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Endogenization of a Prosimian Retrovirus during Lemur Evolution

Studies of viruses that coevolved with lemurs provide an opportunity to understand the basal traits of primate viruses and provide an evolutionary context for host-virus interactions. Germline integration of endogenous retroviruses (ERVs) are fossil evidence of past infections. Hence, characterizati...

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Autores principales: Apakupakul, Kathleen, Deem, Sharon L., Maqsood, Rabia, Sithiyopasakul, Peeti, Wang, David, Lim, Efrem S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7997422/
https://www.ncbi.nlm.nih.gov/pubmed/33673677
http://dx.doi.org/10.3390/v13030383
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author Apakupakul, Kathleen
Deem, Sharon L.
Maqsood, Rabia
Sithiyopasakul, Peeti
Wang, David
Lim, Efrem S.
author_facet Apakupakul, Kathleen
Deem, Sharon L.
Maqsood, Rabia
Sithiyopasakul, Peeti
Wang, David
Lim, Efrem S.
author_sort Apakupakul, Kathleen
collection PubMed
description Studies of viruses that coevolved with lemurs provide an opportunity to understand the basal traits of primate viruses and provide an evolutionary context for host-virus interactions. Germline integration of endogenous retroviruses (ERVs) are fossil evidence of past infections. Hence, characterization of novel ERVs provides insight into the ancient precursors of extant viruses and the evolutionary history of their hosts. Here, we report the discovery of a novel endogenous retrovirus present in the genome of a lemur, Coquerel’s sifaka (Propithecus coquereli). Using next-generation sequencing, we identified and characterized the complete genome sequence of a retrovirus, named prosimian retrovirus 1 (PSRV1). Phylogenetic analyses indicate that PSRV1 is a gamma-type betaretrovirus basal to the other primate betaretroviruses and most closely related to simian retroviruses. Molecular clock analysis of PSRV1 long terminal repeat (LTR) sequences estimated the time of endogenization within 4.56 MYA (±2.4 MYA), placing it after the divergence of Propithecus species. These results indicate that PSRV1 is an important milestone of lemur evolution during the radiation of the Propithecus genus. These findings may have implications for both human and animal health in that the acquisition of a gamma-type env gene within an endogenized betaretrovirus could facilitate a cross-species jump between vertebrate class hosts.
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spelling pubmed-79974222021-03-27 Endogenization of a Prosimian Retrovirus during Lemur Evolution Apakupakul, Kathleen Deem, Sharon L. Maqsood, Rabia Sithiyopasakul, Peeti Wang, David Lim, Efrem S. Viruses Article Studies of viruses that coevolved with lemurs provide an opportunity to understand the basal traits of primate viruses and provide an evolutionary context for host-virus interactions. Germline integration of endogenous retroviruses (ERVs) are fossil evidence of past infections. Hence, characterization of novel ERVs provides insight into the ancient precursors of extant viruses and the evolutionary history of their hosts. Here, we report the discovery of a novel endogenous retrovirus present in the genome of a lemur, Coquerel’s sifaka (Propithecus coquereli). Using next-generation sequencing, we identified and characterized the complete genome sequence of a retrovirus, named prosimian retrovirus 1 (PSRV1). Phylogenetic analyses indicate that PSRV1 is a gamma-type betaretrovirus basal to the other primate betaretroviruses and most closely related to simian retroviruses. Molecular clock analysis of PSRV1 long terminal repeat (LTR) sequences estimated the time of endogenization within 4.56 MYA (±2.4 MYA), placing it after the divergence of Propithecus species. These results indicate that PSRV1 is an important milestone of lemur evolution during the radiation of the Propithecus genus. These findings may have implications for both human and animal health in that the acquisition of a gamma-type env gene within an endogenized betaretrovirus could facilitate a cross-species jump between vertebrate class hosts. MDPI 2021-02-27 /pmc/articles/PMC7997422/ /pubmed/33673677 http://dx.doi.org/10.3390/v13030383 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Apakupakul, Kathleen
Deem, Sharon L.
Maqsood, Rabia
Sithiyopasakul, Peeti
Wang, David
Lim, Efrem S.
Endogenization of a Prosimian Retrovirus during Lemur Evolution
title Endogenization of a Prosimian Retrovirus during Lemur Evolution
title_full Endogenization of a Prosimian Retrovirus during Lemur Evolution
title_fullStr Endogenization of a Prosimian Retrovirus during Lemur Evolution
title_full_unstemmed Endogenization of a Prosimian Retrovirus during Lemur Evolution
title_short Endogenization of a Prosimian Retrovirus during Lemur Evolution
title_sort endogenization of a prosimian retrovirus during lemur evolution
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7997422/
https://www.ncbi.nlm.nih.gov/pubmed/33673677
http://dx.doi.org/10.3390/v13030383
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