Law Carmen Oi Kwan, Huang Chuan, Pan Qing, Lee Joseph, Hao Qin, Chan Ting-Fung, Lo Norman Wai Sing, Ang Irene Ling, Koon Alex, Ip Margaret, Chan Edwin, Lau Terrence Chi Kong
Department of Biomedical Sciences, College of Veterinary Medicine and Life Science, City University of Hong Kong, Kowloon, Hong Kong Special Administrative Region, China; School of Life Sciences, The Chinese University of Hong Kong, Hong Kong Special Administrative Region, China.
Department of Biomedical Sciences, College of Veterinary Medicine and Life Science, City University of Hong Kong, Kowloon, Hong Kong Special Administrative Region, China.
Mol Ther Nucleic Acids. 2019 Jun 7;16:218-228. doi: 10.1016/j.omtn.2019.02.011. Epub 2019 Feb 22.
Bacteria with multiple drug resistance (MDR) have become a global issue worldwide, and hundreds of thousands of people's lives are threatened every year. The emergence of novel MDR strains and insufficient development of new antimicrobial agents are the major reasons that limit the choice of antibiotics for the treatment of bacterial infection. Thus, preserving the clinical value of current antibiotics could be one of the effective approaches to resolve this problem. Here we identified numerous novel small RNAs that were downregulated in the MDR clinical isolates of Pseudomonas aeruginosa (P. aeru), and we demonstrated that overexpression of one of these small RNAs (sRNAs), AS1974, was able to transform the MDR clinical strain to drug hypersusceptibility. AS1974 is the master regulator to moderate the expression of several drug resistance pathways, including membrane transporters and biofilm-associated antibiotic-resistant genes, and its expression is regulated by the methylation sites located at the 5' UTR of the gene. Our findings unravel the sRNA that regulates the MDR pathways in clinical isolates of P. aeru. Moreover, transforming bacterial drug resistance to hypersusceptibility using sRNA could be the potential approach for tackling MDR bacteria in the future.
多重耐药细菌(MDR)已成为全球范围内的一个全球性问题,每年威胁着数十万人的生命。新型MDR菌株的出现以及新型抗菌药物开发不足是限制用于治疗细菌感染的抗生素选择的主要原因。因此,保留当前抗生素的临床价值可能是解决这一问题的有效方法之一。在这里,我们鉴定了许多在铜绿假单胞菌(P. aeru)的MDR临床分离株中下调的新型小RNA,并且我们证明其中一种小RNA(sRNA)AS1974的过表达能够将MDR临床菌株转变为药物超敏性。AS1974是调节几种耐药途径表达的主要调节因子,包括膜转运蛋白和生物膜相关的抗生素抗性基因,其表达受位于该基因5'UTR的甲基化位点调控。我们的研究结果揭示了调节P. aeru临床分离株中MDR途径的sRNA。此外,使用sRNA将细菌耐药性转变为超敏性可能是未来应对MDR细菌的潜在方法。