Antibacterial Activity of LCB10-0200 against Klebsiella pneumoniae

Klebsiella pneumoniae is one of the important clinical organisms that causes various infectious diseases, including urinary tract infections, necrotizing pneumonia, and surgical wound infections. The increase in the incidence of multidrug-resistance K. pneumoniae is a major problem in public healthcare. Therefore, a novel antibacterial agent is needed to treat this pathogen. Here, we studied the in vitro and in vivo activities of a novel antibiotic LCB10-0200, a siderophore-conjugated cephalosporin, against clinical isolates of K. pneumoniae. In vitro susceptibility study found that LCB10-0200 showed potent antibacterial activity against K. pneumoniae, including the beta-lactamase producing strains. The in vivo efficacy of LCB10-0200 was examined in three different mouse infection models, including systemic, thigh, and urinary tract infections. LCB10-0200 showed more potent in vivo activity than ceftazidime in the three in vivo models against the drug-susceptible and drug-resistant K. pneumoniae strains. Taken together, these results show that LCB10-0200 is a potential antibacterial agent to treat infection caused by K. pneumoniae.

Automated summary

Klebsiella pneumoniae is a significant clinical pathogen causing various infections, with growing concern over multidrug-resistant strains. The novel antibiotic LCB10-0200, a siderophore-conjugated cephalosporin, demonstrated potent antibacterial activity against K. pneumoniae in vitro and in vivo, surpassing ceftazidime in efficacy. These findings highlight the potential of LCB10-0200 as a promising antibacterial agent against K. pneumoniae infections.