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Phylogenetics of HIV-1 subtype G env: Greater complexity and older origins than previously reported
•Subtype G dates to ∼1953, approximately 13years older than previously reported.•Subtype G env phylogeny has a complex structure including 7 distinct, old lineages.•The G-attributed portion of CRF25_cpx env is derived from a lineage older than G. HIV-1 subtype G has played an early and central role...
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Published in: | Infection, genetics and evolution genetics and evolution, 2015-10, Vol.35, p.9-18 |
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creator | Tongo, Marcel Essomba, René G. Nindo, Frederick Abrahams, Fatima Nanfack, Aubin Joseph Fokam, Joseph Takou, Desire Torimiro, Judith N. Mpoudi-Ngole, Eitel Burgers, Wendy A. Martin, Darren P. Dorfman, Jeffrey R. |
description | •Subtype G dates to ∼1953, approximately 13years older than previously reported.•Subtype G env phylogeny has a complex structure including 7 distinct, old lineages.•The G-attributed portion of CRF25_cpx env is derived from a lineage older than G.
HIV-1 subtype G has played an early and central role in the emergent complexity of the HIV-1 group M (HIV-1M) epidemic in central/west Africa. Here, we analysed new subtype G env sequences sampled from 8 individuals in Yaoundé, Cameroon during 2007–2010, together with all publically available subtype G-attributed full-length env sequences with known sampling dates and locations. We inferred that the most recent common ancestor (MRCA) of the analysed subtype G env sequences most likely occurred in ∼1953 (95% Highest Posterior Density interval [HPD] 1939–1963): about 15years earlier than previous estimates. We found that the subtype G env phylogeny has a complex structure including seven distinct lineages, each likely dating back to the late 1960s or early 1970s. Sequences from Angola, Gabon and the Democratic Republic of Congo failed to group consistently in these lineages, possibly because they are related to more ancient sequences that are poorly sampled. The circulating recombinant form (CRF), CRF06_cpx env sequences but not CRF25_cpx env sequences are phylogenetically nested within the subtype G clade. This confirms that the CRF06_cpx env plausibly was derived through recombination from a subtype G parent, and suggests that the CRF25_cpx env was likely derived from an HIV-1M lineage related to the MRCA of subtype G that has remained undiscovered and may be extinct. Overall, this fills important gaps in our knowledge of the early events in the spread of HIV-1M. |
doi_str_mv | 10.1016/j.meegid.2015.07.017 |
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HIV-1 subtype G has played an early and central role in the emergent complexity of the HIV-1 group M (HIV-1M) epidemic in central/west Africa. Here, we analysed new subtype G env sequences sampled from 8 individuals in Yaoundé, Cameroon during 2007–2010, together with all publically available subtype G-attributed full-length env sequences with known sampling dates and locations. We inferred that the most recent common ancestor (MRCA) of the analysed subtype G env sequences most likely occurred in ∼1953 (95% Highest Posterior Density interval [HPD] 1939–1963): about 15years earlier than previous estimates. We found that the subtype G env phylogeny has a complex structure including seven distinct lineages, each likely dating back to the late 1960s or early 1970s. Sequences from Angola, Gabon and the Democratic Republic of Congo failed to group consistently in these lineages, possibly because they are related to more ancient sequences that are poorly sampled. The circulating recombinant form (CRF), CRF06_cpx env sequences but not CRF25_cpx env sequences are phylogenetically nested within the subtype G clade. This confirms that the CRF06_cpx env plausibly was derived through recombination from a subtype G parent, and suggests that the CRF25_cpx env was likely derived from an HIV-1M lineage related to the MRCA of subtype G that has remained undiscovered and may be extinct. Overall, this fills important gaps in our knowledge of the early events in the spread of HIV-1M.</description><identifier>ISSN: 1567-1348</identifier><identifier>EISSN: 1567-7257</identifier><identifier>DOI: 10.1016/j.meegid.2015.07.017</identifier><identifier>PMID: 26190450</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Africa, Central ; Angola ; CRF ; env Gene Products, Human Immunodeficiency Virus - genetics ; HIV Infections - virology ; HIV-1 ; HIV-1 - classification ; HIV-1 - genetics ; HIV-1 - isolation & purification ; HIV-1 - metabolism ; Humans ; Molecular Sequence Data ; Phylogenetic analysis ; Phylogeny ; Phylogeography ; Recombination, Genetic ; Subtype G</subject><ispartof>Infection, genetics and evolution, 2015-10, Vol.35, p.9-18</ispartof><rights>2015 Elsevier B.V.</rights><rights>Copyright © 2015 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c362t-c629998089821465b7568fae93a58139cd2c3b6dd60c9090dd430ef774305c5c3</citedby><cites>FETCH-LOGICAL-c362t-c629998089821465b7568fae93a58139cd2c3b6dd60c9090dd430ef774305c5c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26190450$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tongo, Marcel</creatorcontrib><creatorcontrib>Essomba, René G.</creatorcontrib><creatorcontrib>Nindo, Frederick</creatorcontrib><creatorcontrib>Abrahams, Fatima</creatorcontrib><creatorcontrib>Nanfack, Aubin Joseph</creatorcontrib><creatorcontrib>Fokam, Joseph</creatorcontrib><creatorcontrib>Takou, Desire</creatorcontrib><creatorcontrib>Torimiro, Judith N.</creatorcontrib><creatorcontrib>Mpoudi-Ngole, Eitel</creatorcontrib><creatorcontrib>Burgers, Wendy A.</creatorcontrib><creatorcontrib>Martin, Darren P.</creatorcontrib><creatorcontrib>Dorfman, Jeffrey R.</creatorcontrib><title>Phylogenetics of HIV-1 subtype G env: Greater complexity and older origins than previously reported</title><title>Infection, genetics and evolution</title><addtitle>Infect Genet Evol</addtitle><description>•Subtype G dates to ∼1953, approximately 13years older than previously reported.•Subtype G env phylogeny has a complex structure including 7 distinct, old lineages.•The G-attributed portion of CRF25_cpx env is derived from a lineage older than G.
HIV-1 subtype G has played an early and central role in the emergent complexity of the HIV-1 group M (HIV-1M) epidemic in central/west Africa. Here, we analysed new subtype G env sequences sampled from 8 individuals in Yaoundé, Cameroon during 2007–2010, together with all publically available subtype G-attributed full-length env sequences with known sampling dates and locations. We inferred that the most recent common ancestor (MRCA) of the analysed subtype G env sequences most likely occurred in ∼1953 (95% Highest Posterior Density interval [HPD] 1939–1963): about 15years earlier than previous estimates. We found that the subtype G env phylogeny has a complex structure including seven distinct lineages, each likely dating back to the late 1960s or early 1970s. Sequences from Angola, Gabon and the Democratic Republic of Congo failed to group consistently in these lineages, possibly because they are related to more ancient sequences that are poorly sampled. The circulating recombinant form (CRF), CRF06_cpx env sequences but not CRF25_cpx env sequences are phylogenetically nested within the subtype G clade. This confirms that the CRF06_cpx env plausibly was derived through recombination from a subtype G parent, and suggests that the CRF25_cpx env was likely derived from an HIV-1M lineage related to the MRCA of subtype G that has remained undiscovered and may be extinct. Overall, this fills important gaps in our knowledge of the early events in the spread of HIV-1M.</description><subject>Africa, Central</subject><subject>Angola</subject><subject>CRF</subject><subject>env Gene Products, Human Immunodeficiency Virus - genetics</subject><subject>HIV Infections - virology</subject><subject>HIV-1</subject><subject>HIV-1 - classification</subject><subject>HIV-1 - genetics</subject><subject>HIV-1 - isolation & purification</subject><subject>HIV-1 - metabolism</subject><subject>Humans</subject><subject>Molecular Sequence Data</subject><subject>Phylogenetic analysis</subject><subject>Phylogeny</subject><subject>Phylogeography</subject><subject>Recombination, Genetic</subject><subject>Subtype G</subject><issn>1567-1348</issn><issn>1567-7257</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNp9kEtr3DAQgEVJaR7tPyhBx1zs6GFJVg6FEppNIJAe2l6FVxpvtNiWK2mX-N9XYTc95jTD8M3rQ-grJTUlVF5v6xFg413NCBU1UTWh6gM6o0KqSjGhTo455U17is5T2pJCENZ-QqdMUk0aQc6Q_fm8DGEDE2RvEw49vn_4U1Gcduu8zIBXGKb9DV5F6DJEbMM4D_Di84K7yeEwuFIM0W_8lHB-7iY8R9j7sEvDgiPMIWZwn9HHvhsSfDnGC_T77sev2_vq8Wn1cPv9sbJcslxZybTWLWl1y2gjxVoJ2fYdaN6JlnJtHbN8LZ2TxGqiiXMNJ9ArVYKwwvILdHWYO8fwdwcpm9EnC8PQTVAuMlRR1bScMl7Q5oDaGFKK0Js5-rGLi6HEvOo1W3PQa171GqJMkVfaLo8bdusR3P-mN58F-HYAoPy59xBNsh4mC85HsNm44N_f8A-584z5</recordid><startdate>201510</startdate><enddate>201510</enddate><creator>Tongo, Marcel</creator><creator>Essomba, René G.</creator><creator>Nindo, Frederick</creator><creator>Abrahams, Fatima</creator><creator>Nanfack, Aubin Joseph</creator><creator>Fokam, Joseph</creator><creator>Takou, Desire</creator><creator>Torimiro, Judith N.</creator><creator>Mpoudi-Ngole, Eitel</creator><creator>Burgers, Wendy A.</creator><creator>Martin, Darren P.</creator><creator>Dorfman, Jeffrey R.</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></search><sort><creationdate>201510</creationdate><title>Phylogenetics of HIV-1 subtype G env: Greater complexity and older origins than previously reported</title><author>Tongo, Marcel ; Essomba, René G. ; Nindo, Frederick ; Abrahams, Fatima ; Nanfack, Aubin Joseph ; Fokam, Joseph ; Takou, Desire ; Torimiro, Judith N. ; Mpoudi-Ngole, Eitel ; Burgers, Wendy A. ; Martin, Darren P. ; Dorfman, Jeffrey R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c362t-c629998089821465b7568fae93a58139cd2c3b6dd60c9090dd430ef774305c5c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Africa, Central</topic><topic>Angola</topic><topic>CRF</topic><topic>env Gene Products, Human Immunodeficiency Virus - genetics</topic><topic>HIV Infections - virology</topic><topic>HIV-1</topic><topic>HIV-1 - classification</topic><topic>HIV-1 - genetics</topic><topic>HIV-1 - isolation & purification</topic><topic>HIV-1 - metabolism</topic><topic>Humans</topic><topic>Molecular Sequence Data</topic><topic>Phylogenetic analysis</topic><topic>Phylogeny</topic><topic>Phylogeography</topic><topic>Recombination, Genetic</topic><topic>Subtype G</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tongo, Marcel</creatorcontrib><creatorcontrib>Essomba, René G.</creatorcontrib><creatorcontrib>Nindo, Frederick</creatorcontrib><creatorcontrib>Abrahams, Fatima</creatorcontrib><creatorcontrib>Nanfack, Aubin Joseph</creatorcontrib><creatorcontrib>Fokam, Joseph</creatorcontrib><creatorcontrib>Takou, Desire</creatorcontrib><creatorcontrib>Torimiro, Judith N.</creatorcontrib><creatorcontrib>Mpoudi-Ngole, Eitel</creatorcontrib><creatorcontrib>Burgers, Wendy A.</creatorcontrib><creatorcontrib>Martin, Darren P.</creatorcontrib><creatorcontrib>Dorfman, Jeffrey R.</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>Tongo, Marcel</au><au>Essomba, René G.</au><au>Nindo, Frederick</au><au>Abrahams, Fatima</au><au>Nanfack, Aubin Joseph</au><au>Fokam, Joseph</au><au>Takou, Desire</au><au>Torimiro, Judith N.</au><au>Mpoudi-Ngole, Eitel</au><au>Burgers, Wendy A.</au><au>Martin, Darren P.</au><au>Dorfman, Jeffrey R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phylogenetics of HIV-1 subtype G env: Greater complexity and older origins than previously reported</atitle><jtitle>Infection, genetics and evolution</jtitle><addtitle>Infect Genet Evol</addtitle><date>2015-10</date><risdate>2015</risdate><volume>35</volume><spage>9</spage><epage>18</epage><pages>9-18</pages><issn>1567-1348</issn><eissn>1567-7257</eissn><abstract>•Subtype G dates to ∼1953, approximately 13years older than previously reported.•Subtype G env phylogeny has a complex structure including 7 distinct, old lineages.•The G-attributed portion of CRF25_cpx env is derived from a lineage older than G.
HIV-1 subtype G has played an early and central role in the emergent complexity of the HIV-1 group M (HIV-1M) epidemic in central/west Africa. Here, we analysed new subtype G env sequences sampled from 8 individuals in Yaoundé, Cameroon during 2007–2010, together with all publically available subtype G-attributed full-length env sequences with known sampling dates and locations. We inferred that the most recent common ancestor (MRCA) of the analysed subtype G env sequences most likely occurred in ∼1953 (95% Highest Posterior Density interval [HPD] 1939–1963): about 15years earlier than previous estimates. We found that the subtype G env phylogeny has a complex structure including seven distinct lineages, each likely dating back to the late 1960s or early 1970s. Sequences from Angola, Gabon and the Democratic Republic of Congo failed to group consistently in these lineages, possibly because they are related to more ancient sequences that are poorly sampled. The circulating recombinant form (CRF), CRF06_cpx env sequences but not CRF25_cpx env sequences are phylogenetically nested within the subtype G clade. This confirms that the CRF06_cpx env plausibly was derived through recombination from a subtype G parent, and suggests that the CRF25_cpx env was likely derived from an HIV-1M lineage related to the MRCA of subtype G that has remained undiscovered and may be extinct. Overall, this fills important gaps in our knowledge of the early events in the spread of HIV-1M.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>26190450</pmid><doi>10.1016/j.meegid.2015.07.017</doi><tpages>10</tpages></addata></record> |
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subjects | Africa, Central Angola CRF env Gene Products, Human Immunodeficiency Virus - genetics HIV Infections - virology HIV-1 HIV-1 - classification HIV-1 - genetics HIV-1 - isolation & purification HIV-1 - metabolism Humans Molecular Sequence Data Phylogenetic analysis Phylogeny Phylogeography Recombination, Genetic Subtype G |
title | Phylogenetics of HIV-1 subtype G env: Greater complexity and older origins than previously reported |
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