TY - JOUR
T1 - Clades of huge phages from across Earth’s ecosystems
AU - Al-Shayeb, Basem
AU - Sachdeva, Rohan
AU - Chen, Lin Xing
AU - Ward, Fred
AU - Munk, Patrick
AU - Devoto, Audra
AU - Castelle, Cindy J.
AU - Olm, Matthew R.
AU - Bouma-Gregson, Keith
AU - Amano, Yuki
AU - He, Christine
AU - Méheust, Raphaël
AU - Brooks, Brandon
AU - Thomas, Alex
AU - Lavy, Adi
AU - Matheus-Carnevali, Paula
AU - Sun, Christine
AU - Goltsman, Daniela S.A.
AU - Borton, Mikayla A.
AU - Sharrar, Allison
AU - Jaffe, Alexander L.
AU - Nelson, Tara C.
AU - Kantor, Rose
AU - Keren, Ray
AU - Lane, Katherine R.
AU - Farag, Ibrahim F.
AU - Lei, Shufei
AU - Finstad, Kari
AU - Amundson, Ronald
AU - Anantharaman, Karthik
AU - Zhou, Jinglie
AU - Probst, Alexander J.
AU - Power, Mary E.
AU - Tringe, Susannah G.
AU - Li, Wen Jun
AU - Wrighton, Kelly
AU - Harrison, Sue
AU - Morowitz, Michael
AU - Relman, David A.
AU - Doudna, Jennifer A.
AU - Lehours, Anne Catherine
AU - Warren, Lesley
AU - Cate, Jamie H.D.
AU - Santini, Joanne M.
AU - Banfield, Jillian F.
N1 - Funding Information:
Acknowledgements Funding for this project was provided by the National Institutes of Health (NIH) under awards RAI092531A and R01-GM109454 and the Alfred P. Sloan Foundation under grant APSF-2012-10-05 to J.F.B. and M.M.; National Science Foundation (NSF) Sustainable Chemistry grant 1349278 to J.F.B., NSF Graduate Research Fellowships to B.A.-S. (DGE 1752814) and M.R.O. (DGE 1106400); the Paul Allen Foundation Frontiers Group; Chan Zuckerberg Biohub; Innovative Genomics Institute; The Novo Nordisk Foundation (NNF16OC0021856) to P.M.; NASA 13R-0043 and CA AES to K.R.A. and K.F.; German Science Foundation postdoctoral scholarship to A.J.P. (DFG PR 1603/1-1); Camille & Henry Dreyfus Postdoctoral Fellowship in Environmental Chemistry to C.H.; Watershed Function Scientific Focus Area funded by the US Department of Energy, Office of Science, Office of Biological and Environmental Research (DE-AC02-05CH11231) to A.L., P.M.-C. and A.T.; NSF grants GRT00048468 and 1342701 to K.C.W. and M.B., and CHE-1740549 to J.H.D.C.; the Ministry of Economy, Trade and Industry of Japan to Y.A.; the March of Dimes Prematurity Research Center at Stanford University School of Medicine, the Thomas C. and Joan M. Merigan Endowment at Stanford University to D.A.R.; the National Research Foundation of South Africa (UID 64877) to S.T.L.H. and NSF CZO funding. We acknowledge the scientists who generated the public database sequences and thank J. Tung, E. Archie, F. Aarestrup and R. Kruger for contributing data and P. Pausch and G. Knott for discussions. The phage icon used in the graphics was created by Two Photon Art and the Innovative Genomics Institute.
Publisher Copyright:
© 2020, The Author(s).
PY - 2020/2/20
Y1 - 2020/2/20
N2 - Bacteriophages typically have small genomes1 and depend on their bacterial hosts for replication2. Here we sequenced DNA from diverse ecosystems and found hundreds of phage genomes with lengths of more than 200 kilobases (kb), including a genome of 735 kb, which is—to our knowledge—the largest phage genome to be described to date. Thirty-five genomes were manually curated to completion (circular and no gaps). Expanded genetic repertoires include diverse and previously undescribed CRISPR–Cas systems, transfer RNAs (tRNAs), tRNA synthetases, tRNA-modification enzymes, translation-initiation and elongation factors, and ribosomal proteins. The CRISPR–Cas systems of phages have the capacity to silence host transcription factors and translational genes, potentially as part of a larger interaction network that intercepts translation to redirect biosynthesis to phage-encoded functions. In addition, some phages may repurpose bacterial CRISPR–Cas systems to eliminate competing phages. We phylogenetically define the major clades of huge phages from human and other animal microbiomes, as well as from oceans, lakes, sediments, soils and the built environment. We conclude that the large gene inventories of huge phages reflect a conserved biological strategy, and that the phages are distributed across a broad bacterial host range and across Earth’s ecosystems.
AB - Bacteriophages typically have small genomes1 and depend on their bacterial hosts for replication2. Here we sequenced DNA from diverse ecosystems and found hundreds of phage genomes with lengths of more than 200 kilobases (kb), including a genome of 735 kb, which is—to our knowledge—the largest phage genome to be described to date. Thirty-five genomes were manually curated to completion (circular and no gaps). Expanded genetic repertoires include diverse and previously undescribed CRISPR–Cas systems, transfer RNAs (tRNAs), tRNA synthetases, tRNA-modification enzymes, translation-initiation and elongation factors, and ribosomal proteins. The CRISPR–Cas systems of phages have the capacity to silence host transcription factors and translational genes, potentially as part of a larger interaction network that intercepts translation to redirect biosynthesis to phage-encoded functions. In addition, some phages may repurpose bacterial CRISPR–Cas systems to eliminate competing phages. We phylogenetically define the major clades of huge phages from human and other animal microbiomes, as well as from oceans, lakes, sediments, soils and the built environment. We conclude that the large gene inventories of huge phages reflect a conserved biological strategy, and that the phages are distributed across a broad bacterial host range and across Earth’s ecosystems.
UR - https://www.scopus.com/pages/publications/85079705302
U2 - 10.1038/s41586-020-2007-4
DO - 10.1038/s41586-020-2007-4
M3 - Article
C2 - 32051592
AN - SCOPUS:85079705302
SN - 0028-0836
VL - 578
SP - 425
EP - 431
JO - Nature
JF - Nature
IS - 7795
ER -