Key Laboratory of Bio-resources and Eco-environment, Ministry of Education, College of Life Sciences, Sichuan University, No. 24, South Section 1, Yihuan Road, Chengdu, 610064, Sichuan, PR China.
Antibiotics Research and Re-evaluation Key Laboratory of Sichuan Province, School of Pharmacy, Chengdu University, No. 2025, Chengluo Avenue, Chengdu, 610106, Sichuan, PR China.
BMC Vet Res. 2022 Mar 24;18(1):114. doi: 10.1186/s12917-022-03216-5.
Trueperella pyogenes and Pseudomonas aeruginosa are two important bacterial pathogens closely relating to the occurrence and development of forest musk deer respiratory purulent disease. Although T. pyogenes is the causative agent of the disease, the subsequently invaded P. aeruginosa will predominate the infection by producing a substantial amount of quorum-sensing (QS)-controlled virulence factors, and co-infection of them usually creates serious difficulties for veterinary treatment. In order to find a potential compound that targets both T. pyogenes and P. aeruginosa, the antibacterial and anti-virulence capacities of 55 compounds, which have similar core structure to the signal molecules of P. aeruginosa QS system, were tested in this study by performing a series of in vitro screening experiments.
We identified that furazolidone could significantly reduce the cell densities of T. pyogenes in mono-culture or in the co-culture with P. aeruginosa. Although the growth of P. aeruginosa could also be moderately inhibited by furazolidone, the results of phenotypic identification and transcriptomic analysis further revealed that sub-inhibitory furazolidone had remarkable inhibitory effect on the biofilm production, motility, and QS system of P. aeruginosa. Moreover, furazolidone could efficiently protect Caenorhabditis elegans models from P. aeruginosa infection under both fast-killing and slow-killing conditions.
This study reports the antibacterial and anti-virulence abilities of furazolidone on T. pyogenes and P. aeruginosa, and provides a promising strategy and molecular basis for the development of novel anti-infectious drugs to dealing with forest musk deer purulent disease, or other diseases caused by T. pyogenes and P. aeruginosa co-infection.
化脓隐秘杆菌和铜绿假单胞菌是与林麝脓性肺炎发生和发展密切相关的两种重要的细菌性病原体。虽然化脓隐秘杆菌是该病的病原体,但随后入侵的铜绿假单胞菌会通过产生大量群体感应(QS)控制的毒力因子而占据优势感染,两者的合并感染通常给兽医治疗带来严重困难。为了寻找一种既能针对化脓隐秘杆菌又能针对铜绿假单胞菌的潜在化合物,本研究通过一系列体外筛选实验,测试了 55 种具有与铜绿假单胞菌 QS 系统信号分子相似核心结构的化合物的抗菌和抗毒力能力。
我们发现呋喃唑酮可显著降低化脓隐秘杆菌在单独培养或与铜绿假单胞菌共培养中的细胞密度。虽然呋喃唑酮也能适度抑制铜绿假单胞菌的生长,但表型鉴定和转录组分析的结果进一步表明,亚抑菌浓度的呋喃唑酮对铜绿假单胞菌生物膜形成、运动性和 QS 系统具有显著的抑制作用。此外,呋喃唑酮在快速杀伤和缓慢杀伤条件下均能有效保护秀丽隐杆线虫模型免受铜绿假单胞菌感染。
本研究报告了呋喃唑酮对化脓隐秘杆菌和铜绿假单胞菌的抗菌和抗毒力作用,为开发新型抗感染药物治疗林麝脓性肺炎或由化脓隐秘杆菌和铜绿假单胞菌合并感染引起的其他疾病提供了有前景的策略和分子基础。