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A truncated anti-CRISPR protein prevents spacer acquisition but not interference

Author

Listed:
  • Cécile Philippe

    (Université Laval
    Université Laval)

  • Carlee Morency

    (Université Laval
    Université Laval)

  • Pier-Luc Plante

    (Université Laval)

  • Edwige Zufferey

    (Université Laval
    Université Laval)

  • Rodrigo Achigar

    (Universidad de la República)

  • Denise M. Tremblay

    (Université Laval
    Université Laval)

  • Geneviève M. Rousseau

    (Université Laval
    Université Laval)

  • Adeline Goulet

    (CNRS UMR7255, Aix-Marseille Université)

  • Sylvain Moineau

    (Université Laval
    Université Laval
    Université Laval)

Abstract

CRISPR-Cas systems in prokaryotic cells provide an adaptive immunity against invading nucleic acids. For example, phage infection leads to addition of new immunity (spacer acquisition) and DNA cleavage (interference) in the bacterial model species Streptococcus thermophilus, which primarily relies on Cas9-containing CRISPR-Cas systems. Phages can counteract this defense system through mutations in the targeted protospacers or by encoding anti-CRISPR proteins (ACRs) that block Cas9 interference activity. Here, we show that S. thermophilus can block ACR-containing phages when the CRISPR immunity specifically targets the acr gene. This in turn selects for phage mutants carrying a deletion within the acr gene. Remarkably, a truncated acrIIA allele, found in a wild-type virulent streptococcal phage, does not block the interference activity of Cas9 but still prevents the acquisition of new immunities, thereby providing an example of an ACR specifically inhibiting spacer acquisition.

Suggested Citation

  • Cécile Philippe & Carlee Morency & Pier-Luc Plante & Edwige Zufferey & Rodrigo Achigar & Denise M. Tremblay & Geneviève M. Rousseau & Adeline Goulet & Sylvain Moineau, 2022. "A truncated anti-CRISPR protein prevents spacer acquisition but not interference," Nature Communications, Nature, vol. 13(1), pages 1-8, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-30310-x
    DOI: 10.1038/s41467-022-30310-x
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    References listed on IDEAS

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    1. 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.
    2. Joe Bondy-Denomy & April Pawluk & Karen L. Maxwell & Alan R. Davidson, 2013. "Bacteriophage genes that inactivate the CRISPR/Cas bacterial immune system," Nature, Nature, vol. 493(7432), pages 429-432, January.
    3. 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.
    4. Sungchul Kim & Luuk Loeff & Sabina Colombo & Slobodan Jergic & Stan J. J. Brouns & Chirlmin Joo, 2020. "Selective loading and processing of prespacers for precise CRISPR adaptation," Nature, Nature, vol. 579(7797), pages 141-145, March.
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    Cited by:

    1. Mingfang Bi & Wenjing Su & Jiafu Li & Xiaobing Mo, 2024. "Insights into the inhibition of protospacer integration via direct interaction between Cas2 and AcrVA5," Nature Communications, Nature, vol. 15(1), pages 1-12, December.

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