College of Basic Medicine, Dali University, Dali, 671000, P.R. China; Department of Laboratory Medicine, The Affiliated Qingyuan Hospital (Qingyuan People's Hospital), Guangzhou Medical University, Qingyuan, 511518, P.R. China.
Department of Laboratory Medicine, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, 510120, P.R. China.
Microb Pathog. 2024 Dec;197:107077. doi: 10.1016/j.micpath.2024.107077. Epub 2024 Oct 29.
Pseudomonas aeruginosa is an important gram-negative pathogen that often causes skin, respiratory, and bloodstream infections. The virulence of P. aeruginosa is regulated by sRNAs through a complex network, which is still incompletely understood. This study employed transcriptome sequencing (RNA-Seq) to screen sRNA 111, and real-time quantitative PCR was conducted for validation. In addition, an overexpression strain of sRNA111 was constructed and the effects of overexpression of sRNA111 on virulence factors such as biofilm formation, pyocyanin, swarming motility, inflammatory factors, and biofilm-associated factors were analyzed. The results revealed that sRNA111 might be closely related to the formation of P. aeruginosa biofilm. Compared to the vector, sRNA111 was found to enhance P. aeruginosa biofilm formation while also suppressing swarming motility, invasive ability, and adhesion capability. Meanwhile, sRNA111 up-regulated the expression of biofilm-related genes, such as Anr, pel family, polB, recA, etc., more significantly in the biofilm environment compared with the wild strain. In addition, sRNA111 effectively promoted the expression of inflammatory factors in the biofilm environment compared with the planktonic environment. These results implied that sRNA111 regulates the formation of P. aeruginosa biofilm and other virulence factors and further modulates the process of infection immunity.
铜绿假单胞菌是一种重要的革兰氏阴性病原体,常引起皮肤、呼吸道和血流感染。铜绿假单胞菌的毒力通过 sRNAs 调节的复杂网络进行调控,但这一网络仍不完全清楚。本研究采用转录组测序(RNA-Seq)筛选 sRNA111,并通过实时定量 PCR 进行验证。此外,构建了 sRNA111 的过表达菌株,并分析了 sRNA111 过表达对生物膜形成、绿脓菌素、泳动运动、炎症因子和生物膜相关因子等毒力因子的影响。结果表明,sRNA111 可能与铜绿假单胞菌生物膜的形成密切相关。与载体相比,sRNA111 增强了铜绿假单胞菌生物膜的形成,同时抑制了泳动运动、侵袭能力和黏附能力。同时,sRNA111 在生物膜环境中比野生株更显著地上调了生物膜相关基因,如 Anr、pel 家族、polB、recA 等的表达。此外,sRNA111 在生物膜环境中比浮游环境更有效地促进了炎症因子的表达。这些结果表明,sRNA111 调节铜绿假单胞菌生物膜和其他毒力因子的形成,并进一步调节感染免疫过程。