Coleman Shannon R, Smith Maren L, Spicer Victor, Lao Ying, Mookherjee Neeloffer, Hancock Robert E W
Center for Microbial Diseases and Immunity Research, Department of Microbiology and Immunology, University of British Columbia, Vancouver, Canada.
Manitoba Center for Proteomics & Systems Biology, University of Manitoba, Winnipeg, Canada.
mSystems. 2020 May 19;5(3):e00204-20. doi: 10.1128/mSystems.00204-20.
is a motile species that initiates swarming motility in response to specific environmental cues, i.e., a semisolid surface with amino acids as a nitrogen source (relevant to the human lung). Swarming is an intricately regulated process, but to date posttranscriptional regulation has not been extensively investigated. Small noncoding RNAs (sRNAs) are hypothesized to play posttranscriptional regulatory roles, largely through suppression of translation, and we previously demonstrated 20 sRNA species that were dysregulated under swarming conditions. One of these, sRNA PA0805.1 (which was 5-fold upregulated under swarming conditions), when cloned, transformed into wild-type (WT) PAO1, and overexpressed, led to broad phenotypic changes, including reduced swarming, swimming, and twitching motilities, as well as increased adherence, cytotoxicity, and tobramycin resistance. A ΔPA0805.1 deletion mutant was more susceptible to tobramycin than the WT under swarming conditions. The strain overexpressing PA0805.1 was compared to the empty-vector strain by transcriptome sequencing (RNA-Seq) and proteomics under swarming conditions to determine sRNA targets. Broad transcriptional and proteomic profiles showed 1,121 differentially expressed genes and 258 proteins with significantly different abundance. Importantly, these included 106 transcriptional regulators, two-component regulatory systems, and sigma and anti-sigma factors. Downstream of these regulators were found downregulated type IV pilus genes, many upregulated adherence and virulence factors, and two multidrug efflux systems, and Therefore, the sRNA PA0805.1 appears to be a global regulator that influences diverse bacterial lifestyles, most likely through a regulatory cascade. is an opportunistic pathogen of humans. With roughly 10% of its genes encoding transcriptional regulators, and hundreds of small noncoding RNAs (sRNAs) interspersed throughout the genome, is able to fine-tune its response to adapt and survive in the host and resist antimicrobial agents. Understanding mechanisms of genetic regulation is therefore crucial to combat pathogenesis. The previously uncharacterized sRNA PA0805.1 was overexpressed in strain PAO1, resulting in decreased motility, increased adherence, cytotoxicity, and tobramycin resistance. In contrast, a ΔPA0805.1 deletion mutant had increased susceptibility to tobramycin under swarming conditions. Omic approaches uncovered 1,121 transcriptomic and 258 proteomic changes in the overexpression strain compared with the empty-vector strain, which included 106 regulatory factors. Downstream of these regulators were upregulated adherence factors, multidrug efflux systems, and virulence factors in both transcriptomics and proteomics. This study provides insights into the role of the sRNA PA0805.1 in modulating bacterial adaptations.
它是一种具有运动性的物种,能响应特定环境线索(即含有氨基酸作为氮源的半固体表面,这与人类肺部相关)启动群体运动。群体运动是一个受到复杂调控的过程,但迄今为止转录后调控尚未得到广泛研究。小非编码RNA(sRNA)被认为在转录后发挥调控作用,主要通过抑制翻译来实现,我们之前证明了20种sRNA在群体运动条件下表达失调。其中之一,sRNA PA0805.1(在群体运动条件下上调了5倍),当被克隆、转化到野生型(WT)PAO1中并过表达时,导致了广泛的表型变化,包括群体运动、游泳运动和颤动运动减少,以及黏附增加、细胞毒性增加和对妥布霉素耐药性增加。在群体运动条件下,ΔPA0805.1缺失突变体比野生型对妥布霉素更敏感。在群体运动条件下,通过转录组测序(RNA-Seq)和蛋白质组学将过表达PA0805.1的菌株与空载体菌株进行比较,以确定sRNA的靶标。广泛的转录组和蛋白质组图谱显示有1121个差异表达基因和258种丰度有显著差异的蛋白质。重要的是,这些包括106个转录调节因子、双组分调节系统以及σ因子和抗σ因子。在这些调节因子的下游发现了下调的IV型菌毛基因、许多上调的黏附因子和毒力因子以及两个多药外排系统。因此,sRNA PA0805.1似乎是一个全局调节因子,很可能通过一个调节级联影响多种细菌生活方式。它是人类的机会致病菌。其大约10%的基因编码转录调节因子,并在整个基因组中散布着数百个小非编码RNA(sRNA),它能够微调其反应以在宿主体内适应和生存并抵抗抗菌剂。因此,了解基因调控机制对于对抗发病机制至关重要。之前未被表征的sRNA PA0805.1在PAO1菌株中过表达,导致运动性降低、黏附增加、细胞毒性增加和对妥布霉素耐药性增加。相比之下,ΔPA0805.1缺失突变体在群体运动条件下对妥布霉素的敏感性增加。组学方法揭示了与空载体菌株相比,过表达菌株中有1121个转录组变化和258个蛋白质组变化,其中包括106个调节因子。在这些调节因子的下游,转录组学和蛋白质组学中黏附因子、多药外排系统和毒力因子均上调。这项研究为sRNA PA0805.1在调节细菌适应性中的作用提供了见解。