Deng Yiqin, Zang Shujun, Lin Ziyang, Xu Liwen, Cheng Changhong, Feng Juan
Key Laboratory of South China Sea Fishery Resources Exploitation & Utilization, Ministry of Agriculture and Rural Affairs, South China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Guangzhou 510300, China.
Microorganisms. 2023 Nov 9;11(11):2741. doi: 10.3390/microorganisms11112741.
Hfq is a global regulator and can be involved in multiple cellular processes by assisting small regulatory RNAs (sRNAs) to target mRNAs. To gain insight into the virulence regulation of Hfq in , the null mutant, ∆, was constructed in strain 345. Compared with the wild-type strain, the mortality of pearl gentian sharply declined from 80% to 0% in ∆ when infected with a dose that was 7.5-fold the median lethal dose (LD50). Additionally, ∆ led to impairments of bacterial growth, motility, and biofilm formation and resistance to reactive oxygen species, chloramphenicol, and florfenicol. A transcriptome analysis indicated that the expression of 16.39% genes on 345 were significantly changed after the deletion of . Without Hfq, the virulence-related pathways, including flagellar assembly and bacterial chemotaxis, were repressed. Moreover, eleven sRNAs, including sRNA0405, sRNA0078, sRNA0419, sRNA0145, and sRNA0097, which, respectively, are involved in chloramphenicol/florfenicol resistance, outer membrane protein synthesis, electron transport, amino acid metabolism, and biofilm formation, were significantly down-regulated. In general, Hfq contributes to the virulence of 345 probably via positively regulating bacterial motility and biofilm formation. It is involved in flagellar assembly and bacterial chemotaxis by binding sRNAs and regulating the target mRNAs.
Hfq是一种全局调节因子,可通过协助小调节RNA(sRNA)靶向mRNA参与多种细胞过程。为了深入了解Hfq在[具体细菌名称未给出]中的毒力调节作用,在[具体细菌名称未给出]菌株345中构建了缺失突变体∆[细菌名称]。与野生型菌株相比,当用7.5倍中位数致死剂量(LD50)的剂量感染时,∆[细菌名称]中珍珠龙胆的死亡率从80%急剧下降到0%。此外,∆[细菌名称]导致细菌生长、运动性、生物膜形成以及对活性氧、氯霉素和氟苯尼考的抗性受损。转录组分析表明,在缺失[细菌名称]后,[具体细菌名称未给出]345上16.39%的基因表达发生了显著变化。没有Hfq时,包括鞭毛组装和细菌趋化性在内的与毒力相关的途径受到抑制。此外,11种sRNA,包括分别参与氯霉素/氟苯尼考抗性、外膜蛋白合成、电子传递、氨基酸代谢和生物膜形成的sRNA0405、sRNA0078、sRNA0419、sRNA0145和sRNA0097,显著下调。总体而言,Hfq可能通过正向调节细菌运动性和生物膜形成来促进[具体细菌名称未给出]345的毒力。它通过结合sRNA并调节靶mRNA参与鞭毛组装和细菌趋化性。