TY - JOUR
T1 - Diversity and classification of cyclic-oligonucleotide-based anti-phage signalling systems
AU - Millman, Adi
AU - Melamed, Sarah
AU - Amitai, Gil
AU - Sorek, Rotem
N1 - We thank the members of the Sorek laboratory for comments on earlier versions of this manuscript. A.M. was supported by a fellowship from the Ariane de Rothschild Women Doctoral Program and, in part, by the Israeli Council for Higher Education via the Weizmann Data Science Research Center. R.S. was supported in part by the Israel Science Foundation (personal grant no. 1360/16), the European Research Council (grant no. ERC-CoG 681203), the German Research Council (DFG) priority program SPP 2002 (grant no. SO 1611/1-1), the Israeli Council for Higher Education through the Weizmann Data Science Research Center, the Ernest and Bonnie Beutler Research Program of Excellence in Genomic Medicine, the Minerva Foundation with funding from the Federal German Ministry for Education and Research and the Knell Family Center for Microbiology. Contributions - A.M. collected and analysed the data and wrote the paper. S.M. and G.A. were involved in the classification of CBASS systems. R.S. supervised the study and wrote the paper.
PY - 2020/12
Y1 - 2020/12
N2 - Cyclic-oligonucleotide-based anti-phage signalling systems (CBASS) are a family of defence systems against bacteriophages (hereafter phages) that share ancestry with the cGAS-STING innate immune pathway in animals. CBASS systems are composed of an oligonucleotide cyclase, which generates signalling cyclic oligonucleotides in response to phage infection, and an effector that is activated by the cyclic oligonucleotides and promotes cell death. Cell death occurs before phage replication is completed, therefore preventing the spread of phages to nearby cells. Here, we analysed 38,000 bacterial and archaeal genomes and identified more than 5,000 CBASS systems, which have diverse architectures with multiple signalling molecules, effectors and ancillary genes. We propose a classification system for CBASS that groups systems according to their operon organization, signalling molecules and effector function. Four major CBASS types were identified, sharing at least six effector subtypes that promote cell death by membrane impairment, DNA degradation or other means. We observed evidence of extensive gain and loss of CBASS systems, as well as shuffling of effector genes between systems. We expect that our classification and nomenclature scheme will guide future research in the developing CBASS field.
AB - Cyclic-oligonucleotide-based anti-phage signalling systems (CBASS) are a family of defence systems against bacteriophages (hereafter phages) that share ancestry with the cGAS-STING innate immune pathway in animals. CBASS systems are composed of an oligonucleotide cyclase, which generates signalling cyclic oligonucleotides in response to phage infection, and an effector that is activated by the cyclic oligonucleotides and promotes cell death. Cell death occurs before phage replication is completed, therefore preventing the spread of phages to nearby cells. Here, we analysed 38,000 bacterial and archaeal genomes and identified more than 5,000 CBASS systems, which have diverse architectures with multiple signalling molecules, effectors and ancillary genes. We propose a classification system for CBASS that groups systems according to their operon organization, signalling molecules and effector function. Four major CBASS types were identified, sharing at least six effector subtypes that promote cell death by membrane impairment, DNA degradation or other means. We observed evidence of extensive gain and loss of CBASS systems, as well as shuffling of effector genes between systems. We expect that our classification and nomenclature scheme will guide future research in the developing CBASS field.
UR - http://www.scopus.com/inward/record.url?scp=85089730509&partnerID=8YFLogxK
U2 - 10.1038/s41564-020-0777-y
DO - 10.1038/s41564-020-0777-y
M3 - مقالة
SN - 2058-5276
VL - 5
SP - 1608
EP - 1615
JO - Nature Microbiology
JF - Nature Microbiology
IS - 12
ER -