Ashwath Priyanka, Sannejal Akhila Dharnappa
Nitte (Deemed to be University), Nitte University Centre for Science Education & Research (NUCSER), Mangaluru, India.
Curr Gene Ther. 2022;22(2):79-88. doi: 10.2174/1566523221666210419084836.
The increasing resistance of the disease-causing pathogens to antimicrobial drugs is a public health concern and a socio-economic burden. The emergence of multi-drug resistant strains has made it harder to treat and combat infectious diseases with available conventional antibiotics. There are currently few effective therapeutic regimens for the successful prevention of infections caused by drug-resistant microbes. Various alternative strategies used in the recent past to decrease and limit antibiotic resistance in pathogens include bacteriophages, vaccines, anti-biofilm peptides, and antimicrobial peptides. However, in this review, we focus on the novel and robust molecular approach of antisense RNA (asRNA) technology and the clustered regulatory interspaced short palindromic repeat (CRISPR)-based antibiotic therapy, which can be exploited to selectively eradicate the drug-resistant bacterial strain in a sequence-specific fashion establishing opportunities in the treatment of multi-drug resistant related infections.
致病病原体对抗菌药物的耐药性不断增强,这是一个公共卫生问题,也是一种社会经济负担。多重耐药菌株的出现使得用现有的传统抗生素治疗和对抗传染病变得更加困难。目前,几乎没有有效的治疗方案能成功预防由耐药微生物引起的感染。过去,为了降低和限制病原体中的抗生素耐药性而采用的各种替代策略包括噬菌体、疫苗、抗生物膜肽和抗菌肽。然而,在本综述中,我们重点关注反义RNA(asRNA)技术这一新颖且强大的分子方法以及基于成簇规律间隔短回文重复序列(CRISPR)的抗生素疗法,它们可被用于以序列特异性方式选择性根除耐药细菌菌株,从而为治疗多重耐药相关感染创造机会。