Genetic and Chemical Engineering of Phages for Controlling Multidrug-Resistant Bacteria.
Dingming GuoJingchao ChenXueyang ZhaoYanan LuoMenglu JinFenxia FanChaiwoo ParkXiaoman YangChuqing SunJin YanWeihua ChenZhi LiuPublished in: Antibiotics (Basel, Switzerland) (2021)
Along with the excessive use of antibiotics, the emergence and spread of multidrug-resistant bacteria has become a public health problem and a great challenge vis-à-vis the control and treatment of bacterial infections. As the natural predators of bacteria, phages have reattracted researchers' attentions. Phage therapy is regarded as one of the most promising alternative strategies to fight pathogens in the post-antibiotic era. Recently, genetic and chemical engineering methods have been applied in phage modification. Among them, genetic engineering includes the expression of toxin proteins, modification of host recognition receptors, and interference of bacterial phage-resistant pathways. Chemical engineering, meanwhile, involves crosslinking phage coats with antibiotics, antimicrobial peptides, heavy metal ions, and photothermic matters. Those advances greatly expand the host range of phages and increase their bactericidal efficiency, which sheds light on the application of phage therapy in the control of multidrug-resistant pathogens. This review reports on engineered phages through genetic and chemical approaches. Further, we present the obstacles that this novel antimicrobial has incurred.
Keyphrases
- multidrug resistant
- gram negative
- pseudomonas aeruginosa
- public health
- drug resistant
- acinetobacter baumannii
- genome wide
- heavy metals
- copy number
- klebsiella pneumoniae
- escherichia coli
- cystic fibrosis
- emergency department
- weight gain
- quantum dots
- bone marrow
- mesenchymal stem cells
- electronic health record
- sewage sludge