Extensive intrasubtype recombination in South African human immunodeficiency virus type 1 subtype C infections.

Recombinant human immunodeficiency virus type 1 (HIV-1) strains containing sequences from different viral genetic subtypes (intersubtype) and different lineages from within the same subtype (intrasubtype) have been observed. A consequence of recombination can be the distortion of the phylogenetic si...

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Hauptverfasser: Rousseau, C, Learn, G, Bhattacharya, T, Nickle, D, Heckerman, D, Chetty, S, Brander, C, Goulder, P, Walker, B, Kiepiela, P, Korber, B, Mullins, J
Format: Journal article
Sprache:English
Veröffentlicht: 2007
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author Rousseau, C
Learn, G
Bhattacharya, T
Nickle, D
Heckerman, D
Chetty, S
Brander, C
Goulder, P
Walker, B
Kiepiela, P
Korber, B
Mullins, J
author_facet Rousseau, C
Learn, G
Bhattacharya, T
Nickle, D
Heckerman, D
Chetty, S
Brander, C
Goulder, P
Walker, B
Kiepiela, P
Korber, B
Mullins, J
author_sort Rousseau, C
collection OXFORD
description Recombinant human immunodeficiency virus type 1 (HIV-1) strains containing sequences from different viral genetic subtypes (intersubtype) and different lineages from within the same subtype (intrasubtype) have been observed. A consequence of recombination can be the distortion of the phylogenetic signal. Several intersubtype recombinants have been identified; however, less is known about the frequency of intrasubtype recombination. For this study, near-full-length HIV-1 subtype C genomes from 270 individuals were evaluated for the presence of intrasubtype recombination. A sliding window schema (window, 2 kb; step, 385 bp) was used to partition the aligned sequences. The Shimodaira-Hasegawa test detected significant topological incongruence in 99.6% of the comparisons of the maximum-likelihood trees generated from each sequence partition, a result that could be explained by recombination. Using RECOMBINE, we detected significant levels of recombination using five random subsets of the sequences. With a set of 23 topologically consistent sequences used as references, bootscanning followed by the interactive informative site test defined recombination breakpoints. Using two multiple-comparison correction methods, 47% of the sequences showed significant evidence of recombination in both analyses. Estimated evolutionary rates were revised from 0.51%/year (95% confidence interval [CI], 0.39 to 0.53%) with all sequences to 0.46%/year (95% CI, 0.38 to 0.48%) with the putative recombinants removed. The timing of the subtype C epidemic origin was revised from 1961 (95% CI, 1947 to 1962) with all sequences to 1958 (95% CI, 1949 to 1960) with the putative recombinants removed. Thus, intrasubtype recombinants are common within the subtype C epidemic and these impact analyses of HIV-1 evolution.
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spelling oxford-uuid:bb4c133b-9d9f-4d6b-8b24-3ccf4c5038fc2022-03-27T05:15:58ZExtensive intrasubtype recombination in South African human immunodeficiency virus type 1 subtype C infections.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:bb4c133b-9d9f-4d6b-8b24-3ccf4c5038fcEnglishSymplectic Elements at Oxford2007Rousseau, CLearn, GBhattacharya, TNickle, DHeckerman, DChetty, SBrander, CGoulder, PWalker, BKiepiela, PKorber, BMullins, JRecombinant human immunodeficiency virus type 1 (HIV-1) strains containing sequences from different viral genetic subtypes (intersubtype) and different lineages from within the same subtype (intrasubtype) have been observed. A consequence of recombination can be the distortion of the phylogenetic signal. Several intersubtype recombinants have been identified; however, less is known about the frequency of intrasubtype recombination. For this study, near-full-length HIV-1 subtype C genomes from 270 individuals were evaluated for the presence of intrasubtype recombination. A sliding window schema (window, 2 kb; step, 385 bp) was used to partition the aligned sequences. The Shimodaira-Hasegawa test detected significant topological incongruence in 99.6% of the comparisons of the maximum-likelihood trees generated from each sequence partition, a result that could be explained by recombination. Using RECOMBINE, we detected significant levels of recombination using five random subsets of the sequences. With a set of 23 topologically consistent sequences used as references, bootscanning followed by the interactive informative site test defined recombination breakpoints. Using two multiple-comparison correction methods, 47% of the sequences showed significant evidence of recombination in both analyses. Estimated evolutionary rates were revised from 0.51%/year (95% confidence interval [CI], 0.39 to 0.53%) with all sequences to 0.46%/year (95% CI, 0.38 to 0.48%) with the putative recombinants removed. The timing of the subtype C epidemic origin was revised from 1961 (95% CI, 1947 to 1962) with all sequences to 1958 (95% CI, 1949 to 1960) with the putative recombinants removed. Thus, intrasubtype recombinants are common within the subtype C epidemic and these impact analyses of HIV-1 evolution.
spellingShingle Rousseau, C
Learn, G
Bhattacharya, T
Nickle, D
Heckerman, D
Chetty, S
Brander, C
Goulder, P
Walker, B
Kiepiela, P
Korber, B
Mullins, J
Extensive intrasubtype recombination in South African human immunodeficiency virus type 1 subtype C infections.
title Extensive intrasubtype recombination in South African human immunodeficiency virus type 1 subtype C infections.
title_full Extensive intrasubtype recombination in South African human immunodeficiency virus type 1 subtype C infections.
title_fullStr Extensive intrasubtype recombination in South African human immunodeficiency virus type 1 subtype C infections.
title_full_unstemmed Extensive intrasubtype recombination in South African human immunodeficiency virus type 1 subtype C infections.
title_short Extensive intrasubtype recombination in South African human immunodeficiency virus type 1 subtype C infections.
title_sort extensive intrasubtype recombination in south african human immunodeficiency virus type 1 subtype c infections
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