Genilloud Olga
Fundacion MEDINA, Parque Tecnologico Ciencias de la Salud, 18100 Armilla, Granada, Spain.
Recent Pat Antiinfect Drug Discov. 2012 Dec 1;7(3):189-204. doi: 10.2174/157489112803521968.
Microbial natural products have been for decades one of the most successful sources of drugs to treat infectious diseases. The high occurrence of resistances to all major classes of known antibiotics represents today a new challenge and new classes of antibacterial compounds are urgently needed to respond to this unmet clinical need. While natural products discovery programs have been gradually abandoned by big pharma, smaller biotechnology companies and other research organizations are taking the lead in the discovery of novel antibacterials. A survey of recent patents has shown that in spite of the efforts, few novel compounds are being developed that can overcome most of the emerging multi-resistant and pan-resistant pathogens. In order to respond to the current challenges of discovering novel antibiotics, new approaches are required to be developed to further exploit the microbial resources and their biosynthetic potential as an untapped source of novel metabolites. Strategies to mine microbial collections for orphan biosynthetic pathways and novel species thought to be uncultivable, are emerging as a need within antibacterial drug discovery programs, in combination with high throughput screening and chemical dereplication of novel compounds. Different innovative methods that are being developed to respond to the new challenges that are faced today by drug discovery programs will ensure the evolution of these strategies into a completely new framework that will address the renovated interest in the discovery of novel classes of antibiotics.
几十年来,微生物天然产物一直是治疗传染病最成功的药物来源之一。如今,对所有主要已知抗生素类别的耐药性高发构成了新的挑战,迫切需要新型抗菌化合物来满足这一未被满足的临床需求。虽然大型制药公司已逐渐放弃天然产物发现项目,但小型生物技术公司和其他研究机构正在引领新型抗菌药物的发现。一项对近期专利的调查表明,尽管付出了努力,但仍很少有新型化合物被开发出来,能够克服大多数新出现的多重耐药和泛耐药病原体。为应对发现新型抗生素的当前挑战,需要开发新方法,以进一步挖掘微生物资源及其生物合成潜力,将其作为新型代谢物的未开发来源。在抗菌药物发现项目中,挖掘微生物库以寻找孤儿生物合成途径和被认为不可培养的新物种的策略正在兴起,同时还结合了新型化合物的高通量筛选和化学去重复。为应对药物发现项目如今面临的新挑战而正在开发的不同创新方法,将确保这些策略演变成一个全新的框架,以满足对发现新型抗生素类别的新兴趣。