Yang Guang, Li Boan, Jia Leili, Qiu Huaiyu, Yang Mingjuan, Zhu Binghua, Xie Jing, Qiu Shaofu, Li Peng, Ma Hui, Song Hongbin, Wang Ligui
Center for Disease Control and Prevention of Chinese People's Liberation Army, Beijing, China.
The 5th Medical Center of General Hospital of Chinese People's Liberation Army, Beijing, China.
Front Cell Infect Microbiol. 2020 Sep 16;10:483. doi: 10.3389/fcimb.2020.00483. eCollection 2020.
Regulation of the environmental stress response and virulence of may involve multiple signaling pathways; however, these mechanisms are not well-defined. In bacteria, small regulatory RNAs (sRNAs) regulate bacterial growth, metabolism, virulence, and environmental stress response. Therefore, identifying novel functional sRNAs in could help elucidate pathogenic adaptations to host micro-environmental stresses and associated virulence. The aim of this study was to confirm the presence of an sRNA, , in and to determine its functions and possible mechanism of action. was found to regulate tolerance and virulence under hyperosmotic pressure. Its expression was verified by qRT-PCR and Northern blotting, and its genomic position was confirmed by 5'-rapid amplification of cDNA ends. expression was significantly decreased (~ 80%) under hyperosmotic conditions (680 mM NaCl), and the survival rate of the deletion strain increased by 20% under these conditions. This suggested that has been selected to promote host survival under hyperosmotic conditions. Additionally, virulence assessment, including guinea pig Sereny test and competitive invasion assays in mouse lungs, revealed that deletion significantly decreased virulence. Two-dimensional gel analyses suggest that may modulate the expression of , and genes, which may affect the virulence and survival of under osmotic pressures. Furthermore, expression has been shown to improve the survival of under osmotic pressures. These results suggest that has a broad range of action in response to hyperosmotic environmental stresses and in controlling its virulence to adapt to environmental stresses encountered during host infection.
[细菌名称]的环境应激反应和毒力调节可能涉及多个信号通路;然而,这些机制尚未明确。在细菌中,小调节RNA(sRNA)可调节细菌生长、代谢、毒力和环境应激反应。因此,鉴定[细菌名称]中新型功能性sRNA有助于阐明其对宿主微环境应激的致病适应性及相关毒力。本研究的目的是证实[细菌名称]中一种sRNA([sRNA名称])的存在,并确定其功能及可能的作用机制。发现[细菌名称]在高渗压力下可调节耐受性和毒力。通过qRT-PCR和Northern印迹验证了其表达,并通过5'-cDNA末端快速扩增确定了其基因组位置。在高渗条件(680 mM NaCl)下,[sRNA名称]的表达显著降低(约80%),在这些条件下,[细菌名称]缺失菌株的存活率提高了20%。这表明[细菌名称]已被选择用于在高渗条件下促进宿主存活。此外,包括豚鼠角膜结膜炎试验和小鼠肺部竞争性侵袭试验在内的毒力评估表明,[细菌名称]缺失显著降低了[细菌名称]的毒力。二维凝胶分析表明,[sRNA名称]可能调节[相关基因名称1]、[相关基因名称2]和[相关基因名称3]的表达,这可能影响[细菌名称]在渗透压下的毒力和存活。此外,已证明[细菌名称]的表达可提高[细菌名称]在渗透压下的存活率。这些结果表明,[sRNA名称]在[细菌名称]应对高渗环境应激以及控制其毒力以适应宿主感染期间遇到的环境应激方面具有广泛作用。