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Discovery of a new human T-cell lymphotropic virus (HTLV-3) in Central Africa

Human T-cell Leukemia virus type 1 (HTLV-1) and type 2 (HTLV-2) are pathogenic retroviruses that infect humans and cause severe hematological and neurological diseases. Both viruses have simian counterparts (STLV-1 and STLV-2). STLV-3 belongs to a third group of lymphotropic viruses which infect num...

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Autores principales: Calattini, Sara, Chevalier, Sébastien Alain, Duprez, Renan, Bassot, Sylviane, Froment, Alain, Mahieux, Renaud, Gessain, Antoine
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1142341/
https://www.ncbi.nlm.nih.gov/pubmed/15882466
http://dx.doi.org/10.1186/1742-4690-2-30
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author Calattini, Sara
Chevalier, Sébastien Alain
Duprez, Renan
Bassot, Sylviane
Froment, Alain
Mahieux, Renaud
Gessain, Antoine
author_facet Calattini, Sara
Chevalier, Sébastien Alain
Duprez, Renan
Bassot, Sylviane
Froment, Alain
Mahieux, Renaud
Gessain, Antoine
author_sort Calattini, Sara
collection PubMed
description Human T-cell Leukemia virus type 1 (HTLV-1) and type 2 (HTLV-2) are pathogenic retroviruses that infect humans and cause severe hematological and neurological diseases. Both viruses have simian counterparts (STLV-1 and STLV-2). STLV-3 belongs to a third group of lymphotropic viruses which infect numerous African monkeys species. Among 240 Cameroonian plasma tested for the presence of HTLV-1 and/or HTLV-2 antibodies, 48 scored positive by immunofluorescence. Among those, 27 had indeterminate western-blot pattern. PCR amplification of pol and tax regions, using HTLV-1, -2 and STLV-3 highly conserved primers, demonstrated the presence of a new human retrovirus in one DNA sample. tax (180 bp) and pol (318 bp) phylogenetic analyses demonstrated the strong relationships between the novel human strain (Pyl43) and STLV-3 isolates from Cameroon. The virus, that we tentatively named HTLV-3, originated from a 62 years old Bakola Pygmy living in a remote settlement in the rain forest of Southern Cameroon. The plasma was reactive on MT2 cells but was negative on C19 cells. The HTLV 2.4 western-blot exhibited a strong reactivity to p19 and a faint one to MTA-1. On the INNO-LIA strip, it reacted faintly with the generic p19 (I/II), but strongly to the generic gp46 (I/II) and to the specific HTLV-2 gp46. The molecular relationships between Pyl43 and STLV-3 are thus not paralleled by the serological results, as most of the STLV-3 infected monkeys have an "HTLV-2 like" WB pattern. In the context of the multiple interspecies transmissions which occurred in the past, and led to the present-day distribution of the PTLV-1, it is thus very tempting to speculate that this newly discovered human retrovirus HTLV-3 might be widespread, at least in the African continent.
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spelling pubmed-11423412005-06-03 Discovery of a new human T-cell lymphotropic virus (HTLV-3) in Central Africa Calattini, Sara Chevalier, Sébastien Alain Duprez, Renan Bassot, Sylviane Froment, Alain Mahieux, Renaud Gessain, Antoine Retrovirology Short Report Human T-cell Leukemia virus type 1 (HTLV-1) and type 2 (HTLV-2) are pathogenic retroviruses that infect humans and cause severe hematological and neurological diseases. Both viruses have simian counterparts (STLV-1 and STLV-2). STLV-3 belongs to a third group of lymphotropic viruses which infect numerous African monkeys species. Among 240 Cameroonian plasma tested for the presence of HTLV-1 and/or HTLV-2 antibodies, 48 scored positive by immunofluorescence. Among those, 27 had indeterminate western-blot pattern. PCR amplification of pol and tax regions, using HTLV-1, -2 and STLV-3 highly conserved primers, demonstrated the presence of a new human retrovirus in one DNA sample. tax (180 bp) and pol (318 bp) phylogenetic analyses demonstrated the strong relationships between the novel human strain (Pyl43) and STLV-3 isolates from Cameroon. The virus, that we tentatively named HTLV-3, originated from a 62 years old Bakola Pygmy living in a remote settlement in the rain forest of Southern Cameroon. The plasma was reactive on MT2 cells but was negative on C19 cells. The HTLV 2.4 western-blot exhibited a strong reactivity to p19 and a faint one to MTA-1. On the INNO-LIA strip, it reacted faintly with the generic p19 (I/II), but strongly to the generic gp46 (I/II) and to the specific HTLV-2 gp46. The molecular relationships between Pyl43 and STLV-3 are thus not paralleled by the serological results, as most of the STLV-3 infected monkeys have an "HTLV-2 like" WB pattern. In the context of the multiple interspecies transmissions which occurred in the past, and led to the present-day distribution of the PTLV-1, it is thus very tempting to speculate that this newly discovered human retrovirus HTLV-3 might be widespread, at least in the African continent. BioMed Central 2005-05-09 /pmc/articles/PMC1142341/ /pubmed/15882466 http://dx.doi.org/10.1186/1742-4690-2-30 Text en Copyright © 2005 Calattini et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Report
Calattini, Sara
Chevalier, Sébastien Alain
Duprez, Renan
Bassot, Sylviane
Froment, Alain
Mahieux, Renaud
Gessain, Antoine
Discovery of a new human T-cell lymphotropic virus (HTLV-3) in Central Africa
title Discovery of a new human T-cell lymphotropic virus (HTLV-3) in Central Africa
title_full Discovery of a new human T-cell lymphotropic virus (HTLV-3) in Central Africa
title_fullStr Discovery of a new human T-cell lymphotropic virus (HTLV-3) in Central Africa
title_full_unstemmed Discovery of a new human T-cell lymphotropic virus (HTLV-3) in Central Africa
title_short Discovery of a new human T-cell lymphotropic virus (HTLV-3) in Central Africa
title_sort discovery of a new human t-cell lymphotropic virus (htlv-3) in central africa
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1142341/
https://www.ncbi.nlm.nih.gov/pubmed/15882466
http://dx.doi.org/10.1186/1742-4690-2-30
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