Department of Clinical Sciences, Institute of Tropical Medicine Antwerp, 2000, Antwerp, Belgium.
Clinical Reference Laboratory, Department of Clinical Sciences, Institute of Tropical Medicine, 2000, Antwerp, Belgium.
Sci Rep. 2024 Feb 27;14(1):4786. doi: 10.1038/s41598-024-55262-8.
Increasing antimicrobial resistance in Enterococcus faecium necessitates the search for novel treatment agents, such as bacteriocins. In this study, we conducted an in vivo assessment of five bacteriocins, namely Lacticin Z, Lacticin Q, Garvicin KS (ABC), Aureocin A53 and Microbisporicin (NAI-107), against vanB-resistant Enterococcus faecium using a Galleria mellonella model. Our in vitro experiments demonstrated the efficacy of all five bacteriocins against vanB-resistant E. faecium with only NAI-107 demonstrating in vivo efficacy. Notably, NAI-107 exhibited efficacy across a range of tested doses, with the highest efficacy observed at a concentration of 16 µg/mL. Mortality rates in the group treated with 16 µg/mL NAI-107 were lower than those observed in the linezolid-treated group. These findings strongly suggest that NAI-107 holds promise as a potential alternative therapeutic agent for treating infections caused by resistant E. faecium and warrants further investigation.
肠球菌对抗菌药物的耐药性不断增加,需要寻找新的治疗药物,如细菌素。本研究采用大蜡螟模型,对五种细菌素(乳链菌肽 Z、乳链菌肽 Q、葡萄球菌素 KS(ABC)、金黄素 A53 和微球菌素(NAI-107))进行了体内评估,以对抗耐万古霉素肠球菌。我们的体外实验表明,所有五种细菌素对耐万古霉素肠球菌均有效,只有 NAI-107 具有体内疗效。值得注意的是,NAI-107 在一系列测试剂量中均表现出疗效,在 16μg/ml 的浓度下观察到的疗效最高。用 16μg/ml NAI-107 治疗的组的死亡率低于用利奈唑胺治疗的组。这些发现强烈表明,NAI-107 有望成为治疗耐万古霉素肠球菌感染的潜在替代治疗药物,值得进一步研究。