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铜绿假单胞菌 PAO1 对四种不同抗生素的 sRNA 响应的转录组分析。

Transcriptome analysis of sRNA responses to four different antibiotics in Pseudomonas aeruginosa PAO1.

机构信息

School of Basic Medical Sciences, Henan University of Science and Technology, Luoyang, 471003, China.

School of Basic Medical Sciences, Henan University of Science and Technology, Luoyang, 471003, China.

出版信息

Microb Pathog. 2022 Dec;173(Pt A):105865. doi: 10.1016/j.micpath.2022.105865. Epub 2022 Nov 1.

Abstract

A large number of evidence showed that regulatory sRNAs could modulate antibiotic resistance and sensitivity. In this study, we used RNA-sequencing to profile sRNAs in wild type and antibiotic-resistant PAO1 selected by four antibiotics (polymyxin B, ciprofloxacin, doxycycline, and ceftriaxone). Totally, we found 113, 25, 91 and 12 differentially expressed sRNAs in polymyxin B-, ciprofloxacin-, doxycycline-, and ceftriaxone-resistant P. aeruginosa, respectively. To elucidate functions of differentially expressed sRNA, we predicated their target genes and obtained pathways enriched by their target genes. In addition, our results indicated that the downregulated sRNA spae884.1, spae3443.1, and spae5681.1 might involve in polymyxin B resistance by enhancing their target genes arnA, arnD, and arnT expression in PAO1, respectively. The upregulated sRNA spae3443.1 and spae649.2 might implicate in ciprofloxacin resistance by promoting their target gene pslK expression to increase biofilm formation in PAO1. The upregulated spae1558.1 might increase oprJ expression, as well as spae3959.1 and spae3706.1 might increase mexC expression to modulate doxycycline resistance in PAO1. The sRNA novel-N714 might involve in virulence in ceftriaxone-resistant PAO1 by activating its target gene PA1429 expression. Our study might provide bases of the underlying mechanism of sRNA in regulating antibiotic resistance of PAO1 against different antibiotics.

摘要

大量证据表明,调控 sRNA 可以调节抗生素耐药性和敏感性。在这项研究中,我们使用 RNA 测序技术对野生型和四种抗生素(多粘菌素 B、环丙沙星、强力霉素和头孢曲松)选择的耐药 PAO1 中的 sRNA 进行了分析。总共,我们在多粘菌素 B、环丙沙星、强力霉素和头孢曲松耐药的铜绿假单胞菌中分别发现了 113、25、91 和 12 个差异表达的 sRNA。为了阐明差异表达 sRNA 的功能,我们预测了它们的靶基因,并获得了其靶基因富集的途径。此外,我们的结果表明,下调的 sRNA spae884.1、spae3443.1 和 spae5681.1 可能通过分别增强其靶基因 arnA、arnD 和 arnT 的表达而参与多粘菌素 B 耐药。上调的 sRNA spae3443.1 和 spae649.2 可能通过促进其靶基因 pslK 的表达来增加 PAO1 生物膜形成,从而参与环丙沙星耐药。上调的 spae1558.1 可能增加 oprJ 的表达,而上调的 spae3959.1 和 spae3706.1 可能增加 mexC 的表达,从而调节 PAO1 对强力霉素的耐药性。sRNA novel-N714 可能通过激活其靶基因 PA1429 的表达参与头孢曲松耐药 PAO1 的毒力。我们的研究可能为 sRNA 调节 PAO1 对不同抗生素的耐药性的潜在机制提供基础。

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