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Identification of three podoviruses infecting Klebsiella encoding capsule depolymerases that digest specific capsular types
Klebsiella pneumoniae is an important human pathogen causing opportunistic nosocomial and community‐acquired infections. A major public health concern regarding K. pneumoniae is the increasing incidence of multidrug‐resistant strains. Here, we isolated three novel Klebsiella bacteriophages, KN1‐1, K...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465236/ https://www.ncbi.nlm.nih.gov/pubmed/30706654 http://dx.doi.org/10.1111/1751-7915.13370 |
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author | Pan, Yi‐Jiun Lin, Tzu‐Lung Chen, Yi‐Yin Lai, Peng‐Hsuan Tsai, Yun‐Ting Hsu, Chun‐Ru Hsieh, Pei‐Fang Lin, Yi‐Tsung Wang, Jin‐Town |
author_facet | Pan, Yi‐Jiun Lin, Tzu‐Lung Chen, Yi‐Yin Lai, Peng‐Hsuan Tsai, Yun‐Ting Hsu, Chun‐Ru Hsieh, Pei‐Fang Lin, Yi‐Tsung Wang, Jin‐Town |
author_sort | Pan, Yi‐Jiun |
collection | PubMed |
description | Klebsiella pneumoniae is an important human pathogen causing opportunistic nosocomial and community‐acquired infections. A major public health concern regarding K. pneumoniae is the increasing incidence of multidrug‐resistant strains. Here, we isolated three novel Klebsiella bacteriophages, KN1‐1, KN3‐1 and KN4‐1, which infect KN1, KN3 and K56, and KN4 types respectively. We determined their genome sequences and conducted a comparative analysis that revealed a variable region containing capsule depolymerase‐encoding genes. Recombinant depolymerase proteins were produced, and their enzymatic activity and specificity were evaluated. We identified four capsule depolymerases in these phages that could only digest the capsule types of their respective hosts. Our results demonstrate that the activities of these capsule depolymerases were correlated with the host range of each phage; thus, the capsule depolymerases are host specificity determinants. By generating a capsule mutant, we demonstrate that capsule was essential for phage adsorption and infection. Further, capsule depolymerases can enhance bacterial susceptibility to serum killing. The discovery of these phages and depolymerases lays the foundation for the typing of KN1, KN3, KN4 and K56 Klebsiella and could be useful alternative therapeutics for the treatment of K. pneumoniae infections. |
format | Online Article Text |
id | pubmed-6465236 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64652362019-04-23 Identification of three podoviruses infecting Klebsiella encoding capsule depolymerases that digest specific capsular types Pan, Yi‐Jiun Lin, Tzu‐Lung Chen, Yi‐Yin Lai, Peng‐Hsuan Tsai, Yun‐Ting Hsu, Chun‐Ru Hsieh, Pei‐Fang Lin, Yi‐Tsung Wang, Jin‐Town Microb Biotechnol Research Articles Klebsiella pneumoniae is an important human pathogen causing opportunistic nosocomial and community‐acquired infections. A major public health concern regarding K. pneumoniae is the increasing incidence of multidrug‐resistant strains. Here, we isolated three novel Klebsiella bacteriophages, KN1‐1, KN3‐1 and KN4‐1, which infect KN1, KN3 and K56, and KN4 types respectively. We determined their genome sequences and conducted a comparative analysis that revealed a variable region containing capsule depolymerase‐encoding genes. Recombinant depolymerase proteins were produced, and their enzymatic activity and specificity were evaluated. We identified four capsule depolymerases in these phages that could only digest the capsule types of their respective hosts. Our results demonstrate that the activities of these capsule depolymerases were correlated with the host range of each phage; thus, the capsule depolymerases are host specificity determinants. By generating a capsule mutant, we demonstrate that capsule was essential for phage adsorption and infection. Further, capsule depolymerases can enhance bacterial susceptibility to serum killing. The discovery of these phages and depolymerases lays the foundation for the typing of KN1, KN3, KN4 and K56 Klebsiella and could be useful alternative therapeutics for the treatment of K. pneumoniae infections. John Wiley and Sons Inc. 2019-01-31 /pmc/articles/PMC6465236/ /pubmed/30706654 http://dx.doi.org/10.1111/1751-7915.13370 Text en © 2019 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Pan, Yi‐Jiun Lin, Tzu‐Lung Chen, Yi‐Yin Lai, Peng‐Hsuan Tsai, Yun‐Ting Hsu, Chun‐Ru Hsieh, Pei‐Fang Lin, Yi‐Tsung Wang, Jin‐Town Identification of three podoviruses infecting Klebsiella encoding capsule depolymerases that digest specific capsular types |
title | Identification of three podoviruses infecting Klebsiella encoding capsule depolymerases that digest specific capsular types |
title_full | Identification of three podoviruses infecting Klebsiella encoding capsule depolymerases that digest specific capsular types |
title_fullStr | Identification of three podoviruses infecting Klebsiella encoding capsule depolymerases that digest specific capsular types |
title_full_unstemmed | Identification of three podoviruses infecting Klebsiella encoding capsule depolymerases that digest specific capsular types |
title_short | Identification of three podoviruses infecting Klebsiella encoding capsule depolymerases that digest specific capsular types |
title_sort | identification of three podoviruses infecting klebsiella encoding capsule depolymerases that digest specific capsular types |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6465236/ https://www.ncbi.nlm.nih.gov/pubmed/30706654 http://dx.doi.org/10.1111/1751-7915.13370 |
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