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A K-17 serotype specific Klebsiella phage JKP2 with biofilm reduction potential

Klebsiella pneumoniae is an opportunistic pathogen responsible for nearly one-third of all Gram-negative infections. Increasing antibiotic resistance has pushed scientists to look for alternative therapeutics. Bacteriophages have emerged as one of the promising alternatives. In the current study, th...

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Autores principales: Asif, Muhammad, Alvi, Iqbal Ahmad, Waqas, Muhammad, Basit, Abdul, Raza, Faiz Ahmed, Rehman, Shafiq-ur
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10194101/
https://www.ncbi.nlm.nih.gov/pubmed/36996938
http://dx.doi.org/10.1016/j.virusres.2023.199107
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author Asif, Muhammad
Alvi, Iqbal Ahmad
Waqas, Muhammad
Basit, Abdul
Raza, Faiz Ahmed
Rehman, Shafiq-ur
author_facet Asif, Muhammad
Alvi, Iqbal Ahmad
Waqas, Muhammad
Basit, Abdul
Raza, Faiz Ahmed
Rehman, Shafiq-ur
author_sort Asif, Muhammad
collection PubMed
description Klebsiella pneumoniae is an opportunistic pathogen responsible for nearly one-third of all Gram-negative infections. Increasing antibiotic resistance has pushed scientists to look for alternative therapeutics. Bacteriophages have emerged as one of the promising alternatives. In the current study, the Klebsiella phage JKP2 was isolated from a sewage sample and characterized against the K-17 serotype of K. pneumoniae. It produced bulls-eye-shaped clear plaques and has a latent period of 45 min with a burst size of 70 pfu/cell. It remained stable at tested pH (5 to 10) and temperatures (37 to 60 °C). Its optimum temperature for long-term storage is 4 °C and -80 °C. The JKP2 showed its infectivity against the K. pneumoniae K-17 serotype only. It controlled planktonic cells of K. pneumoniae 12 h post-incubation. At MOI-1, it efficiently eliminated 98% of 24 and 96% of 48-hour-old biofilm and 86% and 82% of mature biofilm of day 3 and 4, respectively. The JKP2 has an icosahedral capsid of 54 ± 0.5 nm with a short, non-contractile tail, measuring 12 ± 0.2 nm. It possesses a double-stranded DNA genome of 43.2 kbp with 54.1% GC content and encodes 54 proteins, including 29 with known functions and 25 with unknown functions. JKP2 was classified as Drulisvirus within the Autographiviridae family. It uses a T7-like direct terminal repeat strategy for genome packaging. JKP2 can be applied safely for therapeutic purposes as it does not encode an integrase or repressor genes, antibiotic resistance genes, bacterial virulence factors, and mycotoxins.
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spelling pubmed-101941012023-05-19 A K-17 serotype specific Klebsiella phage JKP2 with biofilm reduction potential Asif, Muhammad Alvi, Iqbal Ahmad Waqas, Muhammad Basit, Abdul Raza, Faiz Ahmed Rehman, Shafiq-ur Virus Res Article Klebsiella pneumoniae is an opportunistic pathogen responsible for nearly one-third of all Gram-negative infections. Increasing antibiotic resistance has pushed scientists to look for alternative therapeutics. Bacteriophages have emerged as one of the promising alternatives. In the current study, the Klebsiella phage JKP2 was isolated from a sewage sample and characterized against the K-17 serotype of K. pneumoniae. It produced bulls-eye-shaped clear plaques and has a latent period of 45 min with a burst size of 70 pfu/cell. It remained stable at tested pH (5 to 10) and temperatures (37 to 60 °C). Its optimum temperature for long-term storage is 4 °C and -80 °C. The JKP2 showed its infectivity against the K. pneumoniae K-17 serotype only. It controlled planktonic cells of K. pneumoniae 12 h post-incubation. At MOI-1, it efficiently eliminated 98% of 24 and 96% of 48-hour-old biofilm and 86% and 82% of mature biofilm of day 3 and 4, respectively. The JKP2 has an icosahedral capsid of 54 ± 0.5 nm with a short, non-contractile tail, measuring 12 ± 0.2 nm. It possesses a double-stranded DNA genome of 43.2 kbp with 54.1% GC content and encodes 54 proteins, including 29 with known functions and 25 with unknown functions. JKP2 was classified as Drulisvirus within the Autographiviridae family. It uses a T7-like direct terminal repeat strategy for genome packaging. JKP2 can be applied safely for therapeutic purposes as it does not encode an integrase or repressor genes, antibiotic resistance genes, bacterial virulence factors, and mycotoxins. Elsevier 2023-04-02 /pmc/articles/PMC10194101/ /pubmed/36996938 http://dx.doi.org/10.1016/j.virusres.2023.199107 Text en © 2023 The Authors. Published by Elsevier B.V. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Asif, Muhammad
Alvi, Iqbal Ahmad
Waqas, Muhammad
Basit, Abdul
Raza, Faiz Ahmed
Rehman, Shafiq-ur
A K-17 serotype specific Klebsiella phage JKP2 with biofilm reduction potential
title A K-17 serotype specific Klebsiella phage JKP2 with biofilm reduction potential
title_full A K-17 serotype specific Klebsiella phage JKP2 with biofilm reduction potential
title_fullStr A K-17 serotype specific Klebsiella phage JKP2 with biofilm reduction potential
title_full_unstemmed A K-17 serotype specific Klebsiella phage JKP2 with biofilm reduction potential
title_short A K-17 serotype specific Klebsiella phage JKP2 with biofilm reduction potential
title_sort k-17 serotype specific klebsiella phage jkp2 with biofilm reduction potential
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10194101/
https://www.ncbi.nlm.nih.gov/pubmed/36996938
http://dx.doi.org/10.1016/j.virusres.2023.199107
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