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Recent increased identification and transmission of HIV-1 unique recombinant forms in Sweden
A temporal increase in non-B subtypes has earlier been described in Sweden by us and we hypothesized that this increased viral heterogeneity may become a hotspot for the development of more complex and unique recombinant forms (URFs) if the epidemics converge. In the present study, we performed subt...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5527090/ https://www.ncbi.nlm.nih.gov/pubmed/28744024 http://dx.doi.org/10.1038/s41598-017-06860-2 |
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author | Neogi, Ujjwal Siddik, Abu Bakar Kalaghatgi, Prabhav Gisslén, Magnus Bratt, Göran Marrone, Gaetano Sönnerborg, Anders |
author_facet | Neogi, Ujjwal Siddik, Abu Bakar Kalaghatgi, Prabhav Gisslén, Magnus Bratt, Göran Marrone, Gaetano Sönnerborg, Anders |
author_sort | Neogi, Ujjwal |
collection | PubMed |
description | A temporal increase in non-B subtypes has earlier been described in Sweden by us and we hypothesized that this increased viral heterogeneity may become a hotspot for the development of more complex and unique recombinant forms (URFs) if the epidemics converge. In the present study, we performed subtyping using four automated tools and phylogenetic analysis by RAxML of pol gene sequences (n = 5246) and HIV-1 near full-length genome (HIV-NFLG) sequences (n = 104). A CD4(+) T-cell decline trajectory algorithm was used to estimate time of HIV infection. Transmission clusters were identified using the family-joining method. The analysis of HIV-NFLG and pol gene described 10.6% (11/104) and 2.6% (137/5246) of the strains as URFs, respectively. An increasing trend of URFs was observed in recent years by both approaches (p = 0·0082; p < 0·0001). Transmission cluster analysis using the pol gene of all URFs identified 14 clusters with two to eight sequences. Larger transmission clusters of URFs (BF1 and 01B) were observed among MSM who mostly were sero-diagnosed in recent time. Understanding the increased appearance and transmission of URFs in recent years could have importance for public health interventions and the use of HIV-NFLG would provide better statistical support for such assessments. |
format | Online Article Text |
id | pubmed-5527090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55270902017-08-02 Recent increased identification and transmission of HIV-1 unique recombinant forms in Sweden Neogi, Ujjwal Siddik, Abu Bakar Kalaghatgi, Prabhav Gisslén, Magnus Bratt, Göran Marrone, Gaetano Sönnerborg, Anders Sci Rep Article A temporal increase in non-B subtypes has earlier been described in Sweden by us and we hypothesized that this increased viral heterogeneity may become a hotspot for the development of more complex and unique recombinant forms (URFs) if the epidemics converge. In the present study, we performed subtyping using four automated tools and phylogenetic analysis by RAxML of pol gene sequences (n = 5246) and HIV-1 near full-length genome (HIV-NFLG) sequences (n = 104). A CD4(+) T-cell decline trajectory algorithm was used to estimate time of HIV infection. Transmission clusters were identified using the family-joining method. The analysis of HIV-NFLG and pol gene described 10.6% (11/104) and 2.6% (137/5246) of the strains as URFs, respectively. An increasing trend of URFs was observed in recent years by both approaches (p = 0·0082; p < 0·0001). Transmission cluster analysis using the pol gene of all URFs identified 14 clusters with two to eight sequences. Larger transmission clusters of URFs (BF1 and 01B) were observed among MSM who mostly were sero-diagnosed in recent time. Understanding the increased appearance and transmission of URFs in recent years could have importance for public health interventions and the use of HIV-NFLG would provide better statistical support for such assessments. Nature Publishing Group UK 2017-07-25 /pmc/articles/PMC5527090/ /pubmed/28744024 http://dx.doi.org/10.1038/s41598-017-06860-2 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Neogi, Ujjwal Siddik, Abu Bakar Kalaghatgi, Prabhav Gisslén, Magnus Bratt, Göran Marrone, Gaetano Sönnerborg, Anders Recent increased identification and transmission of HIV-1 unique recombinant forms in Sweden |
title | Recent increased identification and transmission of HIV-1 unique recombinant forms in Sweden |
title_full | Recent increased identification and transmission of HIV-1 unique recombinant forms in Sweden |
title_fullStr | Recent increased identification and transmission of HIV-1 unique recombinant forms in Sweden |
title_full_unstemmed | Recent increased identification and transmission of HIV-1 unique recombinant forms in Sweden |
title_short | Recent increased identification and transmission of HIV-1 unique recombinant forms in Sweden |
title_sort | recent increased identification and transmission of hiv-1 unique recombinant forms in sweden |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5527090/ https://www.ncbi.nlm.nih.gov/pubmed/28744024 http://dx.doi.org/10.1038/s41598-017-06860-2 |
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