TY - JOUR
T1 - An expanded arsenal of immune systems that protect bacteria from phages
AU - Millman, Adi
AU - Melamed, Sarah
AU - Leavitt, Azita
AU - Doron, Shany
AU - Bernheim, Aude
AU - Hör, Jens
AU - Garb, Jeremy
AU - Bechon, Nathalie
AU - Brandis, Alexander
AU - Lopatina, Anna
AU - Ofir, Gal
AU - Hochhauser, Dina
AU - Stokar-Avihail, Avigail
AU - Tal, Nitzan
AU - Sharir, Saar
AU - Voichek, Maya
AU - Erez, Zohar
AU - Ferrer, Jose Lorenzo M.
AU - Dar, Daniel
AU - Kacen, Assaf
AU - Amitai, Gil
AU - Sorek, Rotem
N1 - Publisher Copyright: © 2022 Elsevier Inc.
PY - 2022/11/9
Y1 - 2022/11/9
N2 - Bacterial anti-phage systems are frequently clustered in microbial genomes, forming defense islands. This property enabled the recent discovery of multiple defense systems based on their genomic co-localization with known systems, but the full arsenal of anti-phage mechanisms remains unknown. We report the discovery of 21 defense systems that protect bacteria from phages, based on computational genomic analyses and phage-infection experiments. We identified multiple systems with domains involved in eukaryotic antiviral immunity, including those homologous to the ubiquitin-like ISG15 protein, dynamin-like domains, and SEFIR domains, and show their participation in bacterial defenses. Additional systems include domains predicted to manipulate DNA and RNA molecules, alongside toxin-antitoxin systems shown here to function in anti-phage defense. These systems are widely distributed in microbial genomes, and in some bacteria, they form a considerable fraction of the immune arsenal. Our data substantially expand the inventory of defense systems utilized by bacteria to counteract phage infection.
AB - Bacterial anti-phage systems are frequently clustered in microbial genomes, forming defense islands. This property enabled the recent discovery of multiple defense systems based on their genomic co-localization with known systems, but the full arsenal of anti-phage mechanisms remains unknown. We report the discovery of 21 defense systems that protect bacteria from phages, based on computational genomic analyses and phage-infection experiments. We identified multiple systems with domains involved in eukaryotic antiviral immunity, including those homologous to the ubiquitin-like ISG15 protein, dynamin-like domains, and SEFIR domains, and show their participation in bacterial defenses. Additional systems include domains predicted to manipulate DNA and RNA molecules, alongside toxin-antitoxin systems shown here to function in anti-phage defense. These systems are widely distributed in microbial genomes, and in some bacteria, they form a considerable fraction of the immune arsenal. Our data substantially expand the inventory of defense systems utilized by bacteria to counteract phage infection.
UR - http://www.scopus.com/inward/record.url?scp=85141241867&partnerID=8YFLogxK
U2 - 10.1016/j.chom.2022.09.017
DO - 10.1016/j.chom.2022.09.017
M3 - مقالة
SN - 1931-3128
VL - 30
SP - 1556-1569.e5
JO - Cell Host and Microbe
JF - Cell Host and Microbe
IS - 11
ER -