Beenker Wouter A G, Hoeksma Jelmer, Bannier-Hélaouët Marie, Clevers Hans, den Hertog Jeroen
Hubrecht Institute-KNAW and University Medical Center Utrecht, Utrecht, The Netherlands.
Oncode Institute, Hubrecht Institute-KNAW and University Medical Center, Utrecht, The Netherlands.
Microbiol Spectr. 2023 Mar 15;11(2):e0509722. doi: 10.1128/spectrum.05097-22.
Pseudomonas aeruginosa is an opportunistic pathogen that causes major health care concerns due to its virulence and high intrinsic resistance to antimicrobial agents. Therefore, new treatments are greatly needed. An interesting approach is to target quorum sensing (QS). QS regulates the production of a wide variety of virulence factors and biofilm formation in P. aeruginosa. This study describes the identification of paecilomycone as an inhibitor of QS in both Chromobacterium violaceum and P. aeruginosa. Paecilomycone strongly inhibited the production of virulence factors in P. aeruginosa, including various phenazines, and biofilm formation. In search of the working mechanism, we found that paecilomycone inhibited the production of 4-hydroxy-2-heptylquinoline (HHQ) and 3,4-dihydroxy-2-heptylquinoline (PQS), but not 2'-aminoacetophenone (2-AA). Therefore, we suggest that paecilomycone affects parts of QS in P. aeruginosa by targeting the PqsBC complex and alternative targets or alters processes that influence the enzymatic activity of the PqsBC complex. The toxicity of paecilomycone toward eukaryotic cells and organisms was low, making it an interesting lead for further clinical research. Antibiotics are becoming less effective against bacterial infections due to the evolution of resistance among bacteria. Pseudomonas aeruginosa is a Gram-negative pathogen that causes major health care concerns and is difficult to treat due to its high intrinsic resistance to antimicrobial agents. Therefore, new targets are needed, and an interesting approach is to target quorum sensing (QS). QS is the communication system in bacteria that regulates multiple pathways, including the production of virulence factors and biofilm formation, which leads to high toxicity in the host and low sensitivity to antibiotics, respectively. We found a compound, named paecilomycone, that inhibited biofilm formation and the production of various virulence factors in P. aeruginosa. The toxicity of paecilomycone toward eukaryotic cells and organisms was low, making it an interesting lead for further clinical research.
铜绿假单胞菌是一种机会致病菌,因其毒力和对抗菌药物的高度固有耐药性而引起重大医疗保健问题。因此,迫切需要新的治疗方法。一种有趣的方法是针对群体感应(QS)。群体感应调节铜绿假单胞菌中多种毒力因子的产生和生物膜形成。本研究描述了拟青霉素作为紫色杆菌和铜绿假单胞菌中群体感应抑制剂的鉴定。拟青霉素强烈抑制铜绿假单胞菌中毒力因子的产生,包括各种吩嗪,并抑制生物膜形成。在寻找作用机制时,我们发现拟青霉素抑制4-羟基-2-庚基喹啉(HHQ)和3,4-二羟基-2-庚基喹啉(PQS)的产生,但不抑制2'-氨基苯乙酮(2-AA)。因此,我们认为拟青霉素通过靶向PqsBC复合物和其他靶点影响铜绿假单胞菌群体感应的部分环节,或改变影响PqsBC复合物酶活性的过程。拟青霉素对真核细胞和生物体的毒性较低,使其成为进一步临床研究的一个有趣线索。由于细菌耐药性的演变,抗生素对细菌感染的疗效越来越低。铜绿假单胞菌是一种革兰氏阴性病原体,引起重大医疗保健问题,由于其对抗菌药物的高度固有耐药性而难以治疗。因此,需要新的靶点,一种有趣的方法是针对群体感应(QS)。群体感应是细菌中的通讯系统,调节多种途径,包括毒力因子的产生和生物膜形成,分别导致在宿主中的高毒性和对抗生素的低敏感性。我们发现一种名为拟青霉素的化合物,它抑制铜绿假单胞菌中的生物膜形成和各种毒力因子的产生。拟青霉素对真核细胞和生物体的毒性较低,使其成为进一步临床研究的一个有趣线索。