Complete Genome Sequence of CG-0018a-01 Establishes HIV-1 Subtype L
Background: The full spectrum of HIV-1 diversity can be found in Central Africa, including 2 divergent HIV-1 strains collected in 1983 and 1990 in Democratic Republic of Congo (DRC) that were preliminarily classified as group M subtype L. However, a third epidemiologically distinct subtype L genome...
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Veröffentlicht in: | Journal of acquired immune deficiency syndromes (1999) 2020-03, Vol.83 (3), p.319 |
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description | Background: The full spectrum of HIV-1 diversity can be found in Central Africa, including 2 divergent HIV-1 strains collected in 1983 and 1990 in Democratic Republic of Congo (DRC) that were preliminarily classified as group M subtype L. However, a third epidemiologically distinct subtype L genome must be identified to designate L as a true subtype. Methods: Specimen CG-0018a-01 was collected in 2001 in DRC as part of an HIV diversity study. Previous subgenomic HIV-1 sequences from this specimen branched closely with proposed subtype L references. Metagenomic next-generation sequencing (mNGS) and HIV-specific target-enriched (HIV-xGen) libraries were combined for NGS to extend genome coverage. mNGS reads were analyzed for the presence of other coinfections with the sequence-based ultrarapid pathogen identification bioinformatics pipeline. Results: A complete HIV-1 genome was generated with an average coverage depth of 47,783×. After bioinformatic analysis also identified hepatitis B virus reads, a complete hepatitis B virus genotype A genome was assembled with an average coverage depth of 73,830×. The CG-0018a-01 HIV-1 genome branched basal to the 2 previous putative subtype L strains with strong bootstrap support of 100. With no evidence of recombination present, the strain was classified as subtype L. Conclusions: The CG-0018a-01 HIV-1 genome establishes subtype L and confirms ongoing transmission in DRC as recently as 2001. Since CG-0018a-01 is more closely related to an ancestral strain than to isolates from 1983 to 1990, additional strains are likely circulating in DRC and possibly elsewhere. |
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However, a third epidemiologically distinct subtype L genome must be identified to designate L as a true subtype. Methods: Specimen CG-0018a-01 was collected in 2001 in DRC as part of an HIV diversity study. Previous subgenomic HIV-1 sequences from this specimen branched closely with proposed subtype L references. Metagenomic next-generation sequencing (mNGS) and HIV-specific target-enriched (HIV-xGen) libraries were combined for NGS to extend genome coverage. mNGS reads were analyzed for the presence of other coinfections with the sequence-based ultrarapid pathogen identification bioinformatics pipeline. Results: A complete HIV-1 genome was generated with an average coverage depth of 47,783×. After bioinformatic analysis also identified hepatitis B virus reads, a complete hepatitis B virus genotype A genome was assembled with an average coverage depth of 73,830×. The CG-0018a-01 HIV-1 genome branched basal to the 2 previous putative subtype L strains with strong bootstrap support of 100. With no evidence of recombination present, the strain was classified as subtype L. Conclusions: The CG-0018a-01 HIV-1 genome establishes subtype L and confirms ongoing transmission in DRC as recently as 2001. Since CG-0018a-01 is more closely related to an ancestral strain than to isolates from 1983 to 1990, additional strains are likely circulating in DRC and possibly elsewhere.</description><identifier>ISSN: 1525-4135</identifier><identifier>EISSN: 1944-7884</identifier><identifier>DOI: 10.1097/QAI.0000000000002246</identifier><language>eng</language><publisher>Hagerstown: Lippincott Williams & Wilkins Ovid Technologies</publisher><subject>Bioinformatics ; Epidemiology ; Genomes ; Genotypes ; Hepatitis ; Hepatitis B ; HIV ; Human immunodeficiency virus ; Metagenomics ; Next-generation sequencing ; Nucleotide sequence ; Recombination ; Strains (organisms) ; Viruses</subject><ispartof>Journal of acquired immune deficiency syndromes (1999), 2020-03, Vol.83 (3), p.319</ispartof><rights>Copyright Lippincott Williams & Wilkins Ovid Technologies Mar 1, 2020</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Yamaguchi, Julie</creatorcontrib><creatorcontrib>Vallari, Ana</creatorcontrib><creatorcontrib>McArthur, Carole</creatorcontrib><creatorcontrib>Sthreshley, Larry</creatorcontrib><creatorcontrib>Cloherty, Gavin A</creatorcontrib><creatorcontrib>Berg, Michael G</creatorcontrib><creatorcontrib>Rodgers, Mary A</creatorcontrib><title>Complete Genome Sequence of CG-0018a-01 Establishes HIV-1 Subtype L</title><title>Journal of acquired immune deficiency syndromes (1999)</title><description>Background: The full spectrum of HIV-1 diversity can be found in Central Africa, including 2 divergent HIV-1 strains collected in 1983 and 1990 in Democratic Republic of Congo (DRC) that were preliminarily classified as group M subtype L. However, a third epidemiologically distinct subtype L genome must be identified to designate L as a true subtype. Methods: Specimen CG-0018a-01 was collected in 2001 in DRC as part of an HIV diversity study. Previous subgenomic HIV-1 sequences from this specimen branched closely with proposed subtype L references. Metagenomic next-generation sequencing (mNGS) and HIV-specific target-enriched (HIV-xGen) libraries were combined for NGS to extend genome coverage. mNGS reads were analyzed for the presence of other coinfections with the sequence-based ultrarapid pathogen identification bioinformatics pipeline. Results: A complete HIV-1 genome was generated with an average coverage depth of 47,783×. After bioinformatic analysis also identified hepatitis B virus reads, a complete hepatitis B virus genotype A genome was assembled with an average coverage depth of 73,830×. The CG-0018a-01 HIV-1 genome branched basal to the 2 previous putative subtype L strains with strong bootstrap support of 100. With no evidence of recombination present, the strain was classified as subtype L. Conclusions: The CG-0018a-01 HIV-1 genome establishes subtype L and confirms ongoing transmission in DRC as recently as 2001. Since CG-0018a-01 is more closely related to an ancestral strain than to isolates from 1983 to 1990, additional strains are likely circulating in DRC and possibly elsewhere.</description><subject>Bioinformatics</subject><subject>Epidemiology</subject><subject>Genomes</subject><subject>Genotypes</subject><subject>Hepatitis</subject><subject>Hepatitis B</subject><subject>HIV</subject><subject>Human immunodeficiency virus</subject><subject>Metagenomics</subject><subject>Next-generation sequencing</subject><subject>Nucleotide sequence</subject><subject>Recombination</subject><subject>Strains (organisms)</subject><subject>Viruses</subject><issn>1525-4135</issn><issn>1944-7884</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqNjEsLgkAYRYcoyB7_oMVA67F5-VqGmAptwmgrGp-UqGOOLvr3zaJFy87mXriHi9COUZvRwDtcjqlNf-BcujNksUBK4vm-nJvucIdIJpwlWmldU8pcKQMLhaFq-wZGwDF0qgWcwWuC7g5YVTiMiRH9glCGIz0WZfPUD9A4SW-E4Wwqx3cP-LxBi6poNGy_uUb7U3QNE9IPypzpMa_VNHRmyrnwmGcQQvxnfQBf6z48</recordid><startdate>20200301</startdate><enddate>20200301</enddate><creator>Yamaguchi, Julie</creator><creator>Vallari, Ana</creator><creator>McArthur, Carole</creator><creator>Sthreshley, Larry</creator><creator>Cloherty, Gavin A</creator><creator>Berg, Michael G</creator><creator>Rodgers, Mary A</creator><general>Lippincott Williams & Wilkins Ovid Technologies</general><scope>7T2</scope><scope>7T5</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope></search><sort><creationdate>20200301</creationdate><title>Complete Genome Sequence of CG-0018a-01 Establishes HIV-1 Subtype L</title><author>Yamaguchi, Julie ; Vallari, Ana ; McArthur, Carole ; Sthreshley, Larry ; Cloherty, Gavin A ; Berg, Michael G ; Rodgers, Mary A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_23717777333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Bioinformatics</topic><topic>Epidemiology</topic><topic>Genomes</topic><topic>Genotypes</topic><topic>Hepatitis</topic><topic>Hepatitis B</topic><topic>HIV</topic><topic>Human immunodeficiency virus</topic><topic>Metagenomics</topic><topic>Next-generation sequencing</topic><topic>Nucleotide sequence</topic><topic>Recombination</topic><topic>Strains (organisms)</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yamaguchi, Julie</creatorcontrib><creatorcontrib>Vallari, Ana</creatorcontrib><creatorcontrib>McArthur, Carole</creatorcontrib><creatorcontrib>Sthreshley, Larry</creatorcontrib><creatorcontrib>Cloherty, Gavin A</creatorcontrib><creatorcontrib>Berg, Michael G</creatorcontrib><creatorcontrib>Rodgers, Mary A</creatorcontrib><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><jtitle>Journal of acquired immune deficiency syndromes (1999)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yamaguchi, Julie</au><au>Vallari, Ana</au><au>McArthur, Carole</au><au>Sthreshley, Larry</au><au>Cloherty, Gavin A</au><au>Berg, Michael G</au><au>Rodgers, Mary A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Complete Genome Sequence of CG-0018a-01 Establishes HIV-1 Subtype L</atitle><jtitle>Journal of acquired immune deficiency syndromes (1999)</jtitle><date>2020-03-01</date><risdate>2020</risdate><volume>83</volume><issue>3</issue><spage>319</spage><pages>319-</pages><issn>1525-4135</issn><eissn>1944-7884</eissn><abstract>Background: The full spectrum of HIV-1 diversity can be found in Central Africa, including 2 divergent HIV-1 strains collected in 1983 and 1990 in Democratic Republic of Congo (DRC) that were preliminarily classified as group M subtype L. However, a third epidemiologically distinct subtype L genome must be identified to designate L as a true subtype. Methods: Specimen CG-0018a-01 was collected in 2001 in DRC as part of an HIV diversity study. Previous subgenomic HIV-1 sequences from this specimen branched closely with proposed subtype L references. Metagenomic next-generation sequencing (mNGS) and HIV-specific target-enriched (HIV-xGen) libraries were combined for NGS to extend genome coverage. mNGS reads were analyzed for the presence of other coinfections with the sequence-based ultrarapid pathogen identification bioinformatics pipeline. Results: A complete HIV-1 genome was generated with an average coverage depth of 47,783×. After bioinformatic analysis also identified hepatitis B virus reads, a complete hepatitis B virus genotype A genome was assembled with an average coverage depth of 73,830×. The CG-0018a-01 HIV-1 genome branched basal to the 2 previous putative subtype L strains with strong bootstrap support of 100. With no evidence of recombination present, the strain was classified as subtype L. Conclusions: The CG-0018a-01 HIV-1 genome establishes subtype L and confirms ongoing transmission in DRC as recently as 2001. Since CG-0018a-01 is more closely related to an ancestral strain than to isolates from 1983 to 1990, additional strains are likely circulating in DRC and possibly elsewhere.</abstract><cop>Hagerstown</cop><pub>Lippincott Williams & Wilkins Ovid Technologies</pub><doi>10.1097/QAI.0000000000002246</doi></addata></record> |
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subjects | Bioinformatics Epidemiology Genomes Genotypes Hepatitis Hepatitis B HIV Human immunodeficiency virus Metagenomics Next-generation sequencing Nucleotide sequence Recombination Strains (organisms) Viruses |
title | Complete Genome Sequence of CG-0018a-01 Establishes HIV-1 Subtype L |
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