Laboratory of Microbiology, Graduate School of Pharmaceutical Sciences, University of Tokyo, Tokyo, Japan.
Laboratory of Synthetic Medicinal Chemistry, Graduate School of Pharmaceutical Sciences, University of Tokyo, Tokyo, Japan.
Nat Chem Biol. 2015 Feb;11(2):127-33. doi: 10.1038/nchembio.1710. Epub 2014 Dec 8.
To obtain therapeutically effective new antibiotics, we first searched for bacterial culture supernatants with antimicrobial activity in vitro and then performed a secondary screening using the silkworm infection model. Through further purification of the in vivo activity, we obtained a compound with a previously uncharacterized structure and named it 'lysocin E'. Lysocin E interacted with menaquinone in the bacterial membrane to achieve its potent bactericidal activity, a mode of action distinct from that of any other known antibiotic, indicating that lysocin E comprises a new class of antibiotic. This is to our knowledge the first report of a direct interaction between a small chemical compound and menaquinone that leads to bacterial killing. Furthermore, lysocin E decreased the mortality of infected mice. To our knowledge, lysocin E is the first compound identified and purified by quantitative measurement of therapeutic effects in an invertebrate infection model that exhibits robust in vivo effects in mammals.
为了获得具有治疗效果的新型抗生素,我们首先在体外筛选具有抗菌活性的细菌培养上清液,然后使用家蚕感染模型进行二次筛选。通过对体内活性的进一步纯化,我们得到了一种具有先前未被描述结构的化合物,并将其命名为“lysocin E”。Lysocin E 与细菌膜中的menaquinone 相互作用,从而实现其强大的杀菌活性,其作用模式与任何其他已知抗生素都不同,这表明 lysocin E 属于一类新型抗生素。据我们所知,这是首次报道小分子化合物与menaquinone 直接相互作用导致细菌死亡。此外,lysocin E 降低了感染小鼠的死亡率。据我们所知,lysocin E 是第一个通过定量测量在无脊椎动物感染模型中的治疗效果来鉴定和纯化的化合物,它在哺乳动物中表现出强大的体内作用。