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T5-like phage BF23 evades host-mediated DNA restriction and methylation
Bacteriophage BF23 is a close relative of phage T5, a prototypical Tequintavirus that infects Escherichia coli. BF23 was isolated in the middle of the XXth century and was extensively studied as a model object. Like T5, BF23 carries long ∼9.7 kb terminal repeats, injects its genome into infected cel...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10644984/ https://www.ncbi.nlm.nih.gov/pubmed/38025991 http://dx.doi.org/10.1093/femsml/uqad044 |
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author | Skutel, Mikhail Andriianov, Aleksandr Zavialova, Maria Kirsanova, Maria Shodunke, Oluwasefunmi Zorin, Evgenii Golovshchinskii, Aleksandr Severinov, Konstantin Isaev, Artem |
author_facet | Skutel, Mikhail Andriianov, Aleksandr Zavialova, Maria Kirsanova, Maria Shodunke, Oluwasefunmi Zorin, Evgenii Golovshchinskii, Aleksandr Severinov, Konstantin Isaev, Artem |
author_sort | Skutel, Mikhail |
collection | PubMed |
description | Bacteriophage BF23 is a close relative of phage T5, a prototypical Tequintavirus that infects Escherichia coli. BF23 was isolated in the middle of the XXth century and was extensively studied as a model object. Like T5, BF23 carries long ∼9.7 kb terminal repeats, injects its genome into infected cell in a two-stage process, and carries multiple specific nicks in its double-stranded genomic DNA. The two phages rely on different host secondary receptors—FhuA (T5) and BtuB (BF23). Only short fragments of the BF23 genome, including the region encoding receptor interacting proteins, have been determined. Here, we report the full genomic sequence of BF23 and describe the protein content of its virion. T5-like phages represent a unique group that resist restriction by most nuclease-based host immunity systems. We show that BF23, like other Tequintavirus phages, resist Types I/II/III restriction–modification host immunity systems if their recognition sites are located outside the terminal repeats. We also demonstrate that the BF23 avoids host-mediated methylation. We propose that inhibition of methylation is a common feature of Tequintavirus and Epseptimavirus genera phages, that is not, however, associated with their antirestriction activity. |
format | Online Article Text |
id | pubmed-10644984 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-106449842023-10-26 T5-like phage BF23 evades host-mediated DNA restriction and methylation Skutel, Mikhail Andriianov, Aleksandr Zavialova, Maria Kirsanova, Maria Shodunke, Oluwasefunmi Zorin, Evgenii Golovshchinskii, Aleksandr Severinov, Konstantin Isaev, Artem Microlife Research Article Bacteriophage BF23 is a close relative of phage T5, a prototypical Tequintavirus that infects Escherichia coli. BF23 was isolated in the middle of the XXth century and was extensively studied as a model object. Like T5, BF23 carries long ∼9.7 kb terminal repeats, injects its genome into infected cell in a two-stage process, and carries multiple specific nicks in its double-stranded genomic DNA. The two phages rely on different host secondary receptors—FhuA (T5) and BtuB (BF23). Only short fragments of the BF23 genome, including the region encoding receptor interacting proteins, have been determined. Here, we report the full genomic sequence of BF23 and describe the protein content of its virion. T5-like phages represent a unique group that resist restriction by most nuclease-based host immunity systems. We show that BF23, like other Tequintavirus phages, resist Types I/II/III restriction–modification host immunity systems if their recognition sites are located outside the terminal repeats. We also demonstrate that the BF23 avoids host-mediated methylation. We propose that inhibition of methylation is a common feature of Tequintavirus and Epseptimavirus genera phages, that is not, however, associated with their antirestriction activity. Oxford University Press 2023-10-26 /pmc/articles/PMC10644984/ /pubmed/38025991 http://dx.doi.org/10.1093/femsml/uqad044 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of FEMS. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Research Article Skutel, Mikhail Andriianov, Aleksandr Zavialova, Maria Kirsanova, Maria Shodunke, Oluwasefunmi Zorin, Evgenii Golovshchinskii, Aleksandr Severinov, Konstantin Isaev, Artem T5-like phage BF23 evades host-mediated DNA restriction and methylation |
title | T5-like phage BF23 evades host-mediated DNA restriction and methylation |
title_full | T5-like phage BF23 evades host-mediated DNA restriction and methylation |
title_fullStr | T5-like phage BF23 evades host-mediated DNA restriction and methylation |
title_full_unstemmed | T5-like phage BF23 evades host-mediated DNA restriction and methylation |
title_short | T5-like phage BF23 evades host-mediated DNA restriction and methylation |
title_sort | t5-like phage bf23 evades host-mediated dna restriction and methylation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10644984/ https://www.ncbi.nlm.nih.gov/pubmed/38025991 http://dx.doi.org/10.1093/femsml/uqad044 |
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