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Multiple recombinant events in human T-cell Leukemia virus Type 1: complete sequences of recombinant African strains
Africa is the largest endemic area for HTLV-1, with many molecular genotypes. We previously demonstrated that some strains from North Africa (a-NA clade) originated from a recombinant event between Senegalese and West African strains. A series of 52 new HTLV-1 strains from 13 North and West African...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7269087/ https://www.ncbi.nlm.nih.gov/pubmed/32249692 http://dx.doi.org/10.1080/22221751.2020.1752117 |
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author | Cassar, Olivier Desrames, Alexandra Marçais, Ambroise Gout, Olivier Taylor, Graham P. Hermine, Olivier Soriano, Vicente de Mendoza, Carmen Dehan, Océane Mener, Margot Le Afonso, Philippe V. Gessain, Antoine |
author_facet | Cassar, Olivier Desrames, Alexandra Marçais, Ambroise Gout, Olivier Taylor, Graham P. Hermine, Olivier Soriano, Vicente de Mendoza, Carmen Dehan, Océane Mener, Margot Le Afonso, Philippe V. Gessain, Antoine |
author_sort | Cassar, Olivier |
collection | PubMed |
description | Africa is the largest endemic area for HTLV-1, with many molecular genotypes. We previously demonstrated that some strains from North Africa (a-NA clade) originated from a recombinant event between Senegalese and West African strains. A series of 52 new HTLV-1 strains from 13 North and West African countries were sequenced in the LTR region and/or a env gene fragment. Four samples from French Guyanese of African origin were also added. Furthermore, 7 complete sequences from different genotypes were characterized. Phylogenetic analyses showed that most of the new African strains belong to the Cosmopolitan a-genotype. Ten new strains from the a-NA clade were found in Morocco, Western Sahara, Mali, Guinea, Côte d'Ivoire and Ghana. A new a-G-Rec clade, which arose from a distinct recombination event between Senegalese and West African strains, was identified in Guinea and Ghana. The complete sequences suggest that recombination occur in the LTR as well as the env/pol region of the genome, thus a-NA and a-G-Rec strains have a mosaic profile with genetic segments from either a-WA or a-Sen strains. Our work demonstrates that recombination in HTLV-1 may not be as rare an event as previously proposed. |
format | Online Article Text |
id | pubmed-7269087 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-72690872020-06-11 Multiple recombinant events in human T-cell Leukemia virus Type 1: complete sequences of recombinant African strains Cassar, Olivier Desrames, Alexandra Marçais, Ambroise Gout, Olivier Taylor, Graham P. Hermine, Olivier Soriano, Vicente de Mendoza, Carmen Dehan, Océane Mener, Margot Le Afonso, Philippe V. Gessain, Antoine Emerg Microbes Infect Article Africa is the largest endemic area for HTLV-1, with many molecular genotypes. We previously demonstrated that some strains from North Africa (a-NA clade) originated from a recombinant event between Senegalese and West African strains. A series of 52 new HTLV-1 strains from 13 North and West African countries were sequenced in the LTR region and/or a env gene fragment. Four samples from French Guyanese of African origin were also added. Furthermore, 7 complete sequences from different genotypes were characterized. Phylogenetic analyses showed that most of the new African strains belong to the Cosmopolitan a-genotype. Ten new strains from the a-NA clade were found in Morocco, Western Sahara, Mali, Guinea, Côte d'Ivoire and Ghana. A new a-G-Rec clade, which arose from a distinct recombination event between Senegalese and West African strains, was identified in Guinea and Ghana. The complete sequences suggest that recombination occur in the LTR as well as the env/pol region of the genome, thus a-NA and a-G-Rec strains have a mosaic profile with genetic segments from either a-WA or a-Sen strains. Our work demonstrates that recombination in HTLV-1 may not be as rare an event as previously proposed. Taylor & Francis 2020-05-13 /pmc/articles/PMC7269087/ /pubmed/32249692 http://dx.doi.org/10.1080/22221751.2020.1752117 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group, on behalf of Shanghai Shangyixun Cultural Communication Co., Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Cassar, Olivier Desrames, Alexandra Marçais, Ambroise Gout, Olivier Taylor, Graham P. Hermine, Olivier Soriano, Vicente de Mendoza, Carmen Dehan, Océane Mener, Margot Le Afonso, Philippe V. Gessain, Antoine Multiple recombinant events in human T-cell Leukemia virus Type 1: complete sequences of recombinant African strains |
title | Multiple recombinant events in human T-cell Leukemia virus Type 1: complete sequences of recombinant African strains |
title_full | Multiple recombinant events in human T-cell Leukemia virus Type 1: complete sequences of recombinant African strains |
title_fullStr | Multiple recombinant events in human T-cell Leukemia virus Type 1: complete sequences of recombinant African strains |
title_full_unstemmed | Multiple recombinant events in human T-cell Leukemia virus Type 1: complete sequences of recombinant African strains |
title_short | Multiple recombinant events in human T-cell Leukemia virus Type 1: complete sequences of recombinant African strains |
title_sort | multiple recombinant events in human t-cell leukemia virus type 1: complete sequences of recombinant african strains |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7269087/ https://www.ncbi.nlm.nih.gov/pubmed/32249692 http://dx.doi.org/10.1080/22221751.2020.1752117 |
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