Cell tropism predicts long-term nucleotide substitution rates of mammalian RNA viruses
The high rates of RNA virus evolution are generally attributed to replication with error-prone RNA-dependent RNA polymerases. However, these long-term nucleotide substitution rates span three orders of magnitude and do not correlate well with mutation rates or selection pressures. This substitution...
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description | The high rates of RNA virus evolution are generally attributed to replication with error-prone RNA-dependent RNA polymerases. However, these long-term nucleotide substitution rates span three orders of magnitude and do not correlate well with mutation rates or selection pressures. This substitution rate variation may be explained by differences in virus ecology or intrinsic genomic properties. We generated nucleotide substitution rate estimates for mammalian RNA viruses and compiled comparable published rates, yielding a dataset of 118 substitution rates of structural genes from 51 different species, as well as 40 rates of non-structural genes from 28 species. Through ANCOVA analyses, we evaluated the relationships between these rates and four ecological factors: target cell, transmission route, host range, infection duration; and three genomic properties: genome length, genome sense, genome segmentation. Of these seven factors, we found target cells to be the only significant predictors of viral substitution rates, with tropisms for epithelial cells or neurons (P |
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However, these long-term nucleotide substitution rates span three orders of magnitude and do not correlate well with mutation rates or selection pressures. This substitution rate variation may be explained by differences in virus ecology or intrinsic genomic properties. We generated nucleotide substitution rate estimates for mammalian RNA viruses and compiled comparable published rates, yielding a dataset of 118 substitution rates of structural genes from 51 different species, as well as 40 rates of non-structural genes from 28 species. Through ANCOVA analyses, we evaluated the relationships between these rates and four ecological factors: target cell, transmission route, host range, infection duration; and three genomic properties: genome length, genome sense, genome segmentation. Of these seven factors, we found target cells to be the only significant predictors of viral substitution rates, with tropisms for epithelial cells or neurons (P<0.0001) as the most significant predictors. Further, one-tailed t-tests showed that viruses primarily infecting epithelial cells evolve significantly faster than neurotropic viruses (P<0.0001 and P<0.001 for the structural genes and non-structural genes, respectively). These results provide strong evidence that the fastest evolving mammalian RNA viruses infect cells with the highest turnover rates: the highly proliferative epithelial cells. Estimated viral generation times suggest that epithelial-infecting viruses replicate more quickly than viruses with different cell tropisms. Our results indicate that cell tropism is a key factor in viral evolvability.</description><identifier>ISSN: 1553-7374</identifier><identifier>ISSN: 1553-7366</identifier><identifier>EISSN: 1553-7374</identifier><identifier>DOI: 10.1371/journal.ppat.1003838</identifier><identifier>PMID: 24415935</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animals ; Biology ; Cell interaction ; Cell research ; Evolution ; Evolution, Molecular ; Genes ; Genes, Viral ; Humans ; Mutation ; Physiological aspects ; Point Mutation ; RNA viruses ; RNA Viruses - physiology ; Tropisms ; Viral Nonstructural Proteins - genetics ; Viral Tropism - genetics ; Viruses</subject><ispartof>PLoS pathogens, 2014-01, Vol.10 (1), p.e1003838-e1003838</ispartof><rights>COPYRIGHT 2014 Public Library of Science</rights><rights>2014 Hicks, Duffy 2014 Hicks, Duffy</rights><rights>2014 Hicks, Duffy. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Hicks AL, Duffy S (2014) Cell Tropism Predicts Long-term Nucleotide Substitution Rates of Mammalian RNA Viruses. 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However, these long-term nucleotide substitution rates span three orders of magnitude and do not correlate well with mutation rates or selection pressures. This substitution rate variation may be explained by differences in virus ecology or intrinsic genomic properties. We generated nucleotide substitution rate estimates for mammalian RNA viruses and compiled comparable published rates, yielding a dataset of 118 substitution rates of structural genes from 51 different species, as well as 40 rates of non-structural genes from 28 species. Through ANCOVA analyses, we evaluated the relationships between these rates and four ecological factors: target cell, transmission route, host range, infection duration; and three genomic properties: genome length, genome sense, genome segmentation. Of these seven factors, we found target cells to be the only significant predictors of viral substitution rates, with tropisms for epithelial cells or neurons (P<0.0001) as the most significant predictors. Further, one-tailed t-tests showed that viruses primarily infecting epithelial cells evolve significantly faster than neurotropic viruses (P<0.0001 and P<0.001 for the structural genes and non-structural genes, respectively). These results provide strong evidence that the fastest evolving mammalian RNA viruses infect cells with the highest turnover rates: the highly proliferative epithelial cells. Estimated viral generation times suggest that epithelial-infecting viruses replicate more quickly than viruses with different cell tropisms. Our results indicate that cell tropism is a key factor in viral evolvability.</description><subject>Animals</subject><subject>Biology</subject><subject>Cell interaction</subject><subject>Cell research</subject><subject>Evolution</subject><subject>Evolution, Molecular</subject><subject>Genes</subject><subject>Genes, Viral</subject><subject>Humans</subject><subject>Mutation</subject><subject>Physiological aspects</subject><subject>Point Mutation</subject><subject>RNA viruses</subject><subject>RNA Viruses - physiology</subject><subject>Tropisms</subject><subject>Viral Nonstructural Proteins - genetics</subject><subject>Viral Tropism - genetics</subject><subject>Viruses</subject><issn>1553-7374</issn><issn>1553-7366</issn><issn>1553-7374</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>DOA</sourceid><recordid>eNqVkluL1TAQx4so7nr0G4gWfNGHHpNO2rQvwuHg5cCywnp5DWkuNYe26Sbpot_edE932YIvkkDC5Df_mcxMkrzEaIuB4vdHO7mBd9tx5GGLEYIKqkfJOS4KyChQ8vjB_Sx55v0RIYIBl0-Ts5wQXNRQnCc_96rr0uDsaHyfjk5JI4JPOzu0WVCuT4dJdMoGI1Xqp8YHE6Zg7JA6HpRPrU573ve8M3xIry536Y1xk1f-efJE886rF8u5SX58-vh9_yW7-Pr5sN9dZKIECBnJuRBE65JURQNVTpqSqLzEuZKaIKmhRBSTBqG8aUhNqJbAicQIQ67ruGGTvD7pjp31bCmJZ5jUFdSAaojE4URIy49sdKbn7g-z3LBbg3Ut4y6Y-EmGMceYKixqygkI3lBRlrIWUBEpalFFrQ9LtKnplRRqCI53K9H1y2B-sdbeMKgqOrdok7xdBJy9npQPrDdexA7wQdnpNm9EEanoHOvNCW15TM0M2kZFMeNsB3O9CBQ4Utt_UHFJ1RthB6VNtK8c3q0cIhPU79DyyXt2-Hb1H-zlmiUnVjjrvVP6vioYsXle75rD5nlly7xGt1cPK3rvdDeg8Bdi0-b2</recordid><startdate>20140101</startdate><enddate>20140101</enddate><creator>Hicks, Allison L</creator><creator>Duffy, Siobain</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISN</scope><scope>ISR</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20140101</creationdate><title>Cell tropism predicts long-term nucleotide substitution rates of mammalian RNA viruses</title><author>Hicks, Allison L ; Duffy, Siobain</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c633t-42acc4ff6485b3824b64e2612edf40df360714b002bb4947fd3a4d10132f92f93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Biology</topic><topic>Cell interaction</topic><topic>Cell research</topic><topic>Evolution</topic><topic>Evolution, Molecular</topic><topic>Genes</topic><topic>Genes, Viral</topic><topic>Humans</topic><topic>Mutation</topic><topic>Physiological aspects</topic><topic>Point Mutation</topic><topic>RNA viruses</topic><topic>RNA Viruses - physiology</topic><topic>Tropisms</topic><topic>Viral Nonstructural Proteins - genetics</topic><topic>Viral Tropism - genetics</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hicks, Allison L</creatorcontrib><creatorcontrib>Duffy, Siobain</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Canada</collection><collection>Gale In Context: Science</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS pathogens</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hicks, Allison L</au><au>Duffy, Siobain</au><au>Sanjuan, Rafael</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cell tropism predicts long-term nucleotide substitution rates of mammalian RNA viruses</atitle><jtitle>PLoS pathogens</jtitle><addtitle>PLoS Pathog</addtitle><date>2014-01-01</date><risdate>2014</risdate><volume>10</volume><issue>1</issue><spage>e1003838</spage><epage>e1003838</epage><pages>e1003838-e1003838</pages><issn>1553-7374</issn><issn>1553-7366</issn><eissn>1553-7374</eissn><abstract>The high rates of RNA virus evolution are generally attributed to replication with error-prone RNA-dependent RNA polymerases. However, these long-term nucleotide substitution rates span three orders of magnitude and do not correlate well with mutation rates or selection pressures. This substitution rate variation may be explained by differences in virus ecology or intrinsic genomic properties. We generated nucleotide substitution rate estimates for mammalian RNA viruses and compiled comparable published rates, yielding a dataset of 118 substitution rates of structural genes from 51 different species, as well as 40 rates of non-structural genes from 28 species. Through ANCOVA analyses, we evaluated the relationships between these rates and four ecological factors: target cell, transmission route, host range, infection duration; and three genomic properties: genome length, genome sense, genome segmentation. Of these seven factors, we found target cells to be the only significant predictors of viral substitution rates, with tropisms for epithelial cells or neurons (P<0.0001) as the most significant predictors. Further, one-tailed t-tests showed that viruses primarily infecting epithelial cells evolve significantly faster than neurotropic viruses (P<0.0001 and P<0.001 for the structural genes and non-structural genes, respectively). These results provide strong evidence that the fastest evolving mammalian RNA viruses infect cells with the highest turnover rates: the highly proliferative epithelial cells. Estimated viral generation times suggest that epithelial-infecting viruses replicate more quickly than viruses with different cell tropisms. Our results indicate that cell tropism is a key factor in viral evolvability.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>24415935</pmid><doi>10.1371/journal.ppat.1003838</doi><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biology Cell interaction Cell research Evolution Evolution, Molecular Genes Genes, Viral Humans Mutation Physiological aspects Point Mutation RNA viruses RNA Viruses - physiology Tropisms Viral Nonstructural Proteins - genetics Viral Tropism - genetics Viruses |
title | Cell tropism predicts long-term nucleotide substitution rates of mammalian RNA viruses |
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