Host genetic requirements for DNA release of lactococcal phage TP901-1

Research output: Contribution to journalJournal articleResearchpeer-review

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Host genetic requirements for DNA release of lactococcal phage TP901-1. / Ruiz-Cruz, Sofía; Erazo Garzon, Andrea; Kelleher, Philip; Bottacini, Francesca; Breum, Solvej Østergaard; Neve, Horst; Heller, Knut J.; Vogensen, Finn K.; Palussière, Simon; Courtin, Pascal; Chapot-Chartier, Marie-Pierre; Vinogradov, Evgeny; Sadovskaya, Irina; Mahony, Jennifer; van Sinderen, Douwe.

In: Microbial Biotechnology, Vol. 15, No. 12, 2022, p. 2875-2889.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Ruiz-Cruz, S, Erazo Garzon, A, Kelleher, P, Bottacini, F, Breum, SØ, Neve, H, Heller, KJ, Vogensen, FK, Palussière, S, Courtin, P, Chapot-Chartier, M-P, Vinogradov, E, Sadovskaya, I, Mahony, J & van Sinderen, D 2022, 'Host genetic requirements for DNA release of lactococcal phage TP901-1', Microbial Biotechnology, vol. 15, no. 12, pp. 2875-2889. https://doi.org/10.1111/1751-7915.14156

APA

Ruiz-Cruz, S., Erazo Garzon, A., Kelleher, P., Bottacini, F., Breum, S. Ø., Neve, H., Heller, K. J., Vogensen, F. K., Palussière, S., Courtin, P., Chapot-Chartier, M-P., Vinogradov, E., Sadovskaya, I., Mahony, J., & van Sinderen, D. (2022). Host genetic requirements for DNA release of lactococcal phage TP901-1. Microbial Biotechnology, 15(12), 2875-2889. https://doi.org/10.1111/1751-7915.14156

Vancouver

Ruiz-Cruz S, Erazo Garzon A, Kelleher P, Bottacini F, Breum SØ, Neve H et al. Host genetic requirements for DNA release of lactococcal phage TP901-1. Microbial Biotechnology. 2022;15(12):2875-2889. https://doi.org/10.1111/1751-7915.14156

Author

Ruiz-Cruz, Sofía ; Erazo Garzon, Andrea ; Kelleher, Philip ; Bottacini, Francesca ; Breum, Solvej Østergaard ; Neve, Horst ; Heller, Knut J. ; Vogensen, Finn K. ; Palussière, Simon ; Courtin, Pascal ; Chapot-Chartier, Marie-Pierre ; Vinogradov, Evgeny ; Sadovskaya, Irina ; Mahony, Jennifer ; van Sinderen, Douwe. / Host genetic requirements for DNA release of lactococcal phage TP901-1. In: Microbial Biotechnology. 2022 ; Vol. 15, No. 12. pp. 2875-2889.

Bibtex

@article{1821a96d50494afdb01958cabd9609cc,
title = "Host genetic requirements for DNA release of lactococcal phage TP901-1",
abstract = "The first step in phage infection is the recognition of, and adsorption to, a receptor located on the host cell surface. This reversible host adsorption step is commonly followed by an irreversible event, which involves phage DNA delivery or release into the bacterial cytoplasm. The molecular components that trigger this latter event are unknown for most phages of Gram-positive bacteria. In the current study, we present a comparative genome analysis of three mutants of Lactococcus cremoris 3107, which are resistant to the P335 group phage TP901-1 due to mutations that affect TP901-1 DNA release. Through genetic complementation and phage infection assays, a predicted lactococcal three-component glycosylation system (TGS) was shown to be required for TP901-1 infection. Major cell wall saccharidic components were analysed, but no differences were found. However, heterologous gene expression experiments indicate that this TGS is involved in the glucosylation of a cell envelope-associated component that triggers TP901-1 DNA release. To date, a saccharide modification has not been implicated in the DNA delivery process of a Gram-positive infecting phage.",
author = "Sof{\'i}a Ruiz-Cruz and {Erazo Garzon}, Andrea and Philip Kelleher and Francesca Bottacini and Breum, {Solvej {\O}stergaard} and Horst Neve and Heller, {Knut J.} and Vogensen, {Finn K.} and Simon Palussi{\`e}re and Pascal Courtin and Marie-Pierre Chapot-Chartier and Evgeny Vinogradov and Irina Sadovskaya and Jennifer Mahony and {van Sinderen}, Douwe",
note = "Publisher Copyright: {\textcopyright} 2022 The Authors. Microbial Biotechnology published by Society for Applied Microbiology and John Wiley & Sons Ltd.",
year = "2022",
doi = "10.1111/1751-7915.14156",
language = "English",
volume = "15",
pages = "2875--2889",
journal = "Microbial Biotechnology",
issn = "1751-7907",
publisher = "Wiley",
number = "12",

}

RIS

TY - JOUR

T1 - Host genetic requirements for DNA release of lactococcal phage TP901-1

AU - Ruiz-Cruz, Sofía

AU - Erazo Garzon, Andrea

AU - Kelleher, Philip

AU - Bottacini, Francesca

AU - Breum, Solvej Østergaard

AU - Neve, Horst

AU - Heller, Knut J.

AU - Vogensen, Finn K.

AU - Palussière, Simon

AU - Courtin, Pascal

AU - Chapot-Chartier, Marie-Pierre

AU - Vinogradov, Evgeny

AU - Sadovskaya, Irina

AU - Mahony, Jennifer

AU - van Sinderen, Douwe

N1 - Publisher Copyright: © 2022 The Authors. Microbial Biotechnology published by Society for Applied Microbiology and John Wiley & Sons Ltd.

PY - 2022

Y1 - 2022

N2 - The first step in phage infection is the recognition of, and adsorption to, a receptor located on the host cell surface. This reversible host adsorption step is commonly followed by an irreversible event, which involves phage DNA delivery or release into the bacterial cytoplasm. The molecular components that trigger this latter event are unknown for most phages of Gram-positive bacteria. In the current study, we present a comparative genome analysis of three mutants of Lactococcus cremoris 3107, which are resistant to the P335 group phage TP901-1 due to mutations that affect TP901-1 DNA release. Through genetic complementation and phage infection assays, a predicted lactococcal three-component glycosylation system (TGS) was shown to be required for TP901-1 infection. Major cell wall saccharidic components were analysed, but no differences were found. However, heterologous gene expression experiments indicate that this TGS is involved in the glucosylation of a cell envelope-associated component that triggers TP901-1 DNA release. To date, a saccharide modification has not been implicated in the DNA delivery process of a Gram-positive infecting phage.

AB - The first step in phage infection is the recognition of, and adsorption to, a receptor located on the host cell surface. This reversible host adsorption step is commonly followed by an irreversible event, which involves phage DNA delivery or release into the bacterial cytoplasm. The molecular components that trigger this latter event are unknown for most phages of Gram-positive bacteria. In the current study, we present a comparative genome analysis of three mutants of Lactococcus cremoris 3107, which are resistant to the P335 group phage TP901-1 due to mutations that affect TP901-1 DNA release. Through genetic complementation and phage infection assays, a predicted lactococcal three-component glycosylation system (TGS) was shown to be required for TP901-1 infection. Major cell wall saccharidic components were analysed, but no differences were found. However, heterologous gene expression experiments indicate that this TGS is involved in the glucosylation of a cell envelope-associated component that triggers TP901-1 DNA release. To date, a saccharide modification has not been implicated in the DNA delivery process of a Gram-positive infecting phage.

U2 - 10.1111/1751-7915.14156

DO - 10.1111/1751-7915.14156

M3 - Journal article

C2 - 36259418

AN - SCOPUS:85140100547

VL - 15

SP - 2875

EP - 2889

JO - Microbial Biotechnology

JF - Microbial Biotechnology

SN - 1751-7907

IS - 12

ER -

ID: 324313207