CRISPR-Cas are prokaryotic defence systems that provide protection against invasion by mobile genetic elements (MGE), including bacteriophages. MGE can overcome CRISPR-Cas defences by encoding anti-CRISPR (Acr) proteins. These proteins are produced in the early stages of the infection and inhibit the CRISPR-Cas machinery to allow phage replication. While research on Acr has mainly focused on their discovery, structure and mode of action, and their applications in biotechnology, the impact of Acr on the ecology of MGE as well as on the coevolution with their bacterial hosts only begins to be unravelled. In this review, we summarise our current understanding on the distribution of anti-CRISPR genes in MGE, the ecology of phages encoding Acr, and their coevolution with bacterial defence mechanisms. We high-light the need to use more diverse and complex experimental models to better understand the impact of anti-CRISPR in MGE-host interactions.(c) 2023 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecom-mons.org/licenses/by/4.0/).
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Indian Agr Res Inst, Div Plant Pathol, Adv Ctr Plant Virol, New Delhi 110012, IndiaIndian Agr Res Inst, Div Plant Pathol, Adv Ctr Plant Virol, New Delhi 110012, India
Chaudhary, Kulbhushan
Chattopadhyay, Anirudha
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SD Agr Univ, Dept Plant Pathol, CP Coll Agr, S K Nagar, Gujrat, IndiaIndian Agr Res Inst, Div Plant Pathol, Adv Ctr Plant Virol, New Delhi 110012, India
Chattopadhyay, Anirudha
Pratap, Dharmendra
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Chaudhary Charan Singh Univ, Dept Genet & Plant Breeding, Meerut, Uttar Pradesh, IndiaIndian Agr Res Inst, Div Plant Pathol, Adv Ctr Plant Virol, New Delhi 110012, India
机构:
Univ Toronto, Dept Mol Genet, Toronto, ON M5S 1A8, CanadaUniv Toronto, Dept Mol Genet, Toronto, ON M5S 1A8, Canada
Stanley, Sabrina Y.
Borges, Adair L.
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Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USAUniv Toronto, Dept Mol Genet, Toronto, ON M5S 1A8, Canada
Borges, Adair L.
Chen, Kuei-Ho
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J David Gladstone Inst, San Francisco, CA 94158 USAUniv Toronto, Dept Mol Genet, Toronto, ON M5S 1A8, Canada
Chen, Kuei-Ho
Swaney, Danielle L.
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J David Gladstone Inst, San Francisco, CA 94158 USA
Univ Calif San Francisco, Quantitat Biosci Inst, San Francisco, CA 94143 USA
Univ Calif San Francisco, Dept Cellular & Mol Pharmacol, San Francisco, CA 94143 USAUniv Toronto, Dept Mol Genet, Toronto, ON M5S 1A8, Canada
Swaney, Danielle L.
Krogan, Nevan J.
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J David Gladstone Inst, San Francisco, CA 94158 USA
Univ Calif San Francisco, Quantitat Biosci Inst, San Francisco, CA 94143 USA
Univ Calif San Francisco, Dept Cellular & Mol Pharmacol, San Francisco, CA 94143 USAUniv Toronto, Dept Mol Genet, Toronto, ON M5S 1A8, Canada
Krogan, Nevan J.
Bondy-Denomy, Joseph
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Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
Univ Calif San Francisco, Quantitat Biosci Inst, San Francisco, CA 94143 USAUniv Toronto, Dept Mol Genet, Toronto, ON M5S 1A8, Canada
Bondy-Denomy, Joseph
Davidson, Alan R.
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Univ Toronto, Dept Mol Genet, Toronto, ON M5S 1A8, Canada
Univ Toronto, Dept Biochem, Toronto, ON M5S 1A8, CanadaUniv Toronto, Dept Mol Genet, Toronto, ON M5S 1A8, Canada
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Univ Otago, Dept Biochem, POB 56, Dunedin 9054, New Zealand
Univ Dhaka, Dept Genet Engn & Biotechnol, Dhaka 1000, BangladeshUniv Otago, Dept Biochem, POB 56, Dunedin 9054, New Zealand
Shehreen, Saadlee
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Birkholz, Nils
Fineran, Peter C.
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Univ Otago, Dept Microbiol & Immunol, Dunedin 9016, New Zealand
Univ Otago, Bioprotect Aotearoa, POB 56, Dunedin 9054, New Zealand
Univ Otago, Genet Otago, POB 56, Dunedin 9054, New ZealandUniv Otago, Dept Biochem, POB 56, Dunedin 9054, New Zealand
Fineran, Peter C.
Brown, Chris M.
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Univ Otago, Dept Biochem, POB 56, Dunedin 9054, New Zealand
Univ Otago, Genet Otago, POB 56, Dunedin 9054, New ZealandUniv Otago, Dept Biochem, POB 56, Dunedin 9054, New Zealand