McCaughey Laura C, Ritchie Neil D, Douce Gillian R, Evans Thomas J, Walker Daniel
Institute of Infection, Immunity and Inflammation, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, G12 8TA, UK.
The ithree institute, University of Technology Sydney, Ultimo, New South Wales, Australia.
Sci Rep. 2016 Jul 22;6:30201. doi: 10.1038/srep30201.
Protein antibiotics, known as bacteriocins, are widely produced by bacteria for intraspecies competition. The potency and targeted action of bacteriocins suggests that they could be developed into clinically useful antibiotics against highly drug resistant Gram-negative pathogens for which there are few therapeutic options. Here we show that Pseudomonas aeruginosa specific bacteriocins, known as pyocins, show strong efficacy in a murine model of P. aeruginosa lung infection, with the concentration of pyocin S5 required to afford protection from a lethal infection at least 100-fold lower than the most commonly used inhaled antibiotic tobramycin. Additionally, pyocins are stable in the lung, poorly immunogenic at high concentrations and efficacy is maintained in the presence of pyocin specific antibodies after repeated pyocin administration. Bacteriocin encoding genes are frequently found in microbial genomes and could therefore offer a ready supply of highly targeted and potent antibiotics active against problematic Gram-negative pathogens.
被称为细菌素的蛋白质抗生素由细菌广泛产生用于种内竞争。细菌素的效力和靶向作用表明,它们可以被开发成临床上有用的抗生素,用于对抗几乎没有治疗选择的高度耐药革兰氏阴性病原体。在这里,我们表明,铜绿假单胞菌特异性细菌素,即绿脓菌素,在铜绿假单胞菌肺部感染的小鼠模型中显示出强大的疗效,提供免受致命感染保护所需的绿脓菌素S5浓度比最常用的吸入性抗生素妥布霉素低至少100倍。此外,绿脓菌素在肺部稳定,高浓度时免疫原性低,并且在重复施用绿脓菌素后,在存在绿脓菌素特异性抗体的情况下仍能保持疗效。细菌素编码基因在微生物基因组中经常被发现,因此可以提供现成的、对有问题的革兰氏阴性病原体具有活性的高度靶向和强效抗生素。