Cargando…

Genome Analysis of Two Novel Synechococcus Phages That Lack Common Auxiliary Metabolic Genes: Possible Reasons and Ecological Insights by Comparative Analysis of Cyanomyoviruses

The abundant and widespread unicellular cyanobacteria Synechococcus plays an important role in contributing to global phytoplankton primary production. In the present study, two novel cyanomyoviruses, S-N03 and S-H34 that infected Synechococcus MW02, were isolated from the coastal waters of the Yell...

Descripción completa

Detalles Bibliográficos
Autores principales: Jiang, Tong, Guo, Cui, Wang, Min, Wang, Meiwen, Zhang, Xinran, Liu, Yundan, Liang, Yantao, Jiang, Yong, He, Hui, Shao, Hongbing, McMinn, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7472177/
https://www.ncbi.nlm.nih.gov/pubmed/32722486
http://dx.doi.org/10.3390/v12080800
_version_ 1783578928540024832
author Jiang, Tong
Guo, Cui
Wang, Min
Wang, Meiwen
Zhang, Xinran
Liu, Yundan
Liang, Yantao
Jiang, Yong
He, Hui
Shao, Hongbing
McMinn, Andrew
author_facet Jiang, Tong
Guo, Cui
Wang, Min
Wang, Meiwen
Zhang, Xinran
Liu, Yundan
Liang, Yantao
Jiang, Yong
He, Hui
Shao, Hongbing
McMinn, Andrew
author_sort Jiang, Tong
collection PubMed
description The abundant and widespread unicellular cyanobacteria Synechococcus plays an important role in contributing to global phytoplankton primary production. In the present study, two novel cyanomyoviruses, S-N03 and S-H34 that infected Synechococcus MW02, were isolated from the coastal waters of the Yellow Sea. S-N03 contained a 167,069-bp genome comprising double-stranded DNA with a G + C content of 50.1%, 247 potential open reading frames and 1 tRNA; S-H34 contained a 167,040-bp genome with a G + C content of 50.1%, 246 potential open reading frames and 5 tRNAs. These two cyanophages contain fewer auxiliary metabolic genes (AMGs) than other previously isolated cyanophages. S-H34 in particular, is currently the only known cyanomyovirus that does not contain any AMGs related to photosynthesis. The absence of such common AMGs in S-N03 and S-H34, their distinct evolutionary history and ecological features imply that the energy for phage production might be obtained from other sources rather than being strictly dependent on the maintenance of photochemical ATP under high light. Phylogenetic analysis showed that the two isolated cyanophages clustered together and had a close relationship with two other cyanophages of low AMG content. Comparative genomic analysis, habitats and hosts across 81 representative cyanomyovirus showed that cyanomyovirus with less AMGs content all belonged to Synechococcus phages isolated from eutrophic waters. The relatively small genome size and high G + C content may also relate to the lower AMG content, as suggested by the significant correlation between the number of AMGs and G + C%. Therefore, the lower content of AMG in S-N03 and S-H34 might be a result of viral evolution that was likely shaped by habitat, host, and their genomic context. The genomic content of AMGs in cyanophages may have adaptive significance and provide clues to their evolution.
format Online
Article
Text
id pubmed-7472177
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-74721772020-09-04 Genome Analysis of Two Novel Synechococcus Phages That Lack Common Auxiliary Metabolic Genes: Possible Reasons and Ecological Insights by Comparative Analysis of Cyanomyoviruses Jiang, Tong Guo, Cui Wang, Min Wang, Meiwen Zhang, Xinran Liu, Yundan Liang, Yantao Jiang, Yong He, Hui Shao, Hongbing McMinn, Andrew Viruses Article The abundant and widespread unicellular cyanobacteria Synechococcus plays an important role in contributing to global phytoplankton primary production. In the present study, two novel cyanomyoviruses, S-N03 and S-H34 that infected Synechococcus MW02, were isolated from the coastal waters of the Yellow Sea. S-N03 contained a 167,069-bp genome comprising double-stranded DNA with a G + C content of 50.1%, 247 potential open reading frames and 1 tRNA; S-H34 contained a 167,040-bp genome with a G + C content of 50.1%, 246 potential open reading frames and 5 tRNAs. These two cyanophages contain fewer auxiliary metabolic genes (AMGs) than other previously isolated cyanophages. S-H34 in particular, is currently the only known cyanomyovirus that does not contain any AMGs related to photosynthesis. The absence of such common AMGs in S-N03 and S-H34, their distinct evolutionary history and ecological features imply that the energy for phage production might be obtained from other sources rather than being strictly dependent on the maintenance of photochemical ATP under high light. Phylogenetic analysis showed that the two isolated cyanophages clustered together and had a close relationship with two other cyanophages of low AMG content. Comparative genomic analysis, habitats and hosts across 81 representative cyanomyovirus showed that cyanomyovirus with less AMGs content all belonged to Synechococcus phages isolated from eutrophic waters. The relatively small genome size and high G + C content may also relate to the lower AMG content, as suggested by the significant correlation between the number of AMGs and G + C%. Therefore, the lower content of AMG in S-N03 and S-H34 might be a result of viral evolution that was likely shaped by habitat, host, and their genomic context. The genomic content of AMGs in cyanophages may have adaptive significance and provide clues to their evolution. MDPI 2020-07-25 /pmc/articles/PMC7472177/ /pubmed/32722486 http://dx.doi.org/10.3390/v12080800 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Jiang, Tong
Guo, Cui
Wang, Min
Wang, Meiwen
Zhang, Xinran
Liu, Yundan
Liang, Yantao
Jiang, Yong
He, Hui
Shao, Hongbing
McMinn, Andrew
Genome Analysis of Two Novel Synechococcus Phages That Lack Common Auxiliary Metabolic Genes: Possible Reasons and Ecological Insights by Comparative Analysis of Cyanomyoviruses
title Genome Analysis of Two Novel Synechococcus Phages That Lack Common Auxiliary Metabolic Genes: Possible Reasons and Ecological Insights by Comparative Analysis of Cyanomyoviruses
title_full Genome Analysis of Two Novel Synechococcus Phages That Lack Common Auxiliary Metabolic Genes: Possible Reasons and Ecological Insights by Comparative Analysis of Cyanomyoviruses
title_fullStr Genome Analysis of Two Novel Synechococcus Phages That Lack Common Auxiliary Metabolic Genes: Possible Reasons and Ecological Insights by Comparative Analysis of Cyanomyoviruses
title_full_unstemmed Genome Analysis of Two Novel Synechococcus Phages That Lack Common Auxiliary Metabolic Genes: Possible Reasons and Ecological Insights by Comparative Analysis of Cyanomyoviruses
title_short Genome Analysis of Two Novel Synechococcus Phages That Lack Common Auxiliary Metabolic Genes: Possible Reasons and Ecological Insights by Comparative Analysis of Cyanomyoviruses
title_sort genome analysis of two novel synechococcus phages that lack common auxiliary metabolic genes: possible reasons and ecological insights by comparative analysis of cyanomyoviruses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7472177/
https://www.ncbi.nlm.nih.gov/pubmed/32722486
http://dx.doi.org/10.3390/v12080800
work_keys_str_mv AT jiangtong genomeanalysisoftwonovelsynechococcusphagesthatlackcommonauxiliarymetabolicgenespossiblereasonsandecologicalinsightsbycomparativeanalysisofcyanomyoviruses
AT guocui genomeanalysisoftwonovelsynechococcusphagesthatlackcommonauxiliarymetabolicgenespossiblereasonsandecologicalinsightsbycomparativeanalysisofcyanomyoviruses
AT wangmin genomeanalysisoftwonovelsynechococcusphagesthatlackcommonauxiliarymetabolicgenespossiblereasonsandecologicalinsightsbycomparativeanalysisofcyanomyoviruses
AT wangmeiwen genomeanalysisoftwonovelsynechococcusphagesthatlackcommonauxiliarymetabolicgenespossiblereasonsandecologicalinsightsbycomparativeanalysisofcyanomyoviruses
AT zhangxinran genomeanalysisoftwonovelsynechococcusphagesthatlackcommonauxiliarymetabolicgenespossiblereasonsandecologicalinsightsbycomparativeanalysisofcyanomyoviruses
AT liuyundan genomeanalysisoftwonovelsynechococcusphagesthatlackcommonauxiliarymetabolicgenespossiblereasonsandecologicalinsightsbycomparativeanalysisofcyanomyoviruses
AT liangyantao genomeanalysisoftwonovelsynechococcusphagesthatlackcommonauxiliarymetabolicgenespossiblereasonsandecologicalinsightsbycomparativeanalysisofcyanomyoviruses
AT jiangyong genomeanalysisoftwonovelsynechococcusphagesthatlackcommonauxiliarymetabolicgenespossiblereasonsandecologicalinsightsbycomparativeanalysisofcyanomyoviruses
AT hehui genomeanalysisoftwonovelsynechococcusphagesthatlackcommonauxiliarymetabolicgenespossiblereasonsandecologicalinsightsbycomparativeanalysisofcyanomyoviruses
AT shaohongbing genomeanalysisoftwonovelsynechococcusphagesthatlackcommonauxiliarymetabolicgenespossiblereasonsandecologicalinsightsbycomparativeanalysisofcyanomyoviruses
AT mcminnandrew genomeanalysisoftwonovelsynechococcusphagesthatlackcommonauxiliarymetabolicgenespossiblereasonsandecologicalinsightsbycomparativeanalysisofcyanomyoviruses