啮齿类柠檬酸杆菌非蛋白编码RNA同源物的比较基因组学鉴定与表征

Kishanraj Selva Raju, Agilandeswarie Kavin Selvam
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摘要

本实验旨在鉴定鼠柠檬酸杆菌(Citrobacter rodentium)中的同源非蛋白编码rna (npcRNA),作为解决该细菌引起的健康问题的替代方案。抗菌药物的滥用导致耐药病原菌的出现。本研究的目的是从已知的啮齿鼠细菌中筛选同源npcRNA,研究同源npcRNA在啮齿鼠中的表达,并预测鉴定出的同源npcRNA在啮齿鼠中的调控作用。首先,从同一属肠杆菌科的伤寒沙门氏菌、大肠杆菌和鼠疫杆菌中收集已知的npcRNA,筛选啮齿类柠檬酸杆菌中同源npcRNA的存在。其次,通过Rfam (RNA family)筛选上一步鉴定的同源npcRNA (BLASTn),鉴定未注释的同源物。然后,利用TargetRNA2 webtool对同源npcRNA进行靶mRNA预测,发现同源序列的互补mRNA结合以及该转录物的调控活性。通过反转录PCR评估预测调控毒力靶mRNA的npcRNA同源物在不同生长阶段的表达谱,并利用Image J工具定量分析条带强度。鼠伤寒沙门氏菌已知的npcRNA Styr-296在鼠伤寒沙门氏菌生长的三个阶段(滞后期、对数期和平稳期)均有表达。迟滞期表达量高,对数和平稳期不表达。预测Styr-296同源物可调节与细菌毒力相关的mRNA翻译调节剂药物活性B。因此,这是一项初步的研究,有望进一步阐明更多毒力相关的npcrna,这些npcrna尚未从啮齿鼠的发展策略中发现,以揭示由该细菌引起的疾病的替代治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification and Characterization of Non-Protein Coding RNA Homologs in Citrobacter rodentium by Comparative Genomics
This experiment was conducted to identify homologous non-protein coding RNAs (npcRNA) in Citrobacter rodentium as an alternate for solving health issues caused by this bacteria. Abuse of antimicrobial leads to the emergence of antimicrobial resistance pathogen. Aim of this research is to screen homologous npcRNAs from known bacteria in C. rodentium, to study the expression of homologous npcRNAs in C. rodentium and to predict the regulatory roles of identified homologous npcRNA in C. rodentium. Firstly, screening for presence of homologous npcRNA in Citrobacter rodentium was conducted by collecting known npcRNAs from S. typhi, E. coli and Y. pestis falling under the same genus of Enterobacteriaceae. Secondly, screening the homolog npcRNA identified from previous step (BLASTn) through Rfam (RNA family) to identify unannotated homologs. Then, target mRNA prediction for homologous npcRNA was done using TargetRNA2 webtool to find the compliment mRNA binding of the homologous sequence and the regulatory activities of this transcript. The npcRNA homologs which predicted to regulate virulence target mRNA were assessed for its expression profile at different growth stages via reverse transcription PCR and the band intensity was quantitatively analysed using Image J tool. The known npcRNA Styr-296 from S. typhi showed expression in C. rodentium during three growth stages (lag, log and stationary). The expression was observed to be high during lag phase followed by no expression during log and stationary phase. This Styr-296 homolog was predicted to regulate mRNA translating modulator drug activity B which is associated with the bacterial virulence. Hence, this is a preliminary study promising for further elucidation of more virulence associated npcRNAs that are yet to be discovered from C. rodentium developing strategy to unveil alternate therapeutic options for diseases caused by this bacterium.
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