Shenzhen National Clinical Research Center for Infectious Disease, Shenzhen Third People's Hospital, The Second Affiliated Hospital of Southern University of Science and Technology, Shenzhen, China.
Department of Pharmacology, Joint Laboratory of Guangdong-Hong Kong Universities for Vascular Homeostasis and Diseases, School of Medicine, Southern University of Science a-nd Technology, Shenzhen, China.
NPJ Biofilms Microbiomes. 2024 Sep 11;10(1):82. doi: 10.1038/s41522-024-00550-4.
Pseudomonas aeruginosa is a widespread nosocomial pathogen with a significant to cause both severe planktonic acute and biofilm-related chronic infections. Small RNAs (sRNAs) are noncoding regulatory molecules that are stabilized by the RNA chaperone Hfq to trigger various virulence-related signaling pathways. Here, we identified an Hfq-binding sRNA in P. aeruginosa PAO1, PqsS, which promotes bacterial pathogenicity and pseudomonas quinolone signal quorum sensing (pqs QS) system. Specifically, PqsS enhanced acute bacterial infections by inducing host cell death and promoting rhamnolipid-regulated swarming motility. Meanwhile, PqsS reduced chronic infection traits including biofilm formation and antibiotic resistance. Moreover, PqsS repressed pqsL transcript, increasing PQS levels for pqs QS. A PQS-rich environment promoted PqsS expression, thus forming a positive feedback loop. Furthermore, we demonstrated that the PqsS interacts and destabilizes the pqsL mRNA by recruiting RNase E to drive degradation. These findings provide insights for future research on P. aeruginosa pathogenesis and targeted treatment.
铜绿假单胞菌是一种广泛存在的医院病原体,可导致严重的浮游急性感染和生物膜相关的慢性感染。小 RNA(sRNA)是一种非编码调节分子,通过 RNA 伴侣蛋白 Hfq 稳定,从而触发各种与毒力相关的信号通路。在这里,我们在铜绿假单胞菌 PAO1 中鉴定出一种 Hfq 结合的 sRNA,即 PqsS,它可促进细菌致病性和铜绿假单胞菌喹诺酮信号群体感应(pqs QS)系统。具体而言,PqsS 通过诱导宿主细胞死亡和促进鼠李糖脂调节的群集运动来增强急性细菌感染。同时,PqsS 降低了生物膜形成和抗生素耐药性等慢性感染特征。此外,PqsS 抑制了 pqsL 转录本,增加了 PQS 水平,从而激活了 pqs QS。富含 PQS 的环境促进了 PqsS 的表达,从而形成了正反馈回路。此外,我们证明 PqsS 通过招募 RNase E 来驱动降解,与 pqsL mRNA 相互作用并使其不稳定。这些发现为铜绿假单胞菌发病机制和靶向治疗的未来研究提供了思路。