Heterogeneous recombination among Hepatitis B virus genotypes
The rapid evolution of Hepatitis B virus (HBV) through both evolutionary forces, mutation and recombination, allows this virus to generate a large variety of adapted variants at both intra and inter-host levels. It can, for instance, generate drug resistance or the diverse viral genotypes that curre...
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description | The rapid evolution of Hepatitis B virus (HBV) through both evolutionary forces, mutation and recombination, allows this virus to generate a large variety of adapted variants at both intra and inter-host levels. It can, for instance, generate drug resistance or the diverse viral genotypes that currently exist in the HBV epidemics. Concerning the latter, it is known that recombination played a major role in the emergence and genetic diversification of novel genotypes. In this regard, the quantification of viral recombination in each genotype can provide relevant information to devise expectations about the evolutionary trends of the epidemic. Here we measured the amount of this evolutionary force by estimating global and local recombination rates in >4700 HBV complete genome sequences corresponding to nine (A to I) HBV genotypes. Counterintuitively, we found that genotype E presents extremely high levels of recombination, followed by genotypes B and C. On the other hand, genotype G presents the lowest level, where recombination is almost negligible. We discuss these findings in the light of known characteristics of these genotypes. Additionally, we present a phylogenetic network to depict the evolutionary history of the studied HBV genotypes. This network clearly classified all genotypes into specific groups and indicated that diverse pairs of genotypes are derived from a common ancestor (i.e., C–I, D–E and, F–H) although still the origin of this virus presented large uncertainty. Altogether we conclude that the amount of observed recombination is heterogeneous among HBV genotypes and that this heterogeneity can influence on the future expansion of the epidemic.
•We quantified recombination in 9 HBV genotypes from >4700 genome sequences.•Recombination is heterogeneous among HBV genotypes at both global and local levels.•Inferences of the evolutionary history of HBV genotypes must consider recombination.•HBV genotypes can be classified with a recombination phylogenetic network. |
doi_str_mv | 10.1016/j.meegid.2017.08.015 |
format | Article |
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•We quantified recombination in 9 HBV genotypes from >4700 genome sequences.•Recombination is heterogeneous among HBV genotypes at both global and local levels.•Inferences of the evolutionary history of HBV genotypes must consider recombination.•HBV genotypes can be classified with a recombination phylogenetic network.</description><identifier>ISSN: 1567-1348</identifier><identifier>EISSN: 1567-7257</identifier><identifier>DOI: 10.1016/j.meegid.2017.08.015</identifier><identifier>PMID: 28827173</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Base Composition ; Evolution, Molecular ; Genome, Viral ; Genotype ; HBV evolution ; HBV genome ; HBV genotypes ; Hepatitis B virus ; Hepatitis B virus - classification ; Hepatitis B virus - genetics ; Phylogeny ; Recombination ; Recombination, Genetic ; Sequence Analysis, DNA</subject><ispartof>Infection, genetics and evolution, 2017-10, Vol.54, p.486-490</ispartof><rights>2017 Elsevier B.V.</rights><rights>Copyright © 2017 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c362t-b326459277d2bd2a7ff5bd7d3876ad6900217689a5b268d87a9fafb404a4d6123</citedby><cites>FETCH-LOGICAL-c362t-b326459277d2bd2a7ff5bd7d3876ad6900217689a5b268d87a9fafb404a4d6123</cites><orcidid>0000-0002-0516-2717</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.meegid.2017.08.015$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28827173$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Castelhano, Nadine</creatorcontrib><creatorcontrib>Araujo, Natalia M.</creatorcontrib><creatorcontrib>Arenas, Miguel</creatorcontrib><title>Heterogeneous recombination among Hepatitis B virus genotypes</title><title>Infection, genetics and evolution</title><addtitle>Infect Genet Evol</addtitle><description>The rapid evolution of Hepatitis B virus (HBV) through both evolutionary forces, mutation and recombination, allows this virus to generate a large variety of adapted variants at both intra and inter-host levels. It can, for instance, generate drug resistance or the diverse viral genotypes that currently exist in the HBV epidemics. Concerning the latter, it is known that recombination played a major role in the emergence and genetic diversification of novel genotypes. In this regard, the quantification of viral recombination in each genotype can provide relevant information to devise expectations about the evolutionary trends of the epidemic. Here we measured the amount of this evolutionary force by estimating global and local recombination rates in >4700 HBV complete genome sequences corresponding to nine (A to I) HBV genotypes. Counterintuitively, we found that genotype E presents extremely high levels of recombination, followed by genotypes B and C. On the other hand, genotype G presents the lowest level, where recombination is almost negligible. We discuss these findings in the light of known characteristics of these genotypes. Additionally, we present a phylogenetic network to depict the evolutionary history of the studied HBV genotypes. This network clearly classified all genotypes into specific groups and indicated that diverse pairs of genotypes are derived from a common ancestor (i.e., C–I, D–E and, F–H) although still the origin of this virus presented large uncertainty. Altogether we conclude that the amount of observed recombination is heterogeneous among HBV genotypes and that this heterogeneity can influence on the future expansion of the epidemic.
•We quantified recombination in 9 HBV genotypes from >4700 genome sequences.•Recombination is heterogeneous among HBV genotypes at both global and local levels.•Inferences of the evolutionary history of HBV genotypes must consider recombination.•HBV genotypes can be classified with a recombination phylogenetic network.</description><subject>Base Composition</subject><subject>Evolution, Molecular</subject><subject>Genome, Viral</subject><subject>Genotype</subject><subject>HBV evolution</subject><subject>HBV genome</subject><subject>HBV genotypes</subject><subject>Hepatitis B virus</subject><subject>Hepatitis B virus - classification</subject><subject>Hepatitis B virus - genetics</subject><subject>Phylogeny</subject><subject>Recombination</subject><subject>Recombination, Genetic</subject><subject>Sequence Analysis, DNA</subject><issn>1567-1348</issn><issn>1567-7257</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kM1LwzAUwIMobk7_A5EevbQmafPRg4IOdcLAi55D2ryOjLWpSTfYf29mp0dP7z34va8fQtcEZwQTfrfOWoCVNRnFRGRYZpiwEzQljItUUCZOjznJCzlBFyGscQQxledoQqWkgoh8iu4XMIB3K-jAbUPioXZtZTs9WNclunXdKllAH8vBhuQp2VkfqUi7Yd9DuERnjd4EuDrGGfp8ef6YL9Ll--vb_HGZ1jmnQ1rllBespEIYWhmqRdOwygiTS8G14SXGlAguS80qyqWRQpeNbqoCF7ownNB8hm7Hub13X1sIg2ptqGGz0T9nK1LmhLKClzKixYjW3oXgoVG9t632e0WwOohTazWKUwdxCksVxcW2m-OGbdWC-Wv6NRWBhxGA-OfOglehttDVYGyUNijj7P8bvgFQLoBZ</recordid><startdate>201710</startdate><enddate>201710</enddate><creator>Castelhano, Nadine</creator><creator>Araujo, Natalia M.</creator><creator>Arenas, Miguel</creator><general>Elsevier B.V</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>7X8</scope><orcidid>https://orcid.org/0000-0002-0516-2717</orcidid></search><sort><creationdate>201710</creationdate><title>Heterogeneous recombination among Hepatitis B virus genotypes</title><author>Castelhano, Nadine ; Araujo, Natalia M. ; Arenas, Miguel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c362t-b326459277d2bd2a7ff5bd7d3876ad6900217689a5b268d87a9fafb404a4d6123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Base Composition</topic><topic>Evolution, Molecular</topic><topic>Genome, Viral</topic><topic>Genotype</topic><topic>HBV evolution</topic><topic>HBV genome</topic><topic>HBV genotypes</topic><topic>Hepatitis B virus</topic><topic>Hepatitis B virus - classification</topic><topic>Hepatitis B virus - genetics</topic><topic>Phylogeny</topic><topic>Recombination</topic><topic>Recombination, Genetic</topic><topic>Sequence Analysis, DNA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Castelhano, Nadine</creatorcontrib><creatorcontrib>Araujo, Natalia M.</creatorcontrib><creatorcontrib>Arenas, Miguel</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Infection, genetics and evolution</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Castelhano, Nadine</au><au>Araujo, Natalia M.</au><au>Arenas, Miguel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Heterogeneous recombination among Hepatitis B virus genotypes</atitle><jtitle>Infection, genetics and evolution</jtitle><addtitle>Infect Genet Evol</addtitle><date>2017-10</date><risdate>2017</risdate><volume>54</volume><spage>486</spage><epage>490</epage><pages>486-490</pages><issn>1567-1348</issn><eissn>1567-7257</eissn><abstract>The rapid evolution of Hepatitis B virus (HBV) through both evolutionary forces, mutation and recombination, allows this virus to generate a large variety of adapted variants at both intra and inter-host levels. It can, for instance, generate drug resistance or the diverse viral genotypes that currently exist in the HBV epidemics. Concerning the latter, it is known that recombination played a major role in the emergence and genetic diversification of novel genotypes. In this regard, the quantification of viral recombination in each genotype can provide relevant information to devise expectations about the evolutionary trends of the epidemic. Here we measured the amount of this evolutionary force by estimating global and local recombination rates in >4700 HBV complete genome sequences corresponding to nine (A to I) HBV genotypes. Counterintuitively, we found that genotype E presents extremely high levels of recombination, followed by genotypes B and C. On the other hand, genotype G presents the lowest level, where recombination is almost negligible. We discuss these findings in the light of known characteristics of these genotypes. Additionally, we present a phylogenetic network to depict the evolutionary history of the studied HBV genotypes. This network clearly classified all genotypes into specific groups and indicated that diverse pairs of genotypes are derived from a common ancestor (i.e., C–I, D–E and, F–H) although still the origin of this virus presented large uncertainty. Altogether we conclude that the amount of observed recombination is heterogeneous among HBV genotypes and that this heterogeneity can influence on the future expansion of the epidemic.
•We quantified recombination in 9 HBV genotypes from >4700 genome sequences.•Recombination is heterogeneous among HBV genotypes at both global and local levels.•Inferences of the evolutionary history of HBV genotypes must consider recombination.•HBV genotypes can be classified with a recombination phylogenetic network.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>28827173</pmid><doi>10.1016/j.meegid.2017.08.015</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0002-0516-2717</orcidid></addata></record> |
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subjects | Base Composition Evolution, Molecular Genome, Viral Genotype HBV evolution HBV genome HBV genotypes Hepatitis B virus Hepatitis B virus - classification Hepatitis B virus - genetics Phylogeny Recombination Recombination, Genetic Sequence Analysis, DNA |
title | Heterogeneous recombination among Hepatitis B virus genotypes |
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