4.8 Article

Anti-CRISPR Phages Cooperate to Overcome CRISPR-Cas Immunity

期刊

CELL
卷 174, 期 4, 页码 908-+

出版社

CELL PRESS
DOI: 10.1016/j.cell.2018.05.058

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资金

  1. Wellcome Trust [109776/Z/15/Z]
  2. Natural Environment Research Council [NE/M018350/1]
  3. BBSRC [BB/N017412/1, BB/R010781/1]
  4. European Research Council [ERC-STG-2016-714478 - EVOIMMECH]
  5. People Programme (Marie Curie Actions) of the European Union's Horizon 2020 (REA) [660039]
  6. Leverhulme Trust
  7. Royal Society
  8. Wellcome Trust [109776/Z/15/Z] Funding Source: Wellcome Trust
  9. BBSRC [BB/N017412/1, BB/R010781/1] Funding Source: UKRI
  10. NERC [NBAF010002, NE/M018350/1] Funding Source: UKRI
  11. Marie Curie Actions (MSCA) [660039] Funding Source: Marie Curie Actions (MSCA)

向作者/读者索取更多资源

Some phages encode anti-CRISPR (acr) genes, which antagonize bacterial CRISPR-Cas immune systems by binding components of its machinery, but it is less clear how deployment of these acr genes impacts phage replication and epidemiology. Here, we demonstrate that bacteria with CRISPR-Cas resistance are still partially immune to Acr-encoding phage. As a consequence, Acr-phages often need to cooperate in order to overcome CRISPR resistance, with a first phage blocking the host CRISPR-Cas immune system to allow a second Acr-phage to successfully replicate. This cooperation leads to epidemiological tipping points in which the initial density of Acr-phage tips the balance from phage extinction to a phage epidemic. Furthermore, both higher levels of CRISPR-Cas immunity and weaker Acr activities shift the tipping points toward higher initial phage densities. Collectively, these data help elucidate how interactions between phage-encoded immune suppressors and the CRISPR systems they target shape bacteria-phage population dynamics.

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