4.7 Review

Reprogrammable microbial cell-based therapeutics against antibiotic-resistant bacteria

期刊

DRUG RESISTANCE UPDATES
卷 27, 期 -, 页码 59-71

出版社

CHURCHILL LIVINGSTONE
DOI: 10.1016/j.drup.2016.06.002

关键词

Synthetic biology; Microbiota; Prophylactic agent; Bacteriocin; Antibiotic-resistant pathogen

资金

  1. National Medical Research Council of Singapore [CBRG11nov109]
  2. Synthetic Biology Initiative of the National University of Singapore [DPRT/943/09/14]
  3. Asian Office of Aerospace Research and Development of U.S. Air Force [FA2386-12-1-4055]
  4. U.S. Defense Threat Reduction Agency [HDTRA1-13-0037]

向作者/读者索取更多资源

The discovery of antimicrobial drugs and their subsequent use has offered an effective treatment option for bacterial infections, reducing morbidity and mortality over the past 60 years. However, the indiscriminate use of antimicrobials in the clinical, community and agricultural settings has resulted in selection for multidrug-resistant bacteria, which has led to the prediction of possible re-entrance to the pre-antibiotic era. The situation is further exacerbated by significantly reduced antimicrobial drug discovery efforts by large pharmaceutical companies, resulting in a steady decline in the number of new antimicrobial agents brought to the market in the past several decades. Consequently, there is a pressing need for new antimicrobial therapies that can be readily designed and implemented. Recently, it has become clear that the administration of broad-spectrum antibiotics can lead to collateral damage to the human commensal microbiota, which plays several key roles in host health. Advances in genetic engineering have opened the possibility of reprogramming commensal bacteria that are in symbiotic existence throughout the human body to implement antimicrobial drugs with high versatility and efficacy against pathogenic bacteria. In this review, we discuss recent advances and potentialities of engineered bacteria in providing a novel antimicrobial strategy against antibiotic resistance. (C) 2016 Elsevier Ltd. All rights reserved.

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