Sun Yuying, Zhang Jiquan, Qin Lei, Yan Cui, Zhang Xiaojun, Liu Dandan
College of Marine Life and Fisheries, Huaihai Institute of Technology, Lianyungang, China.
Jiangsu Marine Resources Development Research Institute, Lianyungang, China.
PLoS One. 2017 Mar 7;12(3):e0172783. doi: 10.1371/journal.pone.0172783. eCollection 2017.
Bacterial small non-coding RNAs (sRNAs) are known as novel regulators involved in virulence, stress responsibility, and so on. Recently, a lot of new researches have highlighted the critical roles of sRNAs in fine-tune gene regulation in both prokaryotes and eukaryotes. Edwardsiella tarda (E. tarda) is a gram-negative, intracellular pathogen that causes edwardsiellosis in fish. Thus far, no sRNA has been reported in E. tarda. The present study represents the first attempt to identify sRNAs in E. tarda S08. Ten sRNAs were validated by RNA sequencing and quantitative PCR (qPCR). ET_sRNA_1 and ET_sRNA_2 were homolous to tmRNA and GcvB, respectively. However, the other candidate sRNAs have not been reported till now. The cellular abundance of 10 validated sRNA was detected by qPCR at different growth phases to monitor their biosynthesis. Nine candidate sRNAs were expressed in the late-stage of exponential growth and stationary stages of growth (36~60 h). And the expression of the nine sRNAs was growth phase-dependent. But ET_sRNA_10 was almost expressed all the time and reached the highest peak at 48 h. Their targets were predicted by TargetRNA2 and each sRNA target contains some genes that directly or indirectly relate to virulence. These results preliminary showed that sRNAs probably play a regulatory role of virulence in E. tarda.
细菌小非编码RNA(sRNA)是参与毒力、应激反应等的新型调节因子。最近,许多新研究强调了sRNA在原核生物和真核生物基因精细调控中的关键作用。迟缓爱德华氏菌(E. tarda)是一种革兰氏阴性细胞内病原体,可导致鱼类患爱德华氏菌病。迄今为止,尚未在迟缓爱德华氏菌中报道过sRNA。本研究首次尝试在迟缓爱德华氏菌S08中鉴定sRNA。通过RNA测序和定量PCR(qPCR)验证了10种sRNA。ET_sRNA_1和ET_sRNA_2分别与tmRNA和GcvB同源。然而,其他候选sRNA至今尚未见报道。通过qPCR在不同生长阶段检测10种已验证sRNA的细胞丰度,以监测它们的生物合成。9种候选sRNA在指数生长后期和稳定生长阶段(36~60小时)表达。这9种sRNA的表达呈生长阶段依赖性。但ET_sRNA_10几乎在所有时间都有表达,并在48小时达到最高峰。通过TargetRNA2预测它们的靶标,每个sRNA靶标都包含一些直接或间接与毒力相关的基因。这些结果初步表明,sRNA可能在迟缓爱德华氏菌中发挥毒力调节作用。