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Strengthening phage resistance of Streptococcus thermophilus by leveraging complementary defense systems

Author

Listed:
  • Audrey Leprince

    (Université Laval)

  • Justine Lefrançois

    (Université Laval)

  • Anne M. Millen

    (3329 Agriculture Dr)

  • Damian Magill

    (CS 10010)

  • Philippe Horvath

    (CS 10010)

  • Dennis A. Romero

    (3329 Agriculture Dr)

  • Geneviève M. Rousseau

    (Université Laval)

  • Sylvain Moineau

    (Université Laval)

Abstract

CRISPR-Cas and restriction-modification systems represent the core defense arsenal in Streptococcus thermophilus, but their effectiveness is compromised by phages encoding anti-CRISPR proteins (ACRs) and other counter-defense strategies. Here, we explore the defensome of 263 S. thermophilus strains to uncover other anti-phage systems. The defense landscape of S. thermophilus is enriched by 21 accessory defense systems, 13 of which have never been investigated in this species. Experimental validation of 17 systems with 14 phages reveals a range of anti-phage activities, highlighting both broad and narrow specificities across the five viral genera infecting S. thermophilus. Synergies are observed when combining CRISPR immunity with accessory systems. We also assess the fitness cost associated with the chromosomal integration of these systems in their native context and find no impact under laboratory or industrial conditions. These findings underscore the potential of these accessory defense systems to enhance the resistance of S. thermophilus, particularly against ACR-encoding phages.

Suggested Citation

  • Audrey Leprince & Justine Lefrançois & Anne M. Millen & Damian Magill & Philippe Horvath & Dennis A. Romero & Geneviève M. Rousseau & Sylvain Moineau, 2025. "Strengthening phage resistance of Streptococcus thermophilus by leveraging complementary defense systems," Nature Communications, Nature, vol. 16(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-62408-3
    DOI: 10.1038/s41467-025-62408-3
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    References listed on IDEAS

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    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. Alexander P. Hynes & Geneviève M. Rousseau & Daniel Agudelo & Adeline Goulet & Beatrice Amigues & Jeremy Loehr & Dennis A. Romero & Christophe Fremaux & Philippe Horvath & Yannick Doyon & Christian Ca, 2018. "Widespread anti-CRISPR proteins in virulent bacteriophages inhibit a range of Cas9 proteins," Nature Communications, Nature, vol. 9(1), pages 1-10, December.
    3. 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.
    4. Donghyun Ka & Hyejin Oh & Eunyoung Park & Jeong-Han Kim & Euiyoung Bae, 2020. "Structural and functional evidence of bacterial antiphage protection by Thoeris defense system via NAD+ degradation," Nature Communications, Nature, vol. 11(1), pages 1-8, December.
    5. Josiane E. Garneau & Marie-Ève Dupuis & Manuela Villion & Dennis A. Romero & Rodolphe Barrangou & Patrick Boyaval & Christophe Fremaux & Philippe Horvath & Alfonso H. Magadán & Sylvain Moineau, 2010. "The CRISPR/Cas bacterial immune system cleaves bacteriophage and plasmid DNA," Nature, Nature, vol. 468(7320), pages 67-71, November.
    6. Marie-Ève Dupuis & Manuela Villion & Alfonso H. Magadán & Sylvain Moineau, 2013. "CRISPR-Cas and restriction–modification systems are compatible and increase phage resistance," Nature Communications, Nature, vol. 4(1), pages 1-7, October.
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