Isolation and Characterization of Klebsiella Phages for Phage Therapy

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Isolation and Characterization of Klebsiella Phages for Phage Therapy. / Townsend, Eleanor M; Kelly, Lucy; Gannon, Lucy et al.
In: PHAGE (New Rochelle, N.Y.), Vol. 2, No. 1, 17.03.2021, p. 26-42.

Research output: Contribution to journalArticlepeer-review

HarvardHarvard

Townsend, EM, Kelly, L, Gannon, L, Muscatt, G, Dunstan, R, Michniewski, S, Sapkota, H, Kiljunen, SJ, Kolsi, A, Skurnik, M, Lithgow, T, Millard, AD & Jameson, E 2021, 'Isolation and Characterization of Klebsiella Phages for Phage Therapy', PHAGE (New Rochelle, N.Y.), vol. 2, no. 1, pp. 26-42. https://doi.org/10.1089/phage.2020.0046

APA

Townsend, E. M., Kelly, L., Gannon, L., Muscatt, G., Dunstan, R., Michniewski, S., Sapkota, H., Kiljunen, S. J., Kolsi, A., Skurnik, M., Lithgow, T., Millard, A. D., & Jameson, E. (2021). Isolation and Characterization of Klebsiella Phages for Phage Therapy. PHAGE (New Rochelle, N.Y.), 2(1), 26-42. https://doi.org/10.1089/phage.2020.0046

CBE

Townsend EM, Kelly L, Gannon L, Muscatt G, Dunstan R, Michniewski S, Sapkota H, Kiljunen SJ, Kolsi A, Skurnik M, et al. 2021. Isolation and Characterization of Klebsiella Phages for Phage Therapy. PHAGE (New Rochelle, N.Y.). 2(1):26-42. https://doi.org/10.1089/phage.2020.0046

MLA

Townsend, Eleanor M et al. "Isolation and Characterization of Klebsiella Phages for Phage Therapy". PHAGE (New Rochelle, N.Y.). 2021, 2(1). 26-42. https://doi.org/10.1089/phage.2020.0046

VancouverVancouver

Townsend EM, Kelly L, Gannon L, Muscatt G, Dunstan R, Michniewski S et al. Isolation and Characterization of Klebsiella Phages for Phage Therapy. PHAGE (New Rochelle, N.Y.). 2021 Mar 17;2(1):26-42. doi: 10.1089/phage.2020.0046

Author

Townsend, Eleanor M ; Kelly, Lucy ; Gannon, Lucy et al. / Isolation and Characterization of Klebsiella Phages for Phage Therapy. In: PHAGE (New Rochelle, N.Y.). 2021 ; Vol. 2, No. 1. pp. 26-42.

RIS

TY - JOUR

T1 - Isolation and Characterization of Klebsiella Phages for Phage Therapy

AU - Townsend, Eleanor M

AU - Kelly, Lucy

AU - Gannon, Lucy

AU - Muscatt, George

AU - Dunstan, Rhys

AU - Michniewski, Slawomir

AU - Sapkota, Hari

AU - Kiljunen, Saija J

AU - Kolsi, Anna

AU - Skurnik, Mikael

AU - Lithgow, Trevor

AU - Millard, Andrew D

AU - Jameson, Eleanor

N1 - © Eleanor M. Townsend et al. 2021; Published by Mary Ann Liebert, Inc.

PY - 2021/3/17

Y1 - 2021/3/17

N2 - Introduction: Klebsiella is a clinically important pathogen causing a variety of antimicrobial resistant infections in both community and nosocomial settings, particularly pneumonia, urinary tract infection, and sepsis. Bacteriophage (phage) therapy is being considered a primary option for the treatment of drug-resistant infections of these types. Methods: We report the successful isolation and characterization of 30 novel, genetically diverse Klebsiella phages. Results: The isolated phages span six different phage families and nine genera, representing both lysogenic and lytic lifestyles. Individual Klebsiella phage isolates infected up to 11 of the 18 Klebsiella capsule types tested, and all 18 capsule-types were infected by at least one of the phages. Conclusions: Of the Klebsiella-infecting phages presented in this study, the lytic phages are most suitable for phage therapy, based on their broad host range, high virulence, short lysis period and given that they encode no known toxin or antimicrobial resistance genes. Phage isolates belonging to the Sugarlandvirus and Slopekvirus genera were deemed most suitable for phage therapy based on our characterization. Importantly, when applied alone, none of the characterized phages were able to suppress the growth of Klebsiella for more than 12 h, likely due to the inherent ease of Klebsiella to generate spontaneous phage-resistant mutants. This indicates that for successful phage therapy, a cocktail of multiple phages would be necessary to treat Klebsiella infections.

AB - Introduction: Klebsiella is a clinically important pathogen causing a variety of antimicrobial resistant infections in both community and nosocomial settings, particularly pneumonia, urinary tract infection, and sepsis. Bacteriophage (phage) therapy is being considered a primary option for the treatment of drug-resistant infections of these types. Methods: We report the successful isolation and characterization of 30 novel, genetically diverse Klebsiella phages. Results: The isolated phages span six different phage families and nine genera, representing both lysogenic and lytic lifestyles. Individual Klebsiella phage isolates infected up to 11 of the 18 Klebsiella capsule types tested, and all 18 capsule-types were infected by at least one of the phages. Conclusions: Of the Klebsiella-infecting phages presented in this study, the lytic phages are most suitable for phage therapy, based on their broad host range, high virulence, short lysis period and given that they encode no known toxin or antimicrobial resistance genes. Phage isolates belonging to the Sugarlandvirus and Slopekvirus genera were deemed most suitable for phage therapy based on our characterization. Importantly, when applied alone, none of the characterized phages were able to suppress the growth of Klebsiella for more than 12 h, likely due to the inherent ease of Klebsiella to generate spontaneous phage-resistant mutants. This indicates that for successful phage therapy, a cocktail of multiple phages would be necessary to treat Klebsiella infections.

U2 - 10.1089/phage.2020.0046

DO - 10.1089/phage.2020.0046

M3 - Article

C2 - 33796863

VL - 2

SP - 26

EP - 42

JO - PHAGE (New Rochelle, N.Y.)

JF - PHAGE (New Rochelle, N.Y.)

SN - 2641-6530

IS - 1

ER -