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Long-Term Infection and Vertical Transmission of a Gammaretrovirus in a Foreign Host Species

Increasing evidence has indicated natural transspecies transmission of gammaretroviruses; however, viral-host interactions after initial xeno-exposure remain poorly understood. Potential association of xenotropic murine leukemia virus-related virus (XMRV) in patients with prostate cancer and chronic...

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Autores principales: Sakuma, Toshie, Tonne, Jason M., Malcolm, Jessica A., Thatava, Tayaramma, Ohmine, Seiga, Peng, Kah-Whye, Ikeda, Yasuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3250474/
https://www.ncbi.nlm.nih.gov/pubmed/22235324
http://dx.doi.org/10.1371/journal.pone.0029682
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author Sakuma, Toshie
Tonne, Jason M.
Malcolm, Jessica A.
Thatava, Tayaramma
Ohmine, Seiga
Peng, Kah-Whye
Ikeda, Yasuhiro
author_facet Sakuma, Toshie
Tonne, Jason M.
Malcolm, Jessica A.
Thatava, Tayaramma
Ohmine, Seiga
Peng, Kah-Whye
Ikeda, Yasuhiro
author_sort Sakuma, Toshie
collection PubMed
description Increasing evidence has indicated natural transspecies transmission of gammaretroviruses; however, viral-host interactions after initial xeno-exposure remain poorly understood. Potential association of xenotropic murine leukemia virus-related virus (XMRV) in patients with prostate cancer and chronic fatigue syndrome has attracted broad interests in this topic. Although recent studies have indicated that XMRV is unlikely a human pathogen, further understanding of XMRV xenoinfection would allow in vivo modeling of the initial steps of gammaretroviral interspecies transmission, evolution and dissemination in a new host population. In this study, we monitored the long-term consequences of XMRV infection and its possible vertical transmission in a permissive foreign host, wild-derived Mus pahari mice. One year post-infection, XMRV-infected mice showed no notable pathological changes, while proviral DNA was detected in three out of eight mice. XMRV-infected mice remained seropositive throughout the study although the levels of gp70 Env- and p30 capsid-specific antibodies gradually decreased. When vertical XMRV transmission was assessed, no viremia, humoral immune responses nor endogenization were observed in nine offspring from infected mothers, yet one offspring was found PCR-positive for XMRV-specific sequences. Amplified viral sequences from the offspring showed several mutations, including one amino acid deletion in the receptor binding domain of Env SU. Our results therefore demonstrate long-term asymptomatic infection, low incidence of vertical transmission and limited evolution of XMRV upon transspecies infection of a permissive new host, Mus pahari.
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spelling pubmed-32504742012-01-10 Long-Term Infection and Vertical Transmission of a Gammaretrovirus in a Foreign Host Species Sakuma, Toshie Tonne, Jason M. Malcolm, Jessica A. Thatava, Tayaramma Ohmine, Seiga Peng, Kah-Whye Ikeda, Yasuhiro PLoS One Research Article Increasing evidence has indicated natural transspecies transmission of gammaretroviruses; however, viral-host interactions after initial xeno-exposure remain poorly understood. Potential association of xenotropic murine leukemia virus-related virus (XMRV) in patients with prostate cancer and chronic fatigue syndrome has attracted broad interests in this topic. Although recent studies have indicated that XMRV is unlikely a human pathogen, further understanding of XMRV xenoinfection would allow in vivo modeling of the initial steps of gammaretroviral interspecies transmission, evolution and dissemination in a new host population. In this study, we monitored the long-term consequences of XMRV infection and its possible vertical transmission in a permissive foreign host, wild-derived Mus pahari mice. One year post-infection, XMRV-infected mice showed no notable pathological changes, while proviral DNA was detected in three out of eight mice. XMRV-infected mice remained seropositive throughout the study although the levels of gp70 Env- and p30 capsid-specific antibodies gradually decreased. When vertical XMRV transmission was assessed, no viremia, humoral immune responses nor endogenization were observed in nine offspring from infected mothers, yet one offspring was found PCR-positive for XMRV-specific sequences. Amplified viral sequences from the offspring showed several mutations, including one amino acid deletion in the receptor binding domain of Env SU. Our results therefore demonstrate long-term asymptomatic infection, low incidence of vertical transmission and limited evolution of XMRV upon transspecies infection of a permissive new host, Mus pahari. Public Library of Science 2012-01-03 /pmc/articles/PMC3250474/ /pubmed/22235324 http://dx.doi.org/10.1371/journal.pone.0029682 Text en Sakuma 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Sakuma, Toshie
Tonne, Jason M.
Malcolm, Jessica A.
Thatava, Tayaramma
Ohmine, Seiga
Peng, Kah-Whye
Ikeda, Yasuhiro
Long-Term Infection and Vertical Transmission of a Gammaretrovirus in a Foreign Host Species
title Long-Term Infection and Vertical Transmission of a Gammaretrovirus in a Foreign Host Species
title_full Long-Term Infection and Vertical Transmission of a Gammaretrovirus in a Foreign Host Species
title_fullStr Long-Term Infection and Vertical Transmission of a Gammaretrovirus in a Foreign Host Species
title_full_unstemmed Long-Term Infection and Vertical Transmission of a Gammaretrovirus in a Foreign Host Species
title_short Long-Term Infection and Vertical Transmission of a Gammaretrovirus in a Foreign Host Species
title_sort long-term infection and vertical transmission of a gammaretrovirus in a foreign host species
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3250474/
https://www.ncbi.nlm.nih.gov/pubmed/22235324
http://dx.doi.org/10.1371/journal.pone.0029682
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