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Transmission of highly virulent CXCR4 tropic HIV-1 through the mucosal route in an individual with a wild-type CCR5 genotype
Nearly all transmitted/founder (T/F) HIV-1 are CCR5 (R5)-tropic. While previous evidence suggested that CXCR4 (X4)-tropic HIV-1 are transmissible, detection was not at the earliest stages of acute infection. Here, we identified an X4-tropic T/F HIV-1 in a participant in acute infection cohort. Corec...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Journal Experts
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10571614/ https://www.ncbi.nlm.nih.gov/pubmed/37841838 http://dx.doi.org/10.21203/rs.3.rs-3359209/v1 |
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author | Song, Hongshuo Marichannegowda, Manukumar Setua, Saini Bose, Meera Sanders-Buell, Eric King, David Zemil, Michelle Wieczorek, Lindsay Diaz-Mendez, Felisa Chomont, Nicolas Thomas, Rasmi Francisco, Leilani Eller, Leigh Anne Polonis, Victoria Tovanabutra, Sodsai Tagaya, Yutaka Michael, Nelson Robb, Merlin |
author_facet | Song, Hongshuo Marichannegowda, Manukumar Setua, Saini Bose, Meera Sanders-Buell, Eric King, David Zemil, Michelle Wieczorek, Lindsay Diaz-Mendez, Felisa Chomont, Nicolas Thomas, Rasmi Francisco, Leilani Eller, Leigh Anne Polonis, Victoria Tovanabutra, Sodsai Tagaya, Yutaka Michael, Nelson Robb, Merlin |
author_sort | Song, Hongshuo |
collection | PubMed |
description | Nearly all transmitted/founder (T/F) HIV-1 are CCR5 (R5)-tropic. While previous evidence suggested that CXCR4 (X4)-tropic HIV-1 are transmissible, detection was not at the earliest stages of acute infection. Here, we identified an X4-tropic T/F HIV-1 in a participant in acute infection cohort. Coreceptor assays demonstrated that this T/F virus is strictly CXCR4 tropic. The participant experienced significantly faster CD4 depletion compared with R5 virus infected participants in the same cohort. Naïve and central memory CD4 subsets declined faster than effector and transitional memory subsets. All CD4 subsets, including naïve, were productively infected. Increased CD4(+) T cell activation was observed over time. This X4-tropic T/F virus is resistant to broadly neutralizing antibodies (bNAbs) targeting V1/V2 and V3 regions. These findings demonstrate that X4-tropic HIV-1 is transmissible through the mucosal route in people with the wild-type CCR5 genotype and have implications for understanding the transmissibility and immunopathogenesis of X4-tropic HIV-1. |
format | Online Article Text |
id | pubmed-10571614 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Journal Experts |
record_format | MEDLINE/PubMed |
spelling | pubmed-105716142023-10-14 Transmission of highly virulent CXCR4 tropic HIV-1 through the mucosal route in an individual with a wild-type CCR5 genotype Song, Hongshuo Marichannegowda, Manukumar Setua, Saini Bose, Meera Sanders-Buell, Eric King, David Zemil, Michelle Wieczorek, Lindsay Diaz-Mendez, Felisa Chomont, Nicolas Thomas, Rasmi Francisco, Leilani Eller, Leigh Anne Polonis, Victoria Tovanabutra, Sodsai Tagaya, Yutaka Michael, Nelson Robb, Merlin Res Sq Article Nearly all transmitted/founder (T/F) HIV-1 are CCR5 (R5)-tropic. While previous evidence suggested that CXCR4 (X4)-tropic HIV-1 are transmissible, detection was not at the earliest stages of acute infection. Here, we identified an X4-tropic T/F HIV-1 in a participant in acute infection cohort. Coreceptor assays demonstrated that this T/F virus is strictly CXCR4 tropic. The participant experienced significantly faster CD4 depletion compared with R5 virus infected participants in the same cohort. Naïve and central memory CD4 subsets declined faster than effector and transitional memory subsets. All CD4 subsets, including naïve, were productively infected. Increased CD4(+) T cell activation was observed over time. This X4-tropic T/F virus is resistant to broadly neutralizing antibodies (bNAbs) targeting V1/V2 and V3 regions. These findings demonstrate that X4-tropic HIV-1 is transmissible through the mucosal route in people with the wild-type CCR5 genotype and have implications for understanding the transmissibility and immunopathogenesis of X4-tropic HIV-1. American Journal Experts 2023-09-25 /pmc/articles/PMC10571614/ /pubmed/37841838 http://dx.doi.org/10.21203/rs.3.rs-3359209/v1 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Song, Hongshuo Marichannegowda, Manukumar Setua, Saini Bose, Meera Sanders-Buell, Eric King, David Zemil, Michelle Wieczorek, Lindsay Diaz-Mendez, Felisa Chomont, Nicolas Thomas, Rasmi Francisco, Leilani Eller, Leigh Anne Polonis, Victoria Tovanabutra, Sodsai Tagaya, Yutaka Michael, Nelson Robb, Merlin Transmission of highly virulent CXCR4 tropic HIV-1 through the mucosal route in an individual with a wild-type CCR5 genotype |
title | Transmission of highly virulent CXCR4 tropic HIV-1 through the mucosal route in an individual with a wild-type CCR5 genotype |
title_full | Transmission of highly virulent CXCR4 tropic HIV-1 through the mucosal route in an individual with a wild-type CCR5 genotype |
title_fullStr | Transmission of highly virulent CXCR4 tropic HIV-1 through the mucosal route in an individual with a wild-type CCR5 genotype |
title_full_unstemmed | Transmission of highly virulent CXCR4 tropic HIV-1 through the mucosal route in an individual with a wild-type CCR5 genotype |
title_short | Transmission of highly virulent CXCR4 tropic HIV-1 through the mucosal route in an individual with a wild-type CCR5 genotype |
title_sort | transmission of highly virulent cxcr4 tropic hiv-1 through the mucosal route in an individual with a wild-type ccr5 genotype |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10571614/ https://www.ncbi.nlm.nih.gov/pubmed/37841838 http://dx.doi.org/10.21203/rs.3.rs-3359209/v1 |
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