» Articles » PMID: 37036571

Phage Therapy of Antibiotic-resistant Strains of Klebsiella Pneumoniae, Opportunities and Challenges from the Past to the Future

Overview
Publisher Springer
Specialty Microbiology
Date 2023 Apr 10
PMID 37036571
Authors
Affiliations
Soon will be listed here.
Abstract

Klebsiella spp. is a commensal gram-negative bacterium and a member of the human microbiota. It is the leading cause of various hospital-acquired infections. The occurrence of multi-drug drug resistance and carbapenemase-producing strains of Klebsiella pneumoniae producing weighty contaminations is growing, and Klebsiella oxytoca is an arising bacterium. Alternative approaches to tackle contaminations led by these microorganisms are necessary as strains enhance opposing to last-stage antibiotics in the way that Colistin. The lytic bacteriophages are viruses that infect and rapidly eradicate bacterial cells and are strain-specific to their hosts. They and their proteins are immediately deliberate as opportunities or adjuncts to antibiotic therapy. There are several reports in vitro and in vivo form that proved the potential use of lytic phages to combat superbug stains of K. pneumoniae. Various reports dedicated that the phage area can be returned to the elimination of multi-drug resistance and carbapenemase resistance isolates of K. pneumoniae. This review compiles our current information on phages of Klebsiella spp. and highlights technological and biological issues related to the evolution of phage-based therapies targeting these bacterial hosts.

Citing Articles

Cutibacterium acnes bacteriophage therapy: exploring a new frontier in acne vulgaris treatment.

Mohammadi M Arch Dermatol Res. 2024; 317(1):84.

PMID: 39644414 DOI: 10.1007/s00403-024-03585-x.


Is It Time to Start Worrying? A Comprehensive Report on the Three-Year Prevalence of ESBL-Producing Bacteria and Their Trends in Antibiotic Resistance from the Largest University Hospital in Slovakia.

Jalali Y, Kolosova A, Liptakova A, Kyselovic J, Olearova A, Jalali M Pharmaceuticals (Basel). 2024; 17(11).

PMID: 39598427 PMC: 11597623. DOI: 10.3390/ph17111517.


Bacteriophages and their potential for treatment of metabolic diseases.

Deng Y, Jiang S, Duan H, Shao H, Duan Y J Diabetes. 2024; 16(11):e70024.

PMID: 39582431 PMC: 11586638. DOI: 10.1111/1753-0407.70024.


Isolation and characterization of two novel bacteriophages against carbapenem-resistant .

Senhaji-Kacha A, Bernabeu-Gimeno M, Domingo-Calap P, Aguilera-Correa J, Seoane-Blanco M, Otaegi-Ugartemendia S Front Cell Infect Microbiol. 2024; 14:1421724.

PMID: 39268483 PMC: 11390652. DOI: 10.3389/fcimb.2024.1421724.


Identification of Lytic Phages Against Multidrug-Resistant : Illuminating Hope on Antimicrobial-Resistance.

Rahman S, Hossain M, Akther J, Mahamud I, Khan T, Haider A Phage (New Rochelle). 2024; 5(2):91-98.

PMID: 39119212 PMC: 11304750. DOI: 10.1089/phage.2023.0038.

References
1.
Ackermann H . Phage classification and characterization. Methods Mol Biol. 2008; 501:127-40. DOI: 10.1007/978-1-60327-164-6_13. View

2.
Anand T, Virmani N, Kumar S, Mohanty A, Pavulraj S, Bera B . Phage therapy for treatment of virulent Klebsiella pneumoniae infection in a mouse model. J Glob Antimicrob Resist. 2019; 21:34-41. DOI: 10.1016/j.jgar.2019.09.018. View

3.
Assafiri O, Song A, Tan G, Hanish I, Hashim A, Yusoff K . Klebsiella virus UPM2146 lyses multiple drug-resistant Klebsiella pneumoniae in vitro and in vivo. PLoS One. 2021; 16(1):e0245354. PMC: 7794032. DOI: 10.1371/journal.pone.0245354. View

4.
Bhattarai Y, Williams B, Battaglioli E, Whitaker W, Till L, Grover M . Gut Microbiota-Produced Tryptamine Activates an Epithelial G-Protein-Coupled Receptor to Increase Colonic Secretion. Cell Host Microbe. 2018; 23(6):775-785.e5. PMC: 6055526. DOI: 10.1016/j.chom.2018.05.004. View

5.
Briers Y, Walmagh M, Grymonprez B, Biebl M, Pirnay J, Defraine V . Art-175 is a highly efficient antibacterial against multidrug-resistant strains and persisters of Pseudomonas aeruginosa. Antimicrob Agents Chemother. 2014; 58(7):3774-84. PMC: 4068523. DOI: 10.1128/AAC.02668-14. View