IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v15y2024i1d10.1038_s41467-024-51915-4.html
   My bibliography  Save this article

Tail assembly interference is a common strategy in bacterial antiviral defenses

Author

Listed:
  • Lingchen He

    (Imperial College London)

  • Laura Miguel-Romero

    (Imperial College London
    CSIC)

  • Jonasz B. Patkowski

    (Imperial College London)

  • Nasser Alqurainy

    (University of Glasgow
    King Saud bin Abdulaziz University for Health Sciences & King Abdullah International Medical Research Centre)

  • Eduardo P. C. Rocha

    (Microbial Evolutionary Genomics)

  • Tiago R. D. Costa

    (Imperial College London)

  • Alfred Fillol-Salom

    (Imperial College London)

  • José R. Penadés

    (Imperial College London
    CEU Universities)

Abstract

Many bacterial immune systems recognize phage structural components to activate antiviral responses, without inhibiting the function of the phage component. These systems can be encoded in specific chromosomal loci, known as defense islands, and in mobile genetic elements such as prophages and phage-inducible chromosomal islands (PICIs). Here, we identify a family of bacterial immune systems, named Tai (for ‘tail assembly inhibition’), that is prevalent in PICIs, prophages and P4-like phage satellites. Tai systems protect their bacterial host population from other phages by blocking the tail assembly step, leading to the release of tailless phages incapable of infecting new hosts. To prevent autoimmunity, some Tai-positive phages have an associated counter-defense mechanism that is expressed during the phage lytic cycle and allows for tail formation. Interestingly, the Tai defense and counter-defense genes are organized in a non-contiguous operon, enabling their coordinated expression.

Suggested Citation

  • Lingchen He & Laura Miguel-Romero & Jonasz B. Patkowski & Nasser Alqurainy & Eduardo P. C. Rocha & Tiago R. D. Costa & Alfred Fillol-Salom & José R. Penadés, 2024. "Tail assembly interference is a common strategy in bacterial antiviral defenses," Nature Communications, Nature, vol. 15(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-51915-4
    DOI: 10.1038/s41467-024-51915-4
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-024-51915-4
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-024-51915-4?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Florian Tesson & Alexandre Hervé & Ernest Mordret & Marie Touchon & Camille d’Humières & Jean Cury & Aude Bernheim, 2022. "Systematic and quantitative view of the antiviral arsenal of prokaryotes," Nature Communications, Nature, vol. 13(1), pages 1-10, December.
    2. Tong Zhang & Hedvig Tamman & Kyo Coppieters ’t Wallant & Tatsuaki Kurata & Michele LeRoux & Sriram Srikant & Tetiana Brodiazhenko & Albinas Cepauskas & Ariel Talavera & Chloe Martens & Gemma C. Atkins, 2022. "Direct activation of a bacterial innate immune system by a viral capsid protein," Nature, Nature, vol. 612(7938), pages 132-140, December.
    3. Jens Hör & Sharon G. Wolf & Rotem Sorek, 2024. "Bacteria conjugate ubiquitin-like proteins to interfere with phage assembly," Nature, Nature, vol. 631(8022), pages 850-856, July.
    4. Pramalkumar H. Patel & Véronique L. Taylor & Chi Zhang & Landon J. Getz & Alexa D. Fitzpatrick & Alan R. Davidson & Karen L. Maxwell, 2024. "Anti-phage defence through inhibition of virion assembly," Nature Communications, Nature, vol. 15(1), pages 1-11, December.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Dimitri Boeckaerts & Michiel Stock & Celia Ferriol-González & Jesús Oteo-Iglesias & Rafael Sanjuán & Pilar Domingo-Calap & Bernard Baets & Yves Briers, 2024. "Prediction of Klebsiella phage-host specificity at the strain level," Nature Communications, Nature, vol. 15(1), pages 1-10, December.
    2. Rubén Barcia-Cruz & David Goudenège & Jorge A. Moura de Sousa & Damien Piel & Martial Marbouty & Eduardo P. C. Rocha & Frédérique Roux, 2024. "Phage-inducible chromosomal minimalist islands (PICMIs), a novel family of small marine satellites of virulent phages," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
    3. Danielle Miller & Adi Stern & David Burstein, 2022. "Deciphering microbial gene function using natural language processing," Nature Communications, Nature, vol. 13(1), pages 1-11, December.
    4. Pedro Leão & Mary E. Little & Kathryn E. Appler & Daphne Sahaya & Emily Aguilar-Pine & Kathryn Currie & Ilya J. Finkelstein & Valerie Anda & Brett J. Baker, 2024. "Asgard archaea defense systems and their roles in the origin of eukaryotic immunity," Nature Communications, Nature, vol. 15(1), pages 1-9, December.
    5. Tom J. Arrowsmith & Xibing Xu & Shangze Xu & Ben Usher & Peter Stokes & Megan Guest & Agnieszka K. Bronowska & Pierre Genevaux & Tim R. Blower, 2024. "Inducible auto-phosphorylation regulates a widespread family of nucleotidyltransferase toxins," Nature Communications, Nature, vol. 15(1), pages 1-20, December.
    6. Carolien Bastiaanssen & Pilar Bobadilla Ugarte & Kijun Kim & Giada Finocchio & Yanlei Feng & Todd A. Anzelon & Stephan Köstlbacher & Daniel Tamarit & Thijs J. G. Ettema & Martin Jinek & Ian J. MacRae , 2024. "RNA-guided RNA silencing by an Asgard archaeal Argonaute," Nature Communications, Nature, vol. 15(1), pages 1-14, December.
    7. Angelina Beavogui & Auriane Lacroix & Nicolas Wiart & Julie Poulain & Tom O. Delmont & Lucas Paoli & Patrick Wincker & Pedro H. Oliveira, 2024. "The defensome of complex bacterial communities," Nature Communications, Nature, vol. 15(1), pages 1-15, December.
    8. Shao-Ming Gao & Han-Lan Fei & Qi Li & Li-Ying Lan & Li-Nan Huang & Peng-Fei Fan, 2024. "Eco-evolutionary dynamics of gut phageome in wild gibbons (Hoolock tianxing) with seasonal diet variations," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
    9. Jan D. Brüwer & Chandni Sidhu & Yanlin Zhao & Andreas Eich & Leonard Rößler & Luis H. Orellana & Bernhard M. Fuchs, 2024. "Globally occurring pelagiphage infections create ribosome-deprived cells," Nature Communications, Nature, vol. 15(1), pages 1-9, December.
    10. Motaher Hossain & Barbaros Aslan & Asma Hatoum-Aslan, 2024. "Tandem mobilization of anti-phage defenses alongside SCCmec elements in staphylococci," Nature Communications, Nature, vol. 15(1), pages 1-14, December.
    11. Yunxue Guo & Kaihao Tang & Brandon Sit & Jiayu Gu & Ran Chen & Xinqi Shao & Shituan Lin & Zixian Huang & Zhaolong Nie & Jianzhong Lin & Xiaoxiao Liu & Weiquan Wang & Xinyu Gao & Tianlang Liu & Fei Liu, 2024. "Control of lysogeny and antiphage defense by a prophage-encoded kinase-phosphatase module," Nature Communications, Nature, vol. 15(1), pages 1-17, December.
    12. Pramalkumar H. Patel & Véronique L. Taylor & Chi Zhang & Landon J. Getz & Alexa D. Fitzpatrick & Alan R. Davidson & Karen L. Maxwell, 2024. "Anti-phage defence through inhibition of virion assembly," Nature Communications, Nature, vol. 15(1), pages 1-11, December.
    13. Jiafeng Huang & Keli Zhu & Yina Gao & Feng Ye & Zhaolong Li & Yao Ge & Songqing Liu & Jing Yang & Ang Gao, 2024. "Molecular basis of bacterial DSR2 anti-phage defense and viral immune evasion," Nature Communications, Nature, vol. 15(1), pages 1-11, December.
    14. Matthieu Haudiquet & Julie Bris & Amandine Nucci & Rémy A. Bonnin & Pilar Domingo-Calap & Eduardo P. C. Rocha & Olaya Rendueles, 2024. "Capsules and their traits shape phage susceptibility and plasmid conjugation efficiency," Nature Communications, Nature, vol. 15(1), pages 1-16, December.
    15. Bogna J. Smug & Krzysztof Szczepaniak & Eduardo P. C. Rocha & Stanislaw Dunin-Horkawicz & Rafał J. Mostowy, 2023. "Ongoing shuffling of protein fragments diversifies core viral functions linked to interactions with bacterial hosts," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
    16. Yong Sheng & Hengyu Wang & Yixin Ou & Yingying Wu & Wei Ding & Meifeng Tao & Shuangjun Lin & Zixin Deng & Linquan Bai & Qianjin Kang, 2023. "Insertion sequence transposition inactivates CRISPR-Cas immunity," Nature Communications, Nature, vol. 14(1), pages 1-19, December.
    17. Eugen Pfeifer & Eduardo P. C. Rocha, 2024. "Phage-plasmids promote recombination and emergence of phages and plasmids," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
    18. Natalia Quinones-Olvera & Siân V. Owen & Lucy M. McCully & Maximillian G. Marin & Eleanor A. Rand & Alice C. Fan & Oluremi J. Martins Dosumu & Kay Paul & Cleotilde E. Sanchez Castaño & Rachel Petherbr, 2024. "Diverse and abundant phages exploit conjugative plasmids," Nature Communications, Nature, vol. 15(1), pages 1-16, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-51915-4. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.