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STLV-1 co-infection is correlated with an increased SFV proviral load in the peripheral blood of SFV/STLV-1 naturally infected non-human primates

Simian T-Leukemia Virus type 1 and Simian Foamy Virus infect non-human primates. While STLV-1, as HTLV-1, causes Adult T-cell Leukemia/lymphoma, SFV infection is asymptomatic. Both retroviruses can be transmitted from NHPs to humans through bites that allow contact between infected saliva and recipi...

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Autores principales: Alais, Sandrine, Pasquier, Amandine, Jegado, Brice, Journo, Chloé, Rua, Réjane, Gessain, Antoine, Tobaly-Tapiero, Joelle, Lacoste, Romain, Turpin, Jocelyn, Mahieux, Renaud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6181429/
https://www.ncbi.nlm.nih.gov/pubmed/30273350
http://dx.doi.org/10.1371/journal.pntd.0006812
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author Alais, Sandrine
Pasquier, Amandine
Jegado, Brice
Journo, Chloé
Rua, Réjane
Gessain, Antoine
Tobaly-Tapiero, Joelle
Lacoste, Romain
Turpin, Jocelyn
Mahieux, Renaud
author_facet Alais, Sandrine
Pasquier, Amandine
Jegado, Brice
Journo, Chloé
Rua, Réjane
Gessain, Antoine
Tobaly-Tapiero, Joelle
Lacoste, Romain
Turpin, Jocelyn
Mahieux, Renaud
author_sort Alais, Sandrine
collection PubMed
description Simian T-Leukemia Virus type 1 and Simian Foamy Virus infect non-human primates. While STLV-1, as HTLV-1, causes Adult T-cell Leukemia/lymphoma, SFV infection is asymptomatic. Both retroviruses can be transmitted from NHPs to humans through bites that allow contact between infected saliva and recipient blood. Because both viruses infect CD4+ T-cells, they might interfere with each other replication, and this might impact viral transmission. Impact of STLV-1 co-infection on SFV replication was analyzed in 18 SFV-positive/STLV-1-negative and 18 naturally SFV/STLV-1 co-infected Papio anubis. Even if 9 animals were found STLV-1-positive in saliva, STLV-1 PVL was much higher in the blood. SFV proviruses were detected in the saliva of all animals. Interestingly, SFV proviral load was much higher in the blood of STLV-1/SFV co-infected animals, compared to STLV-1-negative animals. Given that soluble Tax protein can enter uninfected cells, we tested its effect on foamy virus promoter and we show that Tax protein can transactivate the foamy LTR. This demonstrates that true STLV-1 co-infection or Tax only has an impact on SFV replication and may influence the ability of the virus to be zoonotically transmitted as well as its ability to promote hematological abnormalities.
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spelling pubmed-61814292018-10-25 STLV-1 co-infection is correlated with an increased SFV proviral load in the peripheral blood of SFV/STLV-1 naturally infected non-human primates Alais, Sandrine Pasquier, Amandine Jegado, Brice Journo, Chloé Rua, Réjane Gessain, Antoine Tobaly-Tapiero, Joelle Lacoste, Romain Turpin, Jocelyn Mahieux, Renaud PLoS Negl Trop Dis Research Article Simian T-Leukemia Virus type 1 and Simian Foamy Virus infect non-human primates. While STLV-1, as HTLV-1, causes Adult T-cell Leukemia/lymphoma, SFV infection is asymptomatic. Both retroviruses can be transmitted from NHPs to humans through bites that allow contact between infected saliva and recipient blood. Because both viruses infect CD4+ T-cells, they might interfere with each other replication, and this might impact viral transmission. Impact of STLV-1 co-infection on SFV replication was analyzed in 18 SFV-positive/STLV-1-negative and 18 naturally SFV/STLV-1 co-infected Papio anubis. Even if 9 animals were found STLV-1-positive in saliva, STLV-1 PVL was much higher in the blood. SFV proviruses were detected in the saliva of all animals. Interestingly, SFV proviral load was much higher in the blood of STLV-1/SFV co-infected animals, compared to STLV-1-negative animals. Given that soluble Tax protein can enter uninfected cells, we tested its effect on foamy virus promoter and we show that Tax protein can transactivate the foamy LTR. This demonstrates that true STLV-1 co-infection or Tax only has an impact on SFV replication and may influence the ability of the virus to be zoonotically transmitted as well as its ability to promote hematological abnormalities. Public Library of Science 2018-10-01 /pmc/articles/PMC6181429/ /pubmed/30273350 http://dx.doi.org/10.1371/journal.pntd.0006812 Text en © 2018 Alais et al http://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/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Alais, Sandrine
Pasquier, Amandine
Jegado, Brice
Journo, Chloé
Rua, Réjane
Gessain, Antoine
Tobaly-Tapiero, Joelle
Lacoste, Romain
Turpin, Jocelyn
Mahieux, Renaud
STLV-1 co-infection is correlated with an increased SFV proviral load in the peripheral blood of SFV/STLV-1 naturally infected non-human primates
title STLV-1 co-infection is correlated with an increased SFV proviral load in the peripheral blood of SFV/STLV-1 naturally infected non-human primates
title_full STLV-1 co-infection is correlated with an increased SFV proviral load in the peripheral blood of SFV/STLV-1 naturally infected non-human primates
title_fullStr STLV-1 co-infection is correlated with an increased SFV proviral load in the peripheral blood of SFV/STLV-1 naturally infected non-human primates
title_full_unstemmed STLV-1 co-infection is correlated with an increased SFV proviral load in the peripheral blood of SFV/STLV-1 naturally infected non-human primates
title_short STLV-1 co-infection is correlated with an increased SFV proviral load in the peripheral blood of SFV/STLV-1 naturally infected non-human primates
title_sort stlv-1 co-infection is correlated with an increased sfv proviral load in the peripheral blood of sfv/stlv-1 naturally infected non-human primates
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6181429/
https://www.ncbi.nlm.nih.gov/pubmed/30273350
http://dx.doi.org/10.1371/journal.pntd.0006812
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