Unlocking the next generation of phage therapy: the key is in the receptors

被引:96
作者
Altamirano, Fernando L. Gordillo [1 ]
Barr, Jeremy J. [1 ]
机构
[1] Monash Univ, Sch Biol Sci, 25 Rainforest Walk, Clayton, Vic 3800, Australia
基金
英国医学研究理事会;
关键词
HOST-RANGE; RESISTANCE; TWORT;
D O I
10.1016/j.copbio.2020.10.002
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Phage therapy, the clinical use of viruses that kill bacteria, is a promising strategy in the fight against antimicrobial resistance. Before administration, phages under go a careful examination of their safety and interactions with target bacteria. This characterization seldom includes identifying the receptor on the bacterial surface involved in phage adsorption. In this perspective article, we propose that understanding the function and location of these phage receptors can open the door to improved and innovative ways to use phage therapy. With knowledge of phage receptors, we can design intelligent phage cocktails, discover new phage-derived antimicrobials, and steer the evolution of phage-resistance towards clinically exploitable phenotypes. In an effort to jump-start this initiative, we recommend priority groups of hosts and phages. Finally, were view modern approaches for the identification of phage receptors, including molecular platforms for high-throughput mutagenesis, synthetic biology, and machine learning.
引用
收藏
页码:115 / 123
页数:9
相关论文
共 57 条
[1]   Phage Therapy in the Postantibiotic Era [J].
Altamirano, Fernando L. Gordillo ;
Barr, Jeremy J. .
CLINICAL MICROBIOLOGY REVIEWS, 2019, 32 (02)
[2]  
[Anonymous], 2019, Antibiotic resistance threats in the United States
[3]  
Bernasconi Odette J, 2018, Pathog Immun, V3, P72, DOI 10.20411/pai.v3i1.234
[4]   Genes affecting progression of bacteriophage P22 infection in Salmonella identified by transposon and single gene deletion screens [J].
Bohm, Kaitlynne ;
Porwollik, Steffen ;
Chu, Weiping ;
Dover, John A. ;
Gilcrease, Eddie B. ;
Casjens, Sherwood R. ;
McClelland, Michael ;
Parent, Kristin N. .
MOLECULAR MICROBIOLOGY, 2018, 108 (03) :288-305
[5]   The tail-associated depolymerase of Erwinia amylovora phage L1 mediates host cell adsorption and enzymatic capsule removal, which can enhance infection by other phage [J].
Born, Yannick ;
Fieseler, Lars ;
Klumpp, Jochen ;
Eugster, Marcel R. ;
Zurfluh, Katrin ;
Duffy, Brion ;
Loessner, Martin J. .
ENVIRONMENTAL MICROBIOLOGY, 2014, 16 (07) :2168-2180
[6]   Phage therapy as a potential solution in the fight against AMR: obstacles and possible futures [J].
Brives, Charlotte ;
Pourraz, Jessica .
PALGRAVE COMMUNICATIONS, 2020, 6 (01)
[7]   Pleiotropy complicates a trade-off between phage resistance and antibiotic resistance [J].
Burmeister, Alita R. ;
Fortier, Abigail ;
Roush, Carli ;
Lessing, Adam J. ;
Bender, Rose G. ;
Barahman, Roxanna ;
Grant, Raeven ;
Chan, Benjamin K. ;
Turner, Paul E. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2020, 117 (21) :11207-11216
[8]   Bacteriophage-Resistant Staphylococcus aureus Mutant Confers Broad Immunity against Staphylococcal Infection in Mice [J].
Capparelli, Rosanna ;
Nocerino, Nunzia ;
Lanzetta, Rosa ;
Silipo, Alba ;
Amoresano, Angela ;
Giangrande, Chiara ;
Becker, Karsten ;
Blaiotta, Giuseppe ;
Evidente, Antonio ;
Cimmino, Alessio ;
Iannaccone, Marco ;
Parlato, Marianna ;
Medaglia, Chiara ;
Roperto, Sante ;
Roperto, Franco ;
Ramunno, Luigi ;
Iannelli, Domenico .
PLOS ONE, 2010, 5 (07)
[9]   Phage treatment of an aortic graft infected with ⁢Pseudomonas aeruginosa⁢ [J].
Chan, Benjamin K. ;
Turner, Paul E. ;
Kim, Samuel ;
Mojibian, Hamid R. ;
Elefteriades, John A. ;
Narayan, Deepak .
EVOLUTION MEDICINE AND PUBLIC HEALTH, 2018, (01) :60-66
[10]   Phage selection restores antibiotic sensitivity in MDR Pseudomonas aeruginosa [J].
Chan, Benjamin K. ;
Sistrom, Mark ;
Wertz, John E. ;
Kortright, Kaitlyn E. ;
Narayan, Deepak ;
Turner, Paul E. .
SCIENTIFIC REPORTS, 2016, 6