Functional characteristics of HIV-1 subtype C compatible with increased heterosexual transmissibility.

BACKGROUND: Despite the existence of over 50 subtypes and circulating recombinant forms of HIV-1, subtype C dominates the heterosexual pandemic causing approximately 56% of all infections. OBJECTIVE: To evaluate whether viral genetic factors may contribute to the observed subtype-C predominance. MET...

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Egile Nagusiak: Walter, B, Armitage, A, Graham, S, de Oliveira, T, Skinhøj, P, Jones, E, Stuart, D, Mcmichael, A, Chesebro, B, Iversen, A
Formatua: Journal article
Hizkuntza:English
Argitaratua: 2009
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author Walter, B
Armitage, A
Graham, S
de Oliveira, T
Skinhøj, P
Jones, E
Stuart, D
Mcmichael, A
Chesebro, B
Iversen, A
author_facet Walter, B
Armitage, A
Graham, S
de Oliveira, T
Skinhøj, P
Jones, E
Stuart, D
Mcmichael, A
Chesebro, B
Iversen, A
author_sort Walter, B
collection OXFORD
description BACKGROUND: Despite the existence of over 50 subtypes and circulating recombinant forms of HIV-1, subtype C dominates the heterosexual pandemic causing approximately 56% of all infections. OBJECTIVE: To evaluate whether viral genetic factors may contribute to the observed subtype-C predominance. METHODS: Chimeric viruses were generated using V1-V3 envelope fragments from a subtype-A/C dually infected woman with preferential genital replication of subtype C. Viral adaptation, spread and cell fusion ability were evaluated in vitro using peripheral blood mononuclear cells and HeLa-CD4-CCR5 cell lines, sequencing and cloning. Structural modeling was performed using a crystal structure of gp120-CD4-X5. Phylogenetic analysis was done using subtype-A, subtype-B and subtype-C sequences from blood and cervix of 37 infected women and database sequences. RESULTS: We identified two envelope motifs, compact V1-V2 loops and V3-316T, which are found at high frequency throughout subtype-C evolution and affect gp120 interactions with CD4 and CCR5, respectively. When a V1-Delta5 deletion or V3-A316T was incorporated into subtype A, each increased viral fusion and spread several fold in peripheral blood mononuclear cell and cell lines with low CCR5 expression. Structural modeling suggested the formation of an additional hydrogen bond between V3 and CCR5. Moreover, we found preferential selection of HIV with 316T and/or extremely short V1-V2 loops in cervices of three women infected with subtypes A/C, B or C. CONCLUSION: As CD4-CCR5-T cells are key targets for genital HIV infection and cervical selection can favor compact V1-V2 loops and 316T, which increase viral infectivity, we propose that these conserved subtype-C motifs may contribute to transmission and spread of this subtype.
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spelling oxford-uuid:ba60ea5c-25c8-4571-bf39-b1eb264538b52022-03-27T05:09:19ZFunctional characteristics of HIV-1 subtype C compatible with increased heterosexual transmissibility.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:ba60ea5c-25c8-4571-bf39-b1eb264538b5EnglishSymplectic Elements at Oxford2009Walter, BArmitage, AGraham, Sde Oliveira, TSkinhøj, PJones, EStuart, DMcmichael, AChesebro, BIversen, ABACKGROUND: Despite the existence of over 50 subtypes and circulating recombinant forms of HIV-1, subtype C dominates the heterosexual pandemic causing approximately 56% of all infections. OBJECTIVE: To evaluate whether viral genetic factors may contribute to the observed subtype-C predominance. METHODS: Chimeric viruses were generated using V1-V3 envelope fragments from a subtype-A/C dually infected woman with preferential genital replication of subtype C. Viral adaptation, spread and cell fusion ability were evaluated in vitro using peripheral blood mononuclear cells and HeLa-CD4-CCR5 cell lines, sequencing and cloning. Structural modeling was performed using a crystal structure of gp120-CD4-X5. Phylogenetic analysis was done using subtype-A, subtype-B and subtype-C sequences from blood and cervix of 37 infected women and database sequences. RESULTS: We identified two envelope motifs, compact V1-V2 loops and V3-316T, which are found at high frequency throughout subtype-C evolution and affect gp120 interactions with CD4 and CCR5, respectively. When a V1-Delta5 deletion or V3-A316T was incorporated into subtype A, each increased viral fusion and spread several fold in peripheral blood mononuclear cell and cell lines with low CCR5 expression. Structural modeling suggested the formation of an additional hydrogen bond between V3 and CCR5. Moreover, we found preferential selection of HIV with 316T and/or extremely short V1-V2 loops in cervices of three women infected with subtypes A/C, B or C. CONCLUSION: As CD4-CCR5-T cells are key targets for genital HIV infection and cervical selection can favor compact V1-V2 loops and 316T, which increase viral infectivity, we propose that these conserved subtype-C motifs may contribute to transmission and spread of this subtype.
spellingShingle Walter, B
Armitage, A
Graham, S
de Oliveira, T
Skinhøj, P
Jones, E
Stuart, D
Mcmichael, A
Chesebro, B
Iversen, A
Functional characteristics of HIV-1 subtype C compatible with increased heterosexual transmissibility.
title Functional characteristics of HIV-1 subtype C compatible with increased heterosexual transmissibility.
title_full Functional characteristics of HIV-1 subtype C compatible with increased heterosexual transmissibility.
title_fullStr Functional characteristics of HIV-1 subtype C compatible with increased heterosexual transmissibility.
title_full_unstemmed Functional characteristics of HIV-1 subtype C compatible with increased heterosexual transmissibility.
title_short Functional characteristics of HIV-1 subtype C compatible with increased heterosexual transmissibility.
title_sort functional characteristics of hiv 1 subtype c compatible with increased heterosexual transmissibility
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