Inactivation of CRISPR-Cas systems by anti-CRISPR proteins in diverse bacterial species

被引:4
|
作者
Pawluk, April [1 ]
Staals, Raymond H. J. [2 ]
Taylor, Corinda [2 ]
Watson, Bridget N. J. [2 ]
Saha, Senjuti [3 ]
Fineran, Peter C. [2 ]
Maxwell, Karen L. [4 ]
Davidson, Alan R. [1 ,3 ]
机构
[1] Univ Toronto, Dept Biochem, 1 Kings Coll Circle, Toronto, ON M5S 1A8, Canada
[2] Univ Otago, Dept Microbiol & Immunol, POB 56, Dunedin 9054, New Zealand
[3] Univ Toronto, Dept Mol Genet, 1 Kings Coll Circle, Toronto, ON M5S 1A8, Canada
[4] Univ Toronto, Donnelly Ctr Cellular & Biomol Res, 160 Coll St, Toronto, ON M5S 3E1, Canada
基金
加拿大健康研究院;
关键词
HORIZONTAL GENE-TRANSFER; IMMUNE-SYSTEM; DNA; CLASSIFICATION; PROKARYOTES; BACTERIOPHAGE; PSEUDOMONAS; INHIBITION; RESISTANCE; COMPLEX;
D O I
10.1038/NMICROBIOL.2016.85
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
CRISPR-Cas systems provide sequence-specific adaptive immunity against foreign nucleic acids(1,2). They are present in approximately half of all sequenced prokaryotes(3) and are expected to constitute a major barrier to horizontal gene transfer. We previously described nine distinct families of proteins encoded in Pseudomonas phage genomes that inhibit CRISPR-Cas function(4,5). We have developed a bioinformatic approach that enabled us to discover additional anti-CRISPR proteins encoded in phages and other mobile genetic elements of diverse bacterial species. We show that five previously undiscovered families of anti-CRISPRs inhibit the type I-F CRISPR-Cas systems of both Pseudomonas aeruginosa and Pectobacterium atrosepticum, and a dual specificity anti-CRISPR inactivates both type I-F and I-E CRISPR-Cas systems. Mirroring the distribution of the CRISPR-Cas systems they inactivate, these anti-CRISPRs were found in species distributed broadly across the phylum Proteobacteria. Importantly, anti-CRISPRs originating from species with divergent type I-F CRISPR-Cas systems were able to inhibit the two systems we tested, highlighting their broad specificity. These results suggest that all type I-F CRISPR-Cas systems are vulnerable to inhibition by anti-CRISPRs. Given the widespread occurrence and promiscuous activity of the anti-CRISPRs described here, we propose that anti-CRISPRs play an influential role in facilitating the movement of DNA between prokaryotes by breaching the barrier imposed by CRISPR-Cas systems.
引用
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页数:6
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