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来自地球生态系统的巨型噬菌体的进化枝。

Clades of huge phages from across Earth's ecosystems.

机构信息

Innovative Genomics Institute, University of California Berkeley, Berkeley, CA, USA.

National Food Institute, Technical University of Denmark, Kongens Lyngby, Denmark.

出版信息

Nature. 2020 Feb;578(7795):425-431. doi: 10.1038/s41586-020-2007-4. Epub 2020 Feb 12.

DOI:10.1038/s41586-020-2007-4
PMID:32051592
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7162821/
Abstract

Bacteriophages typically have small genomes and depend on their bacterial hosts for replication. 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.

摘要

噬菌体通常具有较小的基因组,并依赖其细菌宿主进行复制。在这里,我们对来自不同生态系统的 DNA 进行了测序,发现了数百个长度超过 200 千碱基(kb)的噬菌体基因组,其中一个基因组长达 735 kb,据我们所知,这是迄今为止描述的最大的噬菌体基因组。我们对 35 个基因组进行了人工测序,直至完成(无缺口的环形基因组)。扩展的遗传谱包括多样化的、以前未描述过的 CRISPR-Cas 系统、转移 RNA(tRNA)、tRNA 合成酶、tRNA 修饰酶、翻译起始和延伸因子以及核糖体蛋白。噬菌体的 CRISPR-Cas 系统能够沉默宿主转录因子和翻译基因,这可能是作为一个更大的相互作用网络的一部分,该网络可以拦截翻译,从而将生物合成重新定向到噬菌体编码的功能上。此外,一些噬菌体可能会重新利用细菌的 CRISPR-Cas 系统来消除竞争噬菌体。我们从人类和其他动物微生物组以及海洋、湖泊、沉积物、土壤和建筑环境中,对巨噬菌体的主要进化枝进行了系统发育定义。我们得出的结论是,巨噬菌体的大量基因库反映了一种保守的生物学策略,而且这些噬菌体分布在广泛的细菌宿主范围和地球的生态系统中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc9c/7162821/f1fec5ec5081/41586_2020_2007_Fig14_ESM.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc9c/7162821/0f9e8e2dc2df/41586_2020_2007_Fig7_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc9c/7162821/cd7f99f4a060/41586_2020_2007_Fig8_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc9c/7162821/5c79506a33cc/41586_2020_2007_Fig9_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc9c/7162821/25e5e6afa22a/41586_2020_2007_Fig10_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc9c/7162821/774f8e3cc818/41586_2020_2007_Fig11_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc9c/7162821/c0ff9eb05f8c/41586_2020_2007_Fig12_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc9c/7162821/e293363ae8a7/41586_2020_2007_Fig13_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc9c/7162821/f1fec5ec5081/41586_2020_2007_Fig14_ESM.jpg

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