Ghosh Suparna, Dureja Chetna, Khatri Indu, Subramanian Srikrishna, Raychaudhuri Saumya, Ghosh Sagarmoy
Department of Microbiology, University of Calcutta, Kolkata 700 019, India.
CSIR-Institute of Microbial Technology, Chandigarh 160 036, India.
Microbiology (Reading). 2017 Dec;163(12):1924-1936. doi: 10.1099/mic.0.000566.
Small RNA (sRNA)-mediated regulation of gene expression is a major tool to understand bacterial responses to environmental changes. In particular, pathogenic bacteria employ sRNAs to adapt to the host environment and establish infection. Members of the complex, normally present in soil microbiota, cause nosocomial lung infection especially in hospitalized cystic fibrosis patients. We sequenced the draft genome of KC-01, isolated from the coastal saline soil, and identified several potential sRNAs . Expression of seven small RNAs (Bc_KC_sr1-7) was subsequently confirmed. Two sRNAs (Bc_KC_sr1 and Bc_KC_sr2) were upregulated in response to iron depletion by 2,2'-bipyridyl and another two (Bc_KC_sr3 and Bc_KC_sr4) responded to the presence of 60 µM HO in the culture media. Bc_Kc_sr5, 6 and 7 remained unchanged under these conditions. Expression of Bc_KC_sr2, 3 and 4 also altered with a change in temperature and incubation time. A search in the Rfam and BSRD databases identified Bc_Kc_sr4 as candidate738 in D286 and assigned Bc_Kc_sr5 and 6 as tmRNA and 6S RNA, respectively. The novel sRNAs were conserved in but did not have any homologue in other genera. Bc_KC_sr1 and 4 were transcribed independently while the rest were part of the 3' UTR of their upstream genes. TargetRNA2 predicted that these sRNAs could target a host of cellular messages with very high stringency. Intriguingly, regions surrounding the translation initiation site for several enzymes involved in Fe-S cluster and siderophore biosynthesis, ROS homeostasis, porins, transcription and translation regulators, were among the suggested putative binding sites for these sRNAs.
小RNA(sRNA)介导的基因表达调控是理解细菌对环境变化反应的主要工具。特别是,病原菌利用sRNAs来适应宿主环境并建立感染。该复合体的成员通常存在于土壤微生物群中,会引起医院获得性肺部感染,尤其是在住院的囊性纤维化患者中。我们对从沿海盐土中分离出的KC-01的基因组草图进行了测序,并鉴定出了几种潜在的sRNAs。随后证实了7种小RNA(Bc_KC_sr1 - 7)的表达。两种sRNAs(Bc_KC_sr1和Bc_KC_sr2)在受到2,2'-联吡啶诱导的铁缺乏时上调,另外两种(Bc_KC_sr3和Bc_KC_sr4)对培养基中60 μM H₂O₂的存在有反应。在这些条件下,Bc_Kc_sr5、6和7保持不变。Bc_KC_sr2、3和4的表达也随着温度和孵育时间的变化而改变。在Rfam和BSRD数据库中搜索发现,Bc_Kc_sr4在D286中为候选738,Bc_Kc_sr5和6分别被指定为tmRNA和6S RNA。这些新的sRNAs在该属中保守,但在其他属中没有任何同源物。Bc_KC_sr1和4是独立转录的,而其余的是其上游基因3' UTR的一部分。TargetRNA2预测这些sRNAs可以非常严格地靶向许多细胞信息。有趣的是,参与铁硫簇和铁载体生物合成、活性氧稳态、孔蛋白、转录和翻译调节的几种酶的翻译起始位点周围区域,是这些sRNAs建议的假定结合位点之一。