriptional responses to this pathogen. Cellular compartment-specific RNA-sequencing of intestinal tissue from animals infected with EHEC strains containing or lacking Shiga toxins (Stx) revealed that EHEC infection elicits a robust response that is dramatically shaped by Stx, particularly in epithelial cells. Many of the differences in the transcriptional responses elicited by these strains were in genes involved in immune signaling pathways, such as IL23A, and coagulation, including F3, the gene encoding Tissue Factor. RNA FISH confirmed that these elevated transcripts were found almost exclusively in epithelial cells. Collectively, these findings suggest that Stx potently remodels the host innate immune response to EHEC.
肠出血性大肠杆菌(EHEC)是一种食源性病原体,可引起腹泻病和潜在致命的溶血尿毒综合征。我们使用了一种重现人类肠道疾病许多方面的婴儿兔 EHEC 感染模型,全面评估了该病原体对结肠的转录反应。对感染含有或缺乏志贺毒素(Stx)的 EHEC 菌株的动物肠道组织进行细胞区室特异性 RNA-seq 分析表明,EHEC 感染引发了强烈的反应,Stx 对其有显著影响,特别是在上皮细胞中。这些菌株引起的转录反应的许多差异都存在于免疫信号通路相关的基因中,如 IL23A,以及凝血,包括编码组织因子的 F3 基因。RNA FISH 证实,这些上调的转录本几乎只存在于上皮细胞中。总的来说,这些发现表明 Stx 强烈重塑了宿主对 EHEC 的固有免疫反应。