Xanthomonas citri jumbo phage XacN1 exhibits a wide host range and high complement of tRNA genes

Scientific Reports Volume 8 Issue 1 Page 4486- published_at 2018-03-14
アクセス数 : 1524
ダウンロード数 : 79

今月のアクセス数 : 12
今月のダウンロード数 : 4
File
SciRep_8_4486.pdf 3.16 MB 種類 : fulltext
Title ( eng )
Xanthomonas citri jumbo phage XacN1 exhibits a wide host range and high complement of tRNA genes
Creator
Yoshikawa Genki
Askora Ahmed
Blanc-Mathieu Romain
Li Yanze
Ogata Hiroyuki
Source Title
Scientific Reports
Volume 8
Issue 1
Start Page 4486
Abstract
Xanthomonas virus (phage) XacN1 is a novel jumbo myovirus infecting Xanthomonas citri, the causative agent of Asian citrus canker. Its linear 384,670 bp double-stranded DNA genome encodes 592 proteins and presents the longest (66 kbp) direct terminal repeats (DTRs) among sequenced viral genomes. The DTRs harbor 56 tRNA genes, which correspond to all 20 amino acids and represent the largest number of tRNA genes reported in a viral genome. Codon usage analysis revealed a propensity for the phage encoded tRNAs to target codons that are highly used by the phage but less frequently by its host. The existence of these tRNA genes and seven additional translation-related genes as well as a chaperonin gene found in the XacN1 genome suggests a relative independence of phage replication on host molecular machinery, leading to a prediction of a wide host range for this jumbo phage. We confirmed the prediction by showing a wider host range of XacN1 than other X. citri phages in an infection test against a panel of host strains. Phylogenetic analyses revealed a clade of phages composed of XacN1 and ten other jumbo phages, indicating an evolutionary stable large genome size for this group of phages.
Descriptions
This research was supported by JSPS KAKENHI (Grant nos. 24380049, 15H04477, 16KT0020) as well as a Grant-in-Aid for Scientific Research on Innovative Areas from the Ministry of Education, Culture, Science, Sports, and Technology (MEXT) of Japan (No. 16H06429, 16K21723, and 16H06437). Computational work was completed at the SuperComputer System, Institute for Chemical Research, Kyoto University.
Language
eng
Resource Type journal article
Publisher
Nature Research
Date of Issued 2018-03-14
Rights
© The Author(s) 2018. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
Publish Type Version of Record
Access Rights open access
Source Identifier
[ISSN] 2045-2322
[DOI] 10.1038/s41598-018-22239-3
[PMID] 29540765
[DOI] https://doi.org/10.1038/s41598-018-22239-3