Author
Listed:
- Basem Al-Shayeb
(University of California Berkeley)
- Rohan Sachdeva
(University of California Berkeley)
- Lin-Xing Chen
(University of California Berkeley)
- Fred Ward
(University of California Berkeley)
- Patrick Munk
(Technical University of Denmark)
- Audra Devoto
(University of California Berkeley)
- Cindy J. Castelle
(University of California Berkeley)
- Matthew R. Olm
(University of California Berkeley)
- Keith Bouma-Gregson
(University of California Berkeley)
- Yuki Amano
(Japan Atomic Energy Agency)
- Christine He
(University of California Berkeley)
- Raphaël Méheust
(University of California Berkeley)
- Brandon Brooks
(University of California Berkeley)
- Alex Thomas
(University of California Berkeley)
- Adi Lavy
(University of California Berkeley)
- Paula Matheus-Carnevali
(University of California Berkeley)
- Christine Sun
(Stanford University)
- Daniela S. A. Goltsman
(Stanford University)
- Mikayla A. Borton
(Colorado State University)
- Allison Sharrar
(University of California Berkeley)
- Alexander L. Jaffe
(University of California Berkeley)
- Tara C. Nelson
(University of Toronto)
- Rose Kantor
(University of California Berkeley)
- Ray Keren
(University of California Berkeley)
- Katherine R. Lane
(University of California Berkeley)
- Ibrahim F. Farag
(University of California Berkeley)
- Shufei Lei
(University of California Berkeley)
- Kari Finstad
(University of California Berkeley)
- Ronald Amundson
(University of California Berkeley)
- Karthik Anantharaman
(University of California Berkeley)
- Jinglie Zhou
(DOE Joint Genome Institute)
- Alexander J. Probst
(University of California Berkeley)
- Mary E. Power
(University of California Berkeley)
- Susannah G. Tringe
(DOE Joint Genome Institute)
- Wen-Jun Li
(Sun Yat-Sen University)
- Kelly Wrighton
(Colorado State University)
- Sue Harrison
(University of Cape Town)
- Michael Morowitz
(University of Pittsburgh School of Medicine)
- David A. Relman
(Stanford University)
- Jennifer A. Doudna
(University of California Berkeley)
- Anne-Catherine Lehours
(Laboratoire Microorganismes: Génome et Environnement, Université Clermont Auvergne, CNRS)
- Lesley Warren
(University of Toronto)
- Jamie H. D. Cate
(University of California Berkeley)
- Joanne M. Santini
(University College London)
- Jillian F. Banfield
(University of California Berkeley
University of California Berkeley
University of California Berkeley
University of Melbourne)
Abstract
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.
Suggested Citation
Basem Al-Shayeb & Rohan Sachdeva & Lin-Xing Chen & Fred Ward & Patrick Munk & Audra Devoto & Cindy J. Castelle & Matthew R. Olm & Keith Bouma-Gregson & Yuki Amano & Christine He & Raphaël Méheust & Br, 2020.
"Clades of huge phages from across Earth’s ecosystems,"
Nature, Nature, vol. 578(7795), pages 425-431, February.
Handle:
RePEc:nat:nature:v:578:y:2020:i:7795:d:10.1038_s41586-020-2007-4
DOI: 10.1038/s41586-020-2007-4
Download full text from publisher
As the access to this document is restricted, you may want to search for a different version of it.
Citations
Citations are extracted by the
CitEc Project, subscribe to its
RSS feed for this item.
Cited by:
- Yashan Yang & Qianqian Shao & Mingcheng Guo & Lin Han & Xinyue Zhao & Aohan Wang & Xiangyun Li & Bo Wang & Ji-An Pan & Zhenguo Chen & Andrei Fokine & Lei Sun & Qianglin Fang, 2024.
"Capsid structure of bacteriophage ΦKZ provides insights into assembly and stabilization of jumbo phages,"
Nature Communications, Nature, vol. 15(1), pages 1-12, December.
- Xiaoqian Lin & Tongyuan Hu & Jianwei Chen & Hewei Liang & Jianwei Zhou & Zhinan Wu & Chen Ye & Xin Jin & Xun Xu & Wenwei Zhang & Xiaohuan Jing & Tao Yang & Jian Wang & Huanming Yang & Karsten Kristian, 2023.
"The genomic landscape of reference genomes of cultivated human gut bacteria,"
Nature Communications, Nature, vol. 14(1), pages 1-11, December.
- Samantha L. Peters & Adair L. Borges & Richard J. Giannone & Michael J. Morowitz & Jillian F. Banfield & Robert L. Hettich, 2022.
"Experimental validation that human microbiome phages use alternative genetic coding,"
Nature Communications, Nature, vol. 13(1), pages 1-7, December.
- Eliza S. Nieweglowska & Axel F. Brilot & Melissa Méndez-Moran & Claire Kokontis & Minkyung Baek & Junrui Li & Yifan Cheng & David Baker & Joseph Bondy-Denomy & David A. Agard, 2023.
"The ϕPA3 phage nucleus is enclosed by a self-assembling 2D crystalline lattice,"
Nature Communications, Nature, vol. 14(1), pages 1-12, December.
- Yi Yi & Shunzhang Liu & Yali Hao & Qingyang Sun & Xinjuan Lei & Yecheng Wang & Jiahua Wang & Mujie Zhang & Shan Tang & Qingxue Tang & Yue Zhang & Xipeng Liu & Yinzhao Wang & Xiang Xiao & Huahua Jian, 2023.
"A systematic analysis of marine lysogens and proviruses,"
Nature Communications, Nature, vol. 14(1), pages 1-15, December.
- Luis E. Valentin-Alvarado & Kathryn E. Appler & Valerie Anda & Marie C. Schoelmerich & Jacob West-Roberts & Veronika Kivenson & Alexander Crits-Christoph & Lynn Ly & Rohan Sachdeva & Chris Greening & , 2024.
"Asgard archaea modulate potential methanogenesis substrates in wetland soil,"
Nature Communications, Nature, vol. 15(1), pages 1-16, December.
- Zongzhi Wu & Tang Liu & Qian Chen & Tianyi Chen & Jinyun Hu & Liyu Sun & Bingxue Wang & Wenpeng Li & Jinren Ni, 2024.
"Unveiling the unknown viral world in groundwater,"
Nature Communications, Nature, vol. 15(1), pages 1-12, December.
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:nature:v:578:y:2020:i:7795:d:10.1038_s41586-020-2007-4. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.