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Brief Report: 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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Autores principales: Yamaguchi, Julie, Vallari, Ana, McArthur, Carole, Sthreshley, Larry, Cloherty, Gavin A., Berg, Michael G., Rodgers, Mary A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JAIDS Journal of Acquired Immune Deficiency Syndromes 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7012332/
https://www.ncbi.nlm.nih.gov/pubmed/31693506
http://dx.doi.org/10.1097/QAI.0000000000002246
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author Yamaguchi, Julie
Vallari, Ana
McArthur, Carole
Sthreshley, Larry
Cloherty, Gavin A.
Berg, Michael G.
Rodgers, Mary A.
author_facet Yamaguchi, Julie
Vallari, Ana
McArthur, Carole
Sthreshley, Larry
Cloherty, Gavin A.
Berg, Michael G.
Rodgers, Mary A.
author_sort Yamaguchi, Julie
collection PubMed
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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spelling pubmed-70123322020-02-19 Brief Report: Complete Genome Sequence of CG-0018a-01 Establishes HIV-1 Subtype L Yamaguchi, Julie Vallari, Ana McArthur, Carole Sthreshley, Larry Cloherty, Gavin A. Berg, Michael G. Rodgers, Mary A. J Acquir Immune Defic Syndr Basic Science 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. JAIDS Journal of Acquired Immune Deficiency Syndromes 2020-03-01 2019-11-06 /pmc/articles/PMC7012332/ /pubmed/31693506 http://dx.doi.org/10.1097/QAI.0000000000002246 Text en Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Basic Science
Yamaguchi, Julie
Vallari, Ana
McArthur, Carole
Sthreshley, Larry
Cloherty, Gavin A.
Berg, Michael G.
Rodgers, Mary A.
Brief Report: Complete Genome Sequence of CG-0018a-01 Establishes HIV-1 Subtype L
title Brief Report: Complete Genome Sequence of CG-0018a-01 Establishes HIV-1 Subtype L
title_full Brief Report: Complete Genome Sequence of CG-0018a-01 Establishes HIV-1 Subtype L
title_fullStr Brief Report: Complete Genome Sequence of CG-0018a-01 Establishes HIV-1 Subtype L
title_full_unstemmed Brief Report: Complete Genome Sequence of CG-0018a-01 Establishes HIV-1 Subtype L
title_short Brief Report: Complete Genome Sequence of CG-0018a-01 Establishes HIV-1 Subtype L
title_sort brief report: complete genome sequence of cg-0018a-01 establishes hiv-1 subtype l
topic Basic Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7012332/
https://www.ncbi.nlm.nih.gov/pubmed/31693506
http://dx.doi.org/10.1097/QAI.0000000000002246
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