TY - JOUR
T1 - Mycobacteriophages as potential therapeutic agents against drug-resistant tuberculosis
AU - Allué-Guardia, Anna
AU - Saranathan, Rajagopalan
AU - Chan, John
AU - Torrelles, Jordi B.
N1 - Funding Information:
Funding: This work has been partially supported by the Robert J. Kleberg and Helen C. Kleberg Foundation to J.B.T., and by the National Institutes of Health/National Institute of Allergy and Infectious Diseases (NIH/NIAID) grant numbers R01 AI146340 to J.C. and J.B.T, R01 AI-137344 and R01 AI-139297 to J.C., and R01 AI-026170 and R21 AI-156853 to R.S.
Publisher Copyright:
© 2021 by the authors. Li-censee MDPI, Basel, Switzerland.
PY - 2021/1/2
Y1 - 2021/1/2
N2 - The current emergence of multi-, extensively-, extremely-, and total-drug resistant strains of Mycobacterium tuberculosis poses a major health, social, and economic threat, and stresses the need to develop new therapeutic strategies. The notion of phage therapy against bacteria has been around for more than a century and, although its implementation was abandoned after the introduction of drugs, it is now making a comeback and gaining renewed interest in Western medicine as an alternative to treat drug-resistant pathogens. Mycobacteriophages are genetically diverse viruses that specifically infect mycobacterial hosts, including members of the M. tuberculosis complex. This review describes general features of mycobacteriophages and their mechanisms of killing M. tuberculosis, as well as their advantages and limitations as therapeutic and prophylactic agents against drug-resistant M. tuberculosis strains. This review also discusses the role of human lung micro-environments in shaping the availability of mycobacteriophage receptors on the M. tuberculosis cell envelope surface, the risk of potential development of bacterial resistance to mycobacteriophages, and the interactions with the mammalian host immune system. Finally, it summarizes the knowledge gaps and defines key questions to be addressed regarding the clinical application of phage therapy for the treatment of drug-resistant tuberculosis.
AB - The current emergence of multi-, extensively-, extremely-, and total-drug resistant strains of Mycobacterium tuberculosis poses a major health, social, and economic threat, and stresses the need to develop new therapeutic strategies. The notion of phage therapy against bacteria has been around for more than a century and, although its implementation was abandoned after the introduction of drugs, it is now making a comeback and gaining renewed interest in Western medicine as an alternative to treat drug-resistant pathogens. Mycobacteriophages are genetically diverse viruses that specifically infect mycobacterial hosts, including members of the M. tuberculosis complex. This review describes general features of mycobacteriophages and their mechanisms of killing M. tuberculosis, as well as their advantages and limitations as therapeutic and prophylactic agents against drug-resistant M. tuberculosis strains. This review also discusses the role of human lung micro-environments in shaping the availability of mycobacteriophage receptors on the M. tuberculosis cell envelope surface, the risk of potential development of bacterial resistance to mycobacteriophages, and the interactions with the mammalian host immune system. Finally, it summarizes the knowledge gaps and defines key questions to be addressed regarding the clinical application of phage therapy for the treatment of drug-resistant tuberculosis.
KW - Drug-resistance
KW - Lung mucosa
KW - Mycobacteriophages
KW - Mycobacterium tuberculosis
KW - Phage therapy
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U2 - 10.3390/ijms22020735
DO - 10.3390/ijms22020735
M3 - Review article
C2 - 33450990
AN - SCOPUS:85099389641
SN - 1661-6596
VL - 22
SP - 1
EP - 28
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
IS - 2
M1 - 735
ER -