Khandige Surabhi, Kronborg Tina, Uhlin Bernt Eric, Møller-Jensen Jakob
Department of Biochemistry and Molecular Biology, University of Southern Denmark, Odense, Denmark.
Department of Molecular Biology and Laboratory for Molecular Infection Medicine Sweden (MIMS), Umeå Centre for Microbial Research (UCMR), Umeå University, Umeå, Sweden.
PLoS Pathog. 2015 Aug 20;11(8):e1005109. doi: 10.1371/journal.ppat.1005109. eCollection 2015 Aug.
Uropathogenic Escherichia coli (UPEC) are capable of occupying physiologically distinct intracellular and extracellular niches within the urinary tract. This feat requires the timely regulation of gene expression and small RNAs (sRNAs) are known to mediate such rapid adjustments in response to changing environmental cues. This study aimed to uncover sRNA-mediated gene regulation in the UPEC strain UTI89, during infection of bladder epithelial cells. Hfq is an RNA chaperone known to facilitate and stabilize sRNA and target mRNA interactions with bacterial cells. The co-immunoprecipitation and high throughput RNA sequencing of Hfq bound sRNAs performed in this study, revealed distinct sRNA profiles in UPEC in the extracellular and intracellular environments. Our findings emphasize the importance of studying regulatory sRNAs in a biologically relevant niche. This strategy also led to the discovery of a novel virulence-associated trans-acting sRNA-PapR. Deletion of papR was found to enhance adhesion of UTI89 to both bladder and kidney cell lines in a manner independent of type-1 fimbriae. We demonstrate PapR mediated posttranscriptional repression of the P-fimbriae phase regulator gene papI and postulate a role for such regulation in fimbrial cross-talk at the population level in UPEC. Our results further implicate the Leucine responsive protein (LRP) as a transcriptional activator regulating PapR expression. Our study reports, for the first time, a role for sRNAs in regulation of P-fimbriae phase variation and emphasizes the importance of studying pathogenesis-specific sRNAs within a relevant biological niche.
尿路致病性大肠杆菌(UPEC)能够在泌尿道内占据生理上不同的细胞内和细胞外生态位。这一过程需要及时调控基因表达,已知小RNA(sRNA)可介导这种快速调节以应对不断变化的环境线索。本研究旨在揭示在膀胱上皮细胞感染期间,UPEC菌株UTI89中sRNA介导的基因调控。Hfq是一种RNA伴侣,已知其可促进和稳定sRNA与靶mRNA在细菌细胞中的相互作用。本研究对与Hfq结合的sRNA进行了免疫共沉淀和高通量RNA测序,揭示了UPEC在细胞外和细胞内环境中不同的sRNA谱。我们的研究结果强调了在生物学相关生态位中研究调控sRNA的重要性。这一策略还导致发现了一种新型的与毒力相关的反式作用sRNA——PapR。研究发现,缺失papR可增强UTI89对膀胱和肾细胞系的黏附,且这种增强作用与1型菌毛无关。我们证明了PapR介导对P菌毛相位调节基因papI的转录后抑制,并推测这种调节在UPEC群体水平的菌毛相互作用中发挥作用。我们的结果进一步表明,亮氨酸应答蛋白(LRP)作为转录激活因子调节PapR的表达。我们的研究首次报道了sRNA在P菌毛相位变异调节中的作用,并强调了在相关生物学生态位中研究发病机制特异性sRNA的重要性。