Diversity and evolutionary relationships of T7-like podoviruses infecting marine cyanobacteria
Summary Phages are extremely abundant in the oceans, influencing the population dynamics, diversity and evolution of their hosts. Here we assessed the diversity and phylogenetic relationships among T7‐like cyanophages using DNA polymerase (replication), major capsid (structural) and photosynthesis p...
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Veröffentlicht in: | Environmental microbiology 2013-05, Vol.15 (5), p.1476-1491 |
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creator | Dekel-Bird, Naama P. Avrani, Sarit Sabehi, Gazalah Pekarsky, Irina Marston, Marcia F. Kirzner, Shay Lindell, Debbie |
description | Summary
Phages are extremely abundant in the oceans, influencing the population dynamics, diversity and evolution of their hosts. Here we assessed the diversity and phylogenetic relationships among T7‐like cyanophages using DNA polymerase (replication), major capsid (structural) and photosynthesis psbA (host‐derived) genes from isolated phages. DNA polymerase and major capsid phylogeny divided them into two discrete clades with no evidence for gene exchange between clades. Clade A phages primarily infect Synechococcus while clade B phages infect either Synechococcus or Prochlorococcus. The major capsid gene of one of the phages from clade B carries a putative intron. Nearly all clade B phages encode psbA whereas clade A phages do not. This suggests an ancient separation between cyanophages from these two clades, with the acquisition or loss of psbA occurring around the time of their divergence. A mix and match of clustering patterns was found for the replication and structural genes within each major clade, even among phages infecting different host genera. This is suggestive of numerous gene exchanges within each major clade and indicates that core phage functions have not coevolved with specific hosts. In contrast, clustering of phage psbA broadly tracks that of the host genus. These findings suggest that T7‐like cyanophages evolve through clade‐limited gene exchanges and that different genes are subjected to vastly different selection pressures. |
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Phages are extremely abundant in the oceans, influencing the population dynamics, diversity and evolution of their hosts. Here we assessed the diversity and phylogenetic relationships among T7‐like cyanophages using DNA polymerase (replication), major capsid (structural) and photosynthesis psbA (host‐derived) genes from isolated phages. DNA polymerase and major capsid phylogeny divided them into two discrete clades with no evidence for gene exchange between clades. Clade A phages primarily infect Synechococcus while clade B phages infect either Synechococcus or Prochlorococcus. The major capsid gene of one of the phages from clade B carries a putative intron. Nearly all clade B phages encode psbA whereas clade A phages do not. This suggests an ancient separation between cyanophages from these two clades, with the acquisition or loss of psbA occurring around the time of their divergence. A mix and match of clustering patterns was found for the replication and structural genes within each major clade, even among phages infecting different host genera. This is suggestive of numerous gene exchanges within each major clade and indicates that core phage functions have not coevolved with specific hosts. In contrast, clustering of phage psbA broadly tracks that of the host genus. These findings suggest that T7‐like cyanophages evolve through clade‐limited gene exchanges and that different genes are subjected to vastly different selection pressures.</description><identifier>ISSN: 1462-2912</identifier><identifier>EISSN: 1462-2920</identifier><identifier>DOI: 10.1111/1462-2920.12103</identifier><identifier>PMID: 23461565</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Cyanobacteria ; Cyanobacteria - virology ; Evolution ; Genes ; Genes, Viral - genetics ; Genetic Variation ; Host Specificity ; Microscopy, Electron, Transmission ; Oceans and Seas ; Phylogeny ; Podoviridae - classification ; Podoviridae - genetics ; Podoviridae - ultrastructure ; Prochlorococcus ; Synechococcus ; Water Microbiology</subject><ispartof>Environmental microbiology, 2013-05, Vol.15 (5), p.1476-1491</ispartof><rights>2013 Society for Applied Microbiology and Blackwell Publishing Ltd</rights><rights>2013 Society for Applied Microbiology and Blackwell Publishing Ltd.</rights><rights>Copyright © 2013 Society for Applied Microbiology and Blackwell Publishing Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2F1462-2920.12103$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2F1462-2920.12103$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23461565$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dekel-Bird, Naama P.</creatorcontrib><creatorcontrib>Avrani, Sarit</creatorcontrib><creatorcontrib>Sabehi, Gazalah</creatorcontrib><creatorcontrib>Pekarsky, Irina</creatorcontrib><creatorcontrib>Marston, Marcia F.</creatorcontrib><creatorcontrib>Kirzner, Shay</creatorcontrib><creatorcontrib>Lindell, Debbie</creatorcontrib><title>Diversity and evolutionary relationships of T7-like podoviruses infecting marine cyanobacteria</title><title>Environmental microbiology</title><addtitle>Environ Microbiol</addtitle><description>Summary
Phages are extremely abundant in the oceans, influencing the population dynamics, diversity and evolution of their hosts. Here we assessed the diversity and phylogenetic relationships among T7‐like cyanophages using DNA polymerase (replication), major capsid (structural) and photosynthesis psbA (host‐derived) genes from isolated phages. DNA polymerase and major capsid phylogeny divided them into two discrete clades with no evidence for gene exchange between clades. Clade A phages primarily infect Synechococcus while clade B phages infect either Synechococcus or Prochlorococcus. The major capsid gene of one of the phages from clade B carries a putative intron. Nearly all clade B phages encode psbA whereas clade A phages do not. This suggests an ancient separation between cyanophages from these two clades, with the acquisition or loss of psbA occurring around the time of their divergence. A mix and match of clustering patterns was found for the replication and structural genes within each major clade, even among phages infecting different host genera. This is suggestive of numerous gene exchanges within each major clade and indicates that core phage functions have not coevolved with specific hosts. In contrast, clustering of phage psbA broadly tracks that of the host genus. These findings suggest that T7‐like cyanophages evolve through clade‐limited gene exchanges and that different genes are subjected to vastly different selection pressures.</description><subject>Cyanobacteria</subject><subject>Cyanobacteria - virology</subject><subject>Evolution</subject><subject>Genes</subject><subject>Genes, Viral - genetics</subject><subject>Genetic Variation</subject><subject>Host Specificity</subject><subject>Microscopy, Electron, Transmission</subject><subject>Oceans and Seas</subject><subject>Phylogeny</subject><subject>Podoviridae - classification</subject><subject>Podoviridae - genetics</subject><subject>Podoviridae - ultrastructure</subject><subject>Prochlorococcus</subject><subject>Synechococcus</subject><subject>Water Microbiology</subject><issn>1462-2912</issn><issn>1462-2920</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkTtP5DAUhS0EApalpkOWaGiy-BHbSYkYXiseK-2s6LA8zh0wZOLBTmbJv8dhYAoq3Phc-ztXuvcgtEfJL5rOEc0ly1jJUsko4Wtoe_WyvtKUbaEfMT4RQhVXZBNtMZ5LKqTYRvcjt4AQXdtj01QYFr7uWucbE3ocoDaDjo9uHrGf4rHKavcMeO4rv3ChixCxa6ZgW9c84JkJrgFse9P4ibEtBGd-oo2pqSPsftw76N_Z6fjkIru6Pb88Ob7KXM4Yz2ypKJcMhFSFmdipykFWparSTJZLww0TQlXEqEKVAqRRYHNiLSOVyCVYxXfQ4bLvPPiXDmKrZy5aqGvTgO-iplzIkhVC8m-gnJJCsXzoevAFffJdaNIgiWIFozynLFH7H1Q3mUGl58GlVfT6c8kJEEvgv6uhX_1ToocM9ZCSHhLT7xnq0-vLd5F82dLnYguvK58Jz1qmIIW-uznXZHx2MeJ__urf_A13rZv7</recordid><startdate>201305</startdate><enddate>201305</enddate><creator>Dekel-Bird, Naama P.</creator><creator>Avrani, Sarit</creator><creator>Sabehi, Gazalah</creator><creator>Pekarsky, Irina</creator><creator>Marston, Marcia F.</creator><creator>Kirzner, Shay</creator><creator>Lindell, Debbie</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QH</scope><scope>7QL</scope><scope>7ST</scope><scope>7T7</scope><scope>7TN</scope><scope>7U9</scope><scope>7UA</scope><scope>8FD</scope><scope>C1K</scope><scope>F1W</scope><scope>FR3</scope><scope>H94</scope><scope>H95</scope><scope>H97</scope><scope>L.G</scope><scope>M7N</scope><scope>P64</scope><scope>SOI</scope><scope>7X8</scope></search><sort><creationdate>201305</creationdate><title>Diversity and evolutionary relationships of T7-like podoviruses infecting marine cyanobacteria</title><author>Dekel-Bird, Naama P. ; Avrani, Sarit ; Sabehi, Gazalah ; Pekarsky, Irina ; Marston, Marcia F. ; Kirzner, Shay ; Lindell, Debbie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i4223-c971362e5678abcf74e6d97d210c36a3a2557d0a78795e6a7ec40cc20d546ec73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Cyanobacteria</topic><topic>Cyanobacteria - virology</topic><topic>Evolution</topic><topic>Genes</topic><topic>Genes, Viral - genetics</topic><topic>Genetic Variation</topic><topic>Host Specificity</topic><topic>Microscopy, Electron, Transmission</topic><topic>Oceans and Seas</topic><topic>Phylogeny</topic><topic>Podoviridae - classification</topic><topic>Podoviridae - genetics</topic><topic>Podoviridae - ultrastructure</topic><topic>Prochlorococcus</topic><topic>Synechococcus</topic><topic>Water Microbiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dekel-Bird, Naama P.</creatorcontrib><creatorcontrib>Avrani, Sarit</creatorcontrib><creatorcontrib>Sabehi, Gazalah</creatorcontrib><creatorcontrib>Pekarsky, Irina</creatorcontrib><creatorcontrib>Marston, Marcia F.</creatorcontrib><creatorcontrib>Kirzner, Shay</creatorcontrib><creatorcontrib>Lindell, Debbie</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Aqualine</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Oceanic Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Water Resources Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Environmental microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dekel-Bird, Naama P.</au><au>Avrani, Sarit</au><au>Sabehi, Gazalah</au><au>Pekarsky, Irina</au><au>Marston, Marcia F.</au><au>Kirzner, Shay</au><au>Lindell, Debbie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diversity and evolutionary relationships of T7-like podoviruses infecting marine cyanobacteria</atitle><jtitle>Environmental microbiology</jtitle><addtitle>Environ Microbiol</addtitle><date>2013-05</date><risdate>2013</risdate><volume>15</volume><issue>5</issue><spage>1476</spage><epage>1491</epage><pages>1476-1491</pages><issn>1462-2912</issn><eissn>1462-2920</eissn><abstract>Summary
Phages are extremely abundant in the oceans, influencing the population dynamics, diversity and evolution of their hosts. Here we assessed the diversity and phylogenetic relationships among T7‐like cyanophages using DNA polymerase (replication), major capsid (structural) and photosynthesis psbA (host‐derived) genes from isolated phages. DNA polymerase and major capsid phylogeny divided them into two discrete clades with no evidence for gene exchange between clades. Clade A phages primarily infect Synechococcus while clade B phages infect either Synechococcus or Prochlorococcus. The major capsid gene of one of the phages from clade B carries a putative intron. Nearly all clade B phages encode psbA whereas clade A phages do not. This suggests an ancient separation between cyanophages from these two clades, with the acquisition or loss of psbA occurring around the time of their divergence. A mix and match of clustering patterns was found for the replication and structural genes within each major clade, even among phages infecting different host genera. This is suggestive of numerous gene exchanges within each major clade and indicates that core phage functions have not coevolved with specific hosts. In contrast, clustering of phage psbA broadly tracks that of the host genus. These findings suggest that T7‐like cyanophages evolve through clade‐limited gene exchanges and that different genes are subjected to vastly different selection pressures.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>23461565</pmid><doi>10.1111/1462-2920.12103</doi><tpages>16</tpages></addata></record> |
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subjects | Cyanobacteria Cyanobacteria - virology Evolution Genes Genes, Viral - genetics Genetic Variation Host Specificity Microscopy, Electron, Transmission Oceans and Seas Phylogeny Podoviridae - classification Podoviridae - genetics Podoviridae - ultrastructure Prochlorococcus Synechococcus Water Microbiology |
title | Diversity and evolutionary relationships of T7-like podoviruses infecting marine cyanobacteria |
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