Institute of Molecular Infection Biology (IMIB), University of Würzburg, D-97080, Würzburg, Germany.
Helmholtz Institute for RNA-based Infection Research (HIRI), Helmholtz Centre for Infection Research (HZI), D-97080, Würzburg, Germany.
Nucleic Acids Res. 2022 Jun 24;50(11):6435-6452. doi: 10.1093/nar/gkac362.
Antisense peptide nucleic acids (PNAs) that target mRNAs of essential bacterial genes exhibit specific bactericidal effects in several microbial species, but our mechanistic understanding of PNA activity and their target gene spectrum is limited. Here, we present a systematic analysis of PNAs targeting 11 essential genes with varying expression levels in uropathogenic Escherichia coli (UPEC). We demonstrate that UPEC is susceptible to killing by peptide-conjugated PNAs, especially when targeting the widely-used essential gene acpP. Our evaluation yields three additional promising target mRNAs for effective growth inhibition, i.e.dnaB, ftsZ and rpsH. The analysis also shows that transcript abundance does not predict target vulnerability and that PNA-mediated growth inhibition is not universally associated with target mRNA depletion. Global transcriptomic analyses further reveal PNA sequence-dependent but also -independent responses, including the induction of envelope stress response pathways. Importantly, we show that 9mer PNAs are generally as effective in inhibiting bacterial growth as their 10mer counterparts. Overall, our systematic comparison of a range of PNAs targeting mRNAs of different essential genes in UPEC suggests important features for PNA design, reveals a general bacterial response to PNA conjugates and establishes the feasibility of using PNA antibacterials to combat UPEC.
反义肽核酸 (PNA) 可靶向必需的细菌 mRNA,在多种微生物中表现出特定的杀菌作用,但我们对 PNA 活性及其靶基因谱的机制理解有限。在这里,我们对靶向尿路致病性大肠杆菌 (UPEC) 中表达水平不同的 11 个必需基因的 PNA 进行了系统分析。我们证明了 UPEC 容易被肽偶联 PNA 杀死,尤其是在靶向广泛使用的必需基因 acpP 时。我们的评估还确定了另外三个有希望的有效生长抑制的靶 mRNA,即 dnaB、ftsZ 和 rpsH。分析还表明,转录丰度不能预测靶标易损性,并且 PNA 介导的生长抑制并不普遍与靶标 mRNA 耗竭相关。全转录组分析进一步揭示了 PNA 序列依赖性和非依赖性反应,包括诱导包膜应激反应途径。重要的是,我们表明 9 聚体 PNA 通常与 10 聚体 PNA 一样有效地抑制细菌生长。总体而言,我们对 UPEC 中不同必需基因的 mRNA 进行了一系列 PNA 的系统比较,这表明了 PNA 设计的重要特征,揭示了细菌对 PNA 缀合物的一般反应,并确立了使用 PNA 抗菌剂来对抗 UPEC 的可行性。